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Folate-Conjugated Chitosan-Pluronic P123 Nanogels: Synthesis and Characterizations towards Dual Drug Delivery.

1. Introduction

In the past few decades, polysaccharide-based amphiphilic copolymers have been widely studied as drug and gene delivery systems due to their specific interactions with several kinds of bioactive molecules [1, 2]. Through the orientation of distinctive segments of these amphiphilic copolymers in aqueous solution, their self-assembly models induce various desirable core-shell platforms with a homogeneous particle size. The most substantial advances of core-shell nanoparticles are the ideal location in which hydrophobic agents such as chemotherapy drugs (cisplatin, paclitaxel, etc.), bioactive compounds (curcumin, quercetin, etc.), fluorescent probes (pyrazole, etc.), or genes/proteins can be protected by the hydrophilic segments organizing into the shell, whereas the pharmacokinetics of this compound become more significant [3-7]. Along with the advantage of a core-shell nanostructure, the introduction of natural polymers such as chitosan, heparin, or hyaluronic acid also helps to protect nanoparticles from opsonization due to the imparting of a stealth effect on the shell [8-10]. Moreover, because of the nature of the polysaccharide, the polysaccharide based amphiphilic copolymers could improve the biocompatibility of the nanocarriers as well as enhance the interaction with biological entities such as the surface protein of the cell membrane leading to a viable drug delivery strategy.

Among amphiphilic copolymers, pluronics are well-known as biocompatible polymers. The range application of pluronics has been expanding to include various therapeutic formulations in both academic and industrial fields. Several pluronics are listed in U.S. pharmacopoeia and are approved for various medical uses as excipients [11-13]. Among them, pluronic P123 (P123) is particularly appropriate as a carrier for water-insoluble drugs, e.g., paclitaxel, docetaxel, and curcumin [14, 15]. Due to the low value of CMC (4.4 x [10.sup.-6] mol/l) and a higher ratio of hydrophobic segments (hydrophilic-lipophilic balance, HLB = 8), P123 provides a strong capacity for hydrophobic drug loading [16]. Despite its effectiveness in the entrapment of hydrophobic drugs, the use of P123 as a carrier is still unpopular due to a potential dissolution of the cell membrane [15-17]. To eliminate the remaining problem of P123 related to its solubility and biological compatibility, P123 is usually fabricated with other drugs analogous to P123 with higher CMC and HLB values [15, 17]. For example, pharmacokinetic and biodistribution studies demonstrated that PTX-loaded P123/F127 could significantly increase the blood circulation time of PTX as compared to PTX loading P123 alone [18]. As another strategy to overcome the above problem, the modification of polysaccharides has recently been a popular approach [16]. Through a grafting method, the pluronic-conjugated polysaccharide resulted in the increased bioavailability of the carrier along with a high capacity for drug packaging. A pluronic F127-grafted chitosan (CP) was successfully published in our previous study [16]. A colloidal dispersion of pluronic F127-grafted chitosan was under a core-shell structure with good biocompatibility, an immense capacity for packaging drugs, as well as excellent stability of micelles [19-23]. In addition, a chemically modified pluronic F127 with heparin [24] was successfully developed for a dual-drug delivery system in which the synergistic anticancer efficacy of curcumin and cisplatin was well-displaced in in vivo experiments [25]. However, despite the positive results of pluronic F127-grafted polysaccharide nanogels in drug delivery, there was a lack of reports related to this approach to the remaining problem of P123 in a drug delivery system. Moreover, by using an appropriate nano-carrier, the synergistic effect against cancer cell growth may improve effectiveness in cancer treatment [26]. Gao et al. [27] established that the codelivery of PTX and Cur in single-carrier-based MPEG-PCL was a powerful strategy for cancer treatment as compared to a single Cur or PTX-loaded micelles at the same dose. The combination of Cur and PTX in PLGA-phospholipid nanoparticles [28] or PEG-PNB-TC nanoformulation [29] strongly supports this point. Based on the aforementioned backgrounds, a cotherapy using Cur and PTX can not only palliate drug resistance but also amplify their anticancer capacity by reason of a synergistic therapeutic effect [27-29].

In this study, a new amphiphilic folate-conjugated chitosan-pluronic P123 nanogel was developed as an effective drug carrier system. It was proposed, therefore, that the use of a CP-FA nanocarrier to codeliver PTX and curcumin (Cur) would lead to an improvement in drug efficacy. The incorporation of a new amphiphilic CP copolymer with the synergistic PTX and Cur drugs could be a potential dual-drug delivery system in the future.

2. Materials and Methods

2.1. Materials. Chitosan from shrimp shells with low-viscosity (code 50494-25G-F), pluronic P123 (P123, 5.800 MW), folic acid, curcumin, and paclitaxel were purchased from Sigma-Aldrich. 3-Amino-1-propanol (Ami), p-nitrophenyl chloroformate (NPC), 1-ethyl-3-3-dimethyl aminopropyl carbodiimide (EDC), and N-hydroxysuccinimide (NHS) were supplied by Acros Organics. Solvents were obtained from Scharlau's Chemicals. Cellulose dialysis membranes (MWCO 14 kDa and MWCO 3.5 kDa) were bought from Spectrum Laboratories (USA).

2.2. Methods

2.2.1. Synthesis of Folate-Conjugated Chitosan-Pluronic P123 Nanogels. Folate-conjugated chitosan-pluronic P123 (CP-FA) was prepared via four stages as presented in Figure 1. P123 pluronic was first activated by NPC to obtain NPC-P123-NPC. Then, NPC-P123-NPC was partially substituted with Ami to produce NPC-P123-OH, followed by conjugation with chitosan to obtain an amphiphilic CP copolymer through carbamate formation. In the final stage, folic acid was conjugated with a CP copolymer using a carbodiimide coupling reagent.

(1) Synthesis of NPC-P123-NPC. P123 (15gram, 2.59mmol) was activated with NPC (1.06 gram, 5.31 mmol) at 65[degrees]C under stirring. After 24 h, the temperature of the reaction was reduced to R.T. before adding chloroform. Then, the product was collected by precipitation in a diethyl ether/hexane mixture (1:1 v/v). The obtained paste precipitant was dried in a vacuum oven to obtain NPC-P123-NPC.

(2) Synthesis of NPC-P123-OH. NPC-P123-NPC (12 gram, 1.94 mmol) was dissolved in chloroform solution (1: 20 w/v). Then, the solution of Ami (2.04 mmol) in chloroform (1:20 v/v) was added dropwise into the NPC-P123-NPC solution (molar ratio of NPC-P123-NPC and Ami was 1 : 1.05). After 24 hours, the resultant was precipitated in a diethyl ether/hexane mixture (1 : 1 v/v). The paste precipitant was dried under vacuum condition to obtain NPC-P123-OH.

(3) Synthesis of Chitosan-Grafted P123 (CP). Chitosan (100 mg) was dissolved in 20 ml of acidic media (pH~5.0). NPC-P123-OH (1 gram) was dissolved in 20 ml of ethanol and then added dropwise into the chitosan solution under stirring at room temperature for 24 hours. Finally, the product was dialyzed against cold distilled water using a cellulose membrane (MWCO = 12 kDa) for 7 days and then lyophilized to obtain a powdery product of CP. To evaluate the loading ability of hydrophobic drugs, various feed weight ratios of P123 were conducted to graft onto chitosan (chitosan : 123 =1 : 5, 1: 10, 1: 15, and 1:20 by mass).

(4) Synthesis of Folic Acid-Conjugated CP. A solution of folic acid was activated by EDC and NHS (molar ratio =1 : 1 : 1) in anhydrous DMSO (1 mg of folic acid/1 ml DMSO). The activated folic acid was then dropped slowly to a CP solution (100mg/1 ml DI water) and stirred at room temperature in the dark for 12 h to obtain a folate-conjugated CP. Regarding the grafting degree of P123 onto chitosan (by TGA calculation), the molar ratio of folic acid and glucosamine used was used 1: 2. Finally, the product was dialyzed against DI water for 7 days using a cellulose membrane (MWCO = 12 kDa) and then lyophilized to obtain a powdery product of CP-FA. [sup.1]H-NMR (Bruker AMX-500) measurements were used to identify the chemical structure of copolymers. TGA (PerkinElmer TGA-7) was also used to assess compositions of the grafted copolymers.

2.2.2. Preparation and Characterizations of Nanogels. P123 micelles and CP nanogels were prepared in DI water. CMC values of the amphiphilic copolymers were determined via the iodine method using a UV-Visible spectrophotometer (Shimadzu UV-1700 PharmaSpec, Japan) at wavelengths from 300 to 400 nm. The CMC values of the copolymer solution were calculated from the intersection of the two regression lines at which the vertical axis presented the absorption intensity, whereas the logarithm copolymer concentration was in a horizontal coordination [28]. Morphology and size distribution of the nanoparticles were characterized by transmission electron thermal stability microscopy (JEM-1400 JEOL) and dynamic light scattering (Nano Particle Analyzer SZ-100), respectively.

2.2.3. Preparation of Drug-Loaded Micelles (Nanogels) and Their Release Behavior. For drug encapsulation, a different amount of curcumin or PTX ethanol solution was added dropwise into 100 mg carriers (CP or CP-FA) that were soluble in DI water under stirring condition. Ethanol solvent was evaporated to form drug-encapsulated nanogels via a hydrophobic interaction with the hydrophobic PPO blocks of P123. Subsequently, the mixtures were hydrated in 10 ml of DI water and kept for 24 hours at RT to allow free drugs to settle down; this was followed by lyophilizing to obtain a powdery product of drug/copolymer mixtures. The amount of curcumin and/or PTX was determined by using UV absorbance at a wavelength of 420 nm and 254 nm, respectively. The encapsulation efficiency percent (EE (%)) and drug loading percent (DL (%)) in the micelles were calculated using the following equation:

EE(%) = weight of the drug in micelles/weight of the feeding drugs x 100%, DL (%) = weight of the drug in micelles/weight of copolymers and drugs x 100%. (1)

An in vitro drug release study was conducted by a diffusion method [24,25]. Briefly, four milligrams of a drug/copolymer was dispersed in 2 ml of fresh phosphate-buffered saline (PBS; pH = 7.4) and then transferred into a dialysis bag (MWCO = 3.5 kDa). Each dialysis bag was immersed in single vials containing 50 ml of the release medium under mild shaking at 37[degrees]C. For each sample, 5 ml of the release medium was withdrawn at predetermined time intervals and replaced by the fresh medium at the same volume.

2.2.4. In Vitro Cytotoxicity. The cytotoxic effects of CP-FA, free PTX, PTX-loaded CP-FA (pTX-CP-FA), PTX/Cur-loaded CP-FA (PTX/Cur-CP-FA), and Cur-loaded CP-FA (Cur-CP-FA) were determined by the sulforhodamine B (SRB) colorimetric assay, using MCF-7 cells as the cancer cell model. All tested samples were first screened at 100 [micro]g/ml before making a serial dilution in order to identify the half-maximal inhibitory concentration (IC50) values. Briefly, MCF-7 cells were cultured in 96-well plates at a density of [10.sup.4] cells per well for 24 h; then, various concentrations of drugs or its encapsulated nanocarriers were added, while the same volume of pure culture media was added into negative control wells. After 48 h of culture, all wells were fixed with 50% (w/v) trichloroacetic acid (Merck) solution for 1-3 h before being stained with 0.2% (w/v) SRB (Sigma-Aldrich) for 60 min. 10 mM Tris base solution (Promega) was applied after the unbound dye was removed by 1% acetic acid (Merck) (in mM). The percentage of growth inhibition (%I) was calculated according to the optical density values of 492 nm and 620 nm according to the following formula:

%I =(1 - O[D.sub.t]/O[D.sub.c]) x 100, (2)

where O[D.sub.t] and O[D.sub.c] are the optical density values of the test sample and the control sample, respectively. Camptothecin (Calbiochem) was used as a positive control. All trials were repeated at least 3 times (n = 3) and the data was presented as the mean [+ or -] SD.

3. Results and Discussions

3.1. Characterization of the Activated P123, CP, and CP-FA. Figure 2(a) shows the [sup.1]H-NMR spectrum of NPC-P123-NPC revealing the first success of the modified P123. Along with the proton signals on aromatic groups of NPC at [delta]-8.3 ppm (a) and [delta]-7.4 ppm (b), the proton of P123 was also exhibited. The resonance peak at [delta]~3.6 ppm (c) was characteristic of the protons on the -C[H.sub.2]- group in the PEO block, whereas the resonance peaks at [delta]~1.1 ppm (d), 3.4 ppm (e), and 3.5 ppm (f) were characteristic of the protons of the -C[H.sub.3], -C[H.sub.2]-, and -CH- groups on PPO chains, respectively. The successfully activated P123 was disclosed via the chemical shift at [delta]~4.4 ppm (g) according to the proton on the terminal methylene ester group on C[H.sub.2]-O-NPC. By using integral areas of the resonance peak at [delta]~7.4 ppm (b) and 1.1 ppm (d), approximately 100% of the terminal hydroxyl groups were activated by NPC. The [sup.1]H-NMR spectrum of NPC-P123-OH also clearly shows resonance peaks characteristic of the protons of the P123 chain as in the spectrum of NPC-P123-NPC (Figure 2(b)). The appearance of the peak at [delta]~4.2 ppm (h) assigned to the methylene proton of Ami proved the success of the partially substituted step. From this spectrum, only 48.7% of the NPC groups remained in the NPC-P123-OH.

Grafting NPC-P123-OH onto a chitosan backbone was conducted at pH 5.0 to enhance the formation of the covalent bond between the NPC moiety and the amine groups on chitosan. The [sup.1]H-NMR spectrum of CP (Figure 3(a)) clearly exposes the resonance peaks of protons on P123 structures to accompany the appearance of two peaks at [delta]~2.7 ppm (i) and [delta]~2.0 ppm (j), which were assigned to protons at C2 carbon and the acetyl proton unit in chitosan. Besides, the disappearance of chemical signals of NPC at [delta]~8.3 ppm (a) and [delta]~7.4 ppm (b) indicated that P123 had been successfully grafted onto chitosan.

The [sup.1]H-NMR spectrum of CP-FA (Figure 3(b)) presented the appearance of three peaks at [delta]~8.8 ppm (m), [delta]~7.4 ppm (k), and [delta]~6.7 ppm (L), attributed to the proton resonance of the folate aromatic. The result could confirm that the CP-FA copolymer was obtained for targeted application towards the MCF-7 cancer cell in a further study.

The thermal stabilities of P123, chitosan, CP, and CP-FA were analyzed by TGA (Figure 4). The initial thermal decomposition of chitosan was at 100[degrees]C corresponding to the removal of absorbed water and following a main step at 250[degrees]C. This further process happened slowly at 500[degrees]C. P123 exhibited one-step decomposition; the initial thermal decomposition point started at 340[degrees]C and almost completed weight loss at 420[degrees]C. The TGA curves of CP(1: 10) contained features of both chitosan and P123 resulting in two steps of weight loss; the first was at 250[degrees]C inheriting from chitosan and rapid thermal decomposition at 340[degrees]C following the nature of P123. This patent was similar as other ratio grafting (the TGA curves of CP(1: 5), CP(1: 15), and CP(1:20) were not shown). The weight loss behavior of folic acid was partially similar to chitosan, but it had a lower thermal decomposition than that of chitosan. The initial thermal decomposition of folic acid was at 200[degrees]C and slowly decomposed according to the increase of the temperature. In addition, the TGA curves of CP-FA showed a slightly higher thermal stability as compared to CP in the range of 100 to 370[degrees]C and of 420 to 550[degrees]C. The difference revealed the evidence for the presence of the conjugated FA moieties in a CP copolymer.

The composition of each polymer could be identified through the thermal behavior of P123 and of chitosan as well as various CP samples at 420[degrees]C at which P123 was fully decomposed [25]. The content of the pluronic grafted onto a chitosan chain was in the range from 73.92 to 89.90 wt/wt% (Table 1) and reached the equilibrium of grafting reaction when the initial feeding amount of P123 was at 93.75% (CP(1:15)). Even with a further increase, the grafted efficiency of a fed P123 was nonsignificantly changed due to the steric effect of the prior P123-grafted moieties.

3.2. Characterization of Micelle and Nanogel Formation. The relationship between the CMC value and the hydrophobic drug loading efficiency of the micelles or nanogels was investigated in previous reports [16, 30, 31]. Moreover, the stability of the compound-loaded micelles also depends on the value of CMC [31]. In this study, CMC values were determined using the iodine method [30]. Solubilized iodine ion is involved in the hydrophobic environment of the PPO blocks, causing the conversion of [I.sup.-.sub.3] into [I.sub.2] from the residual KI in the solution [30]. Under CMC values, surfactants exhibit as unimers rather than in micelles; thus, no conversion of [I.sup.-.sub.3] into [I.sub.2] induces the constant in the absorption intensity of the mixture solution. After micelle formation, [I.sup.-.sub.3] is transformed into [I.sub.2] that is entrapped into the hydrophobic space of PPO blocks leading to a dramatic increase in the absorption intensity as demonstrated in Figure 5(a). The absorption intensity of [I.sub.2] had been plotted as a function of copolymer CP concentration (Figure 5(b)). Figure 5(c) indicates that the CMC values of various CP and CP-FA formulations were much lower than that of pure P123. An increasing amount of the grafted P123 or a high content of P123 in the CP copolymer contributed to enlarging the CMC value. Many previous studies have also shown that conjugation with polysaccharides leads to a reduction of the CMC value of pluronics [6, 32]. Chitosan attacks pluronic chains and shields the hydrophobic blocks from interaction with water reducing the interfacial free energy of the polymer-water system. Minimizing interfacial free energy helps to reduce the concentration at which micelle formation begins [33]. Hence, the lower CMC values were expected.

Along with the changing CMC as the amount of the grafted P123 increased, the size distribution of the pluronic-based nanogels was also reduced as the P123 content increased in the CP copolymer because a compacted core structure occurred when a hydrophobic force is predominant (Table 2). The zeta potentials of CP and CP-FA formulation micelles indicated that the surface charges were positive as a result of the N[H.sup.3+] groups of chitosan. In the case of the higher grafted ratio, a decrement in zeta potential could be seen due to the loss of the functional N[H.sub.2] groups of chitosan by binding to P123. The high zeta potentials of CP nanogels imply that the core-shell structure was produced in high stability forms.

Transmission electron microscopy (TEM) images of the P123, CP, and CP-FA nanogels (Figures 6(a1)-6(f1)) show that the nanoparticles (P123, CP(1:5), CP(1:10), CP(1: 15), CP(1: 20), and CP-FA) were in a spherical shape with a size diameter of 40.05 [+ or -]7.50, 38.00 [+ or -]6.62, 32.17[+ or -] 2.31,28.63 [+ or -] 2.34,26.70 [+ or -] 2.36, and 24.27 [+ or -] 2.01 nm, respectively. However, TEM images in Figures 6(a3)-6(f3) show that the diameter of the nanoparticles are much smaller than that from DLS (Figures 6(a1)-6(f1)). This is because the basis for the measurement of the particle size of DLS is hydrodynamic diameter, which includes polymer shells and hydration layers as well as the swelling of chitosan and PEO block in a water environment leading to a larger particle size [16]. Moreover, in Figures 6(a3)-6(f3), the normalized intensity autocorrelation functions [g.sub.2]([tau]) fit to stretched exponential forms which could indicate that the nanoparticles were produced at the spherical micelles without free unimers [34]. Together with a moderate positive value of the zeta potential (Table 2), the results could confirm that the nanoparticles showed a high stability in colloidal solution without any dissolution or aggregation.

3.3. Characterization and Encapsulation Efficiency of Drug-Loaded CP Nanogels. The CP with very low CMC values should select an appropriate vehicle for encapsulating a drug into the core of micelles. At concentrations above CMC values, micelles are protected by a hydrophilic outer shell that limits the attraction of hydrophobic drugs into the core of micelles when the emulsion methods are used. The thin film method seems to have more advantages for encapsulating a drug into micelles [35-37]. As shown in Figure 7(a), the highest encapsulation efficiencies (EE) could be seen in a range of Cur concentrations from 5 to 10%. EE did not increase when the Cur concentration was elevated further. The CP(1:10) performed with the highest EE reaching approximately 100%. This copolymer also showed the highest drug loading capacity as seen in Figure 7(b). It is interesting that an increment in hydrophobic P123 moieties in CP(1:15) and CP(1:20) did not lead to improving the entrapment and loading capacity of hydrophobic Cur. The results offer that a positively charged chitosan backbone could have an impact on the EE and DL values via the electrostatic interaction of the protonated chitosan and partially negatively charged Cur [16]. This suggested that a high encapsulation of Cur contributed by both hydrophobic and electrostatic interactions of CP copolymers and the bioactive molecule. Due to a well-performed encapsulation ability, CP(1: 10) was selected as an appropriate platform for further studies.

For further study, CP(1: 10) was also investigated for the encapsulation of PTX. As shown in Table 3, the loading ability was the most effective at concentrations of 2 wt/wt%. When the concentrations of PTX were fed at 4 and 8 wt/wt%, PTX encapsulation efficiencies decreased significantly. In our hypothesis, the PTX loading capacity was low despite a high amount of feeding. This might be due to its strong hydrophobicity as compared to Cur. The average size of the PTX-loaded CP(1:10) was dependent on the PTX loading amount. The mean size increased gradually in the range of the fed PTX from 1 to 8 wt/wt%. This behavior could be explained by the bulky structure of PTX resulting in an increase of the PTX-loaded nanoparticles. The zeta potential result of samples showed that all nanogels formed under the positively charged form. Regarding Cur and PTX loading in a single investigation, the CP(1: 10) formulation could be selected for encapsulating 10 and 2 wt/wt%, respectively. Furthermore, CP(1 : 10) was selected to conjugate folic acid towards the fabrication of targeted delivery in inhibitory cancer cell growth.

3.4. Characterizations of Dual Cur/PTX-Loaded CP-FA. According to the optimal encapsulating content of Cur- (or PTX-) loaded CP, dual-loading PTX and Cur were at 2 and 10 wt/wt% onto CP-FA, respectively. The results showed that the encapsulating ability was not significantly changed for each drug as seen in Table 4. In the PTX-loaded formulations, an increment of size distribution could be observed from DLS measurement. The size distribution of the drug-loaded nanocarriers also followed the trend of TEM results, in which dual drug-loaded nanogels appeared in the biggest spherical shape as compared to single-loading CP-FA (Figure 8). These obtained results were strongly supported for discussion related to the bulky structure of PTX.

3.5. In Vitro Release Behavior. The drug release profile is a critical parameter for evaluating the effectiveness of a delivery system. The CP-FA nanogels were investigated for the release profile behavior of single and dual drugs at physiological condition (pH 5.6 and pH 7.4). In general, all drugs performed in a sustained-release manner as seen in Figure 9. The cumulative release rate of PTX from PTX/Cur-loaded CP-FA was slightly higher than that of its release rate from PTX-loaded CP-FA. The cumulative release profile of Cur from a dual PTX/Cur-loaded CP-FA was lower than that of a single-loaded CP-FA. This could be explained by a higher hydrophobic interaction of PTX or PTX/Cur with a hydrophobic domain in CP-FA resulting in the well-controlled release of the loaded PTX or PTX and Cur. The behavior is similar to that found in Nguyen et al.'s study in which a hydrophobic drug had a slightly slower release behavior from a higher hydrophobic platform [25]. In addition, Figures 9(a) and 9(b) show the release profile of PTX and Cur affected by the incubated media that exhibited a faster release rate at pH 5.6 as compared to pH 7.4. For instance, the PTX cumulative release rates increased from 16.08% at pH 7.4 to 23.80% at pH 5.6 for PTX/Cur-CP-FA after 48 h. At the same time, the Cur cumulative release rates performed in a similar behavior. This pH-dependent PTX and Cur release could be explained by the protonation of the CP-FA platform resulting in the swelling behavior of nanogels that lead to a higher release rate of PTX and Cur. The sustained and pH-dependent release of PTX and Cur could be significant for enhancing drug accumulation at the tumor site and for achieving intracellular release of the combined anticancer drugs.

3.5.1. In Vitro Cytotoxicity. In recent years, there have been several reports on the synergistic effect of phytocompounds and anticancer drugs in clinical treatment [38, 39]. A combination of the effect in nanocarriers has also received much attention [27-29]. In this study, CP-FA, free PTX, PTXCP-FA, PTX/Cur-CP-FA, and Cur-CP-FA were evaluated for inhibitory activity against MCF-7 cancer cell growth using a sulforhodamine B (SRB) colorimetric assay. After 48 h of incubation, the result showed that CP-FA exhibited an inhibitory value at 18 [+ or -]0.5% at 100 [micro]g/ml of screening concentration. Free PTX exhibited very high cytotoxicity with an IC50 value of 4.04 [+ or -] 1.02 nM. However, after loading in a CP-FA nanogel, the cytotoxicity of PTX was significantly reduced to a IC50 value of 8.20 [+ or -] 1.41 nM. In the case of a single-loaded Cur, Cur-CP-FA performed a low anticancer activity (IC50 = 13.00 [+ or -] 1.42 [micro]M). It is highly attractive that the dual-drug-loaded nanogel (PTX/Cur-CP-FA) significantly enhanced toxicity against MCF-7 cancer cell growth (IC50 = 5.74 [+ or -]0.23 nM) as compared to a single-PTX-loaded platform. Free PTX exhibited a better cytotoxic activity with a lower IC50 value than PTX-CP-FA and PTX/Cur-CP-FA, owing to a different amount of PTX present in the cytoplasm of MCF-7 cells. According to the release profiles, only 19.46% or 13.05% PTX was released from CP-FA at pH 5.6 and pH 7.4 after 48 h, respectively. This means that the concentration of PTX from CP-FA in MCF-7 cells is lower than that of free PTX in MCF-7 cells. Moreover, free PTX could readily deliver into the cytosol via passive diffusion and be quickly effective, whereas the drug-loaded platforms were mainly taken up by cells via the endocytic pathway (due to the charge surface of vesicles) and then the drugs released PTX in a sustained manner resulting in certain cytotoxicity. The results also agreed with some previous reports in which a free drug is more cytotoxic than a drug-loaded platform [40, 41]. As seen in Figure 10, the dual-loading formulation exhibits a higher activity than that of a single-loading sample (PTX-CP-FA) starting from 1.17 nM of PTX-loaded concentration. These results could confirm a synergistic effect of Cur and PTX in the new CP-FA nanogel. The work should also be studied further to clarify the role of the FA targeting ligand in the specific delivery of Cur and PTX towards cancer cells.

4. Conclusions

In this paper, we successfully developed a series of differently amphiphilic-grafted chitosan-P123 copolymers characterized towards drug delivery. The current results indicated that CP(1: 10) performs highly efficiently in Cur and PTX drug loading. The CP formulation was utilized for conjugating the FA-targeted ligand. The CP-FA nanogels exhibited great behavior with a hydrophobic drug encapsulation efficiency that was up to 98.63 [+ or -] 0.42 of PTX and 97.82 [+ or -] 0.48 of Cur. The size of the dual-loaded CP-FA nanogels were distributed at 60.57 [+ or -] 0.21 nm which may be appropriate for cell endocytosis. The release profile behavior of drug-loaded CPFA depended on pH. Moreover, the combination of the dual drugs in the CP-FA delivery platform could offer a synergistic effect against cancer cell growth. The dual-drug-loaded nanogel (PTX/Cur-CP-FA) significantly enhanced toxicity against MCF-7 cancer cell growth (IC50 = 5.74 [+ or -] 0.23 nM) that was better than that of the PTX-loaded platform (IC50 = 8.20 [+ or -] 1.41 nM). Regarding these obtained results, the work exhibited some positive facets that could pave a way for further studies to clarify the effectiveness of PTX/Cur-loaded CP-FA in the specific delivery for cancer treatment in vivo.

https://doi.org/10.1155/2019/1067821

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was funded by the Vietnam National Foundation for Science and Technology Development (NAFOSTED) under grant number 104.02-2017.60.

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Van Toan Nguyen, (1,2) Thi Huong Nguyen, (3) Le Hang Dang, (4) Hieu Vu-Quang [ID], (5) and Ngoc Quyen Tran [ID] (2,4)

(1) Institute of Research and Development, Duy Tan University, Da Nang City 550000, Vietnam

(2) Graduate University of Science and Technology, Vietnam Academy of Science and Technology, Ho Chi Minh City 700000, Vietnam

(3) Institute of Chemistry and Material, Hanoi City 100000, Vietnam

(4) Institute of Applied Materials Science, Vietnam Academy of Science and Technology, Ho Chi Minh City 700000, Vietnam

(5) NTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City 700000, Vietnam

Correspondence should be addressed to Hieu Vu-Quang; vqhieu@ntt.edu.vn and Ngoc Quyen Tran; tnquyen979@gmail.com

Received 16 July 2019; Revised 16 October 2019; Accepted 1 November 2019; Published 21 December 2019

Academic Editor: Hassan Karimi-Maleh

Caption: Figure 1: Preparation of chitosan-P123 copolymers.

Caption: Figure 2: [sup.1]H-NMR spectra of NPC-P123-NPC (a) and NPC-P123-OH (b).

Caption: Figure 3: [sup.1]H-NMR spectrum of CP (a) and CP-FA (b).

Caption: Figure 4: TGA of P123 (a), folic acid (b), chitosan (c), CP(1: 10) (d), and CP-FA (e).

Caption: Figure 5: Illustration of [I.sub.2] micellization (a), plot of UV-Vis intensity of [I.sub.2] versus copolymer concentrations (b), and CMC value of various copolymers (c) (n = 3).

Caption: Figure 6: TEM micrographs and DLS of P123 (a), CP(1: 5) (b), CP(1: 10) (c), CP(1: 15) (d), CP(1:20) (e), and CP-FA (f).

Caption: Figure 7: Encapsulation efficiencies (a) and drug loading (b) of various Cur-loaded CP formulations (n = 3).

Caption: Figure 8: TEM images of PTX-CP-FA (a), PTX/Cur-CP-FA (b), Cur-CP-FA (c), and CP-FA nanogels.

Caption: Figure 9: In vitro release of Cur (a) and PTX (b) from CP-FA at various pH values (7.4 and 5.6) (n = 3).

Caption: Figure 10: Cytotoxicity of PTX-CP-FA and PTX/Cur-CP-FA on MCF-7 cancer cells (n = 3).
Table 1: Composition and grafted degree of the CP copolymers
calculated from TGA curves.

               Chitosan   Pluronic   Grafted ratio    Grafted
Formulations   content    content    chitosan: P123   degree
                 (%)        (%)                         (%)

CP(1 : 5)       26.08      73.92        1 : 3.5        56.69
CP(1 : 10)      16.05      83.95        1 : 5.09       52.29
CP(1 : 15)      11.91      88.09        1 : 7.39       49.31
CP(1 :20)       10.01      89.90        1 : 8.98       44.51

Table 2: DLS, zeta potentials, and CMC of P123 and various CP
micelles in DI water (n = 3).

Formulations   DLS (nm)   Zeta potential (mV)       CMC (mg/ml)

P123            104.80    -8.77 [+ or -] 0.52   0.085 [+ or -] 0.003
CP(1 : 5)       97.20     60.77 [+ or -] 1.60   0.036 [+ or -] 0.002
CP(1 : 10)      78.60     58.40 [+ or -] 0.54   0.038 [+ or -] 0.002
CP(1 : 15)      69.63     57.00 [+ or -] 1.10   0.076 [+ or -] 0.003
CP(1 :20)       64.70     51.43 [+ or -] 0.92   0.078 [+ or -] 0.002
CP-FA           51.10     39.43 [+ or -] 3.45   0.036 [+ or -] 0.002

Table 3: EE, DL, DLS, and zeta potentials of various PTX-loaded
CP(1: 10) formulations (n = 3).

Sample   CP (mg)   PTX (mg)         EE (%)                DL (%)

1          100        1       97.5 [+ or -] 0.48    0.97 [+ or -] 0.01
2          100        2       97.65 [+ or -] 1.35   1.91 [+ or -] 0.03
3          100        4       61.07 [+ or -] 0.40   2.35 [+ or -] 0.02
4          100        8       41.29 [+ or -] 0.59   3.06 [+ or -] 0.04

Sample     Size (DLS, nm)      Zeta potentials (mV)

1        49.60 [+ or -] 1.10   36.27 [+ or -] 1.60
2        52.80 [+ or -] 1.85   34.03 [+ or -] 0.86
3        53.90 [+ or -] 0.57   31.23 [+ or -] 0.09
4        63.47 [+ or -] 0.60   24.30 [+ or -] 1.02

Table 4: EE, DL, and DLS of various Cur and PTX-loaded CP-FA
formulations (n = 3).

Samples   CP-FA (mg)   PTX (mg)   Cur (mg)            EE (%)

1            100          2          --         98.21 [+ or -] 0.49
2            100          2          10      98.63 [+ or -] 0.42 (PTX)
                                             97.82 [+ or -] 0.48 (Cur)
3            100          --         10         99.13 [+ or -] 0.35

Samples            DL (%)                 DLS (nm)

1            1.93 [+ or -] 0.01      53.93 [+ or -] 0.65
2         1.76 [+ or -] 0.01 (PTX)   60.57 [+ or -] 0.21
          8.83 [+ or -] 0.01 (Cur)
3            9.01 [+ or -] 0.01      44.83 [+ or -] 0.25
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Title Annotation:Research Article
Author:Nguyen, Van Toan; Nguyen, Thi Huong; Dang, Le Hang; Vu-Quang, Hieu; Tran, Ngoc Quyen
Publication:Journal of Nanomaterials
Geographic Code:9VIET
Date:Dec 1, 2019
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