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Effect of Excipients on Lag Time of Press Coated Tablets in Pulsatile Drug Delivery For The Treatment of Rheumatoid Arthritis.

机译:赋形剂对治疗类风湿关节炎的脉冲药物递送中压制包衣片的延迟时间的影响。

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A tablet system consisting of cores coated with insoluble coating was prepared and evaluated as pulsatile drug delivery system for the treatment of rheumatoid arthritis. The dry-coated tablet with optimal lag time was designed to simulate the drug dosing time according to physiological needs. Press coated tablet was prepared with meloxicam, the drug of choice for the treatment of rheumatoid arthritis, in the core tablet & Ethyl cellose powder (EC) with fine particles , in the whole layer of the outer shell as insoluble coating . Along with this Spray Dried Lactose (SDL) and Hydroxy Propyl Methyl Cellulose ( HPMC) were mixed in different weight ratios with EC individually and its effect on the lag time of the drug release was investigated. The release profile exhibited a lag time followed by a rapid and complete release phase, in which the outer shell ruptured or broke into two halves and found that the lag time was dependent on the weight ratios of EC / SDL or EC/HPMC in the outer shell.
机译:制备了由包有不溶性包衣的核组成的片剂系统,并将其评价为用于治疗类风湿性关节炎的脉动药物递送系统。设计具有最佳滞后时间的干包衣片剂,以根据生理需要模拟给药时间。用美洛昔康(一种用于治疗类风湿性关节炎的药物)在核心片剂和乙基纤维素粉(EC)中制成细颗粒,并在外壳的整个层中以不溶性涂层的形式制备压片片剂。与该喷雾干燥的乳糖(SDL)和羟丙基甲基纤维素(HPMC)分别以不同的重量比与EC混合,并研究其对药物释放滞后时间的影响。释放曲线表现出滞后时间,随后是快速且完全的释放阶段,其中外壳破裂或分成两半,发现滞后时间取决于外壳中EC / SDL或EC / HPMC的重量比贝壳。

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