Hydrotalcite-Embedded Magnetite Nanoparticles for Hyperthermia-Triggered Chemotherapy

A magnetic nanocomposite, consisting of Fe3O4 nanoparticles embedded into a Mg/Al layered double hydroxide (LDH) matrix, was developed for cancer multimodal therapy, based on the combination of local magnetic hyperthermia and thermally induced drug delivery. The synthesis procedure involves the sequential hydrolysis of iron salts (Fe2+, Fe3+) and Mg2+/Al3+ nitrates in a carbonate-rich mild alkaline environment followed by the loading of 5-fluorouracil, an anionic anticancer drug, in the interlayer LDH space. Magnetite nanoparticles with a diameter around 30 nm, dispersed in water, constitute the hyperthermia-active phase able to generate a specific loss of power of around 500 W/g-Fe in an alternating current (AC) magnetic field of 24 kA/m and 300 kHz as determined by AC magnetometry and calorimetric measurements. Heat transfer was found to trigger a very rapid release of drug which reached 80% of the loaded mass within 10 min exposure to the applied field. The potential of the Fe3O4/LDH nanocomposites as cancer treatment agents with minimum side-effects, owing to the exclusive presence of inorganic phases, was validated by cell internalization and toxicity assays.


Introduction
Magnetic fluid hyperthermia (MH) has been developed as an alternative approach for the heat-mediated treatment of cancer cells at a controllably localized level [1]. MH stands on the energy losses of magnetic nanoparticle (MNP) dispersion subjected to AC magnetic fields (H AC ), resulting in a temperature elevation of the dispersion medium. In recent years, significant research effort has been devoted to the synthesis of MNPs with high heating efficiency, their successful incorporation into biological matrices (cells or tissues), the treatment optimization based on theoretical models and the technical improvement of field generation devices and error-free measuring protocols [2,3]. Thanks to their facile and low-cost availability in various geometries, their chemical stability, affordable biocompatibility and magnetic response, iron oxide nanoparticles are widely considered as the most efficient agents for magnetic hyperthermia applications [4,5]. The best heating In all these cases, magnetic featuring of the drug-loaded nanocomposites was only used for the magnetically assisted delivery through the application of a static magnetic field.
Here, we report an attempt to illustrate the potential incorporation of inorganic magnetic nanohybrids, consisting of Fe 3 O 4 nanoparticles and Mg-Al LDH loaded with anticancer 5-fluorouracil (C 4 H 3 FN 2 O 2 , FU), as a way to improve therapeutic efficiency by combining magnetic hyperthermia and chemotherapy. Importantly, a major milestone was to go beyond the parallel occurrence of the two therapeutic modalities as described elsewhere for doxorubicin-loaded nanocomposites [32], and provide their coupling, i.e., the drug release switch-on upon application of the AC magnetic field (Figure 1). The main advantage of the proposed nanocomposites is their fully inorganic nature which is able to combine the heating capability of magnetic nanoparticles with the drug hosting capacity of the layered double hydroxide, considering also that the Mg/Al layered double hydroxide is already recognized for its compatibility for human use as an antacid.

Nanocomposite Synthesis
The synthesis of the nanocomposite consisting of Fe 3 O 4 nanoparticles (IONPs) distributed into a matrix of Mg/Al layered double hydroxide was carried out in a continuousflow sequence of two stirring reactors (operating volume 1 L) by the combined precipitation of iron, magnesium and aluminium salts ( Figure S1). In the first reactor, Fe 3 O 4 seeds were prepared after the coprecipitation of FeSO 4 ·7H 2 O and Fe 2 (SO 4 ) 3 ·9H 2 O, which were pumped in the form of aqueous solutions (5 mM), under alkaline conditions (pH 11) regulated by the continuous addition of NaOH solution (2 g/L) in drops. The blackcoloured suspension was directed into the second reactor in which the coprecipitation of Mg(NO 3 ) 2 ·6H 2 O and Al(NO 3 ) 3 ·9H 2 O took place. The two reagents were pumped as aqueous solutions with concentration 10 mM and hydrolyzed at a pH 9 maintained by the addition of a 1:1 mixture of NaOH/Na 2 CO 3 (3.5 g/L). Sodium carbonate was introduced in this step to serve also as the source of CO 3 2− which participated in the building up of the layered hydrotalcite structure. Each reactor operated with a residence time of 1 h. The final product was received in the outflow of the second reactor and then, centrifuged and washed several times to remove soluble residuals. The described reactions can be realized with similar success in batch reactors, however, advantages such as the good reproducibility, the achievement of constant concentrations in all ionic and solid forms, the minimization of operation cost and the scale-up potential to mass production would not be covered. A schematic summary of the process is presented in Figure 2 while a picture of the laboratory continuous-flow system appears in Supplementary Materials. Using such proportions, the Mg-to-Al molecular ratio was adjusted to 3. Under such conditions, the production rate of the nanocomposite in terms of dry solid varied between 0.35−0.55 g/h.

Characterization
An overview of produced nanocomposites' morphology and separately of their constituting phases was obtained by electron microscopy. For more clarity on the distribution of IONPs, high magnification images were taken by transmission electron microscopy (TEM) using JEM-1210 (JEOL, Tokyo, Japan), operating at 120 kV. TEM samples were prepared by dropping a diluted aqueous dispersion of the material onto a carbon coated copper grid. Quasi-static magnetic properties of the samples were measured using a superconducting quantum interference device (SQUID) MPMS XL-7T magnetometer (Quantum Design, San Diego, CA, USA). Structural-phase identification was performed by powder X-ray diffractometry (XRD) using a water-cooled Ultima+ diffractometer (Rigaku, Tokyo, Japan) with CuKa radiation, a step size of 0.05 • and a step time of 3 s, operating at 40 kV and 30 mA.
Average elemental content of the nanocomposites was determined by graphite furnace atomic absorption spectrophotometry, using a AAnalyst 800 instrument (Perkin Elmer, Waltham, MA, USA). The actual ratio of Fe 2+ /Fe 3+ in the Fe 3 O 4 fraction was defined after digestion of a weighted quantity of each sample in 7 M H 2 SO 4 under heating and titration with 0.05 M KMnO 4 solution till the appearance of a pink colour. The percentage of carbonates (CO 3 2− ) located in the interlayer space of hydrotalcite was quantified using a FOGL bench-top soil calcimeter (BD Inventions, Thessaloniki, Greece) with a determination error of less than 5%.
The potentiometric mass titration method was applied to define the positive charge density of the solid. In the first step, the point of zero charge (PZC) was determined after equilibrating water suspensions of the nanocomposites (10 g/L) in 0.001, 0.01 and 0.1 M NaNO 3 solutions and adjusting pH to 11 by adding 0.1 M NaOH. Then, suspensions were titrated by adding stepwise small quantities of a 0.1 N HNO 3 solution and recording equilibrium pH until pH 3 was reached. For the three ionic strengths, the plotting of surface charge density, which is proportional to the difference of acid volume used to set the same pH in the dispersion and a blank titration, indicates the PZC as the point of intersection.

Magnetic Heat Losses
Calorimetry measurements of magnetic suspensions under H AC were performed using a commercial AC magnetic field generator (SPG-06-III 6 kW High Frequency Induction Heating Machine, Shenzhen Shuangping Ltd., Shenzhen, China) working at 765 kHz frequency and 24 kA/m magnetic field intensity. The specific loss power (SLP), referred to as specific absorption rate (SAR) hereafter, was derived from the slope of the temperature versus time curve after subtracting water background signal and heat losses to the environment [33].
Temperature variations during the application of AC field were recorded using a commercial optical fibre thermal probe located in the centre of the sample and connected to an PicoM device (Opsens, Quebec, QC, Canada) with an experimental error of ±0.1 • C. SAR values under non-adiabatic conditions were determined through the temperature increment as a function of time (dT/dt) using the following expression: where C d is the mass specific heat of the dispersion media, m d is the dispersion's mass, m Fe is the iron mass related to the IONPs diluted in the dispersion and dT/dt is the effective slope upon switching H AC on, after subtracting the contributions of coil surface heating and environment cooling. The value of C d considered in this study was 4.18 J/g K for water dispersion. AC magnetometry measurements of the magnetic colloids were carried out by commercial inductive magnetometers (AC Hyster Series; Nanotech Solutions, Madrid, Spain). The AC Hyster Series magnetometer offers a wider field frequency range from 10 kHz up to 300 kHz and field intensities up to 24 kA/m which are automatically selected. Hyster Series measure magnetization cycles from IONPs dispersed in liquid media at room temperature, consisting of three repetitions to obtain an average of the magnetization cycles and the related magnetic parameters (H C , M R , Area). In order to accurately quantify the magnetic losses of IONP suspensions, the specific absorption rate (SAR) values were calculated according to SAR = A·f, where A is the magnetic area and f is AC magnetic field frequency [34].

Drug Loading and Release
Loading of 5-fluorouracil in the interlayer space of the Mg-Al LDH part of the nanocomposite was carried out by equilibrating a quantity of the samples with a solution of the drug in phosphate-buffered saline (PBS). The obtained FU-loaded nanocomposite sample is referred as Fe 3 O 4 /LDH-FU. In these experiments, a freshly prepared 20 mM stock solution of 5-fluorouracil in PBS was used after proper dilution. Exchange between 5-fluorouracil molecules and carbonates was maximized when experiment took place at pH 9. In these conditions, the kinetic behavior of loading was studied using a 2 g/L dispersion of MGT-35 in a 0.5 mM 5-fluorouracil PBS solution and measuring the residual concentration in different time intervals till equilibrium was reached. The adsorption capacity variation (isotherm) as a function of residual 5-fluorouracil was determined after equilibrating 2-20 g/L of nanocomposite with a 15 mM drug solution.
After drug loading, the leaching behavior under different pH values was evaluated. Sample loaded with around 1 mmol/g of 5-florouracil was dispersed in PBS adjusted to pH 4.0, 7.4 and 8.5, and the released drug was monitored for a period of up to 60 min. Similarly, the release of drugs was examined for various temperatures, 10, 20 and 35 • C, while in another experiment the temperature of the sample was increased at 40 • C by the application of AC magnetic field and kept at this value for 10 min.

Cell Internalization
Human colon cancer cells (HT29) were cultured in a microscope coverslip placed in the wells of a 12-well plate containing DMEM/F-12 (Dulbecco's Modified Eagle Medium/Nutrient Mixture) basal medium supplemented with 10% fatal bovine serum (FBS), 1% l-glutamine and 1% penicillin/streptomycin. After 24 h, they were incubated with the nanoparticles (IONPs, Fe 3 O 4 /LDH and Fe 3 O 4 /LDH-FU) at a concentration of 0.1 mg/mL in growth media for two days. Then, the cells were washed and incubated with lysotracker red (0.25 µM dispersed in basal media for 25 min) to stain the lysosomes. The cells were then washed with PBS, dispersed in PBS and observed under a LSP2 Leica Confocal Laser Scanning Microscope. Samples were excited with a 543 nm Green Helium-Neon laser and collected emitted light from 555 nm to 620 nm.

Toxicity
A resazurin-based cytotoxicity assay was used for checking the biocompatibility of the nanoparticles (IONPs and Mg-Al LDH-FU) in HT29. A number of 20,000 cells/well in 100 µL growth medium were seeded in a 96-well plate. After growth for two days, cells were incubated with different nanoparticle concentrations ranging from 0 to 256 mg/mL for one day. As negative control for cell viability, cells were incubated with dimethyl sulfoxide (DMSO) inducing cell death. Three wells were used per sample tested. Afterwards, resazurin (10%) was added for three hours and measured for its fluorescent metabolite (resorufin) (λ ex 560 nm; λ em 572-650 nm). First, the maximum intensity emission wavelength value was taken and the maximum intensity value obtained for the negative control to remove background signal was subtracted. Then, data was normalized with the highest value. Finally, the normalized values (relative cell viability, %) were plotted towards the logarithm of the concentrations. GraphPad Prism 6 was used to obtain the logIC 50 . This experiment was replicated three times.

Material Properties
The structural characterization of the developed nanocomposite indicated the preservation of the constituting phases, LDH and iron oxide, in the final product. Figure 3 shows the XRD diagrams of the pure components when separately prepared in comparison to their sequential preparation as a hybrid in the two-stage reaction setup. The observed diffraction peaks for IONPs fitted well to those expected for the inverse spinel structure of Fe 3 O 4 whereas the layered formation of the Mg-Al LDH was signified by the strong low-angle peaks which were identified as hydrotalcite. Chemical analysis indicated that Mg/Al molecular ratio was 2.9/1 which is very close to the nominal value for the R3m space group of hydrotalcite. For initially formed hydrotalcite, the unit cell parameters of its 3R stacking sequence were calculated to be α = 0.3055 nm and c = 2.2725 nm respectively, whereas the interlamellar distance estimated by the reflection (003)  The nanocomposites showed relatively high specific surface areas, 78 m 2 /g for MGT-20 and 65 m 2 /g for MGT-35, although they appeared significantly decreased in comparison to the pure Mg-Al LDH (175 m 2 /g). The nanocomposites indicated also a significant surface charge density which was maintained at around 0.7 mmol OH − /g. The nanocomposites showed relatively high specific surface areas, 78 m 2 /g for MGT-20 and 65 m 2 /g for MGT-35, although they appeared significantly decreased in comparison to the pure Mg-Al LDH (175 m 2 /g). The nanocomposites indicated also a significant surface charge density which was maintained at around 0.7 mmol OH − /g.
The TEM images shown in Figure 4 provide a representative view on the nanoscale morphology and distribution of the nanocomposites in comparison to the separately prepared pure LDH and IONPs. Following the described precipitation method, Mg-Al LDH form very thin nanosheets, while IONPs have a nearly spherical shape with an average diameter of 31 ± 6 nm. The sequential synthesis of the two phases resulted in a good distribution of the nanoparticles onto the surface of the LDH sheets. Magnetic interactions between nanoparticles and the absence of any stabilizing agent during synthesis contributed to the observed aggregation effects. The lower magnification images of the sample MGT-35 ( Figure S7), recorded with scanning electron microscopy, indicate that in the powder form, the layered matrix appears as a continuous substrate without obvious limits of the separation that occurs when dispersed. This effect may be attributed to the secondary self-organization of the layered structure by weak forces during dewatering and it is fully reversible considering that a hydrodynamic diameter of samples was measured around 500 nm.
The magnetic response of the nanocomposites was attributed to the participation of Fe3O4 and its intensity appeared to be proportional to the magnetic phase percentage. The hysteresis loops under quasi-static conditions shown in Figure 5 indicated that samples MGT-20 and MGT-35 had saturation magnetisation values around 17 and 30 Am 2 /kg respectively, in good accordance to the measured magnetisation for pure IONPs (90 Am 2 /kg) and the mass percentage of Fe3O4 in each case. The TEM images shown in Figure 4 provide a representative view on the nanoscale morphology and distribution of the nanocomposites in comparison to the separately prepared pure LDH and IONPs. Following the described precipitation method, Mg-Al LDH form very thin nanosheets, while IONPs have a nearly spherical shape with an average diameter of 31 ± 6 nm. The sequential synthesis of the two phases resulted in a good distribution of the nanoparticles onto the surface of the LDH sheets. Magnetic interactions between nanoparticles and the absence of any stabilizing agent during synthesis contributed to the observed aggregation effects. The lower magnification images of the sample MGT-35 ( Figure S7), recorded with scanning electron microscopy, indicate that in the powder form, the layered matrix appears as a continuous substrate without obvious limits of the separation that occurs when dispersed. This effect may be attributed to the secondary self-organization of the layered structure by weak forces during dewatering and it is fully reversible considering that a hydrodynamic diameter of samples was measured around 500 nm.
The magnetic response of the nanocomposites was attributed to the participation of Fe 3 O 4 and its intensity appeared to be proportional to the magnetic phase percentage. The hysteresis loops under quasi-static conditions shown in Figure 5 indicated that samples MGT-20 and MGT-35 had saturation magnetisation values around 17 and 30 Am 2 /kg respectively, in good accordance to the measured magnetisation for pure IONPs (90 Am 2 /kg) and the mass percentage of Fe 3 O 4 in each case.

Hyperthermia Performance
The temperature increase during the AC field application indicated a significantly high potential of the samples to deliver heat flow to the environment ( Figure S3). For instance, a temperature increase from room temperature to around 35 • C within 2 min of field application was obtained for a 2 g/L aqueous dispersion of sample MGT-35, yielding a SAR value of 1970 W/g Fe (±10%). Keeping the same field strength, SAR values seemed to follow an exponentially increasing trend in the frequency range from 30 to 765 kHz succeeding in relatively high performances even for frequencies below 100 kHz ( Figure 6). The uncertainty of the determined SAR values in the lower frequencies range was quite small (typically below 3%) following the accuracy of the AC magnetometry measurements. Importantly, it was found that the addition of the Mg-Al LDH phase did not appear to modify the heating performance of IONPs and therefore, temperature rise was proportional to the content of the magnetic phase.  Compared to other studies on single iron oxide nanoparticles or LDH composites, the obtained SAR values were among the highest reported, covering a very wide frequency range. Typically, Fe 3 O 4 nanoparticles prepared by the oxidative precipitation method, showed efficiency of around 2 kW/g at 765 kHz, translated into 2.3 W/g Fe when produced by a continuous flow process [35], but less than half when produced in batches [36]. Aiming to achieve higher SAR values (up to 10 kW/g at 500 kHz), combined ferrite phases were employed but the requirement for using hazardous reagents for their synthesis and the toxicity of elements such as Mn and Co inhibit their potential for clinical application [37][38][39]. Research reports on the heating performance of magnetic nanoparticle-decorated LDH systems are only scarce. For example, Fe 3 O 4 /Mg-Al LDH nanohybrids were found to reach an SAR of 73.5 W/g at 425 kHz and 30 kA/m [32]. The same study provided promising results concerning the combined hyperthermia and drug delivery with doxorubicin as well as the therapeutic efficiency in HeLa cells.

Drug Release Behavior
The capacity of the Mg-Al LDH structure to host 5-fluorouracil molecules after exchange with structural carbonates was first demonstrated through the kinetic experiments ( Figure S2). Within less than 1 h, MGT-35 was able to capture significant quantities from the equilibrated drug solution overcoming a loading of 6.5 mmol/g and approaching the 75% of its maximum ability (~8.7 mmol/g) into PBS at pH 9. The procedure is described as: Mg 6 Al 2 (OH) 16  It should be noted that the loss of carbonate content at the end of this experiment, which validates the presence of the ion exchange mechanism, was around 1 wt.% Considering the uptake capacity values for 5-fluorouracil, carbonate losses appeared much higher than the stoichiometrically expected ones, suggesting that the incorporation of drug's voluminous molecule caused the release of multiple carbonate ions in order to fit in the interlayer space. The partial replacement of the structural carbonates by 5-fluorouracil was also reflected in the expansion of Mg-Al LDH unit cell which was revealed by the shift of the XRD diffractogram to smaller angles in the drug-loaded sample ( Figure S6). The uptake capacity can be adjusted by varying the dispersion's concentration and therefore, the residual 5-fluorouracil concentration as shown in the adsorption isotherm of Figure S4.
The stability of loaded 5-fluorouracil and the release rate can be evaluated by modifying the pH of the dispersion medium ( Figure S5). At pH 8.5, slightly below the loading acidity, the release rate was very low with less than 20 wt.% of the drug to be found in soluble state. However, the loss percentage within 1 h of contact, reached 50 wt.% when the pH was adjusted to 7.4. The weakening of the layered structure by the increase of metal component solubility was the reason for the increasingly observed drug release. Under more acidic conditions, the whole quantity of drug was completely released immediately, however, a significant part was captured back to the nanocomposite within less than 1 h of contact. The last observation could be of high importance when stimuli-responsive drug delivery systems are required.
The temperature of the studied medium was another important parameter which defined the release rate even in the short term (Figure 7). More specifically, the loading loss at temperatures of 10, 20 and 35 • C (close to the human body temperature) after 5 h of contact at pH 7.4 was found to be 45, 55 and 70 wt.%, respectively. The temperature-dependence study provides a general view of the release kinetics in a wide temperature range indicating the behavior of the drug-loaded nanocomposite during storage in a refrigerator or its application in cancer treatment. Importantly, even at the higher temperature, around 20% of the initial load was stabilized into the nanocomposite for several hours. A very interesting finding that validates the motivation of this study was that the drug release was very rapid and reached 80 wt.% only by applying the AC magnetic field for 10 min and reaching a temperature of 40 • C by means of magnetic hyperthermia. This result should be attributed to the high localized temperature increase within the nanocomposite mass which was able to initiate a fast release response to the LDH phase.

Cellular Uptake and Biocompatibility
The biological characterization of the pure and drug-loaded MGT-35, in comparison to the corresponding IONPs, involved cell internalization and the induced cellular toxicity. The physicochemical properties of nanoparticles (e.g., size, shape, charge) are known to affect cellular responses such as internalization (rates and mechanisms) or cytotoxicity [40][41][42][43] and, therefore, knowledge of these parameters is crucial to predict the nanoparticle potential for the magnetic hyperthermia treatment of cancer in real biological conditions that may interfere with performance. For example, previous results showed differences in the uptake of magnetic nanoparticles depending on the surface charge (positive vs. negative) [44]. Quantitative analysis indicated that positively charged magnetic nanoparticles avoid the early endosomes and they are preferentially located in the lysosomes. On the other hand, negatively charged nanoparticles were first accumulated in early endosomes and then, transferred to the lysosomes with time. In general, positively charged nanoparticles are considered as more toxic (at least, acutely) than their negatively charged counterparts due to their stronger interaction with cellular components [43,45].
HT29 cells were incubated with the three tested systems, i.e., Fe 3 O 4 nanoparticles, pure MGT-35 and drug-loaded MGT-35 (MGT-35-FU). Figure 8 shows that the nanoparticles were steadily taken up by the cells located in the lysosomes after two days of incubation. The nanomaterials provided a high contrast in the transmitted channel of the confocal microscope, mostly due to a strong intracellular accumulation. This high contrast enabled their tracking inside the cells and colocalization inside the lysosomes (labelled in red). Figure 9 illustrates the toxicity profile at the level of mitochondrial activity of the three samples when exposed at different concentrations ranging from 256 to 0.5 mg/mL for 24 h. Reference IONPs practically exhibited no toxicity at the given concentrations and exposure time. Iron oxide nanoparticles are known to be metabolized with the iron metabolism in the spleen and liver [46]. MGT-35 and MGT-35-FU showed a sigmoidal curve for toxicity. The IC 50 values of Fe 3 O 4 , MGT-35 and MGT-35-FU, which indicate the concentrations needed for each system to kill half of the cell population, were 476 mg/mL, 12 mg/mL, and 18 mg/mL, respectively. It appears that the presence of the Mg-Al LDH modifies the toxicity profile of the sample, although the provided concentration range for safe use without chemically induced side-effects still remains wide. Such observations should be attributed to the relatively good structural stability which favours membrane damage and the higher release of metal ions and carbonates at the acidic conditions occurring in endosomes or lysosomes [47]. Noteworthy, MGT-35-FU and MGT-35 exhibited similar IC 50 values. Their toxic profile appeared to be dominated by the Mg/Al layered double hydroxide matrix while the effect of the 5-fluorouracil presence was minor. Such a finding was attributed to the drug release of around 80% (Figure 7) which took place during the initial washing of the nanocomposite before contact with the cells. The remaining 20% could be stabilized into the structure for the time window of the experiment, as explained by the temperature-dependent kinetic data. The application of localized heating by magnetic hyperthermia enabled this barrier to be overcome and rapidly promoted the complete release of this fraction which appeared to be the most strongly captured. Another possible explanation is that the presence of serum protein corona around the nanoparticles may influence the short-term release kinetics of 5-fluorouracil [41,44].

Conclusions
A 100% inorganic-based drug carrier was developed to be used for the controllable delivery and release of anticancer molecules. In particular, a nanocomposite built from iron oxide nanoparticles and a matrix of Mg/Al layer double hydroxide was produced by an environmentally friendly and scalable procedure which provides very stable synthesis conditions, high production rates and an affordable cost for an engineered drug-delivery system. The nanocomposite is capable of loading up to several mmol/g of anionic molecules, such as 5-fluorouracil, which is then released very rapidly when an AC magnetic field is externally applied, due to the high heat generation at the microstructure level. Importantly, such advantages are combined with sufficient cell internalization of the nanocomposite and very limited toxicity, even for relatively high applied concentrations.
Supplementary Materials: The following are available online at https://www.mdpi.com/article/ 10.3390/nano11071796/s1, Figure S1, Laboratory setup for the continuous-flow production of the hydrotalcite/magnetite nanocomposites. Figure S2, Kinetic of drug loading. Figure S3, Temperature increase during AC field application. Figure S4, Uptake capacity versus residual 5-fluorouracil concentration. Figure S5, Time dependent leaching behavior of 5-fluorouracil. Figure S6, XRD diagrams of pure hydrotalcite before and after loading with 5-fluorouracil. Figure S7, Scanning electron microscopy images and elemental analysis.