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药物在水溶液中的溶解度。第4部分。基于稀释近似法的药物溶解度

Solubility of drugs in aqueous solutions. Part 4. Drug solubility by the dilute approximation.

作者信息

Ruckenstein E, Shulgin I

机构信息

Department of Chemical Engineering, State University of New York at Buffalo, Amherst 14260, USA.

出版信息

Int J Pharm. 2004 Jul 8;278(2):221-9. doi: 10.1016/j.ijpharm.2004.03.007.

Abstract

As in our previous publications in this journal [Int. J. Pharm. 258 (2003a) 193; Int. J. Pharm. 260 (2003b) 283; Int. J. Pharm. 267 (2003c) 121], this paper is concerned with the solubility of poorly soluble drugs in aqueous mixed solvents. In the previous publications, the solubilities of drugs were assumed to be low enough for the so-called infinite dilution approximation to be applicable. In contrast, in the present paper, the solubilities are considered to be finite and the dilute solution approximation is employed. As before, the fluctuation theory of solutions is used to express the derivatives of the activity coefficient of a solute in a ternary solution (dilute solute concentrations in a binary solvent) with respect to the concentrations of the solvent and cosolvent. The expressions obtained are combined with a theoretical equation for the activity coefficient of the solute. As a result, the activity coefficient of the solute was expressed through the activity coefficients of the solute at infinite dilution, solute mole fraction, some properties of the binary solvent (composition, molar volume and activity coefficients of the components) and parameters reflecting the nonidealities of binary species. The expression thus obtained was used to derive an equation for the solubility of poorly soluble drugs in aqueous binary solvents which was applied in two different ways. First, the nonideality parameters were considered as adjustable parameters, determined from experimental solubility data. Second, the obtained equation was used to correct the solubilities of drugs calculated via the infinite dilution approximation. It was shown that both procedures provide accurate correlations for the drug solubility.

摘要

正如我们之前在本期刊上发表的文章[《国际药学杂志》258 (2003a) 193;《国际药学杂志》260 (2003b) 283;《国际药学杂志》267 (2003c) 121]一样,本文关注难溶性药物在水性混合溶剂中的溶解度。在之前的文章中,假设药物的溶解度足够低,以至于所谓的无限稀释近似法适用。相比之下,在本文中,溶解度被认为是有限的,并采用了稀溶液近似法。和以前一样,溶液的涨落理论用于表示三元溶液(二元溶剂中的稀溶质浓度)中溶质活度系数相对于溶剂和助溶剂浓度的导数。所得到的表达式与溶质活度系数的理论方程相结合。结果,溶质的活度系数通过溶质在无限稀释时的活度系数、溶质摩尔分数、二元溶剂的一些性质(组成、摩尔体积和各组分的活度系数)以及反映二元物种非理想性的参数来表示。由此得到的表达式被用于推导难溶性药物在二元水性溶剂中溶解度的方程,该方程以两种不同方式应用。首先,将非理想性参数视为可调参数,根据实验溶解度数据确定。其次,所得到的方程用于校正通过无限稀释近似法计算的药物溶解度。结果表明,这两种方法都能为药物溶解度提供准确的相关性。

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