卡培他滨
PLGA公司
结直肠癌
乙醇酸
细胞毒性
药理学
药品
化学
纳米颗粒
癌症研究
癌症
医学
体外
纳米技术
材料科学
乳酸
内科学
生物化学
生物
遗传学
细菌
作者
Sonia Pandey,Sanganala Mattha Vijayendra Swamy,Udhshu Mansha Ubaid Ulla,Arti Gupta,Hetal Patel,Jitendra Singh Yadav
标识
DOI:10.2174/1567201813666160817150621
摘要
Capecitabine, an anti cancer drug, has a very short drug elimination half-life (0.49 to 0.89 h). High doses and absence of targeting ability in the colon region may lead to more side effects to the patients with colon cancer.To develop and optimize sustained release nanoparticles for effective treatment of colon cancer.Eudragit S100-PLGA(poly (lactic-co-glycolic acid)) nanoparticles were prepared by a double emulsification, solvent evaporation method followed by high-pressure homogenisation evaluated and the particles were evaluated for surface morphology, particle size analysis, polydispersity index, drug content, % entrapment efficiency and in vitro drug release. To optimize the batch a 32 full factorial design was applied. The optimized batch was evaluated for cytotoxicity and cellular uptake study.The optimized formulation exhibited 179.25 nm mean particle size, 71.27% of drug entrapment efficiency and 81.824% drug release up to 72 h. When the concentration of capecitabine was increased from 50-500 μg/ml, the % cytotoxicity of nanoparticles and capecitabine (pure drug) increased from 8.5 to 97.70% and 2.7 to 82.23%, respectively. As per a cellular uptake study, the optimized nanoparticles were completely uptaken by HT 29 adenocarcinoma cells within 2 to 4 h.Optimized Eudragit S100-PLGA nanoparticles are a promising delivery system for colon targeting.
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