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使用三元研磨混合物提高克拉霉素的溶出速率:纳米晶体的形成

Dissolution rate enhancement of clarithromycin using ternary ground mixtures: nanocrystal formation.

作者信息

Shahbaziniaz Malihe, Foroutan Seyed Mohsen, Bolourchian Noushin

机构信息

Department of Pharmaceutics, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran. ; Student Research Committee, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Department of Pharmaceutics, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Pharm Res. 2013 Fall;12(4):587-98.

Abstract

Clarithromycin (CLA), a broad-spectrum macrolide, is a poorly soluble drug with dissolution rate limited absorption. The aim of this investigation was to prepare CLA nanoparticles from a ternary ground mixture in the presence of sodium lauryl sulfate (SLS) and polyvinyl pyrrolidone (PVP) as co-grinding water-soluble compounds, in order to improve the drug dissolution rate. Different weight ratios of CLA: SLS: PVP were ground in a dry process by planetary ball mill using different grinding ball size. Following the dissolution rate study, physical properties of the best dissolved co-ground formulation was studied. The accelerated stability studies were also conducted on the co-ground formulation. The results revealed that the dissolution rate of ternary ground mixtures was much higher than that of the intact drug (p < 0.001). Decreasing the grinding ball size and weight with the same rotation speed resulted in particles with decreased dissolution. On the other hand, increasing the PVP concentration in the formulations reduced the drug dissolution. Dissolution efficiencies (DE10 and DE30) for the best dissolved formulation, which consisted of the equal ratio of each co-ground component, were 8.7 and 5 folds higher than the untreated CLA, respectively. This formulation formed nanocrystals with enhanced solubility after dispersing in water. X-ray diffraction, differential scanning calorimetry and infrared spectrophotometry confirmed no chemical interaction and phase transition during the process. Accelerated stability studies confirmed that the co-ground mixture almost remained unchanged in terms of dissolution rate, drug assay and particle size after exposing in stability conditions for three months.

摘要

克拉霉素(CLA)是一种广谱大环内酯类药物,是一种难溶性药物,其溶解速率限制了吸收。本研究的目的是在月桂基硫酸钠(SLS)和聚乙烯吡咯烷酮(PVP)作为共研磨水溶性化合物存在的情况下,由三元研磨混合物制备CLA纳米颗粒,以提高药物溶解速率。采用不同尺寸的研磨球,通过行星式球磨机干法研磨CLA、SLS和PVP的不同重量比混合物。在进行溶解速率研究后,对溶解效果最佳的共研磨制剂的物理性质进行了研究。还对共研磨制剂进行了加速稳定性研究。结果表明,三元研磨混合物的溶解速率远高于完整药物(p < 0.001)。在相同转速下减小研磨球尺寸和重量会导致颗粒溶解速率降低。另一方面,增加制剂中PVP的浓度会降低药物溶解。溶解效果最佳的制剂由各共研磨成分等比例组成,其10分钟和30分钟的溶出效率(DE10和DE30)分别比未处理的CLA高8.7倍和5倍。该制剂分散在水中后形成了溶解度增强的纳米晶体。X射线衍射、差示扫描量热法和红外分光光度法证实该过程中没有化学相互作用和相变。加速稳定性研究证实,共研磨混合物在稳定性条件下暴露三个月后,其溶解速率、药物含量和粒径几乎保持不变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdc5/3920702/4b35d659e8ea/ijpr-12-587-g001.jpg

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