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球磨固体分散体中灰黄霉素和羟丙甲纤维素醋酸琥珀酸酯的混溶性研究。

Investigation of griseofulvin and hydroxypropylmethyl cellulose acetate succinate miscibility in ball milled solid dispersions.

机构信息

Institute of Pharmaceutical Science, King's College London, Franklin Wilkins Building, 150 Stamford Street, London SE1 9NH, United Kingdom.

出版信息

Int J Pharm. 2013 Feb 25;443(1-2):95-102. doi: 10.1016/j.ijpharm.2012.12.045. Epub 2013 Jan 6.

Abstract

Solid dispersions of varying weight ratios compositions of the nonionic drug, griseofulvin and the hydrophilic, anionic polymer, hydroxylpropylmethyl cellulose acetate succinate, have been prepared by ball milling and the resulting samples characterized using a combination of Fourier transform infra-red spectroscopy, X-ray powder diffraction and differential scanning calorimetry. The results suggest that griseofulvin forms hydrogen bonds with the hydroxylpropylmethyl cellulose acetate succinate polymer when prepared in the form of a solid dispersion but not when prepared in a physical mixture of the same composition. As anticipated, the actual measured glass transition temperature of the solid dispersions displayed a linear relationship between that predicted using the Gordon-Taylor and Fox equations assuming ideal mixing, but interestingly only at griseofulvin contents less than 50 wt%. At griseofulvin concentrations greater than this, the measured glass transition temperature of the solid dispersions was almost constant. Furthermore, the crystalline content of the solid dispersions, as determined by differential scanning calorimetry and X-ray powder diffraction followed a similar trend in that the crystalline content significantly decreased at ratios less than 50 wt% of griseofulvin. When the physical mixtures of griseofulvin and the hydroxylpropylmethyl cellulose acetate succinate polymer were analyzed using the Flory-Huggins model, a negative free energy of mixing with an interaction parameter of -0.23 were obtained. Taken together these results suggest that anionic hydrophilic hydroxylpropylmethyl cellulose acetate succinate polymer is a good solvent for crystalline nonionic griseofulvin with the solubility of griseofulvin in the solid dispersion being was estimated to be within the range 40-50 wt%. Below this solubility limit, the amorphous drug exists as amorphous glassy solution while above these values the system is supersaturated and glassy suspension and solution may coexist.

摘要

已通过球磨制备了不同重量比组成的非离子药物灰黄霉素和亲水性阴离子聚合物羟丙甲纤维素醋酸琥珀酸酯的固体分散体,并使用傅里叶变换红外光谱、X 射线粉末衍射和差示扫描量热法对所得样品进行了表征。结果表明,灰黄霉素在以固体分散体形式制备时与羟丙甲纤维素醋酸琥珀酸酯聚合物形成氢键,但在以相同组成的物理混合物形式制备时则不会。正如预期的那样,实际测量的固体分散体的玻璃化转变温度显示出与 Gordon-Taylor 和 Fox 方程预测的线性关系,假设为理想混合,但有趣的是仅在灰黄霉素含量小于 50wt%时。在灰黄霉素浓度大于此值时,固体分散体的测量玻璃化转变温度几乎保持不变。此外,通过差示扫描量热法和 X 射线粉末衍射确定的固体分散体的结晶含量也呈现出相似的趋势,即在灰黄霉素含量小于 50wt%的比例下,结晶含量显着降低。当使用 Flory-Huggins 模型分析灰黄霉素和羟丙甲纤维素醋酸琥珀酸酯聚合物的物理混合物时,获得了负混合自由能和 -0.23 的相互作用参数。这些结果表明,阴离子亲水性羟丙甲纤维素醋酸琥珀酸酯聚合物是结晶性非离子灰黄霉素的良好溶剂,固体分散体中灰黄霉素的溶解度估计在 40-50wt%范围内。在此溶解度极限以下,无定形药物以无定形玻璃溶液的形式存在,而在这些值以上,体系是过饱和的,玻璃状悬浮液和溶液可能共存。

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