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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >PROCESS OPTIMIZATION, FORMULATION AND EVALUATION OF HYDROGEL {GUARGUM-G-POLY (ACRYLAMIDE)} BASED DOXOFYLLINE MICROBEADS
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PROCESS OPTIMIZATION, FORMULATION AND EVALUATION OF HYDROGEL {GUARGUM-G-POLY (ACRYLAMIDE)} BASED DOXOFYLLINE MICROBEADS

机译:基于水凝胶{GUAGGUM-G-POLY(丙烯酰胺)}的DOXOFYLLINE微珠的工艺优化,配方和评价

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Objective: The objective of the present study was to improve the physical and chemical properties of natural polymers and to reduce the cost of product by graft copolymerization techniques using a natural polymer (Guar gum) and a synthetic polymer {poly (acrylamide)}. The optimized formulation of hydrogel was formulated as microbeads and loaded with Doxofylline and characterized with different parameters. Methods: Graft copolymer of guar gum-g-poly (acrylamide) was prepared by free radical polymerization technique in a specially designed jacked reaction vessel under constant flow of nitrogen. To initiate the reaction, Ceric ammonium nitrate (CAN) was used as reaction initiator. The graft co-polymer was characterised by using FTIR, TGA, and SEM. Polymeric blend beads of the grafted copolymer with sodium alginate were prepared by cross linking with calcium chloride in ionic gelation method and used to deliver a model new generation anti asthmatic drug, Doxofylline. Preparation condition of beads was optimized by considering the percentage entrapment efficiency, particle size, swelling capacity of beads in different P H conditions and their release data. Results: The formation of grafted copolymers is confirmed by FTIR studies and TGA studies showed a comparatively higher thermal stability of grafted copolymer. The pAAm-g-GG/sodium alginate microbeads were almost spherical in shape as indicated by the SEM studies. Swelling index was found to be maximum in Phosphate buffer P H 7.4 and minimum in Phosphate buffer P H 9.2. Release of doxofylline was found to be in a controlled manner with increasing polyacrylamide content in the copolymer and sodium alginate content in microbeads and higher release was observed in P H 7.4 medium than that of P H 1.2. In vitro release kinetics of doxofylline from the polymeric beads followed Higuchi kinetics model. Conclusion: Hydrogel based Doxofylline microbeads were successfully developed by using optimized batches of Guar gum-g-poly (acrylamide) and sodium alginate by free radical ionization technique. All the characterization parameters came under acceptance criteria.
机译:目的:本研究的目的是通过使用天然聚合物(瓜尔胶)和合成聚合物{聚(丙烯酰胺)}的接枝共聚技术来改善天然聚合物的物理和化学性质,并降低产品成本。将优化的水凝胶制剂配制成微珠,并装载多索茶碱,并用不同的参数进行表征。方法:在特殊设计的顶升反应容器中,在恒定的氮气流下,通过自由基聚合技术制备瓜耳胶-g-聚丙烯酰胺共聚物(丙烯酰胺)。为了引发反应,硝酸铈铵(CAN)用作反应引发剂。通过使用FTIR,TGA和SEM表征了接枝共聚物。通过离子凝胶法与氯化钙交联制备接枝共聚物与海藻酸钠的聚合物共混珠,并用于生产新型抗哮喘药物多索茶碱。通过在不同的PH条件下考虑包封率,颗粒大小,溶胀能力以及释放数据来优化微珠的制备条件。结果:FTIR研究证实了接枝共聚物的形成,TGA研究表明接枝共聚物的热稳定性相对较高。 SEM研究表明,pAAm-g-GG /藻酸钠微珠的形状几乎为球形。发现溶胀指数在磷酸盐缓冲液PH 7.4中最大,而在磷酸盐缓冲液PH 9.2中最小。发现多索茶碱的释放是受控的,随着共聚物中聚丙烯酰胺含量的增加和微珠中藻酸钠含量的增加,在P H 7.4介质中观察到的释放高于P H 1.2。遵循Higuchi动力学模型,从聚合物珠中体外释放多索茶碱的动力学。结论:通过自由基电离技术,优化使用了瓜尔胶-g-聚丙烯酰胺和藻酸钠,成功开发了基于水凝胶的多索茶碱微珠。所有表征参数均符合验收标准。

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