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提高难溶性药物的溶出速率:盐酸氨基葡萄糖作为固体分散体制剂中的潜在载体。

To enhance dissolution rate of poorly water-soluble drugs: glucosamine hydrochloride as a potential carrier in solid dispersion formulations.

机构信息

Medway School of Pharmacy, University of Kent, Kent, UK.

出版信息

Colloids Surf B Biointerfaces. 2010 Mar 1;76(1):170-8. doi: 10.1016/j.colsurfb.2009.10.030. Epub 2009 Nov 11.

Abstract

The solid dispersion technique is the most effective method for improving the dissolution rate of poorly water-soluble drugs, however this is reliant on a suitable carrier and solvent being selected. The work presented explores D-glucosamine HCl (G-HCl) as a potential hydrophilic carrier to improve dissolution rate of a poorly water-soluble drug, carbamazepine (CBZ), from physical mixtures and solid dispersion formulations. The effect of different solvents in the preparation of solid dispersion formulations was also investigated. Solid dispersions of the drug and G-HCl were prepared using different ratios by the conventional solvent evaporation method. Different solvents (ethanol, acetone and water) were used as second variable in the preparation of solid dispersions. Physical mixtures of CBZ and G-HCl were also prepared for comparison. The properties of all solid dispersions and physical mixtures were studied using a dissolution tester, FT-IR, SEM and DSC. These results showed that the presence of glucosamine can increase dissolution rate of CBZ compared to pure CBZ. All solid dispersions of CBZ-G-HCl showed considerably a higher dissolution rate than the corresponding physical mixtures. The presence of water during preparation of the solid dispersions reduced the dissolution rate of CBZ due to formation of carbamazepine dihydrate during the preparation of solid dispersion, as proved by DSC and FT-IR studies. To facilitate comparison, the dissolution efficiency was calculated for solid dispersions prepared with different solvents and the dissolution efficiency can generally be ranked as follows: ethanol>acetone>ethanol-water>acetone-water when the ratios of drug to carrier were 4:1 and 2:1. It has thus been shown that the use of G-HCl in solid dispersion formulations can significantly enhance the dissolution rate of poorly water-soluble drugs such as carbamazepine. This amino sugar could be used as a new carrier in solid dispersion formulations and would have significant commercial potential.

摘要

固体分散技术是提高难溶性药物溶出度最有效的方法,但这依赖于选择合适的载体和溶剂。本工作探索了盐酸氨基葡萄糖(G-HCl)作为一种潜在的亲水性载体,以提高难溶性药物卡马西平(CBZ)的溶出度,从物理混合物和固体分散体配方。还研究了不同溶剂在制备固体分散体配方中的作用。采用常规溶剂蒸发法,以不同比例制备药物和 G-HCl 的固体分散体。不同的溶剂(乙醇、丙酮和水)被用作制备固体分散体的第二变量。还制备了 CBZ 和 G-HCl 的物理混合物进行比较。使用溶出度测试仪、FT-IR、SEM 和 DSC 研究所有固体分散体和物理混合物的性质。结果表明,与纯 CBZ 相比,氨基葡萄糖的存在可以提高 CBZ 的溶出度。所有 CBZ-G-HCl 的固体分散体都显示出比相应的物理混合物更高的溶出度。在制备固体分散体过程中存在水会降低 CBZ 的溶出度,因为在制备固体分散体过程中形成了卡马西平二水合物,这一点通过 DSC 和 FT-IR 研究得到了证明。为了便于比较,计算了用不同溶剂制备的固体分散体的溶出效率,当药物与载体的比例为 4:1 和 2:1 时,溶出效率通常可以按以下顺序排列:乙醇>丙酮>乙醇-水>丙酮-水。因此,已经表明,在固体分散体配方中使用 G-HCl 可以显著提高难溶性药物如卡马西平的溶出度。这种氨基糖可以用作固体分散体配方中的新型载体,具有重要的商业潜力。

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