Using a Laser Monitoring Technique for Dissolution and Thermodynamic Study of Celecoxib in 2-Propanol and Propylene Glycol Mixtures

IF 1 4区 医学 Q4 PHARMACOLOGY & PHARMACY Dissolution Technologies Pub Date : 2023-01-01 DOI:10.14227/dt300223p80
V. Jouyban-Gharamaleki, F. Martínez, M. Kuentz, E. Rahimpour, A. Jouyban
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Abstract

In the current work, a laser monitoring technique was used to study dissolution and solubility of celecoxib (CBX) in 2-propanol and propylene glycol mixtures at temperatures of 293.2–313.2 K. The solubility data were fitted to mathematical models, i.e., the van’t Hoff model, the mixture surface model, the Jouyban-Acree and Jouyban-Acree-van’t Hoff equations, and the modified Wilson model. Model accuracy was evaluated by mean relative deviation (MRD%) for back-calculated solubility values. The thermodynamic behavior of CBX dissolution was evaluated according to the van’t Hoff and Gibbs equations. CBX exhibited maximum solubility in 2-propanol with a mass fraction of 0.8 at all temperatures. CBX dissolution was identified as an endothermic and enthalpy-driven process, which was more favorable in mixtures with high drug solubilizing capacity. The various models described solubility data from the laser monitoring technique adequately, and the studied cosolvent mixtures have the potential to be used in analytical pharmaceutical development or as intermediate bulk solutions for CBX products.
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用激光监测技术研究塞来昔布在2-丙醇和丙二醇混合物中的溶解和热力学
本文采用激光监测技术研究了塞来昔布(CBX)在293.2-313.2 K温度下在2-丙醇和丙二醇混合物中的溶解和溶解度。将溶解度数据拟合到数学模型中,即van 't Hoff模型、混合表面模型、Jouyban-Acree和Jouyban-Acree-van 't Hoff方程以及修正的Wilson模型。用反演溶解度值的平均相对偏差(MRD%)来评价模型的准确性。根据范霍夫方程和吉布斯方程评价了CBX溶解的热力学行为。CBX在2-丙醇中的溶解度最大,质量分数为0.8。CBX的溶解是一个吸热焓驱动的过程,在高药物增溶能力的混合物中更有利。各种模型充分描述了激光监测技术的溶解度数据,并且所研究的共溶剂混合物具有用于分析药物开发或作为CBX产品的中间散装溶液的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dissolution Technologies
Dissolution Technologies 医学-药学
CiteScore
1.20
自引率
33.30%
发文量
14
审稿时长
3 months
期刊介绍: Dissolution Technologies is a peer reviewed quarterly publication reporting ongoing, useful information on dissolution testing of pharmaceuticals. It provides an international forum for dissolution analysts to receive and exchange information on various dissolution topics. Dissolution Technologies welcomes submissions related to dissolution, in vitro release, and disintegration testing. These topics should be the major focus of the article. Do not submit articles where the focus is formulation development with dissolution testing as one of many tests.
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