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首页> 外文期刊>Journal of Drug Delivery and Therapeutics >FORMULATION AND EVALUATION OF COLON TARGETED DRUG DELIVERY SYSTEM OF BUSULFAN: USING COMBINATION OF pH AND TIME DEPENDANT SYSTEMS
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FORMULATION AND EVALUATION OF COLON TARGETED DRUG DELIVERY SYSTEM OF BUSULFAN: USING COMBINATION OF pH AND TIME DEPENDANT SYSTEMS

机译:pH和时间依赖系统的结合对busulfan结肠靶向药物输送系统的形成和评价

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摘要

In present work Colon targeting drug delivery system was developed for Busulfan an anticancer drug by using combination of delayed systems one is pH dependant and other is time dependant delayed system. Rapid release core tablet (RRCT) formulations were prepared using Busulfan drug with different disintegrating agents in different concentrations. The pre-compression and post-compression parameters of all formulations were determined and the values were found to be satisfactory. From the In-vitro dissolution studies, F6 formulation with 12% Hydroxy propyl cellulose (HPC) was the best formulation. For optimized RRCT formulation press coat was done by using Xanthum Gum and Ethyl Cellulose (EC) in different ratios. Press coated tablet delays the drug release up to 8 hours based on the nature and concentrations of the polymer. Each press coated tablet was coated using enteric solution made of HPMC phthalate, Myvacet and color dissolved in ethanol. Enteric press coated tablets (EPCT) were delayed drug release up to 2hrs in fed condition due to pH dependant delayed system. Based on dissolution studies of EPCT formulations, C3OPF formulation was optimized and showed delayed release pattern in a much customized manner. As a result of this study it may be concluded that the colon targeted drug delivery tablets using a combination of two polymers in optimized concentrations can be used to increase the delayed action of drug release to deliver the drug in a delayed manner.
机译:在当前的工作中,通过使用延迟系统的组合开发了用于白消安的抗结肠癌药物结肠靶向药物输送系统,其中延迟系统是pH依赖性的,而其他是时间依赖性的延迟系统。使用白消安药物与不同浓度的不同崩解剂一起制备了速释核心片剂(RRCT)制剂。测定所有制剂的压缩前和压缩后参数,发现该值令人满意。从体外溶出度研究来看,含12%羟丙基纤维素(HPC)的F6配方是最佳配方。为了优化RRCT配方,通过使用不同比例的黄原胶和乙基纤维素(EC)进行压涂。压制包衣的片剂根据聚合物的性质和浓度将药物释放延迟最多8个小时。使用由邻苯二甲酸HPMC,Myvacet和溶于乙醇的色素制成的肠溶溶液对每种压制包衣的片剂进行包衣。由于依赖pH的延迟系统,肠溶压制片剂(EPCT)在进食条件下延迟药物释放长达2小时。根据EPCT制剂的溶出度研究,对C3OPF制剂进行了优化,并以非常定制的方式显示了延迟释放模式。这项研究的结果可以得出结论,使用两种浓度优化的聚合物结合的结肠靶向药物输送片可用于增加药物释放的延迟作用,从而以延迟的方式输送药物。

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