Alange Vijaykumar V, Birajdar Ravindra P, Kulkarni Raghavendra V
Department of Pharmaceutics, BLDEA's SSM College of Pharmacy and Research Centre, BLDE University Campus, Vijayapur (Bijapur), 586103, Karnataka, India.
Department of Pharmaceutics, BLDEA's SSM College of Pharmacy and Research Centre, BLDE University Campus, Vijayapur (Bijapur), 586103, Karnataka, India.
Int J Biol Macromol. 2017 Sep;102:829-839. doi: 10.1016/j.ijbiomac.2017.04.023. Epub 2017 Apr 6.
An effort was made to formulate and evaluate pH-sensitive spray dried microspheres using hydrolyzed polyacrylamide-graft-gum karaya (PAAm-g-GK) for colon specific delivery of an anti-cancer agent, capecitabine. The synthesis of pH-sensitive PAAm-g-GK copolymer was done by free radical polymerization followed by alkaline hydrolysis and characterized satisfactorily. The microspheres were spherical in shape; drug entrapment efficiency was found to be in the range of 77.30% to 88.74%. Pulsatile swelling study indicates that the PAAm-g-GK consists of considerable pH-sensitivity. The in-vitro drug release suggested that the microspheres prepared using native GK were incapable to retard the drug release within 5h in the environment of stomach and small intestine. While, those microspheres prepared using pH-sensitive PAAm-g-GK copolymer having crosslinked with glutaraldehyde (GA), released little amount of drug within 5h, but maximum amount of drug was targeted to colonic region in a controlled manner up to 24h. For example, GK10 Microspheres showed only 19.16% drug release at the end of 5th h, while about 80.14% of drug was targeted to colonic region. Cross-linking with GA reduced the early drug release in the upper part of gastrointestinal tract and guaranteed maximum drug release in the colonic region. A rapid enhancement in drug release was witnessed in rat caecal content medium due to the action of colonic bacteria on PAAm-g-GK copolymer.
研究人员尝试使用水解聚丙烯酰胺接枝刺梧桐树胶(PAAm-g-GK)制备并评估pH敏感型喷雾干燥微球,用于抗癌药物卡培他滨的结肠特异性递送。通过自由基聚合反应随后进行碱性水解合成了pH敏感型PAAm-g-GK共聚物,并对其进行了令人满意的表征。微球呈球形;药物包封率在77.30%至88.74%之间。脉冲溶胀研究表明,PAAm-g-GK具有相当的pH敏感性。体外药物释放研究表明,使用天然刺梧桐树胶制备的微球在胃和小肠环境中无法在5小时内延缓药物释放。而使用与戊二醛(GA)交联的pH敏感型PAAm-g-GK共聚物制备的微球,在5小时内释放少量药物,但最大量的药物在24小时内以可控方式靶向结肠区域。例如,GK10微球在第5小时末仅释放了19.16%的药物,而约80.14%的药物靶向结肠区域。与GA交联减少了胃肠道上部的早期药物释放,并保证了结肠区域的最大药物释放。由于结肠细菌对PAAm-g-GK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迅速增加。