共磨对水溶性差药物克拉霉素溶出度影响的评价

Z. Iqbal, Amjid Khan, Nabeela Niaz
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引用次数: 2

摘要

新发明的活性药物成分原料药大多水溶性较差,溶出度是压缩固体剂型生物利用度的限制步骤。目的:研究亲水性载体对水溶性较差药物溶出度的影响及克拉霉素在直接压缩片剂制备中的利用。根据美国药典测定克拉霉素的内在溶出度为提高克拉霉素的溶出率,采用共磨技术,将克拉霉素与微晶纤维素的润滑物理混合物压缩到鼻涕虫中,然后用直接压片技术制备含有共磨克拉霉素的颗粒剂,并对其进行评价在最大释药不相似因子f相似因子f和溶出效率的基础上,比较两种制剂与市售片的物理参数、机械强度、崩解行为和体外释药溶出度特征。克拉霉素是水溶性较差的二类药物与固有溶出度相比,亲水性载体共磨可显著提高克拉霉素的溶出度,其溶出度随亲水性载体浓度的增加而增加,药载比(重量比)的增加幅度最大。进一步增加载体比,由于缓释作用,含共磨片的溶出度降低与市售片剂相比,共磨克拉霉素片剂的min最大释药量、Q - plusmn、Q - plusmn、Q - plusmn和溶出效率均高于市售片剂,含共磨克拉霉素片剂的水溶性较差药物克拉霉素的溶出率可通过亲水载体微晶纤维素共磨提高,共磨技术是一种环保型技术,可用于提高克拉霉素的溶出度水溶性差原料药的溶出率,与性质和剂量无关
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Evaluation of the effect of co‒grinding on dissolution rate of poor water soluble drug (clarithromycin)
Most of the newly invented active pharmaceutical ingredients APIs are poor water soluble and dissolution rate is the limiting step in bioavailability from compressed solid dosage forms Objective of the study was to elucidate the effect of hydrophilic carriers on dissolution rate of poor water soluble drug and utilization of co grinded Clarithromycin in preparation of tablets by direct compression Intrinsic dissolution rate of Clarithromycin was determined according to United States Pharmacopeia USP using rotating disk method Hydrophilic carrier micro crystalline cellulose was applied in varying ratios and drug to carrier ratio by weight for enhancement of dissolution rate of Clarithromycin by co grinding technique Co grinded Clarithromycin was prepared by compressing lubricated physical mixture blend of Clarithromycin and micro crystalline cellulose to slugs followed by granulation Tablets containing co grinded Clarithromycin were prepared by direct compression technique and evaluated for various official and unofficial parameters at pre compression and post compression level The prepared tablets were compared with marketed tablets in terms of physical parameters mechanical strength disintegration behavior and in vitro drug release Dissolution profiles of both types of the tablets were compared on the basis of maximum drug release dissimilarity factor f similarity factor f and dissolution efficiency Clarithromycin is a class II drug with poor water solubility Its intrinsic dissolution rate is very low mg cm min In comparison to intrinsic dissolution rate significant increase in dissolution rate of Clarithromycin was observed by co grinding with hydrophilic carriers Dissolution rate of Clarithromycin enhanced with concentration of hydrophilic carrier and maximum increase was observed at drug to carrier ratio by weight By further increasing ratio of the carrier resulted in decrease in dissolution rate due to cushioning effect Tablets containing co grinded Clarithromycin showed better dissolution profile compared with marketed tablets In comparison with marketed tablets maximum drug release in min Q plusmn Q plusmn Q plusmn and dissolution efficiency were higher for tablets containing co grinded Clarithromycin Dissolution rate of poor water soluble drug Clarithromycin can be enhanced by co grinding with hydrophilic carrier micro crystalline cellulose Co grinding is an environment friendly technique that can be applied for enhancement of dissolution rate of poor water soluble APIs irrespective of nature and dose
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