Preparation and In vitro Evaluation of Enteric Coated Oral Vancomycin Hydrochloride Sustained Release Formulation with Mucoadhesive Properties

Lana Alsharkas, Vijayaraj Kumar Palanirajan, Y. Wei
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引用次数: 2

Abstract

Clostridium difficile is a species of gram-positive bacteria thought to infect patients with weakened immune response resulting in colitis. Oral vancomycin hydrochloride is given four times a day to treat Clostridium difficile colitis and is commercially available in the form of capsule and solution. Patient’s compliance is the main issue in this treatment due to the multiple dosing frequencies. Accordingly, replacement of such dose regimen with a once daily dosage will enhance patient compliance. In this study, mucoadhesive vancomycin hydrochloride tablets were prepared with the use of chitosan to exert a local effect in the colon. Sustained release property was also imparted by chitosan. Enteric coating with Eudragit® S 100 was applied to prevent the sticking of chitosan tablets in the stomach and small intestine and deliver the tablets intact to the colon. The prepared tablets were evaluated for In vitro drug release for 24 hours and compared with the marketed formulation. The formulation was found to release in a sustained manner in pH 7.4 buffer allowing the colon delivered oral vancomycin hydrochloride to be a promising formulation in the development of a once daily treatment for Clostridium difficile colitis.
肠溶包衣口服盐酸万古霉素黏附缓释片的制备及体外评价
艰难梭菌是一种革兰氏阳性细菌,被认为感染免疫反应减弱的患者,导致结肠炎。口服盐酸万古霉素每天四次用于治疗艰难梭菌结肠炎,市售胶囊和溶液形式。由于多次给药频率,患者的依从性是该治疗的主要问题。因此,用每日一次的剂量替代这种剂量方案将提高患者的依从性。本研究利用壳聚糖制备盐酸万古霉素黏附片,使其在结肠内发挥局部作用。壳聚糖还具有缓释性能。采用Eudragit®s100肠溶包衣,防止壳聚糖片剂在胃和小肠的粘附,并将片剂完整地输送到结肠。对所制片剂进行了24小时体外释药评价,并与市售制剂进行了比较。该制剂被发现在pH 7.4缓冲液中持续释放,允许结肠递送口服盐酸万古霉素,是一种有前景的制剂,用于开发每日一次治疗艰难梭菌结肠炎。
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