Poloxamer 407/TPGS mixed micelles for delivery of gambogic acid to breast and multidrug-resistant cancer

被引:152
作者
Saxena, Vipin [1 ]
Hussain, M. Delwar [1 ]
机构
[1] Texas A&M Hlth Sci Ctr, Dept Pharmaceut Sci, Irma Lerma Rangel Coll Pharm, Kingsville, TX USA
关键词
gambogic acid; Poloxamer; 407; TPGS; P-glycoprotein; multidrug resistance; breast cancer; POLYMERIC MICELLES; P-GLYCOPROTEIN; POLYETHYLENE-GLYCOL; BLOCK-COPOLYMERS; CARCINOMA CELLS; PLURONIC P123; IN-VITRO; DRUG; APOPTOSIS; SUCCINATE;
D O I
10.2147/IJN.S28745
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Delivery of a high concentration of anticancer drugs specifically to cancer cells remains the biggest challenge for the treatment of multidrug-resistant cancer. Poloxamers and D-alpha-Tocopheryl polyethylene glycol 1000 succinate (TPGS) are known inhibitors of P-glycoprotein (P-gp). Mixed micelles prepared from Poloxamer 407 and TPGS may increase the therapeutic efficacy of the drug by delivering high concentrations inside the cells and inhibiting P-gp. Gambogic acid (GA) is a naturally derived novel anticancer agent, but poor solubility and toxic side effects limit its use. In this study, we have developed Poloxamer 407 and TPGS mixed micelle-encapsulating GA for the treatment of breast and multidrug-resistant cancer. Methods: GA-loaded Poloxamer 407/TPGS mixed micelles were prepared using a thin film hydration method, and their physicochemical properties were characterized. Cellular accumulation and cytotoxicity of the GA-loaded Poloxamer 407/TPGS mixed micelles were studied in breast cancer cells, MCF-7 cells, and multidrug-resistant NCI/ADR-RES cells. Results: The diameter of GA-loaded Poloxamer 407/TPGS mixed micelles was about 17.4 +/- 0.5 nm and the zeta potential -13.57 mV. The entrapment efficiency of GA was 93.1% +/- 0.5% and drug loading was about 9.38% +/- 0.29%. Differential scanning calorimetry and X-ray powder diffraction studies confirmed that GA is encapsulated by the polymers. The in vitro release studies showed that mixed micelles sustained the release of GA for more than 4 days. Results from cellular uptake studies indicated that GA-loaded Poloxamer 407/TPGS mixed micelles had increased cellular uptake of GA in NCI/ADR-RES cells. Cytotoxicity of GA-loaded Poloxamer 407/TPGS mixed micelles was found to be 2.9 times higher in multidrug-resistant NCI/ADR-RES cells, and 1.6 times higher in MCF-7 cells, as compared with unencapsulated GA. Conclusion: This study suggests that Poloxamer 407/TPGS mixed micelles can be used as a delivery system for GA to treat breast and multidrug-resistant cancer.
引用
收藏
页码:713 / 721
页数:9
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