Fluorescent Sensors for Detecting and Imaging Metal Ions in Biological Systems: Recent Advances and Future Perspectives

: Metal ions play a crucial role in many biochemical processes, and when in a state of scarcity or surplus, they can lead to various diseases. Therefore, the development of a selective, sensitive, cost-effective, and fast-responding sensor to detect metal ions is critical for in vitro medical diagnostics. In recent years, ﬂuorescent sensors have been extensively investigated as potent kits for the effective assessment of metal ions in living systems due to their high sensitivity, selectivity, ability to perform real-time, non-invasive monitoring, and versatility. This review is an overview of recent advances in ﬂuorescent sensors for the detection and imaging of metal ions in biosystems from 2018 to date. Speciﬁcally, we discuss their application in detecting essential metal ions and non-essential metal ions for in vitro diagnostics, living cell imaging, and in vivo imaging. Finally, we summarize remaining challenges and offer a future outlook on the above topics.


Introduction
Metal ions are known to play indispensable roles in many critical biochemical processes.The amount and dispersion of metal ions in body fluids have a significant impact on the normal physiological function of the human body.In terms of their effects in biosystems, the general public generally classifies metals into two categories: essential and non-essential.Currently, it is widely recognized that there are ten essential metal ions for life, and our body must have appropriate amounts of them [1][2][3][4], including potassium (K), sodium (Na), calcium (Ca), magnesium (Mg), cobalt (Co), molybdenum (Mo), iron (Fe), copper (Cu), zinc (Zn), and manganese (Mn).Among them, K, Na, Ca, and Mg make up over 99% of the total metal elements in the human body, while the remaining six elements are present in small amounts.When essential metal ions are maintained at normal levels (Table 1), they play a crucial role in various physiological functions, including catalyzing enzymes, participating in oxidative metabolism, and contributing to DNA synthesis [5][6][7].Their absence or disruption of homeostasis can lead to various diseases and health disorders.On a different note, non-essential metal ions, such as mercury (Hg), silver (Ag), gold (Au), and lead (Pb), are often harmful to human health.They are not easily biodegraded and can accumulate in the human body through the biological amplification of the food chain.These non-essential metal ions can react with and deactivate proteins and enzymes in the human body, leading to chronic poisoning.It is important to note that the distinction between essential and non-essential metal ions is somewhat relative, as even essential metal ions can become toxic if their concentrations become too high [8].Therefore, a selective, facile, sensitive, cost-effective, and fast-responding sensor to detect metal ions is of great significance for in vitro healthcare diagnostics and biological system imaging.
The last decade has seen unprecedented advances in the techniques of fluorescent sensors.In addition, considerable progress has been achieved in the exploitation of fluorescent probes with organic fluorescent dyes, benefiting from new fluorescent imaging techniques because of their good biocompatibility, high spatiotemporal resolution, and accessibility to chemical modifications.These features allow for the monitoring of the cellular localization and dynamics of many of the biotargets.Although many reviews have been published regarding fluorescent sensors that detect small molecules, including carbonyl species [26], sulfite derivatives [27], glutathione [28,29], hydrogen peroxide [30], peroxynitrite [31], and metal ions [32,33], only a few reviews have covered the advancement of metal ion sensors in biological systems in detail.To fill this gap, we here provide a comprehensive review that covers recent progress in metal ion sensors in the past five years, including reaction-based, nucleic acid-based, and material-based sensors.We discuss their application in detecting metal ions, including monovalent, divalent, and other metal ions, for in vitro diagnostics, living cell imaging, and in vivo imaging.Finally, we outline the current limitations and future directions in these areas.

Categorization of Fluorescent Sensors for Metal Ions
Numerous metal-ion sensors have been explored in the past five years.Despite some ambiguity in the literature regarding these terms, we are guided by the widely accepted consensus to divide new metal ion sensing systems into four categories, which are genetically encoded biosensors, molecular probes, chemosensors, and nanosensors.
Genetically encoded biosensors consist of sensing elements and transduction elements.The sensing element is used to receive input messages, which may come from metabolites, chemistry, or the environment, and the transduction element converts the inputs to an output signal, usually fluorescent [34].There are different kinds of genetically encoded biosensors, among which the most widely used in metal ion detection are fluorescent protein-based biosensors [35] and nucleic acid-based biosensors [36].Fluorescent proteinbased biosensors utilize a peptide or protein domain that functions as a metal binding site (Figure 1A(a)).For single fluorescent protein-based sensors, upon metal ion binding, a change occurs in the chemical or electronic environment surrounding the chromophore, resulting in either a shift in the excitation or emission spectrum or a change in intensity [37,38].
In biosensors with two fluorescent proteins, fluorescent resonance energy transfer (FRET) is utilized to detect metal binding-induced conformational changes or protein-protein interactions.To detect metal ions in living systems, fluorescent protein-based biosensors are commonly used.However, this biosensor is not ideal for in vitro detection due to its reliance on a highly stable intracellular environment.
Chemosensors 2023, 11, x FOR PEER REVIEW 3 of 34 binding, a change occurs in the chemical or electronic environment surrounding the chromophore, resulting in either a shift in the excitation or emission spectrum or a change in intensity [37,38].In biosensors with two fluorescent proteins, fluorescent resonance energy transfer (FRET) is utilized to detect metal binding-induced conformational changes or protein-protein interactions.To detect metal ions in living systems, fluorescent proteinbased biosensors are commonly used.However, this biosensor is not ideal for in vitro detection due to its reliance on a highly stable intracellular environment.In contrast, the sensing element of nuclear acid-based sensors is usually designed based on functional nucleic acids (FNA) [36,39] and DNA mismatch [40] (Figure 1A(b)).Two primary types of functional DNA have been developed for metal sensing: G-quadruplex (GQ) [41] and DNAzymes [42], which has a number of desirable properties to de- In contrast, the sensing element of nuclear acid-based sensors is usually designed based on functional nucleic acids (FNA) [36,39] and DNA mismatch [40] (Figure 1A(b)).Two primary types of functional DNA have been developed for metal sensing: G-quadruplex (GQ) [41] and DNAzymes [42], which has a number of desirable properties to detect metal ions [43].First, FNAs are critically separated from a large DNA library containing 10 14 -10 15 DNA molecules, which means that they are extremely selective.Second, DNA can be produced from any designed nucleotide sequence and is easily functionalized with the required chemical tags.Third, DNA is highly stable and can be denatured multiple times before apparently losing its binding activity to metal ions.Finally, FNAs do not require the deliberate design of metal binding sites, which are indispensable for fluorescent protein-based biosensors.Moreover, genetically encoded DNA-based optical sensors can be assembled continuously and efficiently through carefully designed DNA sequences to generate signal amplification strategies such as hybrid chain reactions (HCR), thus improving sensitivity and reducing detection limits.Therefore, genetically encoded biosensors are widely used in metal ion biosensors and biological imaging in vitro and in vivo.
Molecular probes are systems that form strong, largely irreversible bonds with their target analytes (Figure 1B).These specific interactions often result in a distinct optical response, such as fluorescence emission or changes in absorbance bands [44].Typically, molecular probes are covalently bonded to their targets through organic reaction mechanisms, allowing them to exhibit optical signals for in vivo imaging.In recent years, molecular probes have been extensively developed because of their higher sensitivity, improved detection accuracy, and relative simplicity of operation [45].Particularly, they have attracted great interest in the field of ion detection and have become promising tools for visualizing ion migration, distribution, and concentration changes in biological systems [46][47][48][49].
Chemosensors reversibly bind metal ions in a reactive manner via a combination of non-covalent binding interactions with the analyte in a selective and reversible manner, and then alter one or more characteristics of the system in the form of color, fluorescence, or redox potential (Figure 1C).The kinetics of binding and unbinding are frequently rapid on the experimental/assay time scale, and the selection of the chromophore has a dramatic effect with respect to these features.In recent years, two major classes of organic dyes have been incorporated into organic molecule-based chemosensors as signal-reporting units, including classic organic dyes and new organic dyes with aggregation-induced emission (AIE).The former become quenched at higher concentrations or in the aggregated state, such as BODIPY [50], porphyrins [51], coumarins [52], naphthalimides [53], and rhodamines [54].In contrast, the AIE dyes are strongly emitted in the aggregate or solidstate [55].These unique fluorescent properties give fluorescent chemosensors remarkable capabilities in monitoring biologically relevant species in vitro and/or in vivo.Therefore, the exploitation of fluorescent chemosensors for the sensing of metal ions has become a highly active area of research.
Nanosensors are small-scale sensing devices with dimensions in the nanometer range, which are small yet powerful tools (Figure 1D).These sensors boast high sensitivity, making them ideal for the detection of low concentrations of target analytes in various fields [56][57][58], including environmental monitoring, medical diagnosis, food and beverage analysis, and industrial process control.In the design of nanosensors, the selection of the recognition element is crucial, as it determines the specificity and sensitivity of nanosensors.This element may take the form of a specific antibody, aptamer, or small molecule that is selectively bound to the metal ion of interest [59].Moreover, nanosensors can be fabricated from a range of materials, including organic molecules, inorganic materials, and biomolecules.At the same time, the choice of material depends on the desired properties of the sensor, such as biocompatibility, stability, and sensitivity.One of the greatest advantages of nanosensors is their ability to simultaneously detect multiple metal ions in a single assay.This feature provides researchers with a complete picture of the status of metal ions in biological systems and allows them to make informed decisions based on the data.Furthermore, the recent advances in nanotechnology have enhanced the versatility and power of nanosensors, making them vital for the measurement of metal ions in complex environments.

In Vitro Detection of Metal Ions
The presence and distribution of various metal ions in human body fluids, such as blood, sweat, and urine, have a critical impact on human health [60][61][62].Hence, in vitro detection of these metal ions through analysis of human body fluid samples plays a crucial role in disease prevention and early detection.Blood was previously the most common type of sample taken as part of a routine physical examination.Recently, saliva, urine, and sweat have gained attention due to their abundant presence, diagnostic ability, and non-invasive sample extraction.
3.1.Fluorescent Sensors for Essential Metal Ions 3.1.1.Na + Sodium is considered to be the most common and critical metal ion in the environment and in biology [63].High sodium levels are reflections of physiological disorders, such as hypertension and edema.In order to detect sodium ions, Liu and his co-workers obtained a mutant of the NaA43 DNAzyme through in vitro selection with a slightly acidic pH optimum and the same excellent specificity for Na + [64].This makes it particularly useful for sodium sensing in environments such as the endosome and within cancer cells.Additionally, preliminary work has shown that this DNAzyme can detect sodium in serum, with a minimum detection threshold of 676 µM and a linear response at concentrations below 20 mM.
The Lu group developed a novel CRISPR-Cas12a-based sensor, employing a Na +specific DNAzyme [65], as shown in Figure 2A.To link the DNAzyme recognition to Cas12a activation, the DNA activator was embedded in the DNAzyme sequences and labeled with biotin at the tail end.After Na + -catalyzed DNAzyme cleavage, the activation strand dissociates from the binding arm.Recognition of the activation strand by the Cas12a-crRNA complex triggers its trans-cleavage activity, which results in a turn-on fluorescence signal.The sensor has a detection limit of 0.10 mM, which is well below the sodium level normally found in human serum.Moreover, the sensor has been compared to a commercial sodium meter and found to be highly accurate (Figure 2B).Additionally, the Kaur group developed a highly selective fluorescent organic nanoparticle sensor based on Biginelli [66], which can measure Na + even in the presence of interfering K + .The sensor displayed a linear detection range of 0-25 µM and a minimum detection concentration of 22 nM.The practical applicability of this sensor has been demonstrated by successfully monitoring Na + concentrations in sweat samples from the lower back and urine samples.

K +
Potassium is a vital cation for metabolic activity in living cells and is intimately mediated through a variety of cellular mechanisms.Li's team developed a transparent and stable G-2FPB-K + hydrogel for detecting K + [67].The hydrogel is highly selective for K + and utilizes berberine to detect its formation during self-assembly.GQ is a unique nucleic acid structure consisting of a guanine-rich sequence with four helices formed by several stacked GQs [41].Moreover, GQ manifests unique catalytic features upon interacting with hemin, a cofactor typically present in hemoproteins [68].Given that the assembly of GQ requires cations, it could serve as a natural biosensor for specific cations.In another work, Cheng and co-workers created a K + -specific biosensor based on a dimerized GQ, whose enzymatic activity depends on the K + concentration [69].When K + is available, the monomer, acted on by three G-quartets, will assemble into a dimer of six G-quartets.The sensor can detect K + selectively in the range of 1-200 mM, even in the presence of up to 140 mM Na + at ambient temperatures up to 45 • C.
Thioflavin T, or 4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethylaniline chloride, first used to detect misfolded proteins, was later found to emit intense fluorescence emission when combined with GQ.Subsequently, Buranachai discovered that low concentrations of K + (25.0-500 nM) can reduce Thioflavin T fluorescence by replacing the dye in Thioflavin T-bimolecular GQ or Thioflavin T-tetramolecular GQ, as illustrated in Figure 2C [70].Therefore, they developed a label-free turn-off fluorescent sensor for the detection of low K + concentrations.This simple and low-cost sensor only requires sample dilution and can be used with high accuracy for the direct detection of K + in normal urine samples, as shown in Figure 2D.Thioflavin T, or 4-(3,6-dimethyl-1,3-benzothiazol-3-ium-2-yl)-N,N-dimethylaniline chloride, first used to detect misfolded proteins, was later found to emit intense fluorescence emission when combined with GQ.Subsequently, Buranachai discovered that low concentrations of K + (25.0-500 nM) can reduce Thioflavin T fluorescence by replacing the dye in Thioflavin T-bimolecular GQ or Thioflavin T-tetramolecular GQ, as illustrated in Figure 2C [70].Therefore, they developed a label-free turn-off fluorescent sensor for the detection of low K + concentrations.This simple and low-cost sensor only requires sample dilution and can be used with high accuracy for the direct detection of K + in normal urine samples, as shown in Figure 2D.

Zn 2+
Zinc is a vital micronutrient essential for numerous biological processes.Globally, approximately 20% of the human race is considered to be at risk for zinc scarcity, which can have a range of negative effects on growth, neurological function, reproduction, and the immune response.The high selectivity of DNAzyme for metal ions makes it a classical metal ion sensor.Despite the Zn 2+ -specific DNAzyme being first screened in 2009 [71], achieving in vitro detection of metal ions bound to biological macromolecules remains a major challenge.To address this limitation, Xing et al. developed a photocaged chelator, XDPAdeCage, which can extract the Zn 2+ from the blood serum [72].Upon 365 nm light irradiation, the chelated Zn 2+ was released into the buffer and finally quantified by 8-17 DNAzymes.The sensor showed high selectivity, accuracy, and reusability, demonstrating its potential for biological applications.On the other hand, the bioluminescent proteinbased sensor is another attractive tool for Zn 2+ in complex media, such as blood serum.Merkx and colleagues developed two new bioluminescent sensor platforms that enable fast and accurate quantification of free Zn 2+ in serum [17].In the first platform, the LuZi

Zn 2+
Zinc is a vital micronutrient essential for numerous biological processes.Globally, approximately 20% of the human race is considered to be at risk for zinc scarcity, which can have a range of negative effects on growth, neurological function, reproduction, and the immune response.The high selectivity of DNAzyme for metal ions makes it a classical metal ion sensor.Despite the Zn 2+ -specific DNAzyme being first screened in 2009 [71], achieving in vitro detection of metal ions bound to biological macromolecules remains a major challenge.To address this limitation, Xing et al. developed a photocaged chelator, XDPAdeCage, which can extract the Zn 2+ from the blood serum [72].Upon 365 nm light irradiation, the chelated Zn 2+ was released into the buffer and finally quantified by 8-17 DNAzymes.The sensor showed high selectivity, accuracy, and reusability, demonstrating its potential for biological applications.On the other hand, the bioluminescent protein-based sensor is another attractive tool for Zn 2+ in complex media, such as blood serum.Merkx and colleagues developed two new bioluminescent sensor platforms that enable fast and accurate quantification of free Zn 2+ in serum [17].In the first platform, the LuZi sensors use a modular design based on split NLuc complementation and BRET to a red fluorescent Cy3 dye, producing a strong shift from red to blue upon binding to Zn 2+ .The second platform, BLZinCh-Pro, replaces the long GGS linker with rigid polyproline linkers, resulting in four different sensor proteins with 3-4 times better emission ratios and Zn 2+ affinities.These sensors were applied for measuring cytosolic free Zn 2+ concentrations between 543 and 992 pM.Both sensors yielded similar results for free Zn 2+ concentration in (diluted) serum of 1-3 nM.

Cu 2+
Copper (Cu) is an indispensable component of human life and is involved in various biological processes, including metalloprotein composition and gene expression.Wu's team synthesized a series of near-infrared (NIR) luminescent ruthenium complexes, which can be rapidly quenched by Cu 2+ , with remarkable selectivity for Cu 2+ detection in human serum [73].In the same way, a new NIR BODIPY compound was reported by He et al. [74], which can be induced to undergo fluorescence bursts by Cu 2+ , while Mn 2+ can specifically cause fluorescence enhancement.
Cu I -catalyzed azide/alkyne cycloaddition (CuAAC) is commonly used for the detection of copper ions.The reaction of azide and alkyne is extremely slow, but the reaction rate can be greatly improved with the catalysis of Cu + .Moreover, the reaction takes place at room temperature, does not require an inert atmosphere, and the products are stable.These features make the CuAAC reaction a mild sensing strategy, and its main advantage is its dependence on the catalytic activity of copper.Jiang et al. introduced a quick and simple fluorescent assay based on CuAAC for detecting free Cu ions in patient urine samples without complex pretreatment [75], as shown in Figure 3A.The assay utilizes a click reaction between graphene oxide and a fluorescent dye.This reaction can be triggered promptly by Cu 2+ , thus allowing the detection of Cu ions with outstanding sensitivity and selectivity in under a minute.Additionally, the system can be read values with a smartphone using color scan software (Figure 3B).Similarly, Chen et al. developed a cascade signal amplification strategy to detect Cu 2+ [76], which is combined with a substrate consisting of gold nanorods coupled with silver nanoislands to enhance fluorescence.In addition, the Raibaut group proposed a turn-off luminescent peptide for Cu 2+ [77], which proved suitable for the detection of copper ions by time-resolved luminescence detection.
Zn 2+ affinities.These sensors were applied for measuring cytosolic free Zn 2+ concentrations between 543 and 992 pM.Both sensors yielded similar results for free Zn 2+ concentration in (diluted) serum of 1-3 nM.

Cu 2+
Copper (Cu) is an indispensable component of human life and is involved in various biological processes, including metalloprotein composition and gene expression.Wu's team synthesized a series of near-infrared (NIR) luminescent ruthenium complexes, which can be rapidly quenched by Cu 2+ , with remarkable selectivity for Cu 2+ detection in human serum [73].In the same way, a new NIR BODIPY compound was reported by He et al. [74], which can be induced to undergo fluorescence bursts by Cu 2+ , while Mn 2+ can specifically cause fluorescence enhancement.
Cu I -catalyzed azide/alkyne cycloaddition (CuAAC) is commonly used for the detection of copper ions.The reaction of azide and alkyne is extremely slow, but the reaction rate can be greatly improved with the catalysis of Cu + .Moreover, the reaction takes place at room temperature, does not require an inert atmosphere, and the products are stable.These features make the CuAAC reaction a mild sensing strategy, and its main advantage is its dependence on the catalytic activity of copper.Jiang et al. introduced a quick and simple fluorescent assay based on CuAAC for detecting free Cu ions in patient urine samples without complex pretreatment [75], as shown in Figure 3A.The assay utilizes a click reaction between graphene oxide and a fluorescent dye.This reaction can be triggered promptly by Cu 2+ , thus allowing the detection of Cu ions with outstanding sensitivity and selectivity in under a minute.Additionally, the system can be read values with a smartphone using color scan software (Figure 3B).Similarly, Chen et al. developed a cascade signal amplification strategy to detect Cu 2+ [76], which is combined with a substrate consisting of gold nanorods coupled with silver nanoislands to enhance fluorescence.In addition, the Raibaut group proposed a turn-off luminescent peptide for Cu 2+ [77], which proved suitable for the detection of copper ions by time-resolved luminescence detection.Reproduced from [18] with permission from Elsevier, copyright 2019.

Ca 2+
Calcium (Ca 2+ ) is the most abundant signal transduction messenger in cells, and calmodulin (CaM) is a widespread Ca 2+ sensor in eukaryotic cells [78].Carbon dots (CDs) are a class of zero-dimensional fluorescent carbon nanomaterials.Motivated by the Ca 2+ sensing process of CaM, Lin et al. explored a new CD-based Ca 2+ sensor by using a CaM mimetic peptide as a functional group [79].CDs functionalized with synthetic peptides can target Ca 2+ specifically in biologically relevant media, leading to an effective fluorescence burst.In addition, the f-CD sensor is highly biocompatible and can be used for the quantitative detection of free Ca 2+ in serum.
Metal-organic frameworks (MOFs) are a relatively new type of chemical sensor with internal pores that can be used to interact with different analytes [80,81].Masoomi's team first reported MOFs-based calcium-sensitive probes (TMU-5S) by introducing rhodamine B into the framework of TMU-5 [82].As a ratiometric fluorescent sensor, this dye-sensitized MOF allows Ca 2+ signaling in the presence of interfering cations similar to plasma ion concentrations and exhibits exceptional sensitivity and selectivity for Ca 2+ in the blood.

Fe 3+
The iron content of human serum ranges from 14-32 µM.Since iron is critical for hemoglobin synthesis and oxidation reactions in the body, iron deficiency and excess can lead to various diseases.Monireh's team developed Mg-Al LDH-SA nanomaterials, which are composed of Mg-Al layered double hydroxides sandwiched by salicylic acid [18], as shown in Figure 3C.The nanosensor emits at 404 nm under excitation at an excitation wavelength of 287 nm.When Mg-Al LDH-SA encounters iron ions, the iron ions and salicylic acid will form a stable complex, which leads to the decrease of its fluorescence signal.In addition, this method was successfully used to measure ferric ions in human serum samples (Figure 3D).Another promising Fe 3+ sensor based on 2,5-dihydroxyterephthalic acid (DOBDC)-Zn 2+ MOFs (ZnMOF-74) was developed by Li et al. [83].The DOBDC phenolic hydroxyl groups are reactive to Fe 3+ , leading to cation conversion between Fe 3+ and Zn 2+ .This results in skeleton collapse, causing quenching of the active fluorescence of ZnMOF-74.This fluorescence probe successfully detected Fe 3+ in human serum with high accuracy and recovery.Later, the Zhang group synthesized fluorescent CDs from brewer's spent grain and used them as label-free probes for Fe 3+ detection [84].The sensor exhibited a linear detection range of 0.3-7 µM with an LOD of 95 nM and was successfully applied for practical Fe 3+ determination in FBS.

Ag +
Ag is a typical heavy metal ion, and its toxic effects on DNA replication and protein function make the detection of Ag of great interest.Particularly, the accurate detection of Ag in biospecimens is crucial through fluorescence analysis.Feng et al. proposed a facile method to synthesize hyperfluorescent N-dots, employing 2-azidazole and hydroxyl compounds as cross-linking additives (Figure 4A) [85].The nanomaterials exhibited excellent stability against various factors and can be used as sensors for Ag + sensing.The sensing mechanism is based on the static quenching effect between N-dots and silver ions.The resulting sensor showed good linearity in the range of concentrations from 20 nM to 6 µM and a detection limit of 6.3 nM, and more importantly, it displayed high specificity for silver ions in human urine.

Pb 2+
Lead ions are a highly toxic type of pollutant that can contaminate soil and water, posing a threat to food safety.Their accumulation in the body is difficult to eliminate and can lead to severe nerve, hematopoietic, and renal damage, ultimately resulting in death.Nucleic acid-based sensors are frequently used for lead ion detection.Xu et al. designed a highly sensitive cascade signal amplification sensor that combines DNAzyme-based strand displacement amplification with HCR to sense Pb 2+ [86], while Jia's group developed a novel strategy for Pb 2+ detection based on a fluorophore-tagged Pb 2+ -binding aptamer [87], as shown in Figure 4B.Since the binding of the aptamer to Pb 2+ leads to a conformational change, the original low-fluorescence "off" state becomes a highfluorescence "on" state.The method enables quantitative detection of lead ions with a minimum detection concentration of 468 nM, maintaining high specificity for Pb 2+ during the detection process.Furthermore, it has been successfully tested in complex biofluids (Figure 4C), making it a promising tool for Pb 2+ detection in practical applications.Tang and colleagues designed an innovative method for the direct detection of K + and Pb 2+ with high selectivity and sensitivity [88], which relies on the assembly and disassembly of a chiral cyanine dye/TBA complex.Lee et al. [89] synthesized fluorescent probes by incorporating a peptide receptor with hard and soft ligands and a benzothiazolylcyanovinylene fluorophore, which were successfully utilized for Pb 2+ quantification in human serum.
Lead ions are a highly toxic type of pollutant that can contaminate soil and water, posing a threat to food safety.Their accumulation in the body is difficult to eliminate and can lead to severe nerve, hematopoietic, and renal damage, ultimately resulting in death.Nucleic acid-based sensors are frequently used for lead ion detection.Xu et al. designed a highly sensitive cascade signal amplification sensor that combines DNAzyme-based strand displacement amplification with HCR to sense Pb 2+ [86], while Jia's group developed a novel strategy for Pb 2+ detection based on a fluorophore-tagged Pb 2+ -binding aptamer [87], as shown in Figure 4B.Since the binding of the aptamer to Pb 2+ leads to a conformational change, the original low-fluorescence "off" state becomes a high-fluorescence "on" state.The method enables quantitative detection of lead ions with a minimum detection concentration of 468 nM, maintaining high specificity for Pb 2+ during the detection process.Furthermore, it has been successfully tested in complex biofluids (Figure 4C), making it a promising tool for Pb 2+ detection in practical applications.Tang and colleagues designed an innovative method for the direct detection of K + and Pb 2+ with high selectivity and sensitivity [88], which relies on the assembly and disassembly of a chiral cyanine dye/TBA complex.Lee et al. [89] synthesized fluorescent probes by incorporating a peptide receptor with hard and soft ligands and a benzothiazolyl-cyanovinylene fluorophore, which were successfully utilized for Pb 2+ quantification in human serum.[87] with permission from the American Chemical Society, copyright 2022.

Hg 2+
Mercury contamination is a global concern due to its toxic and mutagenic effects.A highly sensitive and specific label-free fluorescent sensor for mercury ions was developed by the Wang group [90].This sensor utilized the split GQ/dsDNA assembly and Thioflavin T as a reporter and has been successfully applied to detect Hg 2+ levels in fetal calf serum.Subsequently, they obtained dual fluorescent signals by using two fluorescent dyes and T-rich/G-rich terminal DNA sequences on proportional mercury induction [91].
Nilanjan synthesized a highly sensitive and selective probe for detecting Hg 2+ at ppb levels in aqueous medium [92], as illustrated in Figure 5A.The probe is based on pyridinecoupled dibenzimidazole, which displayed the charge-transfer interactions and coordinated driving of the planarization of the biphenyl backbone.As a result, it exhibited a redshifted absorbance and fluorescence peak in the presence of mercury ions.The dual mode  [87] with permission from the American Chemical Society, copyright 2022.

Hg 2+
Mercury contamination is a global concern due to its toxic and mutagenic effects.A highly sensitive and specific label-free fluorescent sensor for mercury ions was developed by the Wang group [90].This sensor utilized the split GQ/dsDNA assembly and Thioflavin T as a reporter and has been successfully applied to detect Hg 2+ levels in fetal calf serum.Subsequently, they obtained dual fluorescent signals by using two fluorescent dyes and T-rich/G-rich terminal DNA sequences on proportional mercury induction [91].
Nilanjan synthesized a highly sensitive and selective probe for detecting Hg 2+ at ppb levels in aqueous medium [92], as illustrated in Figure 5A.The probe is based on pyridinecoupled dibenzimidazole, which displayed the charge-transfer interactions and coordinated driving of the planarization of the biphenyl backbone.As a result, it exhibited a red-shifted absorbance and fluorescence peak in the presence of mercury ions.The dual mode sensing approach enables accurate and reliable detection of Hg 2+ in the presence of albumin protein (Figure 5B).Moreover, the probe-coated paper strip could remain colorless under normal daylight but exhibit blue fluorescence under UV flashlight irradiation (Figure 5C).This feature can be used for rapid, on-site detection of Hg 2+ , highlighting its potential in environmental monitoring and biomedical research.023, 11, x FOR PEER REVIEW 10 of 34 sensing approach enables accurate and reliable detection of Hg 2+ in the presence of albumin protein (Figure 5B).Moreover, the probe-coated paper strip could remain colorless under normal daylight but exhibit blue fluorescence under UV flashlight irradiation (Figure 5C).This feature can be used for rapid, on-site detection of Hg 2+ , highlighting its potential in environmental monitoring and biomedical research.

Al 3+
Aluminum, the most abundant metallic element in the Earth's crust, has extensive applications in our daily lives.However, excessive intake of aluminum can lead to serious health problems and central nervous system dysfunction.To address this issue, Huang's team developed a highly efficient and versatile bifunctional fluorescence sensor based on benzoindole [93], which can rapidly and accurately detect changes in pH and Al 3+ in aqueous solutions.With a simple and effective detection mode, the sensor can detect Al 3+ in a variety of real samples, including water, food, beverages, drugs, serum, and urine.These promising results demonstrate the sensor's potential for broad applications in the field of metal ion sensing.

Pt 4+
Platinum ion accumulation in the body can lead to toxicity, renal failure, cognitive and motor impairment, and severe neurological disorders.Considering the significant rise in Pt ion chemicals and the associated toxicity, it is crucial for the development of facile and rapid methods to monitor the presence of Pt species in physical and environmental settings.Liang and colleagues designed a highly sensitive and selective nanosensor (PEIMP) for the specific determination of Pt 4+ in aqueous media [94].The nanosensor is based on a novel hydrophilic polymer and shows a linear range of 0.1-10 μM and an ultralow detection limit of 80 nM.The sensing mechanism is based on an "on/off" switching process of photoinduced electron transfer (PET), which allows enhanced fluorescence detection of Pt 4+ .This method has been successfully applied for the quantification of Pt 4+ in wastewater and urine samples and shows great potential for monitoring Pt 4+ in biological systems.

Al 3+
Aluminum, the most abundant metallic element in the Earth's crust, has extensive applications in our daily lives.However, excessive intake of aluminum can lead to serious health problems and central nervous system dysfunction.To address this issue, Huang's team developed a highly efficient and versatile bifunctional fluorescence sensor based on benzoindole [93], which can rapidly and accurately detect changes in pH and Al 3+ in aqueous solutions.With a simple and effective detection mode, the sensor can detect Al 3+ in a variety of real samples, including water, food, beverages, drugs, serum, and urine.These promising results demonstrate the sensor's potential for broad applications in the field of metal ion sensing.

Pt 4+
Platinum ion accumulation in the body can lead to toxicity, renal failure, cognitive and motor impairment, and severe neurological disorders.Considering the significant rise in Pt ion chemicals and the associated toxicity, it is crucial for the development of facile and rapid methods to monitor the presence of Pt species in physical and environmental settings.Liang and colleagues designed a highly sensitive and selective nanosensor (PEIMP) for the specific determination of Pt 4+ in aqueous media [94].The nanosensor is based on a novel hydrophilic polymer and shows a linear range of 0.1-10 µM and an ultra-low detection limit of 80 nM.The sensing mechanism is based on an "on/off" switching process of photoinduced electron transfer (PET), which allows enhanced fluorescence detection of Pt 4+ .This method has been successfully applied for the quantification of Pt 4+ in wastewater and urine samples and shows great potential for monitoring Pt 4+ in biological systems.

Intracellular Imaging of Metal Ions
Our understanding of the effects of metal ions on physiological processes can be deepened by detecting them in living cells.Since the 1960s, the use of fluorescent sensors for cellular and molecular imaging has proliferated due to advances in image processing technology.This imaging technique can be used for disease identification, tracking, and treatment, as well as for the detection of several biomarkers.Fluorescence imaging can expose the structural and physiological characteristics of cells and tissues, and also measure intracellular molecules and molecular structures [39].Recently, there have been significant improvements in the sensitivity and selectivity of metal ion detection by advances in bioimaging.Schiff base ligands possess excellent photochemical properties and can be used to create fluorescent probes, but the use of sodium (I) complexes based on Schiff base ligands is rare [95].Tamilselvi et al. recently designed a sodium ion sensor based on a pyridoxalbearing triazole ring Schiff base [96], which exhibits strong blue-green emission in the solid state and emits a yellow light when Na + is present.They further studied the proportional fluorescence response of this probe with sodium ions in the U87 cell line, indicating its potential application in cell biology protocols.
Potassium and sodium play crucial roles in various biological processes, but their synergies also have important implications for various biological processes.Yang et al. designed the first cell-surface fluorescent probe that can simultaneously detect Na + and K + in the microenvironment of cells [97].The probe utilizes a Y-shaped DNA sensor composed of three distinct DNA sequences: a Na + -specific enzyme strand hybridized with the substrate strand and a GQ strand that binds to K + .The use of this probe to detect Na + /K + concurrently provides a more comprehensive understanding of the dynamic changes of the targets than single-ion assays.The design and use of this probe have great significance in further understanding Na + and K + -related cellular events and biological processes.

K +
For imaging intracellular K + , it is vital to develop a molecular recognition element that can achieve high affinity and selectivity to K + .Tian et al. presented the first polymer-based ratiometric fluorescent K + indicator (PK1), which was modified with a water-soluble polymer skeleton to enable high-throughput monitoring of K + fluctuations in living cells [98].Subsequently, they further enhanced the detection of potassium ions in cells by incorporating a small-molecule K + fluorescent probe into a hydrophilic F127 block and then binding it to cationic liposomes to create modified nanoparticles with enhanced cellular affinity [99].A pioneering chemosensor for the accurate intracellular ratiometric imaging of potassium using a dual fluorophore strategy was introduced by Chang et al. [100].Furthermore, Chen et al. innovated a remotely operated "lock-unlock" nanosystem [101].This nanosystem utilizes a dual-stranded aptamer precursor (DSAP) as the recognition molecule and a SiO 2based gold nanoshell (AuNS) as the nanocarrier, with NIR light as the stimulus for remote application, as shown in Figure 6A.AuNS generates an increased local temperature upon receiving NIR light, which induces the dehybridization of DSAP, activates the binding capability of the aptamer, and enables the monitoring of intracellular K + via changes in the fluorescence signal (Figure 6B).This DSAP-AuNS nanosystem provides a new means to visualize endogenous K + in living cells.

Ca 2+
Fluorescent sensing and imaging have become useful tools to investigate the signaling pathways of calcium ions, which act as a widespread secondary messenger and play an essential role in neurodegenerative diseases.Modified with a specific Ca 2+ chelator ligand with two formaldehyde groups, a copper nanocluster ratiometric fluorescent probe was developed for real-time sensing and imaging of Ca 2+ in neurons [102].In another example, an inner-filter-mediated luminescence probe was developed by using biomass quantum dots as a fluorescent reporter.This probe was initially quenched by a Ca 2+ chelator alizarin red S yet turned on after binding to intracellular Ca 2+ .Despite fluorescent nanoclusters and quantum dots, green fluorescent protein could also be combined with the specific chelator for Ca 2+ imaging [103].Mitochondrial Ca 2+ concentration in living cells is also of great importance.Mt-fura-2, the first ratiometric chemical Ca 2+ probe for mitochondria, was developed by coupling two triphenylphosphonium cations to the molecular backbone of the ratiometric Ca 2+ indicator fura-2 [104].Mt-fura-2 binds calcium ions in vitro with a dissociation constant of ≈1.5 µM and exhibits correct mitochondrial localization and precise measurement of matrix [Ca 2+ ] changes in cells.
Ca 2+ -specific DNAzyme, which was first reported in 2017 [105], was used to construct a SERS-fluorescence dual-mode probe for Ca 2+ imaging in living cells in 2021 by Li and coworkers [106].The Ca 2+ -responsive nanoprobe was constructed by modifying DNAzyme and a Cy5-labelled substrate strand on gold nanostars.When the two chains hybridize, the fluorescence of Cy5 is quenched, which enhances the SERS signal concurrently.The substrate chains could be cleaved and freed from the surface of the gold nanopillar by the catalytic induction of Ca 2+ , which leads to the weakening of the SERS signal, as well as the fluorescence signal recovery.The nanosensor has been successfully used in HeLa cells under the treatment of T-2 toxin, which increased the intracellular free Ca 2+ concentration and caused cell apoptosis.Moreover, the calmodulin domain and its cognate M13 peptide have also been widely used in biological research.Rhodamines are highly bright and photostable fluorophores, and one of their key properties is that they exist in a balance between the non-fluorescent, spirocyclic form and the fluorescent, amphoteric form.The remarkable ability of HaloTag7 to affect rhodamine spirocyclization was used to develop biosensors in which the analyte affects the conformation of HaloTag7 and thus the balance of spirocyclization.The Johnsson group developed a ratiometric biosensor based on spirocyclization in an environmentally sensitive discolored fluorophore that reversibly switches between the green and red fluorescent forms, successfully imaging calcium ions in living cells [107], as shown in Figure 6C.This biosensor combines a HaloTag7 and a Ca 2+ -sensing structural domain (rHCaMP) to enable reversible switching between green and red fluorescent forms through intramolecular spirocyclization by using a color-shifted fluorophore.The biosensor provides precise ratiometric measurements of Ca 2+ both in vitro and intracellularly (Figure 6D).Furthermore, by coupling the CSFs to various protein ligands, the biosensor achieves exceptional sensitivity, with some probes demonstrating up to 2400-fold changes in fluorescence ratios upon binding to the target.The Campbell group developed a NIR genetically encoded indicator using a biliverdin-binding fluorescent protein for multi-color imaging [108].BAPTA could form a chemigenetic indicator due to the interaction between the BAPTA moiety and the GFP chromophore, which provided creative guidance in the design of chemigenetic indicators.In addition to fluorescent intensity-based readout, the Goedhart group also proposed a turquoise fluorescence lifetime-based biosensor for quantitative imaging of intracellular Ca 2+ with a low sensitivity for pH, which was a teaser for traditional intensity-based indicators [109].

Zn 2+
Accurately monitoring the zinc profile and levels in living cells is crucial for various biological studies.Among various developed methods, DNAzyme-based sensors are at the forefront of zinc ion imaging studies.However, their application in cells is limited due to the difficulty in maintaining the activity of RNA-cleaving DNAzymes during delivery and poor biological imaging performance [110,111].To address this issue, Zhang et al. constructed a TP imaging probe based on an RNA-cleaving DNAzyme by modifying the Zn 2+ -specific DNAzyme with TP fluorophores and utilized gold nanoparticles (AuNPs) for efficient intracellular delivery [112].This NIR light-excited probe exhibits exceptional imaging capabilities for Zn 2+ in viable cells and tissues, with remarkable in-depth penetration of tissues reaching depths of 160 µm.The Lu group developed a new fluorescent imaging technique that allows for ratiometric imaging of Mg 2+ and Zn 2+ in living cells [113], using DNAzyme-mediated, genetically encoded fluorescent proteins.The merit of this approach is that Mg 2+ -dependent multi-round cleavage of the target mRNA by DNAzyme activity allows for a correlation between the expression level of fluorescent proteins and the concentration of the target metal ion.This sensor can utilize a variety of metal-specific DNAzyme, greatly expanding the range of metal ions that can be imaged with genetically encoded proteins.Additionally, Luo et al. developed a DNAzyme-based normalized strategy for direct quantification of endogenous zinc in living cells [114].Recently, Li's team described the first example of DNAzyme-based sensors for subcellular metal-ion imaging [115], which combines a photoactivatable DNAzyme sensor probe with upconversion nanotechnology and organelle-localized strategies.Except for DNAzyme-based sensors [116], Schiff base based chemosensors [117,118], peptide-based sensors [119] and single red fluorescent protein-based sensors [120] also offer a variety of options for researchers when studying the distribution and concentration of zinc ions in living cells.Accurately monitoring the zinc profile and levels in living cells is crucial for various biological studies.Among various developed methods, DNAzyme-based sensors are at the forefront of zinc ion imaging studies.However, their application in cells is limited due to the difficulty in maintaining the activity of RNA-cleaving DNAzymes during delivery and poor biological imaging performance [110,111].To address this issue, Zhang et al. constructed a TP imaging probe based on an RNA-cleaving DNAzyme by modifying the Zn 2+ -specific DNAzyme with TP fluorophores and utilized gold nanoparticles (AuNPs) for efficient intracellular delivery [112].This NIR light-excited probe exhibits exceptional imaging capabilities for Zn 2+ in viable cells and tissues, with remarkable in-depth penetration of tissues reaching depths of 160 μm.The Lu group developed a new fluorescent imaging technique that allows for ratiometric imaging of Mg 2+ and Zn 2+ in living cells [113], using DNAzyme-mediated, genetically encoded fluorescent proteins.The merit of this approach is that Mg 2+ -dependent multi-round cleavage of the target mRNA by DNAzyme activity allows for a correlation between the expression level of fluorescent proteins and the concentration of the target metal ion.This sensor can utilize a variety of metal-specific DNAzyme, greatly expanding the range of metal ions that can be imaged

Mg 2+
As the second largest intracellular cation after potassium, the magnesium ion is essential for various biological processes and physiological functions.However, traditional fluorescent chemosensors for the detection of magnesium ions currently face the limitations of low selectivity and poor fluorescence signal enhancement.Yuki et al. overcame this limitation by synthesizing the first highly selective and NIR fluorescent probes for the detection of Mg 2+ [121], as shown in Figure 7A.These probes consisted of charged β-diketones as specific bound spots for Mg 2+ and Si-rhodamine remnants as NIR fluorophores.They are primarily located in the cytoplasm and are localized partially in the lysosomes and mitochondria of cultured rat hippocampal neurons (Figure 7B).Moreover, the Aharon group reported the first example of aqueous CDs with high selectivity for intracellular Mg 2+ detection [122].Furthermore, Ashok's team successfully synthesized novel chromone-based chemosensors (La and Lb) that are highly sensitive to Mg 2+ [123], with La also showing potential for Mn 2+ detection through absorption studies.On the other hand, Lb was found to sense Cu 2+ through absorption studies and also showed sensitivity to Mg 2+ via emission studies.These ligands were successfully used for Mg 2+ imaging in HeLa cancer cells.

Cu 2+
The development of copper ion sensors in recent years has still primarily relied on the design of organic fluorescent probes [124,125] and nanomaterials [126].In the previous section, it was mentioned that the Cu(I)-catalyzed click reaction has a high selectivity for Cu 2+ , making it ideal for complex intracellular environments.Bu et al. developed an innovative "OFF-ON" fluorescent biosensor by combining the Cu(I)-catalyzed click reaction with a 3D DNA walker based on spherical nucleic acid [127].In the initial "OFF" state, the fluorophore (Cy3) on the hairpin is close to the surface of AuNPs, resulting in quenched fluorescence.Cu is rapidly produced in situ from Cu 2+ in the presence of ascorbic acid, triggering the click reaction-based 3D DNA walker.The activated swing arm hybridizes with the neighboring Cy3-hairpin and drives the 3D DNA walker by endonuclease to produce several Cy3-labeled DNA fragments away from the AuNP surface, resulting in a restored fluorescence response (transitioning to the "ON" state).The utilization of this assay provides a means for transducing signals and assessing intracellular Cu 2+ at picomolar concentrations.
intracellular Mg 2+ detection [122].Furthermore, Ashok's team successfully synthesized novel chromone-based chemosensors (La and Lb) that are highly sensitive to Mg 2+ [123], with La also showing potential for Mn 2+ detection through absorption studies.On the other hand, Lb was found to sense Cu 2+ through absorption studies and also showed sensitivity to Mg 2+ via emission studies.These ligands were successfully used for Mg 2+ imaging in HeLa cancer cells.

Cu 2+
The development of copper ion sensors in recent years has still primarily relied on the design of organic fluorescent probes [124,125] and nanomaterials [126].In the previous section, it was mentioned that the Cu(I)-catalyzed click reaction has a high selectivity for Cu 2+ , making it ideal for complex intracellular environments.Bu et al. developed an innovative "OFF-ON" fluorescent biosensor by combining the Cu(I)-catalyzed click reaction with a 3D DNA walker based on spherical nucleic acid [127].In the initial "OFF" state, the fluorophore (Cy3) on the hairpin is close to the surface of AuNPs, resulting in quenched fluorescence.Cu is rapidly produced in situ from Cu 2+ in the presence of ascorbic acid, triggering the click reaction-based 3D DNA walker.The activated swing arm hybridizes with the neighboring Cy3-hairpin and drives the 3D DNA walker by endonuclease to produce several Cy3-labeled DNA fragments away from the AuNP surface, resulting in a restored fluorescence response (transitioning to the "ON" state).The utilization of this assay provides a means for transducing signals and assessing intracellular Cu 2+ at picomolar concentrations.CDs have garnered significant attention in metal ion detection in living cells.To this end, double-emission CDs (NS-CDs) with varying dimensions of nitrogen/sulfur doping were synthesized by solubilizing sodium alginate (SA) and glutathione (GSH) in formamide for heat treatment [128], as shown in Figure 7C.Since Fe 3+ induces the aggregation of NS-CDs, which enhances the fluorescence signal.Therefore, this nanosensor enables ratiometric measurements of iron ions and exhibits remarkable detectability and sensitivity, with detection limits as low as 0.56 µM.Moreover, NS-CDs display unparalleled capability for localized, specific cell membrane imaging (Figure 7D).Similarly, the Guo group proposed the synthesis of N-CDs utilizing fresh tea leaves and urea [129], while Zhang's team fabricated deferoxamine-inspired CDs using L-aspartic acid (Asp) and 2,5-diaminobenzenesulfonic acid (DABSA) as reactants in a single-boiler hydrother-mal synthesis [130].Both N-CDs and deferoxamine-inspired CDs were applied for cell imaging of Fe 3+ and exhibited promising results.Hou et al. developed an innovative "turn-on" fluorescent probe using rhodamine 6G derivatives and spirolactam ring-opening reactions [131].This probe is highly effective in detecting Fe 3+ for fluorescence imaging in living cells.In addition, Wang et al. designed dual-targeting fluorescent probes that combine galactose and imidazole to detect Fe 3+ in the hepatic lysosome [132], enabling both hepatic and lysosomal targeting.Although indole-based fluorescent sensors for Fe 3+ detection are rare, Nantanit reported three new sensors with fluorescence responses to Fe 2+ and Fe 3+ sensing in aqueous buffer systems [133].One of these isomers is an excellent candidate for tracking Fe 3+ in biological systems.

Fluorescent Sensors for Non-Essential Metal Ions 4.2.1. Li +
The lithium-based complex is a widely used and effective drug for the treatment of bipolar disorder (BD) for more than 70 years.The distribution of lithium ions in the patient's cells is crucial to optimize the therapeutic effect.However, imaging lithium selectively in the biomedically relevant concentration range (0.5-2.0 mM) in living cells remains a major challenge.A major breakthrough was recently reported by Lu's team, which developed a lithium-specific DNAzyme with a selectivity exceeding 100-fold that of other biologically relevant metal ions [134], as shown in Figure 8A.This novel sensor allows for the visualization of lithium in HeLa cells, neurons from BD patients, healthy controls (Figure 8B) and human neuronal progenitor cells (Figure 8C) for comparison, making it a promising tool for investigating the therapeutic effects of lithium.
pability for localized, specific cell membrane imaging (Figure 7D).Similarly, the Guo group proposed the synthesis of N-CDs utilizing fresh tea leaves and urea [129], whil Zhang's team fabricated deferoxamine-inspired CDs using L-aspartic acid (Asp) and 2,5 diaminobenzenesulfonic acid (DABSA) as reactants in a single-boiler hydrothermal syn thesis [130].Both N-CDs and deferoxamine-inspired CDs were applied for cell imaging o Fe 3+ and exhibited promising results.Hou et al. developed an innovative "turn-on" fluo rescent probe using rhodamine 6G derivatives and spirolactam ring-opening reaction [131].This probe is highly effective in detecting Fe 3+ for fluorescence imaging in living cells.In addition, Wang et al. designed dual-targeting fluorescent probes that combin galactose and imidazole to detect Fe 3+ in the hepatic lysosome [132], enabling both hepati and lysosomal targeting.Although indole-based fluorescent sensors for Fe 3+ detection ar rare, Nantanit reported three new sensors with fluorescence responses to Fe 2+ and Fe 3 sensing in aqueous buffer systems [133].One of these isomers is an excellent candidate fo tracking Fe 3+ in biological systems.

Li +
The lithium-based complex is a widely used and effective drug for the treatment o bipolar disorder (BD) for more than 70 years.The distribution of lithium ions in the pa tient's cells is crucial to optimize the therapeutic effect.However, imaging lithium selec tively in the biomedically relevant concentration range (0.5-2.0 mM) in living cells re mains a major challenge.A major breakthrough was recently reported by Lu's team which developed a lithium-specific DNAzyme with a selectivity exceeding 100-fold tha of other biologically relevant metal ions [134], as shown in Figure 8A.This novel senso allows for the visualization of lithium in HeLa cells, neurons from BD patients, healthy controls (Figure 8B) and human neuronal progenitor cells (Figure 8C) for comparison making it a promising tool for investigating the therapeutic effects of lithium.[134] with permission from the American Chemical Society, copyright 2021.

Ag +
Dong et al. developed a label-free N-CDs system for the detection of silver ions and GSH through intrinsic ratiometric fluorescence [135].The N-CDs emit a single longwavelength light at 618 nm when excited at 478 nm.When silver ions are present, this nanosensor shows a rising peak at 532 nm and a decrease in emission at 618 nm, enabling the detection of silver ions in the range of 0-140 µM.Yu et al. presented a groundbreaking approach to visualize Ag + in living bacterial cells by utilizing a genetically encoded biosensor (Figure 9B) [136].The sensor incorporates a cytosine-Ag + -cytosine metal base pair into a fluorogenic RNA aptamer, known as Broccoli, which folds and emits a fluorescent signal upon binding to Ag + (Figure 9A).This unique RNA sensor can be further adapted for cellular imaging of other metal ions by implementing a similar design principle based on specific metal base pairs.The Guo group synthesized a novel ratiometric chemosensor called CHa based on the hydrolysis of hydrazone derivatives of coumarin fluorescent moieties induced by Ag + [137].When CHa encounters silver ions, it undergoes hydrolysis, resulting in the release of a 3-formyl-substituted coumarin derivative that acquires blue emission at short wavelengths from yellow emission.Additionally, a phenanthro [9,10-d] imidazole-based fluorescent probe with AIE activity was designed by Bu et al. [138], for simultaneous sensing of Ag + and SCN − .In another example, a sustainably modifiable 1,2-alternating thiacalix [4]arene was synthesized by Yu et al. [139], which displayed a highly sensitive ratio recognition for Ag + .

Ni 2+
Nickel ions play a vital role as a cofactor for a variety of microbial enzymes, supporting essential cellular functions necessary for prokaryotic survival.A FRET-based genetically encoded biosensor was developed by Neha [140], taking enhanced cyan fluorescent protein and Venus (a variant of yellow fluorescent protein) respectively into account as donor and acceptor fluorescent molecules.Such sensors permit concentration-dependent monitoring of nickel ion fluxes within viable cells with a high spatial and temporal resolution to provide in-depth insight into the distribution of nickel ions physiologically at the cellular and subcellular levels.
Reports on fluorescent probes for nickel ions are relatively scarce, and there is still a need to develop simple and effective detection methods.Wang et al. constructed a molecular probe FA-Ni to achieve highly selective and ultrasensitive rapid detection of Ni 2+ , avoiding the interference of other ions [141].Nickel ions were converted to elemental nickel under the reducing conditions of NaBH 4 , and then triphenylphosphine was used as a ligand to detach allyl from the probe FA-Ni, thereby generating a fluorescent signal.They also successfully applied the probe FA-Ni for in situ imaging of nickel ions in living cells.Additionally, Shahzad's team reported AIE active sensors for the detection of Ni 2+ in live cells and acid/base sensing [142].Gu et al. developed a new chemosensor based on a pyrazolopyrimidine core that can simultaneously detect Cu 2+ and Ni 2+ , which has good imaging properties for both Cu 2+ and Ni 2+ in living cells [143].

Pb 2+
The interaction between metals and biomolecules can be found throughout nature and provides a wealth of resources and principles of design in the search for novel, recognizable ligands.Peptides are promising candidates for designing metal-binding ligands due to their rich coordination chemistry, high stability, and availability of optional building blocks.Additionally, their high biocompatibility makes them well-suited for detecting Pb 2+ in biological systems.The Zhao group designed a biomimetic peptide-based fluorescent sensor GSSH-2TPE inspired by the structure of glutathione [144], as shown in Figure 9C.Mechanistic studies confirmed that there is a delicate balancing between the chelating groups and the molecular configuration responsible for the highly selective complexation of Pb 2+ by the sensor.Additionally, the ion-induced supramolecular assembly generates a bright fluorescence signal.Featuring good biocompatibility and the lowest possible disturbance to both endogenous biothiols and background fluorescence, the sensor allows precise imaging of Pb 2+ in vivo (Figure 9D).Similarly, Mehta et al. designed a proportional fluorescent peptide-based sensor by coupling the peptide receptor of Pb(II) with an excimerforming benzothiazolylcyanovinylene fluorophore [145].2TPE, with and without the addition of Pb 2+ .Reproduced from [144] with permission from the American Chemical Society, copyright 2019.

Pb 2+
The interaction between metals and biomolecules can be found throughout nature and provides a wealth of resources and principles of design in the search for novel, recognizable ligands.Peptides are promising candidates for designing metal-binding ligands due to their rich coordination chemistry, high stability, and availability of optional building blocks.Additionally, their high biocompatibility makes them well-suited for detecting Pb 2+ in biological systems.The Zhao group designed a biomimetic peptide-based fluorescent sensor GSSH-2TPE inspired by the structure of glutathione [144], as shown in Figure 9C.Mechanistic studies confirmed that there is a delicate balancing between the chelating groups and the molecular configuration responsible for the highly selective complexation of Pb 2+ by the sensor.Additionally, the ion-induced supramolecular assembly generates a bright fluorescence signal.Featuring good biocompatibility and the lowest possible disturbance to both endogenous biothiols and background fluorescence, the sensor allows precise imaging of Pb 2+ in vivo (Figure 9D).Similarly, Mehta et al. designed a proportional fluorescent peptide-based sensor by coupling the peptide receptor of Pb(II) with an excimer-forming benzothiazolylcyanovinylene fluorophore [145].

Pd 2+
Palladium is a scarce internal transition metal that is widely employed as an extremely potent catalyst in various areas.However, it should be noted that Pd species can disrupt many biological processes and pose significant health hazards.Of particular concern is Pd 2+ , which is the most abundant oxidation state in alive cells, thus the potential for developing validated Pd 2+ detection and imaging approaches are vital for environmental safety and the health of humans.Wen et al. developed a naphthofluorescein-based NIR fluorescent probe called M-PD [146], which boasts exceptional sensing properties for the detection of Pd 2+ .The lower limit of detection for this sensor was found to be 10.8 nM, a value significantly below the drug in threshold values (5-10 ppm).Additionally, M-PD has been successfully utilized for the near-infrared fluorescence imaging of Pd 2+ in living cells.A chemosensor, DCF-MPYM-Pd, featuring a wide stokes shift and an ability for lysosomal targeting was synthesized by Wang et al. [147].It was shown that this sensor can (D) Fluorescence microscopic images of living HeLa cells with GSSH-2TPE, with and without the addition of Pb 2+ .Reproduced from [144] with permission from the American Chemical Society, copyright 2019.

Pd 2+
Palladium is a scarce internal transition metal that is widely employed as an extremely potent catalyst in various areas.However, it should be noted that Pd species can disrupt many biological processes and pose significant health hazards.Of particular concern is Pd 2+ , which is the most abundant oxidation state in alive cells, thus the potential for developing validated Pd 2+ detection and imaging approaches are vital for environmental safety and the health of humans.Wen et al. developed a naphthofluorescein-based NIR fluorescent probe called M-PD [146], which boasts exceptional sensing properties for the detection of Pd 2+ .The lower limit of detection for this sensor was found to be 10.8 nM, a value significantly below the drug in threshold values (5-10 ppm).Additionally, M-PD has been successfully utilized for the near-infrared fluorescence imaging of Pd 2+ in living cells.A chemosensor, DCF-MPYM-Pd, featuring a wide stokes shift and an ability for lysosomal targeting was synthesized by Wang et al. [147].It was shown that this sensor can accurately sense palladium (II) in living cells and can specifically accumulate in lysosomes.To avoid the problem of the multi-step synthesis of a probe, Mareeswaran's group found a simple and well-known organic molecule, coumarin-460 (C460), that can selectively sense palladium ions in aqueous media [148].They went on to validate the binding and sensing properties of C460 for Pd 2+ by absorption and fluorescence spectroscopy techniques, thus demonstrating that the C460 molecule can be used as an "off" probe for Pd 2+ for real-time detection and biological applications.
While most researchers have designed probes to detect only one form of palladium, the ability to discriminate between Pd (0) and Pd (II) has been rarely reported.In this regard, Zhang et al. designed Umb-Pd2, a corymbone-derived sensor that can be used as a tiny, robust, reliable, and detective sensor for the detection of Pd (II) [149], as shown in Figure 10A.In both the stand-alone and co-existing systems, it is distinguished from typical research by its unique selectivity for Pd (II) and Pd (0), which is commonly referred to as Pd (0)-selective.This differentiation capability was further used in the case of living cell imaging (Figure 10B).regard, Zhang et al. designed Umb-Pd2, a corymbone-derived sensor that can be us a tiny, robust, reliable, and detective sensor for the detection of Pd (II) [149], as show Figure 10A.In both the stand-alone and co-existing systems, it is distinguished from ical research by its unique selectivity for Pd (II) and Pd (0), which is commonly refe to as Pd (0)-selective.This differentiation capability was further used in the case of li cell imaging (Figure 10B).[150].When treated with cury ions, the fluorescence of GQDs was quenched.Exploiting the intramolecular ch transfer (ICT) mechanism, Duan's team introduced a new phenothiazine-based se [151], PHE-Ad, for monitoring Hg 2+ .With its excellent fluorescent signaling behavior low cytotoxicity, PHE-Ad proved to be successful in detecting and imaging Hg 2+ in li cells.Furthermore, the same team reported another two novel PET fluorescent pr CH3-R6G and CN-R6G, rationally synthesized by partial doping of rhodamine 6G f ophore with a triazolyl benzaldehyde moiety and applied with great success for Hg 2 aging in breast cancer cells [152].Ding et al. reported the synthesis of ethyl 2,5-diph 2H-1,2,3-triazole-4-carboxylate [153], which was then introduced into rhodamine B to duce a novel derivative, REDTC.This probe exhibited remarkable selectivity for through a chromogenic reaction, without interference from other metal ions.Lastly novel NIR monosulfide probes, MTSQ-1 and MTSQ-2, were designed and used for  [151], PHE-Ad, for monitoring Hg 2+ .With its excellent fluorescent signaling behavior and low cytotoxicity, PHE-Ad proved to be successful in detecting and imaging Hg 2+ in living cells.Furthermore, the same team reported another two novel PET fluorescent probes, CH3-R6G and CN-R6G, rationally synthesized by partial doping of rhodamine 6G fluorophore with a triazolyl benzaldehyde moiety and applied with great success for Hg 2+ imaging in breast cancer cells [152].Ding et al. reported the synthesis of ethyl 2,5-diphenyl-2H-1,2,3triazole-4-carboxylate [153], which was then introduced into rhodamine B to produce a novel derivative, REDTC.This probe exhibited remarkable selectivity for Hg 2+ through a chromogenic reaction, without interference from other metal ions.Lastly, two novel NIR monosulfide probes, MTSQ-1 and MTSQ-2, were designed and used for Hg 2+ imaging based on a mercury deuteration strategy [154].Particularly, the MTSQ-2 was packaged in a β-CD and showed excellent performance for imaging Hg 2+ in HeLa cells as well as a high signal-to-background ratio.

Cd 2+
Cadmium ions, one of the most dangerous heavy metals, can affect various cellular physiological effects.Toxic cadmium ions may lead to acute or chronic toxicity, causing cancer and other diseases.The development of highly sensitive and selective methods for the detection of cadmium ions in cells is still challenging.Lin et al. developed a highly selective probe, (E)-4-(4-([2,2 :6 ,2 -terpyridin]-4 -yl)styryl)-1 octadecylpyridin-1-ium bromide (ZC-F8) [155].The fluorescence spectra of ZC-F8 showed an excellent response to Cd 2+ through both an intramolecular charge transfer effect and an AIE effect.Moreover, the results of cell imaging experiments showed that the probe has ideal membrane permeability and a labeled property for Cd 2+ , indicating its promising application in the detection and tracking of metal ions in living cells.In addition, Liao's team successfully synthesized a new peptide-based probe (DSC) with good water solubility and biocompatibility, showing a fluorescent "turn-on" response to Cd 2+ based on the PET principle [156].Fluorescence imaging experiments showed that DSC can selectively monitor Cd 2+ in living cells.

Au 3+
Gold has a broad range of uses in chemistry, catalysis, and medicine.However, the binding of Au 3+ with certain DNA and enzymes poses severe health risks, causing damage to organs.Guo et al. synthesized carbon dots by a simple solvothermal method using the acetic acid-treated peel of red dragon fruits, called ACDs [157].With their high sp2hybrid carbon and carboxyl group contents, ACDs can efficiently convert Au 3+ to Au 0 and stabilize the resulting AuNPs.Electron transfer from ACD to Au 3+ and the inner filtering effect from ACD to AuNPs synergistically quenched the fluorescence within 30 s.In addition, ACDs possessed promising photo-stability, low cytotoxicity, and favorable biological compatibility, enabling their successful application in intracellular Au 3+ sensing and imaging.

Al 3+
The Nikhil group synthesized a new compound, (E)-2-(benzamido)-N -((2-hydroxynaphthalen-1-yl) methylene) benzohydrazide (BBHAN) [158], which belongs to the Schiff base derivative family and contains a hydrazine-bridged anthranilic acid-naphthalene conjugate.BBHAN is a highly sensitive Al 3+ detection probe with a limit of detection of 1.68 × 10 -9 M. Its detection mechanism is based on the chelation-enhanced fluorescence phenomenon, as demonstrated by time-resolved fluorescence measurements.Moreover, BBHAN is capable of detecting Al 3+ in MDA-MB-468 cells.Later, Jessica et al. designed and synthesized a new series of Schiff base chemosensors to sense Al 3+ [159].The molecular solubility and compatibility of the amino acid Schiff base (A) in the presence and absence of Al 3+ were well demonstrated.Furthermore, in human epithelial cells Hs27, the fluorescent bioimaging applications were demonstrated.In the same way, Wang et al. designed an innovative nanoprobe by co-self-assembling an amphiphilic polymer containing a Schiffbase fluorescent unit [160].This novel nanoprobe not only provides high sensitivity for Al 3+ imaging but also has the potential to be applicable to other ions or biomolecules by adjusting the fluorescent unit incorporated into the amphiphilic polymer.

In Vivo Imaging of Metal Ions
The imaging of living animal models offers the capacity to detect changes in signaling molecules, ions, and other biological components throughout different life stages and in the presence of disease.The information obtained from this imaging technique can be applied to discover novel biological insights or to identify markers of disease progression, thereby facilitating the development and translation of effective therapeutics.In particular, the importance of metal ions in organismal regulation, especially in terms of enzyme activation/deactivation and catalysis, and the close association with disease onset and progression make in vivo metal ion imaging a key priority for fluorescent sensor development.Potassium ions, which fluctuate in concentration, exist inside and outside cells, and can be associated with abnormal physiological functions, including nervous system disorders and cardiac dysfunction [161].Nonetheless, probes for potassium ions perform poorly in real-time monitoring in live animal models and there is still a need to develop more sensitive probes for deep tissue monitoring.Ning et al. designed a potassium ion probe, NK2 [162], which combines colorimetric, fluorescence, and photoacoustic methods for three-channel sensing, utilizing benzylguane-6-string ether as the recognition element.
The probe extended the depotential range of K + from 5 mM to 200 mM.In the exploration of animal models, the probe was further imaged with photoacoustic properties that allowed changes in potassium ion concentration to be monitored in the mouse ear under a photoacoustic microscope.
On the basis of NIR for deep tissue detection in live animals, a mesoporous silica nanocomposite was reported by Liu et al. [163].The material encapsulated upconversion nanoparticles (UNCPs) and potassium ion indicators and was encapsulated within a potassium ion-specific filter membrane, which is used to monitor changes in the concentration of potassium ions in the mouse brain.The presence of the filter membrane effectively shielded the assay from other metal ions and serves to enrich the signal.This "shielded nanoparticle" is expected to be an effective method for monitoring metal ions in the brain, and in combination with endoscopic and photometric methods, could be applied to real-time potassium ion imaging.Relying on shielded nanometers, Liu et al. [164] continued to work on the development of a potassium ion sensor containing mesoporous silica nanoparticles with an embedded optical potassium indicator, as shown in Figure 11A.The nanosensor enables the spatial mapping of potassium ion release in the hippocampus of freely moving mice for precise imaging of epileptic foci in the brain (Figure 11B), also allowing for targeted drug release as needed.

Ca 2+
Genetically encoded calcium indicators (GECIs) of the nervous system are broadly explored for calcium imaging, and the GFP-based GCaMP series of GECIs has undergone iterative updates over nearly 20 years [165].In 2019, on the basis of GCaMP6, Dana et al. optimized jGCaMP7 by utilizing structure-guided mutagenesis and neuron-based screening [166].This calcium sensor optimized parameters including signal-to-noise ratio and speed for in vivo imaging, achieving two-photon and wide-field-of-view imaging.In the subsequent year, Zarowny et al. [167] demonstrated a novel GECI with enhanced brightness of the indicator (compared to GCaMP6s) based on a bright monomeric GFP, mNG, in Figure 11C.Calcium dynamic measurement experiments performed in zebrafish larvae proved that the signal-to-noise ratio, kinetics, and baseline brightness of the indicator of mNG were equivalent to those of GCaMP6s (Figure 11D).Zebrafish, distinguished by their transparent bodies and tiny size, are commonly observed for the in vivo imaging of metal ions.Therefore, mNG is expected to be the next generation of GECI.Shemetov et al. [168] incorporated NIR fluorescent proteins into the development of the iGECI sensor, which in combination with NIR Förster resonance energy transfer, enables the iGECI sensors to simultaneously examine neuronal and haemodynamics in the brains of animal models via hybrid photoacoustic and fluorescent microscopy.

Zn 2+
Intracellular zinc ion disorders are associated with several serious diseases.A twophoton fluorescent probe, CHP-H/CHP-CH3, was designed to monitor the dynamics of zinc ions and HNO (Cyto-JN) in a mouse ischaemia/reperfusion model [169].The synthesized NIR fluorescent probe could recognize Zn 2+ and cyanide, employing the condensation product of isoflurone with p-hydroxybenzaldehyde as the fluorophore while introducing aminourea hydrochloride to increase solubility [170].The rapid responsiveness (20 s), high sensitivity (detection limit: 4.61 × 10 −8 M), and selectivity of this probe led to preliminary confirmation of its Zn 2+ and CN -logical responses in an animal model.Reproduced from [167] with permission from the American Chemical Society, copyright 2020.

Zn 2+
Intracellular zinc ion disorders are associated with several serious diseases.A twophoton fluorescent probe, CHP-H/CHP-CH3, was designed to monitor the dynamics of zinc ions and HNO (Cyto-JN) in a mouse ischaemia/reperfusion model [169].The synthesized NIR fluorescent probe could recognize Zn 2+ and cyanide, employing the condensation product of isoflurone with p-hydroxybenzaldehyde as the fluorophore while introducing aminourea hydrochloride to increase solubility [170].The rapid responsiveness (20 s), high sensitivity (detection limit: 4.61 × 10 −8 M), and selectivity of this probe led to preliminary confirmation of its Zn 2+ and CN -logical responses in an animal model.
The Lu group modified light-activated DNAzyme on lanthanide-doped UCNPs for investigating the distribution of Zn 2+ in both cellular and in vivo models [171].Through the utilization of deeply tissue-penetrating NIR 980 nm light, they were able to achieve spatiotemporal control, providing valuable insights into the dynamic Zn 2+ ion distribution.Recently, the same group designed a novel Zn 2+ probe based on metal-specific DNAzyme and high-intensity focused ultrasound (HIFU) activation to overcome the problem of spatiotemporal control of metal ion detection, as sketched in Figure 12A [172].By using a protector strand to block the formation of the catalytic enzyme structure, a Zn 2+ -selective DNAzyme probe can be deactivated and, subsequently, reactivated by a HIFU-induced increase in local temperature.This design allows for Zn 2+ -specific FRET imaging using the new DNAzyme-HIFU probes, which was successfully demonstrated in both HeLa cells and mice (Figure 12B).[167] with permission from the American Chemical Society, copyright 2020.
The Lu group modified light-activated DNAzyme on lanthanide-doped UCNPs for investigating the distribution of Zn 2+ in both cellular and in vivo models [171].Through the utilization of deeply tissue-penetrating NIR 980 nm light, they were able to achieve spatiotemporal control, providing valuable insights into the dynamic Zn 2+ ion distribution.Recently, the same group designed a novel Zn 2+ probe based on metal-specific DNAzyme and high-intensity focused ultrasound (HIFU) activation to overcome the problem of spatiotemporal control of metal ion detection, as sketched in Figure 12A [172].By using a protector strand to block the formation of the catalytic enzyme structure, a Zn 2+ -selective DNAzyme probe can be deactivated and, subsequently, reactivated by a HIFU-induced increase in local temperature.This design allows for Zn 2+ -specific FRET imaging using the new DNAzyme-HIFU probes, which was successfully demonstrated in both HeLa cells and mice (Figure 12B).

Fe 2+ /Fe 3+
The homeostasis of iron ions within human health is of great relevance, as either too high or too low concentrations can cause various systemic diseases.Researchers have worked to achieve ultra-high sensitivity for imaging iron ions in vivo.Vijay et al. developed a rhodamine-B-armed fluorescent chemosensor (RhBNC) that specifically recognizes iron ions and then emits orange fluorescence [173], as shown in Figure 12C.Following photophysical detection, RhBNC was employed for real-time fluorescence imaging in vivo, and bright red fluorescence was observed in the stomach of zebrafish after 30 min of probe treatment with the addition of iron ions (Figure 12D).The carbon dot-based fluorescence sensor has become a representational platform for the detection of iron ions due to its fast response time, low cost, and stability.Chang et al. prepared high quantum yield CDs (42%) by employing a multiflora polygonum one-step hydrothermal strategy and designed a sensor for multicolor imaging [174], tracking intracellular concentration fluctuations, and in vivo bioimaging based on the fluorescence burst of iron ions on CDs.Meanwhile, the same team reported that the fluorescence burst of iron ions on CDs is based on lysis [175].The homeostasis of iron ions within human health is of great relevance, as either too high or too low concentrations can cause various systemic diseases.Researchers have worked to achieve ultra-high sensitivity for imaging iron ions in vivo.Vijay et al. developed a rhodamine-B-armed fluorescent chemosensor (RhBNC) that specifically recognizes iron ions and then emits orange fluorescence [173], as shown in Figure 12C.Following photophysical detection, RhBNC was employed for real-time fluorescence imaging in vivo, and bright red fluorescence was observed in the stomach of zebrafish after 30 min of probe treatment with the addition of iron ions (Figure 12D).The carbon dot-based fluorescence sensor has become a representational platform for the detection of iron ions due to its fast response time, low cost, and stability.Chang et al. prepared high quantum yield CDs (42%) by employing a multiflora polygonum one-step hydrothermal strategy and designed a sensor for multicolor imaging [174], tracking intracellular concentration fluctuations, and in vivo bioimaging based on the fluorescence burst of iron ions on CDs.Meanwhile, the same team reported that the fluorescence burst of iron ions on CDs is based on lysis [175].For the detection of ferrous ions, Zhu et al. combined an NIR strategy to synthesize (E)-4-(2-(3-(dimethylenimino)-5,5-dimethylcyclohexyl-1-en-1-yl)vinyl-N,Ndiethylaniline oxide (DDED) as a NIR probe [176], which showed a strong imaging capability in zebrafish, emitting intense red fluorescence mainly in the yolk sac and digestive tract.DCI-Fe (II), developed by Zheng et al., allowed for the imaging of ferrous ions within live cell lipid droplets and in mice [177].

Co 2+
Cobalt is a vital mineral needed in small quantities for DNA biosynthesis and is a key component of vitamin B12.Li's team developed an innovative fluorescent CD sensor using frozen tofu, ethylenediamine, and phosphoric acid [178].The resulting CD exhibits

Co 2+
Cobalt is a vital mineral needed in small quantities for DNA biosynthesis and is a key component of vitamin B12.Li's team developed an innovative fluorescent CD sensor using frozen tofu, ethylenediamine, and phosphoric acid [178].The resulting CD exhibits excellent biocompatibility, high stability, low cytotoxicity, and good water solubility.This sensor can selectively and sensitively detect Co 2+ by fluorescence quenching, with a detection limit of 58 nM.Moreover, strong chelating agents such as EDTA can strip the ions from the surface.In zebrafish models, CD was rapidly absorbed from the intestine to the liver and eliminated from the body within 24 h without significant bioaccumulation.

Li +
Lithium is prescribed for the treatment of bipolar disorder.The range of 0.6 to 1.2 mM of lithium in serum has been described as clinically safe and therapeutically effective.Over-ingestion of lithium can lead to toxic and even life-threatening reactions [179].In Figure 13A, Kang et al. reported a fluorescent probe, SP-CE, which was synthesized via introducing an aza-12-crown-4 ether unit into spiropyran for chelation with lithium [180].In the absence of light, the compound undergoes isomerization from SP to MC form upon complexation with lithium in solution, resulting in a significant fluorescence enhancement upon excitation at 550 nm.The fluorescent probe exhibited high sensitivity and selectivity toward lithium in solution.Finally, it was successfully employed for imaging exogenous lithium in living cells and zebrafish (Figure 13B).Among these, SP-CE has a time-dependent fluorescence response to lithium ions (LiCl treatment) in zebrafish.
introducing an aza-12-crown-4 ether unit into spiropyran for chelation with lithium [180].In the absence of light, the compound undergoes isomerization from SP to MC form upon complexation with lithium in solution, resulting in a significant fluorescence enhancement upon excitation at 550 nm.The fluorescent probe exhibited high sensitivity and selectivity toward lithium in solution.Finally, it was successfully employed for imaging exogenous lithium in living cells and zebrafish (Figure 13B).Among these, SP-CE has a time-dependent fluorescence response to lithium ions (LiCl treatment) in zebrafish.Imaging data showed that when this nanosensor was micromanipulated into zebrafish embryos, it could image Pb 2+ in living cells and early zebrafish, demonstrating its remarkable potential for in vivo applications.

Sn 2+
An inadequate Sn 2+ supply can impair hearing and bone growth, while the accumulation of excess can impede zinc metabolism and cause airway and intestinal disorders.A new mitochondria-targeted AIE chemosensor based on naphthoquinone, 2CTA, was synthesized by Palanisamy et al. [182].Its selectivity and sensitivity (79 nM) to Sn 2+ are higher than those of other disruptors.The "turn-on" fluorescence emission of this chemosensor relies on its AIE properties, caused by the binding of larger aggregates to Sn 2+ .2CTA selectively aggregates in mitochondria, producing an image merged with MitoTracker Red.It also detected Sn 2+ in zebrafish larvae and responded rapidly within 10 s, making it a promising legal instrument capable of following Sn 2+ in ambient and physical systems. .This nanosensor consists of UCNPs as energy transfer donor, BHQ1 quencher as energy transfer acceptor and DNAzyme as Pb 2+ specific pattern of target recognition.Following the introduction of Pb 2+ , the DNAzyme cleaves the strand of substrate at the RNA site, resulting in restoration of luminescence.Imaging data showed that when this nanosensor was micromanipulated into zebrafish embryos, it could image Pb 2+ in living cells and early zebrafish, demonstrating its remarkable potential for in vivo applications.

Sn 2+
An inadequate Sn 2+ supply can impair hearing and bone growth, while the accumulation of excess can impede zinc metabolism and cause airway and intestinal disorders.A new mitochondria-targeted AIE chemosensor based on naphthoquinone, 2CTA, was synthesized by Palanisamy et al. [182].Its selectivity and sensitivity (79 nM) to Sn 2+ are higher than those of other disruptors.The "turn-on" fluorescence emission of this chemosensor relies on its AIE properties, caused by the binding of larger aggregates to Sn 2+ .2CTA selectively aggregates in mitochondria, producing an image merged with MitoTracker Red.It also detected Sn 2+ in zebrafish larvae and responded rapidly within 10 s, making it a promising legal instrument capable of following Sn 2+ in ambient and physical systems.

Cd 2+
Wang et al. showed that a very simple fluorescent probe (NIS) could be easily prepared by a one-step, one-pot condensation reaction of 2, 3-naphthalenediamine and imidazole-2carboxaldehyde [183].In addition, the probe was not disturbed by zinc ions and worked well for Cd 2+ detection at physiological pH.Under fluorescence confocal microscopy, the NIS can detect cadmium ions in living cells through two emission channels.In addition, they further applied NIS to the zebrafish to monitor the real-time uptake of cadmium ions in zebrafish larvae by proportional fluorescence bioimaging.

Hg 2+
Wu et al. designed and synthesized a coumarin-based reactive fluorescent probe, PIC, for the detection of Hg 2+ [184].PIC showed greater selectivity for Hg 2+ detection than other metal ions.Specifically, at physiological pH, its fluorescence enhancement for Hg 2+ was 42 times higher than that of other cations.Most importantly, confocal fluorescence microscopy analysis showed that PIC can be used to monitor Hg 2+ in live cells and zebrafish due to its low cytotoxicity.

Ni 2+
The molecular probe based on the nickel-catalyzed deallyl reaction mentioned in the section on nickel ion cell imaging was recently applied to bioimaging in zebrafish.Wang et al. synthesized the probe Ra-Ni by a nucleophilic substitution reaction between rhodamine derivatives and allyl chloride under alkaline conditions [185].The probe has the advantage of a long wavelength and high tissue permeability, making it suitable for use in live cells and zebrafish for nickel ion imaging.

Al 3+
Schiff base ligands with excellent photochemical properties enable the formulation of fluorescent probes with applications in the assay of metal ions [186].In Figure 14A, Tian et al. developed a high-sensitivity fluorescent probe [187], H3L, which is capable of sensing aluminum ions in living zebrafish, on the basis of a previously designed 2hydroxynaphthalene Schiff base compound [188].H3L exhibits blue fluorescence upon exposure to aluminum ions, concentrated in the head and digestive tract of zebrafish (Figure 14B).In particular, blue fluorescence is also observed at the pupil of zebrafish larvae due to the physiological phenomenon of aluminum ion enrichment in their eyes.This probe could be a promising platform for in vivo aluminum ion sensing owing to its high sensitivity and selectivity for the recognition and binding of aluminum ions.Subsequently, the same group improved the 2-hydroxynaphthalene Schiff base fluorescent probe on the basis of modulation in chemical structure [189].The limit of detection of aluminum ions via this fluorescent probe was enhanced by an order of magnitude (10 −8 M) and applied to the in vivo tracing of cells and zebrafish.Repr from [186] with permission from Elsevier, copyright 2018.

Conclusions and Future Directions
In conclusion, this overview highlights the latest advances in fluorescent sens metal ion detection in biological systems since 2018.Nucleic acid-based biosensor vide high recognition selectivity and flexible signal transduction mechanisms for t  [186] with permission from Elsevier, copyright 2018.

Conclusions and Future Directions
In conclusion, this overview highlights the latest advances in fluorescent sensors for metal ion detection in biological systems since 2018.Nucleic acid-based biosensors provide high recognition selectivity and flexible signal transduction mechanisms for the detection of various metal ions.Meanwhile, fluorescent protein-based biosensors are well suited for cellular and in vivo imaging.Molecular probes and chemosensors offer the advantages of cost-effectiveness, wide applicability, and ease of manipulation, making them a promising avenue for future development.Nanosensors have revolutionized the field of nanobiosensing with their desirable properties, including high sensitivity, remarkable selectivity, and biocompatibility.Additionally, combining different sensors can amplify their advantages and reduce their disadvantages.For instance, fusion of nucleic acid sensors with nanomaterials can enhance stability and specificity in vivo, and conjugation of chemical sensors with nanomaterials can simultaneously improve sensitivity and selectivity in living systems.
Despite the advances in designing fluorescence sensors for metal ion detection in biological systems, there are still challenges to overcome.The detection of a wider range of metal ions is necessary, and there is a need for more sensors for in vivo applications.Our future efforts should aim to address the need for improvement in several areas.Specifically, we must focus on improving the toolbox of fluorescent protein-based biosensors and developing more efficient NIR fluorescent proteins with deeper penetration depth, allowing for a significant enhancement of the sensitivity, resolution, and accuracy of in vivo metal ion imaging.Additionally, methods need to be developed to ensure the stability of nucleic acid-based biosensors in serum or plasma.The mechanisms of nanosensors must also be better understood, and the water solubility and sensing behavior of water-based systems for chemosensors need to be improved to better detect living systems.These directions must be pursued in parallel to overcome the challenges and improve the effectiveness of fluorescent sensors in detecting metal ions in biological systems.Although there are some difficulties in this field, based on the exciting advances made so far, we expect to develop better sensors in the future, leading to major breakthroughs in biomedical imaging of living systems.

Figure 1 .
Figure 1.Schematic representation of genetically encoded biosensors, molecular probes, chemosensors, and nanosensors.An emission turn-on response is shown as an exemplary signal response to the presence of an analyte.(A) Genetically encoded biosensors: (a) fluorescent protein-based biosensors; (b) nucleic acid-based biosensors; (B) molecular probes; (C) chemosensors; (D) nanosensors.

Figure 1 .
Figure 1.Schematic representation of genetically encoded biosensors, molecular probes, chemosensors, and nanosensors.An emission turn-on response is shown as an exemplary signal response to the presence of an analyte.(A) Genetically encoded biosensors: (a) fluorescent protein-based biosensors; (b) nucleic acid-based biosensors; (B) molecular probes; (C) chemosensors; (D) nanosensors.

Figure 2 .
Figure 2. Two representative examples of essential metal ion detection in vitro: (A) Design and performance of NaA43 DNAzyme-regulated CRISPR-Cas12a sensor for Na + detection.(B) Comparison of a DNAzyme-regulated CRISPR/Cas12a sensor with a commercial Na + meter for different Na + concentration detection in human plasma.Reproduced from [65] with permission from the American Chemical Society, copyright 2020.(C) Proposed binding mechanism of Thioflavin T on the bimolecular GQ or the tetramolecular GQ formed by oligo-3-T under the influence of K + .(D) Comparison of K + concentrations in a real urine sample measured from the sensor and the reference values obtained from the ion-selective electrode (ISE) method used by the hospital.Reproduced from [70] with permission from Elsevier, copyright 2022.

Figure 2 .
Figure 2. Two representative examples of essential metal ion detection in vitro: (A) Design and performance of NaA43 DNAzyme-regulated CRISPR-Cas12a sensor for Na + detection.(B) Comparison of a DNAzyme-regulated CRISPR/Cas12a sensor with a commercial Na + meter for different Na + concentration detection in human plasma.Reproduced from [65] with permission from the American Chemical Society, copyright 2020.(C) Proposed binding mechanism of Thioflavin T on the bimolecular GQ or the tetramolecular GQ formed by oligo-3-T under the influence of K + .(D) Comparison of K + concentrations in a real urine sample measured from the sensor and the reference values obtained from the ion-selective electrode (ISE) method used by the hospital.Reproduced from [70] with permission from Elsevier, copyright 2022.

Figure 3 .
Figure 3. Two representative examples of essential metal ion detection in vitro: (A) Schematic illustration of the Cu 2+ detection system based on click chemistry and FRET between GO-C2 and Rho-N3.(B) Detection Cu in patient urine by reading the green value of the photo of the samples using the smartphone.Reproduced from [75] with permission from John Wiley and Sons, copyright 2018.(C) Schematic illustration of the Fe 3+ detection system based on nano-structured Mg-Al layered dou-

Figure 3 .
Figure 3. Two representative examples of essential metal ion detection in vitro: (A) Schematic illustration of the Cu 2+ detection system based on click chemistry and FRET between GO-C2 and Rho-N3.(B) Detection Cu in patient urine by reading the green value of the photo of the samples using the smartphone.Reproduced from [75] with permission from John Wiley and Sons, copyright 2018.(C) Schematic illustration of the Fe 3+ detection system based on nano-structured Mg-Al layered double hydroxide intercalated with salicylic acid (Mg-Al LDH-SA).(D) The fluorescence emission spectra of the deproteinized human serum sample before (a) and after adding a standard solution of Fe 3+ (b-d).Reproduced from[18] with permission from Elsevier, copyright 2019.

Figure 4 .
Figure 4. Two representative examples of non-essential metal ion detection in vitro: (A) Illustration of the synthesis process of nitrogen-rich CDs (N-dots) and the detection of Ag + .Reproduced from [85] with permission from the Royal Society of Chemistry, copyright 2019.(B) Concept of Pb 2+ detection using a fluorescent signal-on aptamer sequence (aptaswitch).(C) Detection of Pb 2+ in biological fluids by the aptaswitch probe.Reproduced from[87] with permission from the American Chemical Society, copyright 2022.

Figure 4 .
Figure 4. Two representative examples of non-essential metal ion detection in vitro: (A) Illustration of the synthesis process of nitrogen-rich CDs (N-dots) and the detection of Ag + .Reproduced from [85] with permission from the Royal Society of Chemistry, copyright 2019.(B) Concept of Pb 2+ detection using a fluorescent signal-on aptamer sequence (aptaswitch).(C) Detection of Pb 2+ in biological fluids by the aptaswitch probe.Reproduced from[87] with permission from the American Chemical Society, copyright 2022.

Figure 5 .
Figure 5. (A) Schematic diagram shows simultaneous sensing of Hg 2+ and I − via reversible supramolecular assembly formation.(B) Titration of 1 20 μM) with Hg 2+ (0-1 ppm) in the presence of 0.1 mg/mL HSA at pH 7.0.(C) Hg 2+ induced changes in the color of paper strips (0-2 ppm) under normal daylight and UV light.Reproduced from [92] with permission from Elsevier, copyright 2021.

Figure 5 .
Figure 5. (A) Schematic diagram shows simultaneous sensing of Hg 2+ and I − via reversible supramolecular assembly formation.(B) Titration of 1 20 µM) with Hg 2+ (0-1 ppm) in the presence of 0.1 mg/mL HSA at pH 7.0.(C) Hg 2+ induced changes in the color of paper strips (0-2 ppm) under normal daylight and UV light.Reproduced from [92] with permission from Elsevier, copyright 2021.

3 , 34 Figure 6 .
Figure 6.Two representative examples of essential metal ion detection in living cells: (A) Schematic illustration of the in situ imaging of K + via the DSAP-AuNS nanosystem.(B) Confocal microscopy images of HeLa cells treated with (a) DSAP-AuNS and (b) DSAP-AuNS + NIR.Reproduced from [101] with permission from the American Chemical Society, copyright 2020.(C) Cartoon of the CSFbased semisynthetic Ca 2+ biosensor.Ca 2+ binding induces a conformational change, thereby shifting the equilibrium between red and green fluorescent forms.(D) Live cell Ca 2+ imaging with rHCaMP-8.U2OS cells expressing rHCAMP 8 and treated with ionomycin (1 μM) prior to imaging.Reproduced from [107] with permission from John Wiley and Sons, copyright 2020.

Figure 6 .
Figure 6.Two representative examples of essential metal ion detection in living cells: (A) Schematic illustration of the in situ imaging of K + via the DSAP-AuNS nanosystem.(B) Confocal microscopy images of HeLa cells treated with (a) DSAP-AuNS and (b) DSAP-AuNS + NIR.Reproduced from [101] with permission from the American Chemical Society, copyright 2020.(C) Cartoon of the CSF-based semisynthetic Ca 2+ biosensor.Ca 2+ binding induces a conformational change, thereby shifting the equilibrium between red and green fluorescent forms.(D) Live cell Ca 2+ imaging with rHCaMP-8.U2OS cells expressing rHCAMP 8 and treated with ionomycin (1 µM) prior to imaging.Reproduced from [107] with permission from John Wiley and Sons, copyright 2020.

Figure 7 .
Figure 7. Two representative examples of essential metal ion detection in living cells: (A) Schematic illustration of the intracellular imaging of Mg 2+ via KMG-500 series probes.(B) Intracellular localization of KMG-501 in the whole cell body of cultured hippocampal neurons.Reproduced from [121] with permission from the American Chemical Society, copyright 2020.(C) Schematic illustration of NS-CDs for the ratiometric response to Fe 3+ and cell membrane imaging.(D) NS-CDs for targeted cell membrane imaging.Reproduced from [128] with permission from Elsevier, copyright 2021.

Figure 7 .
Figure 7. Two representative examples of essential metal ion detection in living cells: (A) Schematic illustration of the intracellular imaging of Mg 2+ via KMG-500 series probes.(B) Intracellular localization of KMG-501 in the whole cell body of cultured hippocampal neurons.Reproduced from [121] with permission from the American Chemical Society, copyright 2020.(C) Schematic illustration of NS-CDs for the ratiometric response to Fe 3+ and cell membrane imaging.(D) NS-CDs for targeted cell membrane imaging.Reproduced from [128] with permission from Elsevier, copyright 2021.4.1.7.Fe 2+ /Fe 3+

Figure 8 .
Figure 8. (A) Design of the Li + DNAzyme catalytic beacon.Intracellular Li + imaging in neural progenitor cells of (B) healthy donors; and (C) bipolar disorder patients.Reproduced from [134] with permission from the American Chemical Society, copyright 2021.

Figure 9 .
Figure 9. Two representative examples of non-essential metal ion detection in living cells: (A) Schematic illustration of modified Broccoli.The green region indicates sequences from the original Broccoli and the C-C mismatch is highlighted in blue.(B) Confocal fluorescence imaging of the sensorexpressing BL21 (DE3) * cells.Reproduced from[136] with permission from the Royal Society of Chemistry, copyright 2019.(C) Possible process for the formation of the coordination complex and supramolecular assembling of fluorescent nanoaggregates from GSSH-2TPE and Pb 2+ .(D) Fluorescence microscopic images of living HeLa cells with GSSH-2TPE, with and without the addition of Pb 2+ .Reproduced from[144] with permission from the American Chemical Society, copyright 2019.

Figure 9 .
Figure 9. Two representative examples of non-essential metal ion detection in living cells: (A) Schematic illustration of modified Broccoli.The green region indicates sequences from the original Broccoli and the C-C mismatch is highlighted in blue.(B) Confocal fluorescence imaging of the sensor-expressing BL21 (DE3) * cells.Reproduced from [136] with permission from the Royal Society of Chemistry, copyright 2019.(C) Possible process for the formation of the coordination complex and supramolecular assembling of fluorescent nanoaggregates from GSSH-2TPE and Pb 2+ .(D)Fluorescence microscopic images of living HeLa cells with GSSH-2TPE, with and without the addition of Pb 2+ .Reproduced from[144] with permission from the American Chemical Society, copyright 2019.

Figure 10 .
Figure 10.(A) Schematic illustration of the selective detection for Pd (II) by Umb-Pd2.(B) The focal images of HeLa cells incubated with Umb-Pd2 in different conditions.Reproduced from with permission from Elsevier, copyright 2019.

Figure 10 .
Figure 10.(A) Schematic illustration of the selective detection for Pd (II) by Umb-Pd2.(B) The confocal images of HeLa cells incubated with Umb-Pd2 in different conditions.Reproduced from [149] with permission from Elsevier, copyright 2019.4.2.6.Hg 2+ Sarah et al. developed highly NIR fluorescent graphene quantum dots (GQDs) by pyrolyzing biomass-derived CBDA-2 in basic conditions [150].When treated with mercury ions, the fluorescence of GQDs was quenched.Exploiting the intramolecular charge transfer (ICT) mechanism, Duan's team introduced a new phenothiazine-based sensor[151], PHE-Ad, for monitoring Hg 2+ .With its excellent fluorescent signaling behavior and low cytotoxicity, PHE-Ad proved to be successful in detecting and imaging Hg 2+ in living cells.Furthermore, the same team reported another two novel PET fluorescent probes, CH3-R6G and CN-R6G, rationally synthesized by partial doping of rhodamine 6G fluorophore with a triazolyl benzaldehyde moiety and applied with great success for Hg 2+ imaging in breast cancer cells[152].Ding et al. reported the synthesis of ethyl 2,5-diphenyl-2H-1,2,3triazole-4-carboxylate[153], which was then introduced into rhodamine B to produce a novel derivative, REDTC.This probe exhibited remarkable selectivity for Hg 2+ through a chromogenic reaction, without interference from other metal ions.Lastly, two novel NIR monosulfide probes, MTSQ-1 and MTSQ-2, were designed and used for Hg 2+ imaging based on a mercury deuteration strategy[154].Particularly, the MTSQ-2 was packaged in a β-CD and showed excellent performance for imaging Hg 2+ in HeLa cells as well as a high signal-to-background ratio.

2023, 11 ,
x FOR PEER REVIEW 21 of 34 which in combination with NIR Förster resonance energy transfer, enables the iGECI sensors to simultaneously examine neuronal and haemodynamics in the brains of animal models via hybrid photoacoustic and fluorescent microscopy.

Figure 11 .
Figure 11.Two representative examples of essential metal ion detection in vivo: (A) Schematic showing the design of the K + nanosensor.(B) In vivo experimental scheme for K + sensing in a kindling-induced epileptic mouse model.Reproduced from [164] with permission from Springer Nature, copyright 2020.(C) Topology and in vitro characterization of mNG-GECO1 and GCaMP6s.(D) Schematic representation of the Tol2[HuC-H2B-mNG-GECO1] construct and confocal image of one fish (5-6 days post fertilization) with 7 regions of interest (ROI) circled.Reproduced from[167] with permission from the American Chemical Society, copyright 2020.

Figure 11 .
Figure 11.Two representative examples of essential metal ion detection in vivo: (A) Schematic showing the design of the K + nanosensor.(B) In vivo experimental scheme for K + sensing in a kindling-induced epileptic mouse model.Reproduced from [164] with permission from Springer Nature, copyright 2020.(C) Topology and in vitro characterization of mNG-GECO1 and GCaMP6s.(D) Schematic representation of the Tol2[HuC-H2B-mNG-GECO1] construct and confocal image of one fish (5-6 days post fertilization) with 7 regions of interest (ROI) circled.Reproduced from[167] with permission from the American Chemical Society, copyright 2020.

34 Figure 12 .
Figure 12.Two representative examples of essential metal ion detection in vivo: (A) Schematic of HIFU-activated noninvasive and spatiotemporal control of the DNAzyme-based sensor for Zn 2+ detection in vivo.(B) HIFU-activated metal-ion sensing in vivo.Whole-body fluorescence imaging of mice.Reproduced from [172] with permission from the American Chemical Society, copyright 2022.(C) Proposed sensing mechanism of the probe for the Fe 3+ -sensing event.(D) Confocal fluorescence images of zebrafish embryos (3 days old).

Figure 12 .
Figure 12.Two representative examples of essential metal ion detection in vivo: (A) Schematic of HIFU-activated noninvasive and spatiotemporal control of the DNAzyme-based sensor for Zn 2+ detection in vivo.(B) HIFU-activated metal-ion sensing in vivo.Whole-body fluorescence imaging of mice.Reproduced from [172] with permission from the American Chemical Society, copyright 2022.(C) Proposed sensing mechanism of the probe for the Fe 3+ -sensing event.(D) Confocal fluorescence images of zebrafish embryos (3 days old).

Figure 13 .
Figure 13.(A) Li + fluorescent probe (spirobenzopyrans crowned ether, SP-CE) for in vivo detection of Li + .(B) CLSM images of zebrafish treated by exogenous Li + .Reproduced from [180] with permission from Elsevier, copyright 2019.5.2.2.Pb 2+ Huang et al. designed a highly innovative DNAzyme-assembled nanosensor that can sense and image Pb 2+ at NIR light excitation [181].This nanosensor consists of UCNPs as energy transfer donor, BHQ1 quencher as energy transfer acceptor and DNAzyme as Pb 2+ specific pattern of target recognition.Following the introduction of Pb 2+ , the DNAzyme cleaves the strand of substrate at the RNA site, resulting in restoration of luminescence.Imaging data showed that when this nanosensor was micromanipulated into zebrafish embryos, it could image Pb 2+ in living cells and early zebrafish, demonstrating its remarkable potential for in vivo applications.

Figure 13 .
Figure 13.(A) Li + fluorescent probe (spirobenzopyrans crowned ether, SP-CE) for in vivo detection of Li + .(B) CLSM images of zebrafish treated by exogenous Li + .Reproduced from [180] with permission from Elsevier, copyright 2019.5.2.2.Pb 2+Huang et al. designed a highly innovative DNAzyme-assembled nanosensor that can sense and image Pb 2+ at NIR light excitation[181].This nanosensor consists of UCNPs as energy transfer donor, BHQ1 quencher as energy transfer acceptor and DNAzyme as Pb 2+ specific pattern of target recognition.Following the introduction of Pb 2+ , the DNAzyme cleaves the strand of substrate at the RNA site, resulting in restoration of luminescence.Imaging data showed that when this nanosensor was micromanipulated into zebrafish embryos, it could image Pb 2+ in living cells and early zebrafish, demonstrating its remarkable potential for in vivo applications.

Table 1 .
Normal level range of essential metal ions commonly found in biological systems.