Centre for Nanotechnology & Advanced Biomaterials (CeNTAB), School of Chemical & Biotechnology, SASTRA University, Thanjavur, India.
Centre for Nanotechnology & Advanced Biomaterials (CeNTAB), School of Chemical & Biotechnology, SASTRA University, Thanjavur, India.
Mater Sci Eng C Mater Biol Appl. 2015 Feb;47:40-7. doi: 10.1016/j.msec.2014.11.027. Epub 2014 Nov 8.
Pancreatic cancer is the fourth leading cancer with 85% mortality rate in USA alone and it is prevalent in many other developed and developing countries. Clinically, gemcitabine is prescribed as the first line chemotherapeutic drug for pancreatic cancer treatment. Gemcitabine-loaded poly(lactide-co-glycolide) (PLGA) nanospheres were synthesized and their physico-chemical properties were evaluated. The FESEM images showed that the gemcitabine loaded and blank nanospheres were 180 nm and 200 nm, respectively. The optimized encapsulation efficiency of gemcitabine was 15%. It was observed that 100% of gemcitabine was released from the PLGA nanospheres for 41 days in phosphate buffered saline (PBS) at pH7.4. The uptake of nanospheres in MiaPaCa-2 cells was studied using sulforhodamine B loaded PLGA nanospheres and our results showed that the nanospheres were taken up within 3h. Furthermore, the cytotoxicity of PLGA nanospheres loaded with gemcitabine showed a relative decrease in IC50 in MiaPaCa-2 and ASPC-1 pancreatic cancer cells in comparison to free gemcitabine. The study demonstrates that this system hold promise to improve the therapeutic efficacy of gemcitabine in vitro.
在美国,胰腺癌的死亡率高达 85%,是第四大常见癌症,在许多其他发达国家和发展中国家也很普遍。临床上,吉西他滨被规定为治疗胰腺癌的一线化疗药物。本文合成了负载吉西他滨的聚(乳酸-共-乙醇酸)(PLGA)纳米球,并对其理化性质进行了评价。FESEM 图像显示,负载吉西他滨的和空白纳米球的直径分别为 180nm 和 200nm。吉西他滨的最佳包封效率为 15%。在 pH7.4 的磷酸盐缓冲盐水(PBS)中,观察到 41 天内 100%的吉西他滨从 PLGA 纳米球中释放出来。本文使用负载 sulforhodamine B 的 PLGA 纳米球研究了纳米球在 MiaPaCa-2 细胞中的摄取情况,结果表明纳米球在 3h 内被摄取。此外,与游离吉西他滨相比,负载吉西他滨的 PLGA 纳米球的细胞毒性使 MiaPaCa-2 和 ASPC-1 胰腺癌细胞的 IC50 相对降低。该研究表明,该系统有望提高吉西他滨在体外的治疗效果。