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Characterization and In Vitro Drug Release Studies of a Natural Polysaccharide Terminalia catappa Gum (Badam Gum)

机译:天然多糖榄仁树胶(Badam Gum)的表征和体外药物释放研究

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摘要

The main objective of the present study is the physicochemical characterization of naturally available Terminalia catappa gum (Badam gum [BG]) as a novel pharmaceutical excipient and its suitability in the development of gastroretentive floating drug delivery systems (GRFDDS) to retard the drug for 12 h when the dosage form is exposed to gastrointestinal fluids in the gastric environment. As BG was being explored for the first time for its pharmaceutical application, physicochemical, microbiological, rheological, and stability studies were carried out on this gum. In the present investigation, the physicochemical properties, such as micromeritic, rheological, melting point, moisture content, pH, swelling index, water absorption, and volatile acidity, were evaluated. The gum was characterized by scanning electron microscopy, differential scanning calorimetry (DSC), powder X-ray diffraction studies (PXRD), and Fourier transform infrared spectroscopy (FTIR). Gastroretentive floating tablets of BG were prepared with the model drug propranolol HCl by direct compression methods. The prepared tablets were evaluated for all their physicochemical properties, in vitro buoyancy, in vitro drug release, and rate order kinetics. PBG 04 was selected as an optimized formulation based on its 12-h drug release and good buoyancy characteristics. The optimized formulation was characterized with FTIR, DSC, and PXRD studies, and no interaction between the drug and BG was found. Thus, the study confirmed that BG might be used in the gastroretentive drug delivery system as a release-retarding polymer.
机译:本研究的主要目的是作为一种新型药物赋形剂对天然榄仁木牙龈胶(Badam gum [BG])的理化特性及其在胃滞留漂浮药物传递系统(GRFDDS)的开发中的适应性进行研究,以延迟药物12 h当剂型在胃环境中暴露于胃肠道液体时。由于BG首次用于其药物用途,因此对该胶进行了物理化学,微生物学,流变学和稳定性研究。在本研究中,评估了其物理化学性质,如微团,流变,熔点,水分含量,pH,溶胀指数,吸水率和挥发性酸度。通过扫描电子显微镜,差示扫描量热法(DSC),粉末X射线衍射研究(PXRD)和傅里叶变换红外光谱(FTIR)对口香糖进行表征。用模型药物盐酸普萘洛尔通过直接压片方法制备了BG胃滞留性漂浮片剂。对制备的片剂的所有理化性质,体外浮力,体外药物释放和速率顺序动力学进行评估。基于PBG 04的12小时药物释放和良好的浮力特性,它被选作优化配方。通过FTIR,DSC和PXRD研究对优化的制剂进行了表征,未发现药物与BG之间存在相互作用。因此,该研究证实,BG可以作为缓释聚合物用于胃滞留性药物输送系统。

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