Recent Progress in Technetium-99m-Labeled Nanoparticles for Molecular Imaging and Cancer Therapy

Nanotechnology has played a tremendous role in molecular imaging and cancer therapy. Over the last decade, scientists have worked exceptionally to translate nanomedicine into clinical practice. However, although several nanoparticle-based drugs are now clinically available, there is still a vast difference between preclinical products and clinically approved drugs. An efficient translation of preclinical results to clinical settings requires several critical studies, including a detailed, highly sensitive, pharmacokinetics and biodistribution study, and selective and efficient drug delivery to the target organ or tissue. In this context, technetium-99m (99mTc)-based radiolabeling of nanoparticles allows easy, economical, non-invasive, and whole-body in vivo tracking by the sensitive clinical imaging technique single-photon emission computed tomography (SPECT). Hence, a critical analysis of the radiolabeling strategies of potential drug delivery and therapeutic systems used to monitor results and therapeutic outcomes at the preclinical and clinical levels remains indispensable to provide maximum benefit to the patient. This review discusses up-to-date 99mTc radiolabeling strategies of a variety of important inorganic and organic nanoparticles and their application to preclinical imaging studies.


Introduction
Cancer is a considerable cause of mortality and morbidity in every region of the world, irrespective of medical facilities, human development, and scientific research. According to the GLOBOCAN survey, a total of 19.3 million new cancer cases and more than 10 million deaths from various cancer types were registered in 2020 [1]. Over the past decades, preclinical molecular biology research has provided tremendous results in the exploration of cancer at the cellular level. However, only a few experimental strategies have passed the rigorous clinical trial process to benefit cancer patients in clinics. One of the major obstacles is the lack of availability of facilities and tools to understand different molecular events inside patients [2,3]. The strong demand for the in vivo imaging of different biological events in patients has brought a revolution in molecular imaging. Molecular imaging is a single or combination of various modalities for the non-invasive visualization, characterization, monitoring, and measurement of various biological events at the cellular level in cancer patients [4]. Previously, X-rays [5], ultrasound [6], computed tomography (CT) [7], optical fluorescence [8], magnetic resources imaging (MRI) [9], singlephoton emission computed tomography (SPECT) [10], and positron emission tomography (PET) [11] have been explored for cancer diagnosis and to monitor the efficacy of ongoing treatment procedures. Preclinical and clinical data reveal that each molecular imaging system has its specific utilization, strengths, and limitations (Table 1). For instance, MRI Similarly, therapeutic drugs loaded on different platforms are being monitored using radioisotopes and multimodality imaging systems. The development of new contrast agents such as radiotracers and radiopharmaceuticals is an integral part of the success of multimodality imaging and cancer therapy. Nanotechnology can provide an excellent platform for developing novel tracers to support these hybrid multimodality imaging systems [15]. Nanomedicine has already shown excellent results in diagnostics, gene therapy, drug delivery, and other vital areas of development and clinical research [16]. Nanoparticles (NPs), essential elements of nanotechnology, are materials with an overall size of fewer than a hundred nanometers, typically smaller than human cells and comparable to the size of biomolecules such as antibodies, proteins, and receptors enzymes. Because of this distinctive feature, various well-designed NPs demonstrate long blood circulation, easy and efficient interaction with biological molecules on the target cell surface and cell pene-tration ability [17]. For instance, NPs with typical dimensions ranging from 20 to 100 nm showed enhanced permeability and retention (EPR) effects; they can accumulate at target areas closer to cancer cells. Additionally, NPs possess a high surface area to volume ratio; with this ability, they provide an excellent platform to load a variety of cancer-targeting precursors, therapeutic drugs, imaging, and therapeutic radioisotopes [18].
The radiolabeling of NPs provides a new class of radiotracers for radiotherapy, PET, or SPECT-based imaging. Radiolabeled NPs provide excellent information regarding the pharmacokinetics, biodistribution, and efficiency of the therapeutic drugs delivered to the cancer cell. Therefore, cancer treatment and imaging using radiolabeled NPs holds great potential for preclinical research and clinical applications [19]. This review discusses the current strategies and prospects of 99m Tc labeled NPs for widely available SPECT system-based imaging. This article consists of two categories. The first part describes the 99m Tc radiolabeling of inorganic nanoparticles and the second provides information on the preparation and applications of 99m Tc radiolabeled organic nanoparticles. In addition, the main focus of discussion is radiolabeling strategy and surface modifications, and their impact on the stability and pharmacokinetics of radiolabeled products.

Radiolabeling of Nanomaterials
A variety of radiolabeled nanoparticles have been developed as useful radiotracers, and these materials, such as gamma camera or SPECT imaging (Indium-111, Technetium-99m, Iodine-125, etc.), PET imaging (Flourine-18, Zirconium-89, Copper-64, Gallium-68, etc.), radioisotope therapy (Copper-67, Lutetium-177, Astatine-211, Actinium-225, Yitrium-90, etc.) and dual modality imaging have been applied to nuclear medicine. The selection of an appropriate nanomaterial, radioisotope and radiolabeling strategy depends upon the intended medical application. To introduce a radioisotope to a functional nanomaterial, several methodologies were developed and used in preclinical studies. The surface modifications of a nanomaterial and radiolabeling strategies have great impact on the stability of a radiotracer and its pharmacokinetics in vivo. Herein, technitium-99m, one of the most widely used radioisotope in the field of nuclear medicine has been selected for detailed discussion.

Technetium-99m ( 99m Tc) Properties and Production
After the introduction of positron emission tomography (PET), it was assumed that the more advanced technology would have replaced the old SPECT technology and SPECTbased radiopharmaceuticals. Interestingly, technetium-99m ( 99m Tc)-based radiopharmaceutical production continues, and the number of clinical examinations using 99m Tc and SPECT is still greater than those using PET-based molecular imaging [20]. Despite its great success, PET is still a relatively expensive technology, and the production and radiolabeling of PET radioisotopes are cumbersome tasks in some developing nations. Therefore, 99m Tc is a globally recognized radioisotope, and a major component of day-to-day nuclear imaging procedures. There are many reasons behind this success, such as the low cost and straightforwardness of SPECT procedures, the easy availability of 99m Tc in the form of 99 Mo/ 99m Tc generators, and the worldwide commercial availability of 99m Tc labeling kits. Moreover, its distinguished nuclear properties include a suitable half-life (6.0 h), isomeric decay to a ground state, monochromatic gamma-ray emission (140.5 keV, 98.5%), highly stable coordination chemistry, and high-quality SPECT images make it an ideal radioisotope in the field of nuclear medicine [21]. 99m Tc is eluted from 99 Mo/ 99m Tc generators in the form of pertechnetate (TcO 4 − ), and this is the best strategy to obtain 99m Tc in the clinic. 99 Mo is mainly produced in research reactors by irradiating molybdenum oxide or metallic molybdenum, or by irradiating uranium-235 with thermal or fast neutrons. During a fission reaction, 99 Mo is obtained with other fission products as impurities, and many radiation shielding and purification steps are required to obtain pure parent radionuclide. However, little processing is required for the conversion of 98 Mo to 99 Mo. In a typical  Figure 1) has demonstrated, valuable results at the preclinical and clinical levels.

Inorganic Nanoparticles
Inorganic NPs such as iron oxide, gold, silver copper, cobalt, titanium, silica, manganese gadolinium, quantum dots, and silicon have been extensively used in nanomedicine. Inorganic NPs possess unique size and material-dependent physiochemical properties which are not available in other traditional polymer and lipidbased NPs. Moreover, some unique features such as size-controlled synthesis, easy surface functionalization, and in vitro and in vivo stability in various media make inorganic NPs an excellent platform to synthesize multimodality imaging and therapeutic agents. 99m Tc-radiolabeled nanoparticles are summarized in Table 2.

Iron Oxide Nanoparticles
Iron oxide NPs are classified into three categories depending upon size, such as monocrystalline iron oxide (10-30 nm), ultra-small superparamagnetic iron oxide (5-10 nm), and standard superparamagnetic iron oxide (60-150 nm). Among these iron oxide NPs, standard superparamagnetic iron oxide has been extensively used because of some unique biocompatibility, facile surface functionalization, and enhanced magnetic contrast [26]. Standard superparamagnetic iron oxide NPs can become trapped in the reticuloendothelial system through phagocytosis or endocytosis. However, standard superparamagnetic iron oxide NPs are not harmful to the human body, and can be dissolved under acidic conditions. The resulting iron can be retained in the human body, which has enough iron storage capacity (3-5 g per human adult). Moreover, the toxicity

Inorganic Nanoparticles
Inorganic NPs such as iron oxide, gold, silver copper, cobalt, titanium, silica, manganese gadolinium, quantum dots, and silicon have been extensively used in nanomedicine. Inorganic NPs possess unique size and material-dependent physiochemical properties which are not available in other traditional polymer and lipid-based NPs. Moreover, some unique features such as size-controlled synthesis, easy surface functionalization, and in vitro and in vivo stability in various media make inorganic NPs an excellent platform to synthesize multimodality imaging and therapeutic agents. 99m Tc-radiolabeled nanoparticles are summarized in Table 2.

Iron Oxide Nanoparticles
Iron oxide NPs are classified into three categories depending upon size, such as monocrystalline iron oxide (10-30 nm), ultra-small superparamagnetic iron oxide (5-10 nm), and standard superparamagnetic iron oxide (60-150 nm). Among these iron oxide NPs, standard superparamagnetic iron oxide has been extensively used because of some unique biocompatibility, facile surface functionalization, and enhanced magnetic contrast [26]. Standard superparamagnetic iron oxide NPs can become trapped in the reticuloendothelial system through phagocytosis or endocytosis. However, standard superparamagnetic iron oxide NPs are not harmful to the human body, and can be dissolved under acidic conditions. The resulting iron can be retained in the human body, which has enough iron storage capacity (3-5 g per human adult). Moreover, the toxicity of iron oxide NPs can be avoided by using an organic coating such as synthetic polymers, dextran, or other biocompatible materials. Iron oxide NPs based on single or dual imaging are further coated with tumor-specific biomolecules to increase target accumulation. In the hyperthermia treatment procedure, iron oxide NPs are introduced inside a body and an alternative magnetic field is applied near the tumor area after enough iron oxide NPs have been introduces. The NPs convert magnetic energy into heat energy to damage the cancer cell. In order to assess the efficiency of the hyperthermia procedure, iron oxide NPs were radiolabeled with 99m Tc to confirm maximum accumulation at the tumor area. In a typical procedure, the iron oxide NPs were treated with 99m TcO 4 − in the presence of tetrahydroborate exchange resin as a reducing agent. The 99m Tc was incorporated on the surface of iron oxide NPs via a redox reaction. The radiolabeled NPs showed high in vitro stability. However, the radiolabeled NPs were not subjected to in vivo testing [27]. 99m TcO 4 − does not form a complex with iron oxide NPs in the absence of a reducing agent. Interestingly, a minute amount of stannous chloride dehydrate is enough to reduce pertechnetate to the lower oxidation state and form a stable complex with iron oxide NPs. Stannous chloride-mediated 99m Tc labeled iron oxide demonstrated high stability under physiological conditions, and maximum radioactivity was observed in the liver. In 2009, 99m Tc labeled superparamagnetic iron oxide NPs were synthesized for the dual (magnetic resonance and SPECT) imaging of hepatocytes. The superparamagnetic iron oxide NPs were synthesized, and the surface modification was performed using dopamine. The dopamine arm was used to attach lactobionic acid to the target hepatocyte receptor and 2-(4-Isothiocyanatobenzyl)-diethylenetriamine-pentaacetic acid (DTPA) as 99m Tc chelator ( Figure 2). The lactobionic acid on the surface of the iron oxide NPs efficiently targets hepatocyte receptors in the liver. Both magnetic resonance and SPECT showed high accumulation of the tracer in the target area. The images showed high spatial resolution and sensitivity in the final results. The biodistribution results supported the image data and confirmed that the probe could be used as a dual imaging agent against liver diseases [28]. Iron oxide is an excellent platform for drug loading, and radioisotopes provide an excellent NP surface coating material. Poor surface coating sometimes results in the decomposition of the complex over time, and loss of both the drug and the radioisotope. The literature reveals that phosphonates, monosulfonates, monocarboxylates, citrates, and catechol can form a stable coating on the surface of iron oxide NPs. However, it has been observed that the redox reaction of catechol under a protic environment leads to the precipitation and decomposition of NPs. Interestingly, the development of biocompatible, nonpolymeric methods, such as bisphosphonate-based coating of iron oxide NPs, provides a solution. Recently, a clinically approved magnetic resonance imaging superparamagnetic iron oxide (Endorem) was coated with bisphosphonate chelator (Figure 2). A 99m Tc tricarbonyl kit was used to synthesize radiolabeled Endorem. Initially, the bisphosphonate chelator was radiolabeled with 99m Tc in high radiochemical yield (>95%) and radiochemical purity. In the next step, a 99m Tc chelator was incorporated on the surface of Endorem at elevated temperature. 99m Tc radiolabeled NPs were obtained via bisphosphonate binding on the surface of NPs. The radiolabeled NPs showed excellent in vivo and in vitro stabilities. SPECT/CT and magnetic resonance imaging simultaneously confirmed the presence of tracer, predominantly in the liver and spleen. This dual imaging agent provided magnetic resonance imaging with high spatial resolution, and at the same time, the SPECT/CT data provided crucial quantitative information [29]. The surface modification of iron oxide NPs plays a vital role in reducing toxicity under physiological conditions. Surface coating with biocompatible materials such as aspartic acid, dextran, polyethylene glycol, and dimercaptosuccinic acid (DMSA) increases cell entrance and decreases the toxicity effects. The 99m Tc radiolabeling of DMSA coated iron oxide NPs demonstrated interesting results [30]. DMSA provides an anionic coating on the surface of NPs, which prevents the aggregation of blood proteins on the surface of NPs. Additionally, it increased cell absorption and decreased the removal of NPs by the reticuloendothelial system. The DMSA-based radiolabeling of NPs provided better in vitro and in vivo stability, minimum toxicity, and efficient quantitative information regarding the accumulation of iron oxide NPs in the liver and spleen. Iron oxide NPs have shown great potential for treating liver diseases. Additionally, they provide an excellent platform by which to install tumor-specific biomolecules. Recently, c(RGDyC) peptide-installed iron oxide NPs were synthesized to target α v β 3 -positive tumor cells and tumor angiogenesis. In addition, iron oxide NPs were also radiolabeled with 99m Tc to make a dual-modal SPECT/MRI imaging agent ( 99m Tc-SPION-RGD). NH 2 PEG-modified iron oxide NPs were sequentially treated with c(RGDyC) peptide, the chelating agent DTPA and 99m Tc to synthesize 99m Tc-SPION-RGD ( Figure 3). 99m Tc-SPION-RGD showed excellent in vivo and in vitro selectivity towards H1299 α v β 3 -positive cells. Moreover, radiolabeled NPs provided MRI images with high spatial resolution. SPECT images provided quantitative data for liver uptake. 99m Tc radiolabeled iron oxide NPs have become an irreplaceable emerging tracer for dual imaging, and research is being conducted to improve image quality and sensitivity [31]. The in vivo aggregation of NPs has been exploited to improve image sensitivity. In vivo aggregation of NPs has some clear advantages, such as low dose of contrast agent, prolonged retention of tracers at the tumor site, and an enhanced T 2 effect that improves MRI image quality. c(RGDyC)-installed, glutathione (GSH) sensitive 99m Tc-labeled iron oxide NPs have been synthesized. The aggregation of NPs was observed due to the presence of GSH in the tumor microenvironment. The in vivo aggregation of the tracer improved the sensitivity of MRI and SPECT images. The results were threefold better than normal c(RGDyC) containing iron oxide NPs [32]. Although iron oxide NPs are the most widely used drug carriers due to their biocompatibility, researchers have also attempted other combinations to synthesize superparamagnetic NPs. Recently, cobalt ferrite (CoFe 2 O 4 ) NPs were radiolabeled with 99m Tc to explore their biodistribution and pharmacokinetics. In this study, in vitro and in vivo stabilities, biodistribution, and SPECT images of 99m Tc labeled Fe 3 O 4 and CoFe 2 O 4 were compared in normal mice. Direct radiolabeling of both hybrid NPs provided highly stable radiolabeled tracers with high radiolabeling yield and purity. Interestingly, both NPs had nearly similar biodistribution profiles. A high accumulation of radiotracers was observed in the liver and spleen [33]. Similarly, in 2015, R. Alberto et al. described the synthesis, 99m Tc radiolabeling, and in vitro stability of Au-Fe 3 O 4 NPs (core-shell and dumbbell) [24].

Gold Nanoparticles
Gold nanoparticle (AuNPs)-based contrast agents (MRI or CT) and imaging agents (PET or SPECT) have been extensively studied because of their unique properties, such as surface passivation, simple surface modification, optical properties, and biocompatibility. The first AuNP-based radiotracer was reported in 2004. Over the next decade, comprehensive investigations were performed to optimize radiolabeling procedures, surface chemistry, and pharmacokinetics studies [34]. The surface modification of NPs using tumor-specific peptides can increase image sensitivity. These therapeutic or imaging peptides can target over-expressed peptide receptors in the tumor cells. The overexpressed receptors on the surfaces of cancerous cells represent promising targets for diagnosis or therapy. (GRP-r), the peptide receptor that releases gastrin, is overexpressed in prostate cancer, breast, and metastatic lymph nodes, while a peptide Lys 3 -bombesin binds with GRP-r in high affinity. A multifunctional system was developed, comprised of 20 nm AuNPs having conjugation with Lys 3 -bombesin and HYNIC-Gly-Gly-Cys-NH2 [HYNIC (hydrazinonicotinamide), GGC(Gly-Gly-Cys) peptide] and radiolabeled with 99m Tc. In this multi-model system, HYNIC served as a 99m Tc chelator with a -Gly-Glyspacer, and interactions with the AuNP surfaces were developed by a -Cys-NH2functinal group ( Figure 4). TEM images and spectroscopic techniques reflected the interaction and successful binding of AuNPs with peptide and Lys 3 -bombesin. Afterwards, 99m Tc radiolabeling was successfully performed via the HYNIC-GGC ligand by employing the co-ligands EDDA/tricine and SnCl2, and a radio-chromatogram confirmed more than 95% radiochemical purity. In vitro studies revealed that for overexpressed GRP-rin PC-3 cells, 99m Tc-AuNP-Lys 3 -bombesin exhibits higher specificity with 71% enhanced cellular uptake compared 99m Tc-AuNPs, while in vivo SPECT/CT imaging of this novel multifunctional system displayed tumor uptake of 6.39% ± 0.83% IA/g at one h with significant uptake by spleen and liver. However, the inability of 99m Tc-AuNP-Lys 3 -bombesin to cross narrow blood vessels resulted in significant accumulation in cancerous cells [35]. As per the sentinel lymph node (SLN) concept, this node or its groups are drain cancer. In the light

Gold Nanoparticles
Gold nanoparticle (AuNPs)-based contrast agents (MRI or CT) and imaging agents (PET or SPECT) have been extensively studied because of their unique properties, such as surface passivation, simple surface modification, optical properties, and biocompatibility. The first AuNP-based radiotracer was reported in 2004. Over the next decade, comprehensive investigations were performed to optimize radiolabeling procedures, surface chemistry, and pharmacokinetics studies [34]. The surface modification of NPs using tumor-specific peptides can increase image sensitivity. These therapeutic or imaging peptides can target over-expressed peptide receptors in the tumor cells. The over-expressed receptors on the surfaces of cancerous cells represent promising targets for diagnosis or therapy. (GRPr), the peptide receptor that releases gastrin, is overexpressed in prostate cancer, breast, and metastatic lymph nodes, while a peptide Lys 3 -bombesin binds with GRP-r in high affinity. A multifunctional system was developed, comprised of 20 nm AuNPs having conjugation with Lys 3 -bombesin and HYNIC-Gly-Gly-Cys-NH 2 [HYNIC (hydrazinonicotinamide), GGC(Gly-Gly-Cys) peptide] and radiolabeled with 99m Tc. In this multi-model system, HYNIC served as a 99m Tc chelator with a -Gly-Gly-spacer, and interactions with the AuNP surfaces were developed by a -Cys-NH 2 functinal group ( Figure 4). TEM images and spectroscopic techniques reflected the interaction and successful binding of AuNPs with peptide and Lys 3 -bombesin. Afterwards, 99m Tc radiolabeling was successfully performed via the HYNIC-GGC ligand by employing the co-ligands EDDA/tricine and SnCl 2, and a radio-chromatogram confirmed more than 95% radiochemical purity. In vitro studies revealed that for overexpressed GRP-rin PC-3 cells, 99m Tc-AuNP-Lys 3 -bombesin exhibits higher specificity with 71% enhanced cellular uptake compared 99m Tc-AuNPs, while in vivo SPECT/CT imaging of this novel multifunctional system displayed tumor uptake of 6.39 ± 0.83% IA/g at one h with significant uptake by spleen and liver. However, the inability of 99m Tc-AuNP-Lys 3 -bombesin to cross narrow blood vessels resulted in significant accumulation in cancerous cells [35]. As per the sentinel lymph node (SLN) concept, this node or its groups are drain cancer. In the light of the above assumption, a cancer-free sentinel node is a strong indication of the non-spreading of the tumor. So, the design of a radiolabeled drug composed of 99m Tc based colloids with a size of less than 100 nm with the hydrazinonicotinamide (HYNIC) chelator is a practical approach for peptide radiolabeling to attain enhanced specificity and favorable pharmacokinetics, making such a system a potential imaging tool. A multifunctional model of 99m Tc-labeled AuNPs was stated in which the average size of AuNPs was around 20 nm. In this design, HYNIC served as a 99m Tc chelator, and interactions with the surface of AuNPs were developed with Cys-NH 2 via a spacer (-Gly-Gly-). Afterward, two radiolabeled conjugates: (i) 99m Tc-EDDA/HYNIC-GGC-AuNP ( 99m Tc-AuNP) and (ii) 99m Tc-EDDA/HYNIC-GGC-AuNP mannose ( 99m Tc-AuNP-mannose) were prepared, and a radio-chromatogram confirmed more than 95% radiochemical purity. TEM images and spectroscopic techniques mirrored the interaction and successful binding of AuNPs with the peptide and the mannose. In vitro studies showed a 40% higher uptake of 99m Tc-AuNP-mannose compared to 99m Tc-AuNP. Moreover, in vivo studies also reflect enhanced uptake of 99m Tc-AuNP-mannose by the first lymphatic node (11.58 ± 1.98% ID at 1 h) compared to 99m Tc-AuNP (4.28 ± 1.49% ID at 1 h), thus confirming the specificity and targeted binding of 99m Tc-AuNP-mannose with overexpressed mannose receptors with minimum accumulation in the kidney and insignificant uptake by other tissues. Moreover, the clearance constant (λ) was found to be 0.1527 ± 0.0086 h −1 and 0.1405 ± 0.0047 h −1 for 99m Tc-AuNP-mannose and 99m Tc-AuNP, respectively [36].
Nanomaterials 2021, 11, x FOR PEER REVIEW 9 of 29 of the above assumption, a cancer-free sentinel node is a strong indication of the nonspreading of the tumor. So, the design of a radiolabeled drug composed of 99m Tc based colloids with a size of less than 100 nm with the hydrazinonicotinamide (HYNIC) chelator is a practical approach for peptide radiolabeling to attain enhanced specificity and favorable pharmacokinetics, making such a system a potential imaging tool. A multifunctional model of 99m Tc-labeled AuNPs was stated in which the average size of AuNPs was around 20 nm. In this design, HYNIC served as a 99m Tc chelator, and interactions with the surface of AuNPs were developed with Cys-NH2 via a spacer (-Gly-Gly-). Afterward, two radiolabeled conjugates: (i) 99m Tc-EDDA/HYNIC-GGC-AuNP ( 99m Tc-AuNP) and (ii) 99m Tc-EDDA/HYNIC-GGC-AuNP mannose ( 99m Tc-AuNP-mannose) were prepared, and a radio-chromatogram confirmed more than 95% radiochemical purity. TEM images and spectroscopic techniques mirrored the interaction and successful binding of AuNPs with the peptide and the mannose. In vitro studies showed a 40% higher uptake of 99m Tc-AuNP-mannose compared to 99m Tc-AuNP. Moreover, in vivo studies also reflect enhanced uptake of 99m Tc-AuNP-mannose by the first lymphatic node (11.58% ± 1.98% ID at 1 h) compared to 99m Tc-AuNP (4.28% ± 1.49% ID at 1 h), thus confirming the specificity and targeted binding of 99m Tc-AuNP-mannose with overexpressed mannose receptors with minimum accumulation in the kidney and insignificant uptake by other tissues. Moreover, the clearance constant (λ) was found to be 0.1527 ± 0.0086 h −1 and 0.1405 ± 0.0047 h −1 for 99m Tc-AuNP-mannose and 99m Tc-AuNP, respectively [36]. The angiogenesis process involves the sprouting of existing vessels, followed by the growth of new blood vessels. Thus, it is considered to be the prerequisite for the growth of tumors and metastasis. Overall, this process is controlled by integrins, also known as cell adhesion receptors. On the surface of normal endothelial cells, αvβ3 integrin is barely expressed, but it tends to obtain overexpressed at tumor sites. Arg-Gly-Asp (RGD)-based The angiogenesis process involves the sprouting of existing vessels, followed by the growth of new blood vessels. Thus, it is considered to be the prerequisite for the growth of tumors and metastasis. Overall, this process is controlled by integrins, also known as cell adhesion receptors. On the surface of normal endothelial cells, α v β 3 integrin is barely expressed, but it tends to obtain overexpressed at tumor sites. Arg-Gly-Asp (RGD)-based radiolabeled peptides, particularly with a cyclic RGD (cRGD) sequence, possess selectivity and strong affinity for the α v β 3 integrin, owing to enhanced multivalent sites, thus, making them potentially a radiopharmaceutical for imaging techniques involving non-invasive tumor angiogenesis monitoring. Following this key point, a system of 99m Tc-labeled AuNPs was developed in which the average size of AuNPs was found to be around 20 nm followed by conjugation to two peptides, HYNIC-GGC and cyclic[Arg-Gly-Asp-Phe-Lys(Cys)] {c[RGDfK(C)]}. The 99m Tc labeled peptides HYNIC-GGC and c[RGDfK(C)] were prepared then added to a AuNPs solution (AuNPs/HYNIC-GGC:AuNPs/c[RGDfK(C)] = 1:1250) to yield HYNIC-GGC-AuNP-c[RGDfK(C)] via interactions between -Cys-functionality and the AuNPs' surfaces. Afterwards, 99m Tc-AuNP-RGD ( 99m Tc-EDDA/HYNIC-GGC-AuNPc[RGDfK-(C)]) and 99m Tc-AuNP ( 99m Tc-EDDA/HYNIC-GGC-AuNP) with radiochemical purity of 96 ± 2% were found. TEM and spectroscopic techniques confirmed the successful functionalization of AuNPs with peptides via the thiol moiety. In human serum, 99m Tc-AuNP-RGD showed stability for more than 24 h, and in vitro studies in C6 cells confirmed the recognition of α v β 3 integrins with cellular uptake 2.3 times higher than 99m Tc-AuNP. Micro-SPECT/CT imaging for 99m Tc-AuNP-RGD also reflected higher tumor uptake than 99m Tc-AuNP, making it a potential imaging tool for positive α v β 3 patients. Moreover, the administration mode of the drug (either i.p. or i.v.) was found to significantly affect uptake by liver and spleen, which is decreased by switching administration mode from i.v. to i.p. [37]. The surface of cells' reversible and strong binding between receptors and peptides is governed by the key principle of multivalency that assists in regulating numerous cellular activities. Hence, to achieve a target specified molecular recognition with a stable and biocompatible multimeric system, conjugation between AuNPs and peptides is a well-known strategy. Along this line, receptor-specific multimeric systems for kit formulation were prepared by employing 99m Tc labeled AuNPs followed by conjugation with either Lys 3 -bombesin, thiol-mannose or cyclo[Arg-Gly-Asp-D-Phe-Lys-(Cys)] c[RDGfK(C)] with radiochemical purity of 96 ± 2%. All three radiopharmaceuticals, 99m Tc-AuNP-Lys 3 -bombesin, 99m Tc-AuNP-mannose and 99m Tc-AuNP-c[RDGfK(C)] were found to exhibit suitable properties for be employment as potential target-specific agents for the molecular imaging of GRP-r-positive tumors, SLN detection, and tumor α v β 3 expression, respectively. For GRP-r and α v β 3 positive cells, 99m Tc-AuNP-Lys 3 -bombesin and 99m Tc-AuNP-c[RGDfK(C)] uptake were 1.8 and 2.2 times higher than 99m Tc-AuNP, respectively. Moreover, the kit showed excellent stability for six months when kept at 48 • C [38]. Bombesin and c[RGDfK(C)]-decorated AuNPs demonstrated excellent in vitro and in vivo results; however, these tracers are constrained in the cell membrane and cytoplasm. HIV Tat (49)(50)(51)(52)(53)(54)(55)(56)(57) peptide can penetrate the cell and reach the DNA. Moreover, a combined bombesin and Tat (49)(50)(51)(52)(53)(54)(55)(56)(57) peptide-based 99m Tc-labeled radiotracer showed an ability to penetrate prostate and breast cancer cells. Owing to their large surface area, AuNPs were decorated with bombesin and Tat (49)(50)(51)(52)(53)(54)(55)(56)(57) peptides to increase the stability of peptides and the retention time of the tracer near the cell microenvironment. The tracer was further radiolabeled with 177 Lu via a DOTA chelator for radiotherapy of the cancer cell. An additional HYNIC chelator was incorporated for 99m Tc radiolabeling and in vivo monitoring of the radiotracer. The radiotracer was initially tested against PC3 human cancer cells to provide in vitro plasmonic photothermal therapy and targeted radiotherapy. The radiotracer showed specific accumulation in PC3 cells, which was 52.5% higher than 99m Tc radiolabeled AuNPs. Plasmonic photothermal therapy significantly reduced PC3 cell viability. Similarly, combined plasmonic photothermal and radiotherapy inhibited PC3 cell proliferation significantly more than AuNPs alone [39]. The radiolabeling of AuNPs largely depends upon the type of carrier system. A suitable carrier system not only provides radiolabeling stability but also influences the pharmacokinetics of the tracer. Organic macromolecules such as poly (amidoamine) (PAMAM) dendrimers with appropriate monodispersity are an excellent carrier upon which to load imaging agents. Dendrimer-stabilized AuNPs serve as a CT contrast agent for blood pool or tumor imaging. Recently, dendrimer-stabilized, folic acid-containing gold nanoparticles were radiolabeled with 99m Tc to obtain dual SPECT/CT imaging. The DTPA chelator was attached to the PAMAM dendrimer for the stable radiolabeling of gold nanoparticles. In an in vitro ex-periment, the radiotracer({(Au 0 ) 6 -G2-DTPA( 99m Tc)-mPEG} DENPs) showed high uptake in HeLa-LFAR cells. CT images showed contrast enhancement, and at the same time, SPECT images were obtained with high sensitivity ( Figure 5). For in vivo experiments, the radiotracer was intravenously injected into the xenografted tumor model. High tumor uptake was observed. Moreover, high radioactivity was found in the liver and spleen due to RES clearance. The radiotracer was retained in the tumor for more than 24 h [40]. for blood pool or tumor imaging. Recently, dendrimer-stabilized, folic acid-containing gold nanoparticles were radiolabeled with 99m Tc to obtain dual SPECT/CT imaging. The DTPA chelator was attached to the PAMAM dendrimer for the stable radiolabeling of gold nanoparticles. In an in vitro experiment, the radiotracer({(Au 0 )6-G2-DTPA( 99m Tc)-mPEG} DENPs) showed high uptake in HeLa-LFAR cells. CT images showed contrast enhancement, and at the same time, SPECT images were obtained with high sensitivity ( Figure 5). For in vivo experiments, the radiotracer was intravenously injected into the xenografted tumor model. High tumor uptake was observed. Moreover, high radioactivity was found in the liver and spleen due to RES clearance. The radiotracer was retained in the tumor for more than 24 h [40]. Resveratrol (Res) is a well-known phenolic compound owing to its cancer prevention and antioxidant properties which, upon tagging with a radionuclide, help it serve as a tumor locator. However, the presence of polyphenol aids fast and extensive metabolism making its bioavailability significantly lower in vivo. To overcome this limitation, Res was successfully loaded on AuNPs, and the resulting Res-AuNP exhibited excellent in vitro stability for a period of 48 h and 720 h at 37 °C and 48 °C, respectively. Moreover, at a pH of 7, drug release in PBS was found to be abrupt for the initial 1 h. Afterward, Res-AuNPs were successfully labeled with 99m Tc with greater than 95% labeling efficiency with enhanced shelf life. For HT29 cells, both 99m Tc-Res-AuNP and 99m Tc-AuNP systems showed cell viability above 70%, while cellular uptake was significantly higher for 99m Tc-Res-AuNP during the initial 3 h and was retained afterward, as demonstrated by boosted in vivo targetability and major accumulation in liver, spleen, and kidney. Thus, for 99m Tc-Res-AuNPs, high active uptake and enhanced retention ability in cancer cells made them suitable for in vivo cancer imaging [41]. Hepatic carcinoma, which typically develops after chronic liver disease, is the fifth most common cancer type and the third greatest major death cause worldwide [42]. Therefore, developing an NP system with multiple imaging elements and targeting groups is crucial to achieving precise and accurate imaging. One Resveratrol (Res) is a well-known phenolic compound owing to its cancer prevention and antioxidant properties which, upon tagging with a radionuclide, help it serve as a tumor locator. However, the presence of polyphenol aids fast and extensive metabolism making its bioavailability significantly lower in vivo. To overcome this limitation, Res was successfully loaded on AuNPs, and the resulting Res-AuNP exhibited excellent in vitro stability for a period of 48 h and 720 h at 37 • C and 48 • C, respectively. Moreover, at a pH of 7, drug release in PBS was found to be abrupt for the initial 1 h. Afterward, Res-AuNPs were successfully labeled with 99m Tc with greater than 95% labeling efficiency with enhanced shelf life. For HT29 cells, both 99m Tc-Res-AuNP and 99m Tc-AuNP systems showed cell viability above 70%, while cellular uptake was significantly higher for 99m Tc-Res-AuNP during the initial 3 h and was retained afterward, as demonstrated by boosted in vivo targetability and major accumulation in liver, spleen, and kidney. Thus, for 99m Tc-Res-AuNPs, high active uptake and enhanced retention ability in cancer cells made them suitable for in vivo cancer imaging [41]. Hepatic carcinoma, which typically develops after chronic liver disease, is the fifth most common cancer type and the third greatest major death cause worldwide [42]. Therefore, developing an NP system with multiple imaging elements and targeting groups is crucial to achieving precise and accurate imaging. One approach is to employ a PEI that shows excellent water solubility, due to various amine groups, which can be utilized for drug loading or coating NPs. A PEI surface was modified with DTPA, PEG, and RGD(RGD-Au PENPs), followed by entrapping AuNPs and 99m Tc labeling to develop RGD-99m Tc Au PENPs with 99% radiochemical purity [43]. RGD-Au PENPs exhibited higher a CT value, cytocompatibility (for CCK-8 assay), and presence of RGD-developed specific targeting of overexpressed α v β 3 integrin in vitro, featuring enhanced cellular uptake with major accumulation in the liver and spleen. SPECT imaging with the RGD-99m Tc Au PENPs reflected an intense signal of hepatic carcinoma compared to the unlabeled counterpart that was in good agreement with CT profile, thus making the designed system a potential candidate for SPECT/CT dual imaging. Although SPECT/CT integration is a well-known strategy for tumor imaging and anatomical monitoring, one a recently explored approach is the development of a suitable radiolabeled dendrimer-based NP system with several advantages, such as exceptionally high circulation time in blood, and controlled in vivo behavior.
Furthermore, the surface functionalization of a dendrimer-based AuNPs (Au DENPs) system with duramycin leads to a biodistribution profile. Hence, after chemotherapy, successful monitoring of tumor apoptosis can continue. The surface of G5.NH 2 was successfully modified with DOTA, PEG-duramycin, modified mPEG, and fluorescein isothiocyanate (FI) to develop the template of multifunctional dendrimers that serve to entrap AuNPs radiolabeled with 99m Tc (Figure 6). The DOTA chelator provided high radiochemical stability above 99%. A comparative analysis of Au DENPs and duramycin Au DENPs in C6 cells confirmed higher fluorescence intensity and twice the contrast enhancement with duramycin Au DENPs [44]. After radiolabeling, 99m Tc-duramycin Au DENPs revealed similar trends, with 5.8 times more intense and brighter SPECT images than 99m Tc-Au DENPs. In vivo studies also confirm the high uptake of 99m Tc-duramycin Au DENPs, with major accumulation in the liver and spleen without damaging any organ, thus confirming the developed system was biofriendly and useful for the early monitoring of apoptosis. DENPs in blood. The diffusion rate of 99m Tc-Au-Gly DENPs was greater than that of 99m Tc-Au-Ac DENPs, which was attributed to the lesser hydrodynamic size of the 99m Tc-Au-Gly DENPs. However, HU values indicated a balancing the diffusion rate of both DENPs after 4 h post-injection, and both Au DENPs took 168 h to be cleared from the body. The developed 99m Tc-labeled Au DENPs with various surface functionalities are considered to be a potential contrast agent for LSN SPECT/CT imaging [46].

Silica Nanoparticles
Silica NPs, particularly mesoporous silica NPs, have shown their potential as drug carriers. Their unique structure, chemical stability, biocompatibility, and surface functionalization enable the delivery and the controlled release of various pharmaceuticals. Mesoporous silica NPs have a rigid structure with porous morphology and large surface area, enabling the attachment of various drugs, tumor targeting peptides and proteins, functional groups, chelators, and radioisotopes [47]. Soon after their discovery, mesoporous silica NPs were modified with a variety of drugs and Imaging accuracy and sensitivity are greatly dependent on NPs uptake by tumors, and the most common approach in this regard is the surface modification of NPs to de-velop significant electrostatic interaction between NPs and cell membranes. Following this critical point, a polyethyleneimine (PEI) surface was successfully and sequentially modified by mPEG-COOH, MAL-PEG-SVA (MAL = maleimide, SVA = succinimidylvalerate), DTPA, FI (fluorescein isothiocyanate) followed by entrapping AuNPs, conjugation with alkoxyphenylacylsulfonamide (APAS), and acetylation to yield APAS-Au PENs NPs that were stable, cytocompatible up to 50 • C for 7 days and showed more cellular internalization. Finally, 99m Tc labeling was performed to obtain APAS-99m Tc-AuPENs with radiochemical purity above 95%. PEI led to the successful entrapping of AuNPs, while APAS modification developed pH-responsive charge transformation (neutral charge without APAS) [45] in the resulting NPs that increased cellular uptake (a pH of 5.5), leading to enhanced SPECT/CT imaging. Moreover, for the same radionuclide dose, SPECT intensity was stronger for APAS-99m Tc-Au PENs than for APAS-Au PENs. A novel strategy for SPECT/CT imaging was developed by Wen et al., employing poly(amidoamine) dendrimer (a generation 5 dendrimer, G5-NH 2 ) as a template for the synthesis of AuNPs. To obtain the desired biodistribution profile, the amine group of dendrimers was functionalized with hydroxyl (-OH) and acetyl group (-Ac) via hydroxylation and acetylation followed by surface modification dendrimer. Similarly, the DTPA chelator was used to obtain 99m Tc-Au-Gly DENPs and 99m Tc-Au-Ac DENPs, respectively (Figure 7). 99m Tc-Au DENPs exhibit colloidal stability, radio stability, cytocompatibility, and non-toxicity. The -OH or -Ac functionalization led to different aggregation in aqueous solution, as indicated by their SPR peaks at 510 nm and 530 nm, respectively. Moreover, different surface functionalities also led to a unique in vivo profile, with major accumulation of both -OH and -Ac-functionalized NPs in the liver accompanied by major detection of 99m Tc-Au-Ac DENPs in the lungs and 99m Tc-Au-Gly DENPs in blood. The diffusion rate of 99m Tc-Au-Gly DENPs was greater than that of 99m Tc-Au-Ac DENPs, which was attributed to the lesser hydrodynamic size of the 99m Tc-Au-Gly DENPs. However, HU values indicated a balancing the diffusion rate of both DENPs after 4 h post-injection, and both Au DENPs took 168 h to be cleared from the body. The developed 99m Tc-labeled Au DENPs with various surface functionalities are considered to be a potential contrast agent for LSN SPECT/CT imaging [46].

Silica Nanoparticles
Silica NPs, particularly mesoporous silica NPs, have shown their potential as drug carriers. Their unique structure, chemical stability, biocompatibility, and surface functionalization enable the delivery and the controlled release of various pharmaceuticals. Mesoporous silica NPs have a rigid structure with porous morphology and large surface area, enabling the attachment of various drugs, tumor targeting peptides and proteins, functional groups, chelators, and radioisotopes [47]. Soon after their discovery, mesoporous silica NPs were modified with a variety of drugs and radioisotopes, particularly the most widely used 99m Tc. In the first example, mesoporous silica SBA-15 was prepared and radiolabeled by employing SnCl 2 and mesoporous silica in a reaction for 20 min, followed by 10 min incubation with 99m Tc. The direct radiolabeling provided a highly stable radiotracer with more than 99% labeling stability, as tested over 8 h. Preliminary cytotoxicity results (without 99m Tc radiolabeling) verified non-cytotoxicity. The results showed that aptamer-loaded mesoporous silica NPs are of great practical interest and can be a potential candidate in nuclear medicine [48]. For further investigation, silica NPs were conjugated with Cy5.5 or 99m Tc, followed by characterization and evaluation in vitro and in vivo by scintigraphic imaging. Furthermore, biodistribution studies were performed using intravenous injection or oral administration. The surfaces of as-prepared silica NPs were functionalized with an amine moiety having Cy5.5 fluorescent and 99m Tc radiolabeling possibility (Figure 8). The particle size distribution was around 200-350 nm, while the surface charge was modified from negative to positive after amino functionalization. The NPs' enhanced uptake was observed in kidneys, lungs, liver, spleen, and testis for the fluorescent silica. For the radiolabeled silica NPs, the toxicity level was significantly reduced as shown by the biodistribution profile, thus making radiolabeled silica NPs possible candidates for employment in nuclear medicine as a radiotracer [49]. characterization and evaluation in vitro and in vivo by scintigraphic imaging. Furthermore, biodistribution studies were performed using intravenous injection or oral administration. The surfaces of as-prepared silica NPs were functionalized with an amine moiety having Cy5.5 fluorescent and 99m Tc radiolabeling possibility (Figure 8). The particle size distribution was around 200-350 nm, while the surface charge was modified from negative to positive after amino functionalization. The NPs' enhanced uptake was observed in kidneys, lungs, liver, spleen, and testis for the fluorescent silica. For the radiolabeled silica NPs, the toxicity level was significantly reduced as shown by the biodistribution profile, thus making radiolabeled silica NPs possible candidates for employment in nuclear medicine as a radiotracer [49].  The direct radiolabeling of silica NPs provided satisfactory results regarding in vitro and in vivo stability. However, chelator-based radiolabeling techniques still provide superior results. After synthesis, radiolabeled mesoporous silica NPs (MSNs) were allowed to functionalize with APTES, followed by anchoring through DTPA as a 99m Tc chelator. The product was purified by ultracentrifugation to obtain high radiochemical yields (over 95%) and enhanced stability [50]. For 99m Tc-DTPA-MSN, high uptake in the liver was observed, with fast clearance from the blood, followed by a maximum accumulation of tracer in the lungs, thus making these structures a potential candidate for theranostic purposes. The radiolabeling and biodistribution studies using the silica NP platform demonstrated promising results, and stimulated further development. HER2 is The direct radiolabeling of silica NPs provided satisfactory results regarding in vitro and in vivo stability. However, chelator-based radiolabeling techniques still provide superior results. After synthesis, radiolabeled mesoporous silica NPs (MSNs) were allowed to functionalize with APTES, followed by anchoring through DTPA as a 99m Tc chelator. The product was purified by ultracentrifugation to obtain high radiochemical yields (over 95%) and enhanced stability [50]. For 99m Tc-DTPA-MSN, high uptake in the liver was observed, with fast clearance from the blood, followed by a maximum accumulation of tracer in the lungs, thus making these structures a potential candidate for theranostic purposes. The radiolabeling and biodistribution studies using the silica NP platform demonstrated promising results, and stimulated further development. HER2 is found to be overexpressed in breast cells, and modified silica NPs were synthesized to target HER2. For this, PAMAM was embedded on the exterior of amorphous silica NPs, with a grafting percentage of 55.6%. Moreover, processed NPs (PCSNs) were conjugated to indocyanine green (ICG), a known NIR (Near-infrared) fluorescent dye, by incubation at 37 • C for 30 min. 99m Tc was attached to the PAMAM amine surface via direct chelation to synthesize the dual-imaging probe. Additionally, for better comparison, two chelating agents, DTPA and mercaptoacetyltriglycine (MAG 3 ), were employed. Anti-HER2 antibody was attached to the surface of the PCSNs to increase specificity towards HER2 receptors. The HER2 positive cells exhibited stronger NIR fluorescence compared to HER2 negative cells. The chelator-based radiolabeling showed high in vivo stability as compared with direct radiolabeling using PAMAM. Interestingly, the DTPA chelator showed a high radiolabeling yield as compared with MAG3 [51]. Recombinant humanized monoclonal antibodies, such as Trastuzumab (TZ), can recognize the extracellular domain of HER2 protein and are considered to be among the best cancer therapeutic drugs. Several imaging agents were conjugated with TZ to target HER2-positive breast cancer. Recently, Belloliet et al. explored TZ conjugated silica NPs to target HER2-positive breast cancer. For the radiolabeling of SiNPs, firstly ( 99m Tc[CO] 3 ) + was prepared, followed by ( 99m Tc[CO] 3 ) + -His-Tag prelabeling. Then, the coupling of ( 99m Tc[CO] 3 ) + -His-Tag with SiNP-NTA was achieved. Finally, ( 99m Tc[CO] 3 ) + -His-Tag -SiNP-NTA were conjugated with TZ. Afterward, 99m Tc radiolabeled nanoparticles with or without TZ were tested for breast cancer imaging. Biodistribution studies for HER2+ cells confirmed that, for 99m Tc, the nanosilica uptake was higher than was evident from in vitro results. Moreover, in all cell cultures, toxicity tests confirmed the NPs' safety. Hence, Belloliet et al. emphasized further evaluating 99m Tc-nanoconjugates with silica to introduce safe and multipurpose nano-receptors to analyze and treat aggressive breast cancer [52].
to synthesize the dual-imaging probe. Additionally, for better comparison, two chelating agents, DTPA and mercaptoacetyltriglycine (MAG3), were employed. Anti-HER2 antibody was attached to the surface of the PCSNs to increase specificity towards HER2 receptors. The HER2 positive cells exhibited stronger NIR fluorescence compared to HER2 negative cells. The chelator-based radiolabeling showed high in vivo stability as compared with direct radiolabeling using PAMAM. Interestingly, the DTPA chelator showed a high radiolabeling yield as compared with MAG3 [51]. Recombinant humanized monoclonal antibodies, such as Trastuzumab (TZ), can recognize the extracellular domain of HER2 protein and are considered to be among the best cancer therapeutic drugs. Several imaging agents were conjugated with TZ to target HER2-positive breast cancer. Recently, Belloliet et al. explored TZ conjugated silica NPs to target HER2-positive breast cancer. For the radiolabeling of SiNPs, firstly ( 99m Tc[CO]3) + was prepared, followed by ( 99m Tc[CO]3) + -His-Tag prelabeling. Then, the coupling of ( 99m Tc[CO]3) + -His-Tag with SiNP-NTA was achieved. Finally, ( 99m Tc[CO]3) + -His-Tag -SiNP-NTA were conjugated with TZ. Afterward, 99m Tc radiolabeled nanoparticles with or without TZ were tested for breast cancer imaging. Biodistribution studies for HER2+ cells confirmed that, for 99m Tc, the nanosilica uptake was higher than was evident from in vitro results. Moreover, in all cell cultures, toxicity tests confirmed the NPs' safety. Hence, Belloliet et al. emphasized further evaluating 99m Tc-nanoconjugates with silica to introduce safe and multipurpose nano-receptors to analyze and treat aggressive breast cancer [52]. In an attempt to develop anti-HER2 antibodies, trastuzumab (TZ) is recently employed composition. However, toxicity and development of resistance in a patient are the drawbacks associated with this approach. To overcome these limitations, TZ was installed on radiolabeled silica NPs ( 99m Tc-SiNPs-TZ) for SPECT imaging. An optimized ratio of silica NPs to TZ was found to be 1:2 and 1:8. Higher accumulation was found for SiNPs-TZ with low toxicity; meanwhile, for better comparison, the DOX (doxorubicin)-loaded system DOX-SiNPs-TZ was studied and a similar trend was found. However, the reduction in tumor volume by DOX-SiNPs-TZ (1:8) was more significant than that of DOX-SiNPs, thus signaling its potential to be used as an innovative system for treating HER2-positive breast cancer [53]. 99m Tc radiolabeled silica NP based radiotracers have not only tested for HER2 positive cancer cells, but efforts have also been made to target other cancer types, such as melanoma. Melanoma is considered to be among the most dangerous cancers, and it cannot be detected and treated early. So, there was a need to develop a unique drug delivery system that could detect such tumors. One approach in this regard was utilizing mesoporous silica NPs with magnetic cores followed by dacarbazine doping and 99m Tc labeling supporting subsequent employment as an imaging agent for SPECT. Labeling efficiency was found to be greater than 98%, and the resulting particles exhibited noncytotoxicity and stability for a period of 8 h, entrapment efficiency of more than 98%, and enhanced uptake in the spleen and liver.
Furthermore, the EPR effect of synthesized and labeled NPs was confirmed by in vivo studies. However, targeting time was significantly longer, but the drug adopts two ways to reach the tumor: intratumorally, and by a systemic mode that makes this developed system a reliable and efficient nano-imaging agent for melanoma [54]. Therefore, the silica NP platform was tested for optical and SPECT imaging and also considered for development as a radiotherapy platform. For this, taking advantage of photophysical characteristics of the [M(CO) 3 ] + fragment where M = Re and the radiation characteristics of 186/188 Re and 99m Tc, a multi-model silica platform was developed with 99m Tc/Re as a theranostic pair with high potential for nanomedical applications. Furthermore, to synthesize mesoporous silica NPs, the most suitable mesoporous silica construct was screened, suitable chelate systems were employed and particle surfaces was modified to achieve the required targeting efficiency with no change in the bio profile of the silica platform. Thus, synthetic protocols were successfully employed to develop a target-specific theranostic nano platform by enabling a blend of fluorescence (eosin isothiocyanate (EOITC)) and radio imaging (Figure 9), hence paving the route for chemo and radiotherapy along with SPECT and optical imaging [55].  Silica NPs have demonstrated excellent results when combined with cancer-targeting biomolecules, theranostic radioisotopes, fluorescent imaging agents, and chemotherapeutic drugs. Recently, silica NPs were employed for a dual probe to merge their features of extraordinary SPECT sensitivity and enhanced MRI resolution. Since manganese-based T 1 contrast agents showed lower toxicity than gadolinium-based contrast agents. Here, MnONPs were synthesized and dispersed inside mesoporous silica NPs (MnOx-MSNs), followed by 99m Tc, to be employed for SPECT-MRI dual-modal imaging. Furthermore, DOX was loaded to explore chemotherapeutic efficiency. A novel 99m Tc-Mn-MSNs-PEG material was thus developed (Figure 10) for evaluating pH-responsive MRI and SPECT. The radiolabeling yield was above 99% and, owing to the pH-dependent nature of MnOx-MSNs, the r 1 value for nanoprobe reached 6.60 mM −1 s −1 . Moreover, this nanostructure showed the potential to simultaneously deliver drugs and release them at the tumor location, making it an ideal platform for biological imaging and chemotherapy [56]. A SPECT imaging and biodistribution study confirmed high uptake in the tumor, liver, and lungs.

Titanium Nanoparticles
Titanium dioxide is a common material which has various applications in consumer products. Chemical and radiation stability, low toxicity, and biocompatibility are attractive features that encourage its use in medicine and pharmacy. Additionally, its synthesis is simple and fast, and large-scale production is possible. In nuclear medicine, titanium oxide is used as an adsorbent in a 68 Ge/ 68 Ga generator. In the past, TiO 2 was radiolabeled with various radioisotopes, such as vanadium-48, flourine-18, and astatine-211 for pharmacokinetic studies. Recently TiO 2 NPs were radiolabeled with radium-223 to explore its therapeutic potential of the radiotracer.
Moreover, the NPs were also radiolabeled with 99m Tc to investigate in vivo biodistribution [57]. The TiO 2 NPs were radiolabeled with 99m Tc using surface adsorption and intrinsic radiolabeling techniques. Both strategies showed high radiolabeling efficiency. However, in the in vitro experiments, low radiolabeling stabilities were observed in various media. Therefore, it is expected that surface modification and chelator-based radiolabeling can provide better results.

Silica Nanoparticles
General biodistribution study Without drug Direct radiolabeling using stannous chloride (reducing agent) [48] General biodistribution study Without drug and with Cy5.5 fluorescent agent Direct radiolabeling using stannous chloride (reducing agent) [49] General biodistribution study APTES modified nanoparticles Chelator-based radiolabeling using DTPA and stannous chloride (reducing agent) [50] HER2 receptors targeting in tumors Anti-HER2 antibody Direct radiolabeling using stannous chloride (reducing agent),Chelator-based radiolabeling using DTPA and MAG3 [51] To target HER2 positive breast cancer Trastuzumab (TZ) Chelator-based radiolabeling using His-Tag [52] To target HER2 positive breast cancer Trastuzumab (TZ) and DOX Direct radiolabeling [53] Melanoma treatment Dacarbazine Direct radiolabeling using stannous chloride (reducing agent) [54] General biodistribution study Without the drug, radiotherapy using 186/188 Re and optical imaging using eosin isothiocyanate (EOITC) Direct radiolabeling using a tricarbonyl kit [55] General biodistribution study and dual SPECT and MRI imaging agent DOX drug for chemotherapy and MnO for MRI imaging Direct radiolabeling using stannous chloride (reducing agent) [56] Titanium Nanoparticles General biodistribution study Without drug Direct radiolabeling on the surface of nanoparticles [57]

Organic Nanoparticles
Over the last decade, various organic NPs such as proteins, liposomes, polymeric micelles, and dendrimers have been synthesized and used in various applications of the life sciences. Moreover, organic NPs radiolabeled with various radioisotopes have been studied for molecular imaging and radiotherapy applications. The key 99m Tc radiolabeled organic nanoparticles are summarized in Table 3.

Dendrimers
Dendrimers are homogeneous, highly symmetric, branched polymeric molecules with several applications in the biomedical and pharmaceutical industry. Dendrimers can be synthesized using various chemical compositions in different molecular weights and sizes. Moreover, radioisotopes and drugs can be loaded on the dendrimer surfaces or encapsulated inside them to synthesize multipurpose imaging and therapeutic agents. Recently, dendrimers have been employed to target the folate receptor, which is overexpressed in various human diseases such as lung, kidney, ovary, and breast cancers. The folate receptor has a high affinity towards folic acid moieties, so positively charged PAMAM G4 dendrimers were decorated with folic acid. The surface modification was done using a PEG polymer to stabilize NPs, restrict serum protein binding, and increase biocompatibility. 99m Tc radiolabeling was performed using a HYNIC chelator. The radiolabeled nanomaterial was obtained in high radiochemical yield and purity. The radiotracer showed excellent in vitro stability in mouse serum and PBS buffer solution. Moreover, high cellular uptake was observed in the human breast cancer (MCF-7) cell line, as compared to normal cells. The gamma camera images were obtained using breast cancer-bearing female BALB/c mice. The gamma camera images and biodistribution studies showed high uptake in the liver and spleen. However, only a moderate uptake was observed in the tumor [58]. In another study, the negatively charged dendrimer-G2 was explored. For this, citric acid and polyethylene glycol (PEG) was used to synthesize negatively charged dendrimers. This approach circumvented the need for a chelator for 99m Tc radiolabeling.
Moreover, these negatively charged dendrimers protect against the toxic interaction between the tracer and the healthy cells. Glutamine amino acid, which plays an essential role in metabolic pathways, was installed on these dendrimers to detect cancer cells in vivo. Direct 99m Tc radiolabeling was performed using tin chloride and ascorbic acid. The radiolabeling yield was more than 94%, and the radiotracer showed high in vitro stability in PBS and human serum. The biodistribution study and gamma camera images showed high radioactivity accumulation in the kidneys because of the lipophilicity of the radiotracer. Additionally, the low-level signal in the stomach and thyroid confirmed the in vivo stability of the product. Finally, moderate uptake was observed in the A549 tumor 2 h post intravenous injection. These results promised further studies at the preclinical and clinical levels [59].

Polymeric Nanoparticles
Currently, various non-toxic and biodegradable polymers are being used to synthesize polymeric NPs in the form of nanospheres and nanocapsules. These polymeric NPs have been extensively used in biomedical applications because of their outstanding characteristics such as simple design and synthesis, biocompatibility, facile surface modification, and wide structural varieties. The polymeric NPs showed promising results in preclinical studies, such as the controlled release of the drug, targeted drug delivery for cancer treatment, gene therapy, and multimodality molecular imaging. Recently, biodegradable, biocompatible, FDA-approved polymers such as poly (lactic-co-glycolic) acid (PLGA) and poly-ε-caprolactone (PCL) were used to synthesize polymeric NPs. PLGA and PCL NPs demonstrated promising results in the controlled release of the drugs. However, the in vivo imaging, biodistribution, and pharmacokinetic studies provided crucial data regarding the delivery of the administrated cancer drugs and the efficiency of the ongoing treatment procedure. For this, a study was conducted in which a cancer drug, Etoposide, was loaded on PLGA and PCL NPs ( Figure 11). The biodistribution and pharmacokinetic data were obtained using a 99m Tc radioisotope. Etoposide-loaded polymeric NPs were radiolabeled using a direct radiolabeling strategy where stannous chloride was used as a reducing agent. The radiotracers showed moderate stability in saline and rabbit serum for more than 24 h. Radiolabeled NPs showed high retention in the blood and liver as compared with radiolabeled Etoposide. Overall, polymeric NPs significantly increase the biological half-life of the drug [60].
Nanomaterials 2021, 11, x FOR PEER REVIEW 21 of 29 Figure 11. Schematic diagram of Etoposide-loaded PLGA and PCL nanoparticles and chemical structure of Etoposide [60].
Radiolabeled polymeric NPs were also used as an alternative to classical radiopharmaceuticals. For instance, 99m Tc labeled human serum albumin and sulfur nanocolloid have been used for sentinel lymph node imaging. Both radiopharmaceuticals have few intrinsic limitations. 99m Tc PLGA NPs were synthesized as an alternative radiotracer for sentinel lymph node detection. PLGA NPs were radiolabeled with 99m Tc using a chelator-free approach [61]. The radiolabeling yield was low, and additional purification of the radiotracer was required to achieve high specific activity. However, the Radiolabeled polymeric NPs were also used as an alternative to classical radiopharmaceuticals. For instance, 99m Tc labeled human serum albumin and sulfur nano-colloid have been used for sentinel lymph node imaging. Both radiopharmaceuticals have few Nanomaterials 2021, 11, 3022 20 of 28 intrinsic limitations. 99m Tc PLGA NPs were synthesized as an alternative radiotracer for sentinel lymph node detection. PLGA NPs were radiolabeled with 99m Tc using a chelatorfree approach [61]. The radiolabeling yield was low, and additional purification of the radiotracer was required to achieve high specific activity. However, the biodistribution and scintigraphic imaging showed promising results. High radioactivity was observed in the sentinel lymph node. In another study, efforts were made to improve radiolabeling yield and stability. The carboxylic acid groups on the surface of PLGA NPs were modified with p-aminobenzyldiethlenetriaminepentaacetic acid (p-NH 2 -Bz-DTPA). The DTPA chelator was used to increase the radiochemical yield and stability of the complex.
Interestingly, a highly stable complex was obtained under moderate reaction conditions. A biodistribution study on Wistar rats showed increased uptake in the sentinel lymph nodes. The studies confirmed that chelator-based radiolabeling provides better results in terms of stability and biodistribution. Long blood circulation and low liver uptake were observed after intravenous injection for fluorescent dye or 131 I-labeled PLGA NPs. However, stannous chloride-catalyzed 99m Tc-radiolabeled PLGA NPs showed contrary results, such as high liver uptake and short blood life. Therefore, it was assumed that the production 99m Tc stannic oxide colloid during the radiolabeling of PLGA NPs was influencing the biodistribution results. PLGANPs were radiolabeled using stannous chloride, sodium dithionite, or sodium borohydride as reducing agents to confirm the hypothesis. It was observed that stannous chloride-mediated 99m Tc-labeled PLGA NPs showed high liver uptake because of the formation of a 99m Tc stannic oxide colloid. Sodium borohydride provided a volatile radiolabeled complex.
Sodium dithionite produced highly stable radiolabel NPs without the formation of a 99m Tc colloid. Moreover, biodistribution studies confirmed low liver uptake and high blood circulation time [62]. The literature survey reveals that only a handful of polymeric NPs were radiolabeled with 99m Tc and chitosan-based polymeric NPs. The chitosan polymer demonstrated remarkable properties such as an antibacterial property, low immunogenicity, biodegradability, biocompatibility, and non-toxicity; therefore, this material has found wide applications in various areas, such as food additives, pharmaceuticals, and biomedicine. Recently, poly-gamma glutamic biopolymers and chitosan were used to synthesize polymeric NPs. These polymeric NPs were further decorated with folic acid to target folate receptor-overexpressed tumor cells. The NPs were radiolabeled using a 99m Tc radioisotope and stannous chloride as reducing agents. The radiotracer showed high in vitro and in vivo stability. Moreover, high radioactivity was observed in the liver and in tumor-bearing kidneys. The biodistribution studies and SPECT/CT images were compatible; high uptake was observed in folate receptor-overexpressing tumors [63].
There are only a few examples in the literature where polymeric NPs were modified to target more than one receptor. In an example, PLGA NPs were modified with folic acid (FA) to target folate receptors, and with K237 (HTMYYHHYQHHL) peptide to target vascular endothelial growth factor receptor-2 (VEGFR-2). The NPs were further modified with polyethylene glycol (PEG) as an outer corona to enhance blood circulation time and reduce nonspecific interface with blood components. These K237/FA-PEG-PLGA NPs were radiolabeled with 99m Tc using a direct radiolabeling strategy. The radiotracer showed high in vitro stability in saline and serum, and more than 90% of the radioactivity remained intact after 24 h. The radiolabeled NPs showed high binding specificity to SKOV-3 cell lines. A scintigraphic imaging and biodistribution study was performed in xenografted mice (SKOV-3 cells) using an intravenous injection. High radioactivity was observed in the tumors, liver, kidneys, and blood [64]. The high activity in the blood revealed a prolonged circulation time. Apart from receptor targeting, some chemotherapeutic drugs were also loaded on polymeric NPs to increase biological half-life, control drug release, or increase solubility.
In another example, biocompatible and biodegradable polymers, polylactic acid (PLA), and polyethylene glycol (PEG) were synthesized into polymeric PLA-PEG polymeric NPs. These NPs were loaded with Gemcitabine, a common chemotherapeutic drug used in pancreatic, bladder, lung, ovarian, and breast cancer. Finally, Gemcitabine-loaded PLA-PEG polymeric NPs were radiolabeled with 99m Tc to monitor biodistribution and pharmacokinetics in normal mice. The radiolabeling of NPs was performed using a tricarbonyl kit ([ 99m Tc (CO) 3 (H 2 O) 3 ] + ). The radiolabeled complex showed high in vitro stability in saline. The radiotracer was intravenously injected into normal rats. A uniform distribution of the radiotracer was observed in the body. As shown in SPECT images, high uptake was observed in the liver, lungs, and kidneys [65].

Lipid Nanoparticles
Lipids are hydrophobic biomolecules that include glycerides, fatty acids, phospholipids, sphingolipids, sterols, and prenol (based on their chemically functional backbone). Lipids play a vital role in energy metabolism and storage, signaling, and hormones [66]. Major advantages in drug development associated with lipids are their high biocompatibility and biodegradability, along with their ability to serve as efficient transporters for hydrophobic drugs. Depending upon their structure, lipid-based NPs can be categorized into liquid NPs, solid lipid NPs, lipid nanoemulsions, and nanostructured lipid carriers [67]. For cisplatin, hybrid nucleoside lipids (NLs) allow well-organized encapsulation, so advanced formulations for PEG NLs were prepared, followed by 99m Tc radiolabeling without chelators. The formulation of these NPs involved surface modification of the PEG with targeting agents. Therefore, to achieve active targeting by FA functionalization, uridine was firstly pegylated to aid 99m Tc radiolabeling. The labeling efficiency was found to be more than 97%. Thus, the resulting functionalized and labeled NPs ( 99m Tc-NP-PEGFA) enhanced the half-life of cisplatin in vivo with major accumulation in tumor tissue, improved the pharmacokinetic profile, and had rapid clearance. In vitro, these hybrid NPs were stable, and actively internalized two types of cell lines with overexpressed folic acid receptors, thus making a significant contribution to efficient and non-toxic drug delivery systems [68]. Among well-known radiopharmaceutical and bone imaging agents, 99m Tc-MDP ( 99m Tc labeled methylene diphosphonate) is considered one potential candidate as it accumulates in bone and possesses an easily recognizable biodistribution profile. Radiolabeled 99m Tc-MDP-encapsulated solid lipid NPs (SLNs) less than 500 nm in size were designed that successfully encapsulate the 99m Tc radiotracer. With both administration modes adapted for 99m Tc-MDP-SLNs, SPECT/CT imaging further confirmed biodistribution and high uptake in the bones, with major accumulation in the liver, spleen, and stomach. 99m Tc-MDP oral administration did not show any uptake. However, the use of SLNs still needs to be optimized to avoid non-target uptake and to allow the successful oral administration of 99m Tc based radiopharmaceuticals relative to the traditional i.v. administration mode [69].

Liposomes
A liposome is a small, bio-compatible spherical-shaped vesicle composed of cholesterol and non-toxic phospholipids that can encapsulate hydrophilic or lipophilic drugs. Their properties can be engineered considerably, by varying their composition, size, surface charge, and method of preparation. Moreover, rigidity or fluidity is determined by choice of the bilayer components and the charge of the bilayer [70]. Liposomes are broadly classified as: (i) unilamellar vesicles (UVs) (composed of one phospholipid bilayer), and (ii) multilamellar vesicles (exhibit multiple phospholipid bilayers). UV's can be further subcategorized as: (i) large UVs and (ii) small UVs. When the liposomes are functionalized with PEG, they give steric hindrance to the phagocyte system and prolonged blood circulation time. Moreover, the liposomes' PEGylation reduces radiolabeling efficiency (RE) when the glutathione method is employed for radiolabeling. Therefore, the effect of the liposomal PEG extent (PEGExt) on the in vivo biodistribution profile in Wistar rats and radiolabeling efficiency with 99m Tc was investigated. PEGylated liposomes were prepared, followed by 99m Tc radiolabeling with a labeling efficiency of more than 90% in all compositions. It was found that PEGylated liposome size was reduced by increasing the PEGExt, and with this increased PEGExt, radiolabeling stability was found to significantly enhanced in human serum, with major accumulation in the liver and the spleen, while, with increasing PEGExt, the accumulation in the organs decreased, and uptake was found to be dependent on the liposomal size. Better and improved circulation time was observed for PEGylated liposomes compared to liposomes without PEG chains [71]. Thus, the liposome designs significantly influenced the in vivo biodistribution profile of medicines. Moreover, the radiolabeling of liposomes and their potential application for imaging is a significantly growing area of interest. In this line, a novel approach was developed in which the surfaces of liposomes were labeled with 99m Tc by using the iminothiolane-99m Tc-tricarbonyl complex ( Figure 12) with 95% labeling efficiency, stability of over 2 h in bovine serum, and a highest reported specific activity of 50 MBq, paving the way for quantitative SPECT imaging with the developed system. Afterward, the resulting system was bound to the surface of the liposome. In vivo labeling stability was further confirmed by quantitative SPECT/CT studies showing significant differences between the labeled liposomes and the free 99m Tc-tricarbonyl and non-PEGylated liposomes, resulting in fast clearance from blood with major accumulation in the liver and spleen [72].

Oligomers
Oligomers are a class of polymers whose molecular weight is relatively low, owing to the limited number of repeating units, and this number plays a crucial role in determining their physical properties during polymerization reactions. Oligomers typically form as intermediates. Until now, the diagnosis and effective treatment of proteinopathies is in the early stages, and one promising candidate in this regard is an oligomer that offers significant advances in the treatment of these diseases [73]. Only a single example is available in the literature where oligomer NPs were radiolabeled with 99m Tc for SPECT imaging. The design and synthesis scheme are noted mentioned in Figure  13. 2-cyanobenzothiazole (CBT) was used to synthesize an intermediate compound CKC-CBT and the tris(2-carboxyethyl)phosphine (TCEP)-based condensation reaction of CKC-CBT provided biocompatible oligomer NPs through the π-π interaction. Maleimide-folic acid (Mal-FA) was employed to develop covalent conjugation between folic acid and the SH of the NPs to target the folate receptor. 99m Tc was conjugated with cysteine via amine and the thiol group on the surface of NPs to prepare NPs-FA-99m Tc with more than 97% radiolabeling efficiency and pronounced stability without DOTA, owing to the presence of multiple complexation sites on the NP surfaces. The direct radiolabeling reaction using stannous chloride provided a high radiolabeling yield. NPs-FA-99m Tc demonstrated high in vitro uptake in human HepG2 cells that were folate receptor-positive. The results encouraged further in vivo investigation, such as detailed biodistribution and SPECT imaging in animal models [74].

Protein Nanoparticles
Proteins are large, complex molecules involved in most cellular works and are critical for the building, proper functioning, and regulation of the various tissues and organs. The

Oligomers
Oligomers are a class of polymers whose molecular weight is relatively low, owing to the limited number of repeating units, and this number plays a crucial role in determining their physical properties during polymerization reactions. Oligomers typically form as intermediates. Until now, the diagnosis and effective treatment of proteinopathies is in the early stages, and one promising candidate in this regard is an oligomer that offers significant advances in the treatment of these diseases [73]. Only a single example is available in the literature where oligomer NPs were radiolabeled with 99m Tc for SPECT imaging. The design and synthesis scheme are noted mentioned in Figure 13. 2-cyanobenzothiazole (CBT) was used to synthesize an intermediate compound CKC-CBT and the tris(2-carboxyethyl)phosphine (TCEP)-based condensation reaction of CKC-CBT provided biocompatible oligomer NPs through the π-π interaction. Maleimide-folic acid (Mal-FA) was employed to develop covalent conjugation between folic acid and the SH of the NPs to target the folate receptor. 99m Tc was conjugated with cysteine via amine and the thiol group on the surface of NPs to prepare NPs-FA-99m Tc with more than 97% radiolabeling efficiency and pronounced stability without DOTA, owing to the presence of multiple complexation sites on the NP surfaces. The direct radiolabeling reaction using stannous chloride provided a high radiolabeling yield. NPs-FA-99m Tc demonstrated high in vitro uptake in human HepG2 cells that were folate receptor-positive. The results encouraged further in vivo investigation, such as detailed biodistribution and SPECT imaging in animal models [74].
albumin was coated with four distinct polymers, such as HPMC, GMN2, GPM2, and GTM2 and subsequently radiolabeled with 99m Tc and 67 Ga at different times and temperatures. With both approaches, radiochemical purity was above 97%, and the NPs demonstrated enhanced in vitro stability even after 48 h of labeling, i.e., 70% for 99m Tc and 90% for the 67 Ga-based radiolabeled NP system. Thus, the biodistribution profile of the 99m Tc -GPM2 and 67 Ga -NOTA-GPM2-based NPs systems showed major accumulation in the liver 2 and 24 h after i.v. administration [78]. Figure 13. Synthesis of 99m Tc radiolabeled oligomer nanoparticles [74]. Table 3. Summary of 99m Tc-labeled organic nanoparticles and their applications.

Nanoparticle
Application Drug Loaded on NPs Radiolabeling Method Ref.

Protein Nanoparticles
Proteins are large, complex molecules involved in most cellular works and are critical for the building, proper functioning, and regulation of the various tissues and organs. The transport of insoluble drugs by using NPs is receiving increaded attention because they dissolve quickly in the bloodstream and reach a specific target due to their small size. Proteins exhibit unique properties and functions in biological materials, making them effective base materials for the production of NPs [75]. Therefore, protein NPs are actively employed as medicinal and functional tools due to their abundance in natural sources, costeffectiveness, low toxicity, and biodegradability [76]. Among various available proteins, human serum albumin (HSA) protein-based NPs have demonstrated unique features such as high drug loading capacity and easy surface modification using polymers, finding use in cancer-targeting drugs, SPECT, and PET-based radioisotopes, among others. In the first example, HSA NPs loaded with bevacizumab (NP-Ab) were radiolabeled with 99m Tc, and their biodistribution and SPECT imaging ability was investigated using rodents. In order to obtain an idea about the biodistribution profile of the individual shell and the cargo of NP-Ab, they were functionalized with PEG35000 and studied by SPECT/CT imaging; thus, two formulations were investigated. In the first approach, a desolvation strategy was employed to synthesize NP-Abs, followed by PEG35000 coating and 99m Tc radiolabeling via direct radiolabeling or the tricarbonyl kit methodology ([ 99m Tc] Tc-NP-Ab). In the second approach, Ab radiolabeling via [ 99m Tc] [Tc (CO) 3 (H 2 O) 3 ] + was performed that was further employed to synthesize NP-[ 99m Tc]Tc-Ab. The radiochemical purity of both nano drugs was >95% and more than 87% of radioactivity remained intact when incubated in plasma for 24 h. The biodistribution study and SPECT/CT images confirmed high uptake of the [ 99m Tc] Tc-NP-Ab tracer in the liver and kidneys. On the other hand, NP-[ 99m Tc] Tc-Ab mainly accumulated in the liver, and clearance was slow. Thus, the different clearance rates for the antibody and shell provided the desired imaging information for the drug delivery of nano-systems [77]. In an attempt to optimize the radiolabeling of polymer-coated albumin NPs, the desolvation method was employed to synthesize the NPs using albumin, and NOTA-functionalized albumin was coated with four distinct polymers, such as HPMC, GMN2, GPM2, and GTM2 and subsequently radiolabeled with 99m Tc and 67 Ga at different times and temperatures. With both approaches, radiochemical purity was above 97%, and the NPs demonstrated enhanced in vitro stability even after 48 h of labeling, i.e., 70% for 99m Tc and 90% for the 67 Ga-based radiolabeled NP system. Thus, the biodistribution profile of the 99m Tc -GPM2 and 67 Ga -NOTA-GPM2-based NPs systems showed major accumulation in the liver 2 and 24 h after i.v. administration [78]. Table 3. Summary of 99m Tc-labeled organic nanoparticles and their applications.

Nanoparticle
Application Drug Loaded on NPs Radiolabeling Method Ref.

Conclusions and Future Perspectives
In preclinical and clinical research, the applications of nanoparticles are widely studied for both therapeutic applications and molecular imaging. The radiolabeling of nanoparticles is an accurate and sensitive method to understand their whole-body distribution and pharmacokinetics in both animal models and cancer patients. This review discussed various inorganic and organic nanoparticles, their surface modifications, radiolabeling strategies using 99m Tc, pharmacokinetics, and biodistribution results. Multiple strategies are available that can be used to obtain highly stable and efficiently radiolabeled nanoparticles with 99m Tc. The selection of radiolabeling methodology to obtain highly stable and pure 99m Tc radiolabeled nanoparticles depends entirely on the surface composition and structure of the nanoparticles. In this context, this mini-review will provide an excellent guideline to scientists and researchers working in nanomedicine research to choose the best strategy for the 99m Tc radiolabeling of their product.