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This work has focused on the synthesis of three nanosystems composed of superparamagnetic iron oxide nanoparticles (SPIONs) coated either with a carboxylate platinum(IV) complex (PD = cis, cis, trans-Pt(NH 3) 2Cl 2(HOOCCH 2CH 2COO)(OH)) or with platinum(II) complex functionalized dextrans (DexPt1 = Pt(Dex-NH 2)Cl 3 and DexPt2 = Pt(Dex-NH 2)(NH 3) 2(H 2O)). All nanosystems have shown superparamagnetic behavior. Powder X-ray diffraction (XRD) has confirmed that the SPIONs were iron oxide phase and transmission electron microscopy (TEM) has shown average size of 6 nm (M6). Characterization of the nanosystems by inductively coupled plasma atomic emission spectroscopy (ICP AES) has revealed the presence of platinum on their surface (M6@PD, 0.54 mmol g -1 of Fe and M6@CA@DexPt1-2, 0.32-1.20 mmol g -1 of Fe); infrared spectroscopy (IR) and thermogravimetric and differential thermal analyses (TG-DTA) have confirmed the presence of dextran.
Furthermore, the colloidal properties of these nanosystems (M6@PD and M6@CA@DexPt1-2) have been evaluated in water and in PBS buffer. Although M6@PD has shown good colloidal dispersion in water in the pH range of 2.0-8.0, the system underwent rapid agglomeration in PBS buffer. The M6@CA@DexPt1-2 nanosystems have exhibited improved colloidal behavior both in water and in PBS, where hydrodynamic sizes were kept below 100 nm over a large pH range (2.0-12.0).
Furthermore, the latter systems have displayed isoelectric points below pH 5.0 and low surface charges at pH 7.0 (ζ-potential = -10 mV) and therefore PBS did not affect their colloidal stability.Keywords: colloidal stability; dextran; iron oxide; platinum complexes; superparamagnetism. IntroductionSuperparamagnetic iron oxide nanoparticles (SPIONs) have been widely investigated for biomedical purposes.
Magnetic resonance imaging, - hyperthermia - and drug delivery - are some of the practical applications displayed by SPIONs. These nanomaterials are promising due to the biocompatibility of the iron oxide cores, e.g., magnetite (Fe 3O 4) and maghemite (γ-Fe 2O 3). Furthermore, their surfaces can be easily modified, allowing for the tuning of pharmacokinetic properties.One of the key features for biomedical applications of SPIONs is their aqueous colloidal stability. Therefore, surface functionalization plays a relevant role on the balance of attractive forces, such as dispersion forces and dipole-dipole interactions that determine their agglomeration. Carboxylate-, phosphonate- and aminosilane-based derivatives have been widely used to coat SPIONs in order to prevent aggregation, mainly by electrostatic interactions due to the formation of an electrical double layer. However, this kind of colloidal dispersion is strongly affected by physiological pH and ionic strength. Coating nanoparticles with polymers, such as dextran (Dex) or poly(ethylene glycol) (PEG), is a judicious strategy to prevent SPIONs from aggregation, diminishing opsonization and increasing circulation time.
These polymers can be adsorbed or chemically attached onto the surface of SPIONs, and because the stabilization of these systems is due to steric repulsions, they are less affected by pH and ionic strength changes than SPIONs modified via electrostatic interactions. Nonetheless the colloidal stability of these systems under physiological conditions must be thoroughly investigated before any further in vitro or in vivo studies.Coating SPIONs with dextran has led to improvement of their colloidal stability. Impregnation of cisplatin in the dextran-coated SPIONs has been investigated for the delivery of this drug to cancer cells. However, the drug could be released prematurely before reaching its target. Thus, the use of SPIONs coated with dextran modified with platinum(II) complexes may circumvent this problem. In this work we report the use of two new strategies to attach platinum complexes onto the surface of 6 nm SPIONs (M6): ( i) by coating the SPIONs with platinum(II) complex functionalized dextran (DexPt1-2) and ( ii) by direct coordination of a carboxylate platinum(IV) complex (PD) for comparison.
Furthermore, the colloidal properties of these nanosystems (M6@CA@DexPt1-2 and M6@PD) have been evaluated in aqueous and PBS buffer media. These studies are essential to comprehend their behavior, especially with respect to aggregation and surface charge, which will dictate their future applications. Synthesis of platinum-based and platinum(II) complex functionalized dextran precursorsCisplatin ( cis-Pt(NH 3) 2Cl 2), cis-Pt(NH 3) 2I 2, oxoplatin ( cis, cis, trans-Pt(NH 3) 2Cl 2(OH) 2) and the platinum(IV) complex PD ( cis, cis, trans-Pt(NH 3) 2Cl 2(HOOCCH 2CH 2COO)(OH)) were synthesized according to the literature and their identity, confirmed by melting point measurements and 1H and 195Pt nuclear magnetic resonance (NMR) spectra.For the synthesis of platinum(II) complex functionalized dextran-coated nanoparticles, CM-Dex was first chemically modified with 1 mol L -1 EDA (pH 4.75). Briefly, 160 mL of this solution were added to 16 g of CM-Dex and stirred.
After adjusting the pH to 4.75, EDC (0.32 g) was added and once again the pH was adjusted to 4.75. The solution was kept under stirring for 12 h and then, purified by dialysis using a membrane with a 12,000-14,000 nominal molecular weight cut off. This procedure afforded an amino-modified dextran (Dex-NH 2) solution with an estimated concentration of modified/unmodified dextran of 0.04 g mL -1, which was further modified with platinum derivatives as follows. A sample of this solution was freeze-dried for analysis that showed 14% of functionalized polymer molecules: anal. For (C 8H 12O 7) 6(C 10H 18N 2O 6).12H 2O: C 38.71, H 6.39, N 1.56%. Found: C 39.57, H 6.37, N 1.52%.
Fourier transform infrared spectroscopy (FTIR) (KBr) n max / cm -1: 3434 (O-H), 2924 (C-H), 1595 (C=O), 1280, 1156, 1016 (C-O) and 915, 845 (C-C). KPt(Dex-NH 2)Cl 3 (DexPt1)Potassium tetrachloroplatinate(II) (0.137 g, 0.33 mmol) was added to 30 mL of the Dex-NH 2 solution at pH ca. The light-red solution was stirred for 72 h. This reaction afforded a light yellow solution, which was purified by dialysis, using a membrane with a 12,000-14,000 nominal molecular weight cut off. The estimated concentration of the modified/unmodified dextran polymer was 24 mg mL -1 and the quantity of platinum complex was 71 µmol g -1 of dextran polymer. FTIR (KBr) ν max / cm -1: 3417 (O-H), 3265 (N-H, shoulder), 2927 (C-H), 1598 (C=O), 1278, 1156, 1022 (C-O) and 916, 850 (C-C). Pt(NH 3) 2(Dex-NH 2)(H 2O)(NO 3) 2 (DexPt2)To cis-Pt(NH 3) 2I 2 (0.484 g, 1.0 mmol) in dimethylformamide (DMF, 5 mL), silver nitrate (0.334 g, 1.98 mmol) was added as a solid and the mixture was kept in the dark for 24 h, under stirring.
The pale yellow suspension was centrifuged and the supernatant filtered through a 0.45 µm diameter porous filter. Evaporation of the solvent under vacuum yielded a dark-yellow residue of cis-Pt(NH 3) 2(DMF) 2(NO 3) 2. Then, 25 mL of a previously prepared Dex-NH 2 solution at pH ca. 7 were added to cis-Pt(NH 3) 2(DMF) 2(NO 3) 2 and the mixture, stirred for 72 h. Finally, the pale yellow solution was filtered and purified by dialysis using a membrane with a 12,000-14,000 nominal molecular weight cut off. The estimated concentration of the modified/unmodified dextran polymer was 30 mg mL -1 and the quantity of platinum complex was 318 µmol g -1 of dextran polymer.
FTIR (KBr) ν max / cm -1: 3434 (O-H), 3277 (N-H, shoulder), 2927 (C-H), 1591 (C=O), 1276, 1156, 1014 (C-O) and 913, 847 (C-C). Synthesis of superparamagnetic nanoparticles M6The preparation of maghemite nanoparticles M6 was recently reported in the literature. These particles have been obtained in aqueous medium, following a modified Massart procedure., Briefly, 75 mL of a 25% NH 3 aqueous solution was rapidly added to a solution containing 488 mL of 0.334 mol L -1 FeCl 3 and 0.175 mol L -1 FeCl 2, under vigorous stirring and at room temperature. The particles were isolated by magnetic decantation after 5 min and washed three times with distilled water. They were then treated with HNO 3/Fe(NO 3) 3 to fully oxidize magnetite (Fe 3O 4) to maghemite (γ-Fe 2O 3), which is more biocompatible, by adding 300 mL of 2 mol L -1 HNO 3, and kept under stirring. After 15 min, the supernatant was completely removed and 75 mL of 1 mol L -1 Fe(NO 3) 3 were added, followed by 130 mL of distilled water.
The suspension was refluxed for 30 min and cooled to room temperature. The supernatant was removed, 300 mL of 2 mol L -1 HNO 3 were added and the dispersion, stirred for 15 min. Finally, particles were isolated by magnetic decantation, washed three times with acetone, and redispersed in water.
The acetone residue was removed under vacuum. Coating of M6 nanoparticles with citric acid (M6@CA)A slightly modified procedure was used to prepare M6 nanoparticles coated with citric acid., After addition of 80 mL of a 0.1 mol L -1 citric acid solution to an aqueous dispersion of 50 mL of M6 (Fe ca. 15 mg mL -1), at pH 3.0, the suspension was heated at 80 °C for 30 min under mechanical stirring.
The particles were isolated by centrifugation and redispersed in distilled water. The dispersion was dialyzed using a membrane with a 12,000-14,000 nominal molecular weight cut off. Finally, the pH of the M6@CA dispersion was adjusted to 7.0. Coating of M6@CA nanoparticles with Dex-NH 2 (M6@CA@Dex)To a solution of 10 mL of M6@CA (Fe ca. 7 mg mL -1) at pH 7.0, under sonication, were slowly added 90 mL of a neutral solution of Dex-NH 2 (Dex ca. 0.04 g mL -1). EDC (0.383 g) was added, the pH adjusted to 7.0 and the solution was stirred for 12 h.
The particles were then isolated by centrifugation and redispersed in distilled water. Finally, the M6@CA@Dex particles were purified by dialysis using a membrane with a 50,000 nominal molecular weight cut off. Attachment of the PD onto the surface of M6 nanoparticles (M6@PD)Briefly, to a solution of 25 mL of maghemite M6 (Fe ca. 15 mg mL -1) under sonication was slowly added a suspension of the PD (1 mmol in 60 mL of distilled water). The mixture was heated for 4 h at 80 °C, under mechanical stirring. The particles were isolated by centrifugation and magnetic decantation and then, redispersed in distilled water and purified by dialysis using a membrane of 12,000-14,000 nominal molecular weight cut off. Finally, the pH of the M6@PD dispersion was adjusted to 7.0.
Attachment of platinum(II) complex functionalized dextran derivatives to citrate-coated nanoparticlesGeneral procedure: to a solution of 5 mL of M6@CA (Fe ca. 7 mg mL -1) at pH 7.0, under sonication, was slowly added 55 mL of a neutral solution of DexPt1 (Dex ca. 20 mg mL -1) or DexPt2 (Dex ca. 16 mg mL -1).
The EDC (0.23 g) was added, the pH adjusted to 7.0 and the solution, stirred for 12 h. The particles were then isolated by centrifugation and redispersed in distilled water. Finally, the M6@CA@DexPt1 and M6@CA@DexPt2 particles were purified by dialysis using a membrane with a 50,000 nominal molecular weight cut off. Evaluation of the colloidal propertiesA Zetasizer nano ZS equipment by Malvern Instruments was used to measure both the hydrodynamic diameter (D H, obtained by Z-average size values in the dynamic light scattering measurements) and the ζ-potential. The D H measurements were carried out in water and performed in a large range of pH values (2.0-12.0), as well as in the presence of PBS buffer. Furthermore, ζ-potential measurements were carried out using KNO 3 0.01 mol L -1 as the background electrolyte, and the isoelectric point (IEP) of nanoparticles were determined after measurements in a large range of pH values (2.0-12.0). HNO 3 and KOH were used to change the pH of the dispersions.The aggregation kinetics was evaluated using a Turbiscan Lab apparatus by Formulation.
In this equipment, a laser passes through the sample and the results are reported in transmittance (%). Thus, high transmittance values indicate that the sample undergoes rapid destabilization, followed by decantation. Measurements were performed placing 20 mL of the sample (Fe ca. 1.0 mg mL -1) in a sample holder and collecting data along 72 h.
The experiments were carried out in water and in the presence of PBS buffer at pH 7.4, at different concentrations. Synthesis and general characterizationThe platinum(II) complex functionalized dextran precursors were synthesized by complexation of the amino-modified dextran (Dex-NH 2) with K 2PtCl 4 and cis-Pt(NH 3) 2I 2, affording KPt(Dex-NH 2)Cl 3 (DexPt1) and Pt(NH 3) 2(Dex-NH 2)(H 2O)(NO 3) 2 (DexPt2), respectively. The compounds were purified by dialysis for 5-7 days; their identity was confirmed by FTIR data (see Experimental section) and the amount of platinum, determined by inductively coupled plasma atomic emission spectroscopy (ICP AES) analyses. Due to the low concentration of platinum in the samples the 195Pt NMR spectra could not be obtained and 1H NMR spectra of Dex-NH 2 and DexPt1-2 do not show appreciable differences.Iron oxide nanoparticles (γ-Fe 2O 3, M6) were prepared by acid treatment of magnetite particles (Fe 3O 4), obtained by a modified Massart method., This procedure leads to the oxidation of the Fe 3O 4 core into γ-Fe 2O 3, activating the nanoparticles surface and thus improving their colloidal properties.
The γ-Fe 2O 3 nanoparticles are more stable than Fe 3O 4 and have been approved by the FDA (Food and Drug Administration, USA) for in vivo applications.According to TEM images, the M6 particles exhibit spherical morphology and the particle-size distribution curve shows diameter of 6.5 ± 0.2 nm. The identity of the iron oxide with ferrite structure was confirmed by X-ray diffraction (XRD) data and indexed to an inverse spinel structure (JCPDS 34-1346, maghemite). The average crystallite size of 6 nm was calculated with the Scherrer equation using full-width at half maximum of the (311) X-ray diffraction peak. Good agreement between the XRD and TEM data is observed.
Figure 1 Transmission electron micrographs of M6, M6@CA and M6@PD, and particle-size distributionsModifications on the surface of M6 nanoparticles with citric acid (CA) and the platinum(IV) complex PD ( cis, cis, trans-Pt(NH 3) 2Cl 2(HOOCCH 2CH 2COO)(OH)) were carried out at 80 °C, affording M6@CA and M6@PD, respectively. No significant size changes are observed after this treatment according to the particle-size distribution curves that show mean diameters of 6.2 ± 0.3 nm and 5.8 ± 1.1 nm for M6@CA and M6@PD, respectively. According to TEM images, the spherical morphology of dextran-coated nanoparticles M6@CA@Dex, M6@CA@DexPt1 and M6@CA@DexPt2 is maintained.The FTIR spectra of the maghemite nanoparticles before and after the functionalizations are shown in.
Besides the characteristic maghemite ν(Fe-O) modes observed at 636-630, 584-578, 441-436 and 408-396 cm -1, a sharp intense band at 1385 cm -1, assigned to N-O modes, is observed in the spectrum of M6, due to the presence of residual nitric acid used to oxidize the particles and adjust the pH. The spectra of M6@CA and M6@PD exhibit bands at 1258-1256 and 1065-1040 cm -1 attributed to the vibrations of carboxylic and methylene groups, respectively. FTIR data also confirmed the attachment of amino-modified dextran (Dex-NH 2) and platinum(II) complex functionalized dextran (DexPt1-2) precursors onto M6@CA nanoparticles, affording the M6@CA@Dex and M6@CA@DexPt1-2 nanosystems (, and ). They show the typical amide group ν((C=O)-NH) (1604-1598 cm -1), asymmetric CH 2 (2936-2923 cm -1), carboxylic group ν(C-O) (at around 1280, 1155 and 1015 cm -1) and α-glucopyranose ring deformation modes (917 and 852 cm -1). All spectra show the ν(O-H) modes at 3442-3400 and 1635-1624 cm -1 indicating the presence of physi- and chemisorbed water molecules, respectively. Figure 2 FTIR spectra of M6@PD and M6@CA@DexPt1-2 nanoparticles.Thermal analysis (TG-DTA, -) reveals the organic content of the functionalized nanoparticles.
Total weight loss of 13% is observed for M6@CA nanoparticles, whereas the M6@CA@Dex, M6@CA@DexPt1 and M6@CA@DexPt2 nanosystems show 77, 66 and 62% weight losses, respectively, in one step, starting at around 150 °C, due to decomposition of the dextran coating. These results confirm that the adopted method to attach dextran derivatives onto the surface of M6@CA is effective, affording high amounts of polymer coating.The platinum and iron contents as well as the Pt/Fe ratios (mmol g -1) were determined by ICP AES. In the M6@PD nanomaterial, a concentration of 0.54 mmol of platinum per gram of iron was observed, whereas in the M6@CA@DexPt1 and M6@CA@DexPt2 systems, 0.32 and 1.20 mmol of platinum complex per gram of iron were observed, respectively. Evaluation of the superparamagnetic behaviorThe magnetic behavior of the superparamagnetic nanosystems functionalized with platinum complexes M6@PD and M6@CA@DexPt1-2 was investigated in the solid state. Shows the field dependence of the magnetization per mass of sample at 250 K. According to these data, M6@PD and the uncoated M6 nanoparticles exhibit almost the same saturation magnetization value (M sat ca. 65 emu g -1), due to the low concentration of PD complex attached onto the surface of the nanoparticles., Furthermore, the diamagnetic nature of the coating molecules has a negligible contribution to the magnetic properties of the samples., However, the effect of the dextran coating on the magnetization of the nanoparticles is noticeable, e.g., for M6@CA@DexPt1 a decrease of 54% on the M sat was observed (M sat = 30 emu g -1).
This result is related to the high amount of dextran polymer attached onto the surface of the M6 nanoparticles (according to TG-DTA data). The curves of magnetization versus temperature taking into account the TG-DTA results have been plotted. Thus, the magnetization data are reported in emu per gram of bared nanoparticles, i.e., emu per gram of nanoparticles without organic content. At 250 K the M sat values for M6, M6@PD and M6@CA@DexPt1 are 73, 76 and 89 emu g -1. All systems share the same core, but the M6@PD and M6@CA@DexPt1 samples also contain platinum, which is not lost in the TG-DTA measurements. Therefore, a comparison of these data is not direct, because the quantity of platinum is relatively high, e.g.,%Pt/Fe (m/m) are 9.5 and 5.8% for M6@PD and M6@CA@DexPt1, respectively. Thus, it is not possible to consider that the remaining mass of M6@PD and M6@CA@DexPt1 is composed only of iron oxide.
Figure 3 Field dependence of the magnetization (M) measured at 250 and 5 K (inset) for M6, M6@PD and M6@[email protected] magnetic data at 250 K indicate that M6@PD and M6@CA@DexPt1 are superparamagnetic because the coercivity (H C) values are zero. The uncoated iron oxide core (M6) exhibits same behavior and this is attributed to the small size of the nanoparticles and, even after several modifications on the surface, these systems remain superparamagnetic. At low temperature (5 K, inset), however, M6@PD and M6@CA@DexPt1 show H C values of 170 and 180 Oe, respectively. These similar values suggest that neither the nature nor the amount of coating material on the surface of the nanoparticles significantly affects the interparticle interactions or modify the surface layer. This result is different from previous work of our group in which we observed that functionalizations with distinct phosphonate- and dextran-based derivatives have led to lower H C and higher M sat values when compared to the uncoated nanoparticles.To confirm the superparamagnetic nature of the nanosystems the temperature dependence of the zero-field-cooled (ZFC) and field-cooled (FC) magnetizations was studied.
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According to ZFC/FC curves, these nanosystems show superparamagnetic behavior at room temperature. However, the blocking temperature (T B) determination for the M6@PD, M6@CA@DexPt1 and M6@CA@DexPt2 samples is not accurate (T B values are between 150 and 200 K). All FC curves are flat below T B indicating dipolar interactions even after surface modification. Thus, the results of ZFC and FC curves suggest that the nanosystems exhibit large size distributions, as confirmed by TEM images. Colloidal properties evaluationThe aqueous aggregate sizes of M6 nanoparticles were determined over a large range of pH values. Figure 4 Hydrodynamic diameter (D H) in water and ζ-potential versus pH, in 0.01 mol L -1 KNO 3 for (a) M6@PD; (b) M6@CA@DexPt1 and (c) M6@CA@DexPt2; (d) destabilization kinetic plots of M6 in water and M6@PD and M6@CA@DexPt1-2 in 0.01 mol L -1 PBS.PD attachment onto the surface of M6 shifts the isoelectric point (IEP) to pH 8.1, giving a surface charge of +16 mV at pH 7.0. Despite the low positive surface charge on M6@PD, the system exhibits D H.
Scheme 2 Mechanistic pathway for the synthesis of the Dex-NH 2 precursor.Therefore, the second strategy of SPIONs coating with platinum(II) complexes functionalized dextran yielded superior results, due to a combination of electrostatic interactions and steric repulsions, in comparison with direct attachment of the carboxylate platinum(IV) complex PD, see. Indeed, improved aqueous stability is observed for M6@CA@DexPt1 and M6@CA@DexPt2 with D H values below 100 nm over a large pH range (2.0-12.0) (, and ).Having confirmed the stability of the nanosystems in aqueous medium, their behavior in PBS buffer was evaluated. The M6@PD nanosystem exhibits D H of 46 nm at pH ca. 7 in water, but in PBS buffer aggregation takes place and D H increases to 172 nm ( and ). These results are in agreement with the destabilization plots ( and ), confirming that in PBS buffer rapid agglomeration occurs.
Interestingly, however, the M6@CA@DexPt1-2 nanosystems are unaffected by PBS buffer. Indeed, their D H are almost the same in water and in PBS buffer ( and ) and according to the destabilization kinetic plots (, and ), both nanosystems are stable over 72 h.
ConclusionsBeyond doubt, studies of the ionic strength and the presence of phosphate anions on the colloidal stability of nanosystems is the first step in their evaluation for biomedical applications. Our results show that the attachment of platinum drugs onto the surface of small SPIONs (M6@PD) without a protective coating is not suitable because the PBS buffer fully affects ionic strength, leading to agglomeration of the particles. The platinum(II) complex functionalized dextran-coated SPIONs (M6@CA@DexPt1-2) exhibit good dispersion properties under these conditions, without agglomeration over a large pH range (2.0-12.0). Furthermore, the use of different platinum complexes in the M6@CA@DexPt1-2 systems leads to similar colloidal properties. AcknowledgmentsThe authors would like to thank the Brazilian agencies National Council for Scientific and Technological Development (CNPq: Jovens Pesquisadores em Nanotecnologia grant number 5-0 and G. Da Silva was recipient of Science without borders fellowship grant number 2-9), Brazilian Federal Agency for Support and Evaluation of Graduate Education (CAPES) and Rio de Janeiro Research Foundation (FAPERJ) for financial support.
Vargas and C. Ronconi are recipients of CNPq research fellowships. We also thank the Multiuser Laboratory of Material Characterization (R. Morales would like to thank NANOMAG project (EC FP-7 grant agreement number 604448) for funding. X-ray diffraction, FTIR spectroscopy and thermogravimetric and chemical analysis were carried out in the support laboratories of Instituto de Ciencia de Materiales de Madrid (ICMM/CSIC).
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