A novel paclitaxel-loaded poly(D,L-lactide-co-glycolide)-Tween 80 copolymer nanoparticle overcoming multidrug resistance for lung cancer treatment
Authors Yuan X, Ji W, Chen S, Bao Y, Tan S, Lu S, Wu K, Chu Q
Received 12 July 2015
Accepted for publication 7 March 2016
Published 25 May 2016 Volume 2016:11 Pages 2119—2131
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Dr Lei Yang
Xun Yuan,1,* Wenxiang Ji,2,* Si Chen,1 Yuling Bao,3 Songwei Tan,3 Shun Lu,2 Kongming Wu,1 Qian Chu1
1Department of Oncology, Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 2Lung Tumor Clinical Medical Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, 3School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People’s Republic of China
*These authors contributed equally to this work
Abstract: Drug resistance has become a main obstacle for the effective treatment of lung cancer. To address this problem, a novel biocompatible nanoscale package, poly(D,L-lactide-co-glycolide)-Tween 80, was designed and synthesized to overcome paclitaxel (PTX) resistance in a PTX-resistant human lung cancer cell line. The poly(D,L-lactide-co-glycolide) (PLGA)-Tween 80 nanoparticles (NPs) could efficiently load PTX and release the drug gradually. There was an increased level of uptake of PLGA-Tween 80 in PTX-resistant lung cancer cell line A549/T, which achieved a significantly higher level of cytotoxicity than both PLGA NP formulation and Taxol®. The in vivo antitumor efficacy also showed that PLGA-Tween 80 NP was more effective than Taxol®, indicating that PLGA-Tween 80 copolymer was a promising carrier for PTX in resistant lung cancer.
Keywords: poly(D,L-lactide-co-glycolide), Tween 80, nanoparticle, drug resistance, lung cancer
Due to lack of early detection or screening test, lung cancer patients are often not recognized and diagnosed until they have reached advanced stages, resulting in a poor 5-year overall survival rate of 16.8% in the USA, whereas the outcomes are worse in the developing world.1 Presently, Taxol® is among the first-line formulations of paclitaxel (PTX) that is usually involved in the treatment of non-small-cell lung cancer, which has the highest mortality rate among cancers.2 However, Cremophor EL, an adjuvant used in the formulation of Taxol®, has been associated with severe side effects, including allergic reactions, nephrotoxicity, and neurotoxicity.3 Besides, PTX resistance is seen in over 70% of initially diagnosed patients and almost all recurrent patients. Anticancer drug resistance poses one of the biggest challenging threats to successful lung cancer chemotherapy. It is reported that tumor cells develop chemoresistance through mechanisms such as overexpression of ATP-driven multidrug resistance (MDR) efflux transporters (P-glycoprotein [p-gp]), apoptosis-associated protein Bcl-2, and nuclear factor kappa B.4 Among these, the membrane-bound p-gp-mediated resistance to PTX is frequently observed in cancer.5 p-gp, a product of the ABCB1 (MDR1) gene, is a pump that effluxes out the drug from cells, thus reducing intracellular drug accumulation.6 Some p-gp inhibitors have shown restoration of cancer cell sensitivity to chemotherapy drugs.7 However, a major problem with p-gp inhibitors is that they may also block anticancer drug efflux from normal cells, thus increasing the toxic effects of chemotherapy.8
In order to eliminate the Cremophor EL and in an attempt to reduce the exposure of normal cells to PTX and p-gp inhibitors, alternative formulations have been extensively researched, such as emulsion, micelle, liposome, and nanoparticles (NPs).9–11 Nanomedicine, using NPs to simultaneously deliver p-gp inhibitor along with the anticancer drug, holds the greatest promise for these purposes in cancer treatment.12 It is well known that NPs passively extravasate tumors through capillaries surrounding the tumor tissue via the enhanced permeation and retention effect, leading to the targeted delivery of anticancer drug into the tumor tissue and reducing side effects.13 Besides, NPs could overcome cancer drug resistance by a mechanism of encapsulating drug and reducing their efflux from cells.14 In addition, NPs could be controlled to release the drug gradually and effectively, and prolong the circulation half-life of drug in plasma, which demonstrates that the application of NPs in anticancer drug delivery systems shows superiority over the conventional chemotherapy.15 NPs, made of natural or synthetic macromolecules, have been extensively explored by scientists.16–19 The unique physical properties allow them to be used as imaging probes to locate and identify cancerous lesions. Apart from the application in cancer diagnosis, there has been a great interest in developing new nanomaterials for cancer treatment.20,21 Poly (D,L-lactide-co-glycolide) (PLGA), a biodegradable and biocompatible synthetic polymer approved by the US Food and Drug Administration, is widely used in drug delivery system.22–24 Various studies have reported that multiple drug resistance could be overcome by PLGA NPs codelivering anticancer drug and p-gp inhibitors, indicating that PLGA NPs may be a promising approach to overcome drug resistance.25 Recently, a surge of interest using pluronic block copolymers, which consist of p-gp inhibitors to reverse drug resistance, has emerged due to their unique properties in the inhibition of drug efflux pump.26 Tween 80, a complex mixture of polyoxyethylene ethers used as emulsifiers or dispersing agents in pharmaceuticals, has also been demonstrated to function as a p-gp inhibitor.27,28
In the present work, we successfully synthesized PLGA-Tween 80 copolymer, which combined the advantages of PLGA and Tween 80 to convey chemotherapeutic agent PTX and reverse drug resistance. We investigated the physicochemical properties of PTX-loaded polymeric NPs, including size, zeta potential, and PTX release profile. The in vitro cytotoxicity, cellular uptake, cell cycle assay, and cellular apoptosis of PLGA-Tween 80 NPs in A549 and A549/T cells and in vivo antitumor efficacy in the model of lung cancer exnografts in nude mice were also evaluated. PLGA-Tween 80 NPs were first attempted and prospected to reverse resistance to PTX in lung cancer.
Materials and methods
PTX was purchased from Huafeng United Technology Co., Ltd. (Beijing, People’s Republic of China). PLGA-COOH was purchased from Shandong Institute of Medical Instruments (Jinan, People’s Republic of China). D-alpha tocopheryl polyethyleneglycol 1000 succinate (TPGS), N, N′-dicyclohexylcarbodiimide (DCC), Tween 80, N-hydroxysuccinimide (NHS), propidium iodide (PI), RNase A, Coumarin-6 (C-6), and trypsin-EDTA were obtained from Sigma-Aldrich Co. (St Louis, MO, USA). RPMI 1640 medium, penicillin–streptomycin, fetal bovine serum, and phosphate-buffered saline (PBS) were purchased from Hyclone (Logan, UT, USA). 3-(4,5-Dimethyl-thiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) and 4′,6-Diamidino-2-Phenylindole, Dihydrochloride were purchased from Biosharp (Hefei, People’s Republic of China). Annexin V-FITC/PI double staining assay kit was supplied by KeyGen Biotech Co. Ltd (Nanjing, People’s Republic of China). Trypan blue was purchased from TianGen (Beijing, People’s Republic of China). Taxol® (PTX for injection) was procured from Bristol-Myers Squibb Trading Co., Ltd. (Shanghai, People’s Republic of China). All other reagents were of analytical grade.
The human lung adenocarcinoma cell line (A549) and PTX-resistant human lung cancer cells (A549/T) were purchased from the KeyGen Biotech Co. Ltd. A549 cells were cultured in RPMI 1640 medium supplemented with 10% fetal bovine serum, 100 U mL−1 penicillin G sodium, and 100 μg mL−1 streptomycin sulfate (complete 1640 medium). A549/T cells were cultured in complete 1640 medium with additional 100 ng mL−1 PTX. Cells were maintained at 37°C in a humidified and 5% CO2 incubator. Ethical approval was not deemed necessary for this study according to the Ethical Committee of Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology.
Male Balb/c nude mice, 5 weeks old and weighing 18–20 g, were purchased from Beijing HFK Bio-Technology Co., Ltd. (Beijing, People’s Republic of China; certificate no SCXK 14-01-10-29G). The animals were housed at 25°C±1°C and 60%±10% humidity under a 12-hour light–dark cycle during the experiments. All animal experiments were performed in accordance with the principles of care and use of laboratory animals under the approval of the Ethics Committee of Huazhong University of Science and Technology.
Synthesis and characteristics of PLGA-Tween 80
PLGA-Tween 80 conjugate was synthesized by an esterification reaction (Figure 1). Briefly, 3.9 g of predried PLGA-COOH (0.3 mmol), 0.075 g of DCC (0.36 mmol), and 0.041 g of NHS (0.36 mmol) were dissolved in 20 mL of anhydrous DCM with magnetic stirring for 24 hours at room temperature. Then, 0.78 g of Tween 80 (0.6 mmol) was added in the liquid medium and reacted for 48 hours. The reacted solution was filtered with filter paper and precipitated in methanol two times to remove unreacted DCC and NHS. The structure of polymer was confirmed by 1H-NMR spectra (Bruker AM-400 spectrometer; Bruker, Lausanne, Switzerland) and Fourier transform infrared (FTIR) spectroscopy (Bruker VERTEX 70 spectrophotometer; Bruker, Karlsruhe, Germany).
Figure 1 Synthetic representation of PLGA-Tween 80 copolymer.
Preparation of PTX-loaded NPs
PTX-loaded NPs of PLGA and PLGA-Tween 80 were fabricated by a classical nanoprecipitation technique. Briefly, PLGA or PLGA-Tween 80 (19 mg) and PTX (1 mg) were dissolved in 2 mL of acetone by mild sonication. TPGS was dissolved into aqueous phase to reach 2 mg mL−1 concentration. The organic phase was subsequently added dropwise into the aqueous phase under magnetic stirring and then evaporated after 3 hours under vigorous stirring. The NP suspension was first centrifuged at 1,500 rpm for 10 minutes to remove large particles and aggregations and then filtered with a molecular weight cutoff of 20 kDa to collect the NPs. The resultant NP suspension was then recovered by centrifugation twice at 11,500 rpm for 20 minutes at 4°C. The resultant products were washed twice to remove unloaded PTX and then resuspended in water before lyophilization to get NP powder. The fluorescent NPs were prepared in the same way with PTX replaced by C-6. The sterilized NPs were made with similar method in the superclean bench under sterile conditions. Blank NPs consisting of only PLGA or PLGA-Tween 80 (without PTX loaded) were prepared for the toxicity evaluation.
Characteristics of PTX-loaded NPs
The surface morphology of PLGA and PLGA-Tween 80 was evaluated by transmission electron microscope (Tecnai G2 20, FEI, Eindhoven, the Netherlands). The particle size and surface charge of PTX-loaded PLGA and PLGA-Tween 80 were determined by dynamic light scattering (Zeta Plus; Brookhaven Instruments Corporation, Holtsville, NY, USA). The drug-loading content of the NPs was determined by high-performance liquid chromatography (Hitachi L-2000; Hitachi Ltd., Tokyo, Japan) using a reverse phase Inertsil® ODS-3 C18 column (150 cm ×4.6 mm, pore size 5 μm; Agilent Technologies, Santa Clara, CA, USA) with a mobile phase consisting of acetonitrile and purified water (50/50, v/v) at a flow rate of 1.0 mL min−1. The effluents were monitored three times to detect PTX at 227 nm with a UV/vis detector and quantified by comparing the peak areas with the standard curve.
Drug release experiments were carried out in vitro as follows. In brief, 10 mg samples of PLGA and PLGA-Tween 80 NPs were separately introduced into a dialysis bag (molecular weight cut-off =5,000 Da), and the end-sealed dialysis bag was submerged fully into 25 mL of PBS (pH 7.4) with 1% Tween 80 at 37°C with stirring at 120 rpm. At time intervals (1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 24 hours, 72 hours, 120 hours, and 168 hours), 10 mL of the medium was withdrawn for analysis of PTX concentration. Thereafter, the medium was replaced with an equal volume of fresh PBS. The concentration of PTX released was analyzed by high-performance liquid chromatography as described previously.
Cellular uptake experiment
A549 cells or A549/T cells were seeded at a density of 1×104 cells well−1 in a 24-well plate, which kept cover slips in per well and allowed to attach overnight. Then, the cells were incubated with fresh medium containing 0.125 mg mL−1 C-6-loaded PLGA or PLGA-Tween 80 NPs for different incubation times with 1 hour, 2 hours, and 4 hours at 37°C. C-6 was selected as a model compound based on its high sensitivity of determination in the cell cytoplasm.29 The sample wells were washed twice with PBS to remove the excess NPs that were not taken up by the cells. After fixing with 100 μL 4% paraformaldehyde for 15 minutes, the cells were washed twice again with cold PBS. The intracellular fluorescence was determined using a fluorescence microscope (IX71; Olympus Corporation, Tokyo, Japan). The same imaging parameters were executed. The intensity of fluorescence was determined using a flow cytometer (BD Biosciences, San Jose, CA, USA). Both the qualitative images by fluorescence microscope and the quantitative mean fluorescence intensity analyzed by flow cytometry were done in triplicate.
In vitro cytotoxicity
The in vitro cytotoxicity of the drug-loaded PLGA-Tween 80 NPs was assessed using MTT assay. In brief, A549 cells and A549/T cells were seeded at a density of 5×103 cells/well into a 96-well culture plate and incubated for 24 hours under the condition of 5% CO2 at 37°C. The medium was then replaced with fresh culture media containing Taxol®, PTX-loaded PLGA NPs, and PTX-loaded PLGA-Tween 80 NPs at 1×10−7 mg mL−1, 1×10−5 mg mL−1, 1×10−3 mg mL−1, and 1×10−1 mg mL−1 equivalent PTX concentration. The control group was cells without treatment. After 48 hours, the medium was removed, and the wells were washed twice with PBS. The cells were then incubated with 100 μL of medium and 10 μL of MTT (5 mg mL−1 in PBS) for 4 hours at 37°C, and the precipitant was dissolved in 150 μL of dimethyl sulfoxide using an automated shaker. The absorbance of each well was read at 570 nm by a microplate reader (Multiskan2 MK3; Thermo Fisher Scientific, Waltham, MA, USA). Relative cell viability was calculated as the percentage in relation to untreated control cells. IC50 (concentration resulting in 50% inhibition of cell growth) value for drugs was determined by SPSS software (Version 19.0). The experiment was repeated in triplicate.
Cell apoptosis analysis
The cell apoptosis assay was assessed using Annexin V-FITC/PI double staining assay kit supplied by KeyGEN Biotech Co. Ltd. In brief, A549 cells and A549/T cells were seeded on the 24-well plates and treated with Taxol®, PTX-loaded PLGA NPs, and PTX-loaded PLGA-Tween 80 NPs at an equivalent PTX concentration of 1 μg mL−1 for 48 hours. The control group was cells without treatment. Then, the cells were collected in 400 μL of binding buffer and mixed with 5 μL of Annexin V-FITC and 10 μL of PI for 15 minutes in the dark. The stained cells were analyzed using a flow cytometer (BD Biosciences).
Cell cycle analysis
A549 cells and A549/T cells were seeded on the 24-well plates with 3 mL culture medium containing Taxol®, PTX-loaded PLGA NPs, and PTX-loaded PLGA-Tween 80 NPs at an equivalent PTX concentration of 1 μg mL−1. The control group was cells without treatment. After 48 hours, adherent and nonadherent cells were collected and fixed with 70% cold ethanol at 4°C for overnight. Then, RNase A (0.1 mg mL−1) was used to remove the interferential RNA. PI (1 mg mL−1) was used to dye the nucleus for 30 minutes in the dark. The DNA content was measured by flow cytometry (BD Biosciences), and the percentage of cells in each phase of the cell cycle was evaluated using the ModFit software.
In vivo antitumor efficacy
A total of 5×106 A549 cells were resuspended in 100 μL of PBS and injected subcutaneously into the right armpit of male nude mice (n=40). The length and width of tumor were measured using a caliper, and the tumor volume was calculated by the formula, (length × width2)/2.30 When tumors reached 100–150 mm3 in volume, mice were randomly assigned to four groups (n=10) and injected through the tail vein with saline, Taxol, PTX-loaded PLGA NPs, and PTX-loaded PLGA-Tween 80 NPs at an equivalent PTX concentration of 10 mg mL−1, respectively. Tumor progression in the mice was measured every 2 days, and then animals were sacrificed at the end of the experiment. Tumors were removed and observed by H&E staining.
All experiments were repeated at least three times. For the NP fabrication, in vitro drug release, cellular uptake, and cell cycle/apoptosis analysis, each sample was repeated for three times. As for in vitro cytotoxicity assay and in vivo antitumor efficacy, six wells/each sample and ten mice per group were executed here. The mean ± standard deviation was determined for each data in tables and figures. Statistical analysis was performed using a Student’s t-test. The differences were considered statistically significant with *P<0.05.
Results and discussion
Characterization of synthesized copolymer
PLGA, a polymer well established for enhancing drug solubility and bioavailability, has been widely used in the biomedical field of sustained and controlled release preparation and targeted drug delivery system.31 Various studies have also demonstrated that Tween 80-based NPs could inhibit the exocytosis of p-gp, increasing the concentration of chemotherapeutics in tumor cells.32 In this study, PLGA-Tween 80 conjugate was first synthesized via a one-step esterification reaction. The chemical structure of PLGA-Tween 80 was confirmed by 1H-NMR and FTIR spectra. Figure 2A shows the 1H-NMR spectra of PLGA and PLGA-Tween 80 copolymer. Compared to Tween 80, the newly appearing signals at 3.5 ppm in PLGA-Tween 80 were assigned to the CH2CH2O part of polyoxyethylene group of Tween 80, which verified the successful esterification of Tween 80. The molecular weight of PLGA-Tween 80 copolymers calculated by 1H-NMR results was 35,800 kDa (Figure 2A). Figure 2B shows the FTIR spectra of PLGA and PLGA-Tween 80 copolymers. Compared with PLGA, absorption band at ~3,500 cm−1 was absent in PLGA-Tween 80, which could be attributed to the –COOH of PLGA-COOH, which thus proved the occurrence of successful esterification. All these results indicate that the intended copolymer has been synthesized.
Characteristics of NP
As reported, the hydrophobic segment of PTX can interact with PLGA upon encapsulation in NPs, thus resulting in high encapsulation efficiency and loading content.33 In addition, hydrophilic materials (Tween 80), on the surface of PLGA NPs, could prolong the circulation half-time in plasma.34 We adopted a nanoprecipitation method to prepare PTX-loaded NPs. TPGS was used as a surfactant to facilitate NP formation in an acetone–water system.35 Tween 80 was not appropriate in fabricating PLGA NPs in the similar process as no stable and dispersed NPs can be recovered. Since applying Tween 80 as a surfactant cannot get a stable PLGA NP by the similar nanoprecipitation method in this research, we have not made comparison on following in vitro and in vivo experiment between PTX-loaded PLGA-Tween 80 and PTX-loaded PLGA NP formulated with Tween 80. The size, size distribution, and surface charge of NPs are shown in Table 1. It could be seen that the average size of PLGA-Tween 80 NPs was much smaller, and the particle size distribution was much narrower than those of PLGA NPs. Tween 80 in the copolymer offers a steric stabilization effect, avoiding aggregation of the particles, indicating that Tween 80 could act as a coemulsifier in the fabrication process, resulting in a smaller particle size and a narrow size distribution. Besides, the surface charge of PLGA-Tween 80 NPs was higher than that of PLGA NPs in terms of absolute value, suggesting the presence of a Tween 80 layer on the surface of the NP. As shown in Figure 3A, transmission electron microscopy was used to examine the morphology of PTX-loaded NPs. The transmission electron microscope images revealed that PLGA-Tween 80 NPs were nanometer-sized spherical particles. Furthermore, the particle size observed from transmission electron microscope image was a little smaller than the size measured by particles size analyzer which detected the hydrodynamic diameter.
Table 1 Particle size and zeta potential of PTX-loaded NP
It is known that sustained controlled drug release is essential for effective treatment.36 Figure 3B shows the in vitro release profiles of the PTX-loaded NPs. The results showed that ~70% of PTX was released from the NPs within the first 24 hours, followed by a slow continuous release over the next 6 days. The sustained release of PTX from the NPs at pH 7.4 demonstrates that the PTX-loaded NPs are stable during circulation in the blood. Furthermore, due to the slowly release rate of PTX, the side effects of the drug could be reduced, and the therapeutic efficacy could be greatly enhanced.
Cellular uptake experiment
It is well known that the therapeutic effects depend on the internalization of the drug by cells.37 The cellular uptake of PLGA and PLGA-Tween 80 NPs was performed using C-6-loaded NPs on A549 cells and A549/T cells. C-6, a fluorescence marker, has been reported as a probe for marking NPs in cellular uptake experiments.38 As shown in Figure 4A and B, for both formulations, the cellular uptake of the NPs by A549 cells and A549/T cells was time dependent. The cellular uptake efficiency of PLGA-Tween 80 NPs was seen to be higher than that of PLGA NPs on A549 cells, which suggested that PLGA-Tween 80 could effectively facilitate PTX into cells. But on A549/T cells, the difference between the cellular uptake of C-6-loaded PLGA and that of C-6-loaded PLGA-Tween 80 was larger as exhibited by remarkable brightness in Figure 4A and enhanced mean fluorescence in Figure 4B. It demonstrated that PLGA-Tween 80 could effectively facilitate drug into A549/T cells.
In vitro cytotoxicity experiment
The cytotoxicity of Taxol® and PTX-loaded NPs against A549 and A549/T cells at the equivalent PTX concentrations of 1×10−7 mg mL−1, 1×10−5 mg mL−1, 1×10−3 mg mL−1, and 1×10−1 mg mL−1 (n=4) were evaluated. It was shown in Figure 5 that the IC50 values of free PTX against A549 and A549/T cells were 0.002 mg mL−1 and 0.008 mg mL−1, respectively, which suggested that A549/T cells exhibited high drug resistance to PTX. In addition, the IC50 value of PTX-loaded PLGA-Tween 80 NPs was 0.57 μg mL−1 against A549 cells and showed similar cytotoxicity with free PTX and PTX-loaded PLGA NPs, which suggested that PLGA-Tween 80 copolymer had little effect on the sensitive cells. However, the IC50 of PLGA-Tween 80 NPs against A549/T cells was 1.26 μg mL−1, which was eightfold and threefold lower than that of free PTX and that of PLGA NPs, suggesting that in A549/T cells, PLGA-Tween 80 NPs displayed more remarkable cytotoxicity than free PTX and PLGA NPs. Since that the cellular uptake of PLGA-Tween 80 NPs in A549/T cells was significantly higher than that of PLGA NPs (Figure 4), the increased uptake of PTX in PLGA-Tween 80 caused more cytotoxicity (Figure 5). These could explain why PLGA-Tween 80 showed obvious effects to A549/T cells but showed similar cytotoxicity compared with free PTX on A549 cells. Thus, PLGA-Tween 80 copolymer could increase the anticancer activity of PTX and overcome PTX resistance in lung cancer.
Cell cycle analysis
It has been proved that the antitumor mechanisms of PTX were associated with apoptosis, mitosis inhibition, and cell cycle arrest in G2/M phase.39 Thus, the increased G2/M phase arrest indicated more therapeutic effect of PTX. The cell cycle arrest of Taxol® and PTX-loaded NPs against A549 and A549/T cells at the equivalent PTX concentrations of 1 μg mL−1 was examined. As shown in Figure 6, A549/T cells treated with Taxol® had similar cell cycle distribution (G2/M, 11.1%) compared with control group (G2/M, 4.9%), demonstrating that A549/T cells exhibited high drug resistance to PTX. On the other hand, PTX-loaded PLGA-Tween 80 NPs had relatively larger cell cycle arrest in A549 cells and A549/T cells than PLGA NPs and Taxol® (P<0.05), which suggested that PLGA-Tween 80 could significantly block the cells in the G2/M phase. As shown in Figure 6, cell cycle arrest in G2/M phase was significantly increased from 14.8±4.8 and was 51.1%±10.0% significant for PTX-loaded PLA-Tween 80 NPs on A549 cells, which was ~2.1- and 1.4-fold of Taxol® and PTX-loaded PLGA NPs. On A549/T cells, PTX-loaded PLGA-Tween 80 NPs enhanced the cell cycle arrest on G2/M phase up to 32.5%±8.0%, which was ~5-, 3.0-, and 1.4-fold higher than the control, Taxol®, and PTX-loaded PLGA NPs, respectively (Figure 6J). These results indicated that PLGA-Tween 80 could induce cell cycle arrest in PTX-resistant A549/T cells.
Cell apoptosis assay
To certify that PLGA-Tween 80 NPs could induce multidrug resistant cell apoptosis, Annexin-PI staining assay was performed to analyze the percentage of early cell apoptosis treated with various formulation of PTX. Figure 7 shows that PTX administration for 48 hours displayed limited apoptosis compared with control group in A549/T cells, which demonstrated the strong resistance of A549/T to PTX. On the other hand, PTX-loaded PLGA-Tween 80 NPs caused relatively higher apoptosis in A549 cells and A549/T cells than PLGA NPs and Taxol®, which suggested PLGA-Tween 80 could induce apoptosis significantly. For example, the percentage of early apoptosis of Taxol® and PTX-loaded PLGA NPs in A549/T cells was 6.88% and 11.15%, respectively. However, the percentage of early cell apoptosis of PLGA-Tween 80 NPs was 29.12%. As shown in Figure 7I, the apoptosis induced by Taxol, PTX-loaded PLGA NPs, and PLGA-Tween 80 NPs on A549 cells was 11.8%±4.2%, 22.0%±3.8%, and 31.4%±6.4%, respectively. On the contrary, PTX-loaded PLGA-Tween 80 NPs caused more apoptosis on A549/T cells compared with Taxol and PTX-loaded PLGA NPs as shown in Figure 7J (P<0.01). The ratio of apoptosis was increased from 6.9%±1.7%, 8.5%±1.5%, and 12.6%±1.8% for the control, Taxol, and PLGA NPs, respectively, up to 28.4%±0.9% for PLGA-Tween 80 NPs. These results demonstrated that PLGA-Tween 80 copolymer significantly lowered the apoptosis threshold of drug resistant cells and enhanced PTX-induced apoptosis.
In vivo antitumor efficacy
The average tumor size and body weight were measured during the experiment to monitor the antitumor efficacy and the toxicity (Figure 8). As shown in Figure 8A, weak tumor inhibitory effect was caused by the Taxol group. PLGA-Tween 80 NPs treatment could inhibit the growth of the tumor with final tumor volume =238.5 mm3. The final tumor volume of Taxol group and PLGA group was 273.3 mm3 and 252.6 mm3, which indicated that PLGA-Tween 80 could enhance PTX induced apoptosis. The tumor volume of PLGA-Tween 80 group was only 87% of the Taxol group, that is, the antitumor efficacy of PLGA-Tween 80 NPs was superior to that of PTX treatments, which suggested that PLGA-Tween 80 NPs had significant advantages over Taxol in suppressing A549 solid tumors. However, there is no significant difference between PLGA-Tween 80 NPs and PLGA NPs in antitumor efficacy (P>0.05). Furthermore, the difference among Taxol, PLGA NPs, and PLGA-Tween 80 NPs was not so remarkable, although the difference between Taxol and PLGA-Tween 80 NPs showed significant difference (P<0.05). Moreover, the body weights of mice (Figure 8B) with any treatments had no serious loss, which suggested that no significant toxicity was induced by Taxol or PLGA-Tween 80. Tumor tissue was investigated by HE staining (Figure 8C). It seems that the antitumor efficacy of PTX-loaded PLGA-Tween 80 NPs was the strongest as compared to other groups, which was consistent with the in vitro cell experiment. However, it seems that single drug-loaded NPs demonstrated some kind of efficacy against tumor growth inhibition but not so efficient.21 It may be attributed to the tumor heterogeneity, complexity of drug resistance, and barriers of NPs circulating and crossing in vivo.19,29,30 There are already substantial efforts to incorporate multiple functionalities and moieties within the nanoparticle design. The design for site-specific delivery of therapeutics will be considered in future such as inducing the targeting agent. While there are great strides made in nanomedicine, the nanoparticles formulations for anticancer drug are still limited in clinical evaluation and practice. The considering about the barriers to translation are still absent, such as the blood compartment effect on the in vivo drug retention, tumor extravasation and accumulation, tumor penetration and tumor uptake. The obstacles such as the nonspecific distribution and inadequate drug accumulation remain challenges. The critical features also need further study on the characters of nanoparticles such as the size, zeta potential, shape, stability, surface roughness and functionalization, etc. In future, combinational chemotherapeutic drug treatment or combined with immunotherapy would be recommended to get complete tumor inhibition.40–43
PLGA-Tween 80 NPs delivering PTX to overcome PTX resistance in lung cancer cells were first designed and investigated. PLGA-Tween 80 could effectively deliver PTX, facilitate drug into A549 and A549/T cells, and exhibit detectable cytotoxicity on A549/T cells. The IC50 of PLGA-Tween 80 NPs against A549/T cells was eightfold lower than that of free PTX. Downregulation of p-gp protein by PLGA-Tween 80 could increase PTX accumulation in A549/T cells. Better antitumor efficacy of PLGA-Tween 80 NPs was also observed on nude mice bearing A549 cells. Therefore, the codelivery of PTX by PLGA-Tween 80 could be a more powerful approach for effective chemotherapy in resistant human lung cancer.
This work was supported by NSFC no 81301929 and National Key Scientific Instrument Special Program of China no 2013YQ030923 and Hubei Province Health and Family Planning Scientific Research Project no WJ2015Q009.
The authors report no conflicts of interest in this work.
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