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Drug release from eudragit e-coated mini tablets for colon targeting: in vitro study

机译:eudragit e-coated mini tablet的药物释放用于结肠靶向:体外研究

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Colon-specific drug delivery from solid oral dosage forms may be achieved with enzyme-controlled, time-controlled, and pH-controlled drug release mechanisms, respectively. Recently it has been shown that in severe ulcerative colitis the luminal contents of the colon show a very low pH of 2.3-4.7. A dosage form designed for drug release at this low pH should be able to deliver the drug selectively to the colon of patients with ulcerative colitis. Ou recently developed colonic dosage form consists of drug cores which are coated with the acid-soluble poly(methacrylate) Eudragit~circle R E to provide for drug release only under the acidic conditions of the inflamed colon. The objective of this study was to investigate the influence of hydrodynamic stress and additional coating layers on the drug release from Eudragit E-coated mini tablets.
机译:来自固体口服剂型的结肠特异性药物递送可以分别通过酶控制,时间控制和pH控制的药物释放机制来实现。最近已经显示,在严重的溃疡性结肠炎中,结肠的管腔内容物显示出2.3-4.7的非常低的pH。设计用于在这种低pH值下释放药物的剂型应能够将药物选择性地递送至溃疡性结肠炎患者的结肠。 Ou最近开发的结肠剂型由药物核心组成,这些药物核心被酸溶性聚(甲基丙烯酸酯)Eudragit®环R E包覆,仅在发炎的结肠的酸性条件下提供药物释放。这项研究的目的是研究流体动力学应力和额外的包衣层对Eudragit E包衣迷你片剂释放药物的影响。

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