Department of Pharmaceutics, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences, Brno, Palackého 1/3, 612 42, Brno, Czech Republic,
AAPS PharmSciTech. 2013 Dec;14(4):1341-8. doi: 10.1208/s12249-013-0019-1. Epub 2013 Aug 30.
The solubility of weakly basic drugs within passage though GI tract leads to pH-dependent or even incomplete release of these drugs from extended release formulations and consequently to lower drug absorption and bioavailability. The aim of the study was to prepare and evaluate hydrophilic-lipophilic (hypromellose-montanglycol wax) matrix tablets ensuring the pH-independent delivery of the weakly basic drug verapamil-hydrochloride by an incorporation of three organic acidifiers (citric, fumaric, and itaconic acids) differing in their concentrations, pK a, and solubility. The dissolution studies were performed by the method of changing pH values, which better corresponded to the real conditions in the GI tract (2 h at pH 1.2 and then 10 h at pH 6.8). Within the same conditions, pH of matrix microenvironment was measured. To determine relationships between the above mentioned properties of acidifiers and the monitored effects (the amount of released drug and surface pH of gel layer in selected time intervals-360 and 480 min), the full factorial design method and partial least squares PLS-2 regression were used. The incorporation of the tested pH modifiers significantly increased the drug release rate from matrices. PLS-components explained 75% and 73% variation in the X- and Y-data, respectively. The obtained results indicated that the main crucial points (p < 0.01) were the concentration and strength of acidifier incorporated into the matrix. Contrary, the acid solubility surprisingly did not influence the selected effects except for the surface pH of gel layer in time 480 min.
弱碱性药物在胃肠道中的溶解度导致这些药物从缓释制剂中以 pH 依赖性甚至不完全释放,从而导致药物吸收和生物利用度降低。本研究的目的是制备和评价亲脂性(羟丙甲纤维素-蒙坦戈蜡)基质片剂,通过掺入三种有机酸(柠檬酸、富马酸和衣康酸)来确保弱碱性药物盐酸维拉帕米的 pH 独立传递,这三种有机酸在浓度、pKa 和溶解度方面存在差异。通过改变 pH 值的方法进行溶解研究,该方法更符合胃肠道中的实际条件(在 pH 1.2 下 2 小时,然后在 pH 6.8 下 10 小时)。在相同条件下,测量了基质微环境的 pH 值。为了确定酸化剂的上述特性与监测效果(在选定的时间间隔 360 和 480 分钟内释放的药物量和凝胶层的表面 pH)之间的关系,使用了完全因子设计方法和偏最小二乘 PLS-2 回归。测试的 pH 调节剂的掺入显着增加了基质中药物的释放速率。PLS 成分分别解释了 X 和 Y 数据变化的 75%和 73%。所得结果表明,主要关键点(p <0.01)是掺入基质中的酸的浓度和强度。相反,酸的溶解度除了在 480 分钟的凝胶层表面 pH 值外,出人意料地对所选效果没有影响。