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Colon Targeted Guar Gum Compression Coated Tablets of Flurbiprofen: Formulation, Development, and Pharmacokinetics

机译:氟比洛芬的结肠靶向瓜尔胶压缩包衣片剂:制剂,开发和药代动力学

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摘要

The rationale of the present study is to formulate flurbiprofen colon targeted compression coated tablets using guar gum to improve the therapeutic efficacy by increasing drug levels in colon, and also to reduce the side effects in upper gastrointestinal tract. Direct compression method was used to prepare flurbiprofen core tablets, and they were compression coated with guar gum. Then the tablets were optimized with the support of in vitro dissolution studies, and further it was proved by pharmacokinetic studies. The optimized formulation (F4) showed almost complete drug release in the colon (99.86%) within 24 h without drug loss in the initial lag period of 5 h (only 6.84% drug release was observed during this period). The pharmacokinetic estimations proved the capability of guar gum compression coated tablets to achieve colon targeting. The C max of colon targeted tablets was 11956.15 ng/mL at T max of 10 h whereas it was 15677.52 ng/mL at 3 h in case of immediate release tablets. The area under the curve for the immediate release and compression coated tablets was 40385.78 and 78214.50 ng-h/mL and the mean resident time was 3.49 and 10.78 h, respectively. In conclusion, formulation of guar gum compression coated tablets was appropriate for colon targeting of flurbiprofen.
机译:本研究的基本原理是使用瓜尔豆胶配制氟比洛芬靶向结肠的压缩包衣片剂,以通过增加结肠中的药物水平来提高治疗效果,并减少上消化道的副作用。使用直接压片法制备氟比洛芬核心片剂,并用瓜尔豆胶进行压缩包衣。然后在体外溶出度研究的支持下对片剂进行优化,并通过药代动力学研究进一步证实。优化的制剂(F4)在24小时内显示了几乎完全的结肠内药物释放(99.86%),在最初5h的滞后时间内没有药物损失(在此期间仅观察到6.84%的药物释放)。药代动力学估计证明了瓜尔胶压缩包衣片剂能够实现结肠靶向。结肠靶向片剂的C max在10 max的T max时为11956.15 ng / mL,而对于速释片剂,其在3μh的C max为15677.52 ng / mL。立即释放和压制包衣片剂的曲线下面积为40385.78和78214.50μng-h/ mL,平均停留时间分别为3.49和10.78μh。总之,瓜尔胶压缩包衣片剂的制剂适合于氟比洛芬的结肠靶向。

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