Alange Vijaykumar V, Birajdar Ravindra P, Kulkarni Raghavendra V
a Department of Pharmaceutics , BLDEA's SSM College of Pharmacy and Research Centre, BLDE University Campus , Vijayapur (Bijapur) , India.
J Biomater Sci Polym Ed. 2017 Feb;28(2):139-161. doi: 10.1080/09205063.2016.1257083. Epub 2016 Nov 21.
Unique pH-sensitive spray dried microspheres were formulated employing hydrolyzed polyacrylamide-g-carboxymethylcellulose sodium (PAAm-g-NaCMC) co-polymer for colon targeted delivery of an anticancer drug, capecitabine. Synthesis of PAAm-g-NaCMC was carried out through free radical polymerization, which was supported with an inert atmosphere and then the alkaline hydrolysis was performed and subjected for characterization including FTIR spectroscopic analysis, H NMR spectroscopic analysis, elemental analysis, viscosity measurement, neutralization equivalent and thermo-gravimetric investigation. The swelling data suggested that the PAAm-g-NaCMC possesses significant pH-sensitive property. The microspheres were in the range of 1.00 to 7.34 μ and the drug entrapment efficiency ranged between 70.98 and 94.41%. In vitro drug release suggested the failure of microspheres formulated using native NaCMC which failed to impede drug release in stomach and small intestine, while those prepared with pH-sensitive PAAm-g-NaCMC copolymer and cross-linked with glutaraldehyde are suitable for colon targeting because they retarded release of drug in physiologic atmosphere of stomach and small intestine. Only 12.97% of drug was released from CMC10 formulation by the end of 5th h and rest of drug has been targeted to colonic region. A sudden increase in release of drug was observed in rat caecal contents media because of colonic bacterial action on PAAm-g-NaCMC copolymer.
采用水解聚丙烯酰胺 - g - 羧甲基纤维素钠(PAAm - g - NaCMC)共聚物制备了独特的pH敏感喷雾干燥微球,用于抗癌药物卡培他滨的结肠靶向递送。PAAm - g - NaCMC的合成通过自由基聚合进行,在惰性气氛下进行,然后进行碱性水解并进行表征,包括傅里叶变换红外光谱分析、核磁共振氢谱分析、元素分析、粘度测量、中和当量和热重分析。溶胀数据表明PAAm - g - NaCMC具有显著的pH敏感特性。微球粒径在1.00至7.34μm范围内,药物包封率在70.98%至94.41%之间。体外药物释放表明,使用天然NaCMC制备的微球未能阻止药物在胃和小肠中的释放,而用pH敏感的PAAm - g - NaCMC共聚物制备并用戊二醛交联的微球适用于结肠靶向,因为它们在胃和小肠的生理环境中延缓了药物释放。到第5小时结束时,CMC10制剂中仅12.97%的药物释放,其余药物靶向结肠区域。由于结肠细菌对PAAm - g - NaCMC共聚物的作用,在大鼠盲肠内容物培养基中观察到药物释放突然增加。