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Dissolution Properties and Physical Characterization of Telmisartan–Chitosan Solid Dispersions Prepared by Mechanochemical Activation

机译:机械化学活化法制备替米沙坦-壳聚糖固体分散体的溶出性质和物理表征

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摘要

Solid dispersion systems of telmisartan (a poorly water-soluble antihypertension drug) with biopolymer carrier chitosan have been investigated in this study. The mechanism of solubilization of chitosan for drug has been studied. In addition, the influence of several factors was carefully examined, including the preparation methods, the drug/carrier weight ratios, and the milling time. Drug dissolution and physical characterization of different binary systems were studied by in vitro dissolution test, particle size distribution, Fourier transform infrared spectroscopy, differential scanning calorimetry, powder X-ray diffractometry, and scanning electron microscopy. The results presented that the weak basic property of chitosan appeared as the main driving force for the drug dissolution enhancement. Other effects such as decreased drug crystallinity and size played a positive contributory role. Among the preparation methods, cogrinding was the best method showing strong drug amorphization, reduced particle size, and enhanced dissolution. The drug dissolution markedly improved with increasing the amount of chitosan in solid mixtures. As a result, a significant effect of chitosan increasing telmisartan dissolution has been demonstrated, and cogrinding in a roll ball mill was the best way to prepare solid dispersions, which had high degree of uniformity in drug content and had a practical application in manufacturing.
机译:这项研究研究了替米沙坦(水溶性差的降压药)与生物聚合物载体壳聚糖的固体分散体系。研究了壳聚糖增溶药物的机理。此外,还仔细检查了几个因素的影响,包括制备方法,药物/载体重量比和研磨时间。通过体外溶出试验,粒度分布,傅立叶变换红外光谱,差示扫描量热法,粉末X射线衍射法和扫描电子显微镜研究了不同二元系统的药物溶出度和物理特性。结果表明,壳聚糖的弱碱性是促进药物溶解的主要驱动力。其他影响,例如降低药物的结晶度和大小,也起到了积极的作用。在制备方法中,共研磨是表现出强大的药物无定形性,减小的粒径和增强的溶解性的最佳方法。随着固体混合物中壳聚糖含量的增加,药物的溶出度显着提高。结果,证明了壳聚糖增加替米沙坦溶解的显着效果,并且在辊式球磨机中共研磨是制备固体分散体的最佳方法,该分散体具有高度的药物含量均匀性并且在制造中具有实际应用。

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