Kesharwani Prashant, Tekade Rakesh K, Jain Narendra K
Pharmaceutics Research Laboratory, Department of Pharmaceutical Sciences, Dr. Hari Singh Gour University, Sagar, 470003, MP, India,
Pharm Res. 2015 Apr;32(4):1438-50. doi: 10.1007/s11095-014-1549-2. Epub 2014 Oct 18.
Folate conjugated poly(propyleneimine) (PPI) dendrimer (FPPI) mediated anticancer therapy is being extensively discovered throughout the world. The present investigation was aimed at exploring the targeting potential of Melphalan loaded FPPI of different generations (MP-FPPI) for effective management of cancer.
The MP-FPPI formulations were compared for drug entrapment efficiency, in vitro release profile, toxicology, folate receptor blockage assay, cell uptake assay, stability studies, and in vivo studies.
Upon increasing the dendrimer generation from fourth to fifth, the drug delivery parameters improved negligibly except the toxicological profile that improved exponentially. MTT assay in case of MCF-7 cells depicted the IC 50 values of 8 ± 0.15, 0.9 ± 0.02, 0.2 ± 0.01 and 10 ± 0.17 μM, respectively in case of MP-FPPI3, MP-FPPI4, MP-FPPI5, and free Melphalan suggesting folate based targeting to be the efficacious approach to kill cancer cells. The median survival time for tumor bearing mice treated with MP-FPPI3, MP-FPPI4, MP-FPPI5 and free drug was found to be 23, 59, 62 and 26 days, respectively.
The study concludes fourth generation PPI dendrimer to be superior carrier for folate based tumor targeting compared to third and fifth generation based formulations. This work is expected to provide a significant clue in the selection of "dendrimer generation" for folate mediated cancer targeting therapy.
叶酸偶联聚(丙烯亚胺)(PPI)树枝状大分子(FPPI)介导的抗癌疗法正在全球范围内被广泛探索。本研究旨在探索不同代数的美法仑负载FPPI(MP-FPPI)的靶向潜力,以有效管理癌症。
比较MP-FPPI制剂的药物包封效率、体外释放曲线、毒理学、叶酸受体阻断试验、细胞摄取试验、稳定性研究和体内研究。
随着树枝状大分子代数从第四代增加到第五代,除毒理学特征呈指数改善外,药物递送参数改善可忽略不计。在MCF-7细胞的MTT试验中,MP-FPPI3、MP-FPPI4、MP-FPPI5和游离美法仑的IC50值分别为8±0.15、0.9±0.02、0.2±0.01和10±0.17μM,表明基于叶酸的靶向是杀死癌细胞的有效方法。用MP-FPPI3、MP-FPPI4、MP-FPPI5和游离药物治疗的荷瘤小鼠的中位生存时间分别为23、59、62和26天。
该研究得出结论,与第三代和第五代制剂相比,第四代PPI树枝状大分子是基于叶酸的肿瘤靶向的更优载体。这项工作有望为叶酸介导的癌症靶向治疗中“树枝状大分子代数”的选择提供重要线索。