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Propranolol Hydrochloride Extended-release Matrix Tablets Using Natural Rubber Latex as Binder

机译:使用天然橡胶胶乳作为粘合剂的普萘洛尔盐酸盐延长释放基质片剂

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Matrix is one of the most interesting drug delivery systems to control drug release in pharmaceutical dosage forms. Natural rubber latex (NRL) from Hevea brasiliensis consists of cis-1,4-polyisoprene as the major polymer. It presents interesting physical properties such as easy to manipulate, low cost, high mechanical resistance, and insoluble in water. The aim of this study was to use the NRL as binder in matrix tablets for controlling the release rate of drug. NRL, sodium carboxymethylcellulose, olive oil, Tween 80, and lactose were used as polymer, adsorbent, plasticizer, surfactant, and diluent, respectively. Propranolol hydrochloride was used as a model drug. Propranolol hydrochloride matrix tablets were prepared by conventional heat-melting method. The in vitro release of drug from matrix tablets was determined by UV-Vis method according to dissolution test under Propranolol Hydrochloride Tablets USP30-NF25 monograph. Morphology of propranolol hydrochloride matrix tablet before" and after released study was observed by scanning electron microscopy (SEM). It was found that NRL matrix tablets could control the drug release up to 12 hours. The release profiles were best fitted with Higuchi model. NRL amounts affected the properties of the propranolol hydrochloride matrix tablets. Increasing the NRL quantity in the matrices provided the decrease of release rate of drug. SEM photographs showed the number, size, and distribution of pore in propranolol hydrochloride matrix tablets that depended on amount of NRL addition. These results confirmed that NRL was possible to use as binder for matrix tablets in oral drug delivery systems.
机译:基质是控制药物剂型中药物释放最有趣的药物递送系统之一。来自HEVEA Brasiliensis的天然橡胶胶乳(NRL)由CIS-1,4-聚异戊二烯组成,作为主要聚合物。它呈现有趣的物理性质,例如易于操纵,成本低,机械性高,不溶于水。本研究的目的是在基质片中使用NRL作为粘合剂,用于控制药物的释放速率。使用NRL,羧甲基纤维素,橄榄油,吐温80和乳糖作为聚合物,吸附剂,增塑剂,表面活性剂和稀释剂。盐酸丙醇醇用作模型药物。通过常规的热熔法制备盐酸普萘洛尔盐酸盐基质片。通过根据溶解试验在盐酸普罗兰醇片USP30-NF25专着的溶解试验中,通过UV-Vis方法测定来自基质片的体外释放。通过扫描电子显微镜(SEM)观察到之前“和释放研究”和释放研究“和释放研究”中的形态。发现NRL基质片可以控制药物释放长达12小时。释放型材最适合HIGUCHI模型。NRL量影响了盐酸普萘洛尔罗基基质片剂的性质。增加了基质中的NRL量提供了药物释放速率的降低。SEM照片显示孔中盐酸普罗尔醇孔泊洛洛尼孔的数量,尺寸和分布,依赖于NRL的量。添加。这些结果证实,NRL可以用作口服药物递送系统中基质片剂的粘合剂。

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