Kaushik Dinesh, Sardana Satish, Mishra D N
Department of Pharmaceutics, Hindu College of Pharmacy, Sonepat-131001, India.
Yao Xue Xue Bao. 2009 Nov;44(11):1278-84.
The present investigation is aimed to develop a new formulation containing chemically crosslinked guar gum microspheres loaded with 5-fluorouracil for targeting colorectal cancer. The emulsification polymerization method involving the dispersion of aqueous phase of guar gum in castor oil was used to prepare spherical microspheres. Various processing parameters were studied in order to optimize the formulation. Particle size and surface morphology of the microspheres were determined using optical microscopy and scanning electron microscopy. The in vitro drug release studies performed in simulated gastric fluid (SGF) for 2 h followed by intestinal fluid for 3 h, revealed the retention of the drug inside the microspheres from which only (15.27 +/- 0.56) % of the drug was released in 5 h. In vitro release rate studies were also carried out in simulated colonic fluid (SCF) in the presence of rat caecal contents, which showed improved drug release. The drug release from the formulation was found to be (41.6 +/- 3.5) % with 2% (w/v) caecal matter in 24 h as compared to control study where (25.2 +/- 3.5) % of drug was released. The drug release from the formulation with 2% and 4% rat caecal contents medium after 2 days of enzyme induction was found to be (56.3 +/- 4.1) % and (78.9 +/- 2.8) % in 24 h respectively. Similarly, (61.3 +/- 5.4) % and (90.2 +/- 2.9) % drug was released respectively with 2% and 4% rat caecal matter after 4 days of enzyme induction and (72.1 +/- 2.9) % and (90.2 +/- 3.2) % after 6 days of enzyme induction. In this way, 5-fluorouracil loaded guar gum microspheres have shown promising results in the management of colorectal cancer, warranting thorough in vivo study for scale up technology.
本研究旨在开发一种新制剂,该制剂包含载有5-氟尿嘧啶的化学交联瓜尔胶微球,用于靶向治疗结直肠癌。采用乳化聚合法,即将瓜尔胶水相分散在蓖麻油中,制备球形微球。研究了各种工艺参数以优化制剂。使用光学显微镜和扫描电子显微镜测定微球的粒径和表面形态。在模拟胃液(SGF)中进行2小时,然后在肠液中进行3小时的体外药物释放研究,结果显示药物保留在微球内,在5小时内仅释放了(15.27±0.56)%的药物。还在存在大鼠盲肠内容物的模拟结肠液(SCF)中进行了体外释放速率研究,结果显示药物释放有所改善。与对照研究相比,在24小时内,含有2%(w/v)盲肠物质的制剂的药物释放率为(41.6±3.5)%,而对照研究中药物释放率为(25.2±3.5)%。在酶诱导2天后,含有2%和4%大鼠盲肠内容物培养基的制剂在24小时内的药物释放率分别为(56.3±4.1)%和(78.9±2.8)%。同样,在酶诱导4天后,含有2%和4%大鼠盲肠物质的制剂分别释放了(61.3±5.4)%和(90.2±2.9)%的药物,在酶诱导6天后分别释放了(72.1±2.9)%和(90.2±3.2)%的药物。通过这种方式,载有5-氟尿嘧啶的瓜尔胶微球在结直肠癌治疗中显示出有前景的结果,值得对放大技术进行深入的体内研究。