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Franz Diffusion Cell Approach for Pre-Formulation Characterisation of Ketoprofen Semi-Solid Dosage Forms

机译:Franz扩散池方法用于酮洛芬半固体剂型的预配制表征

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摘要

This study aimed to evaluate and compare, using the methodology of Franz diffusion cells, the ketoprofen (KTP) releasing profiles of two formulations: A gel and a conventional suspension. The second aim was to show that this methodology might be easily applied for the development of semi-solid prototypes and claim proof in pre-formulation stages. Drug release analysis was carried out under physiological conditions (pH: 5.6 to 7.4; ionic strength 0.15 M; at 37 °C) for 24 h. Three independent vertical Franz cells were used with a nominal volume of the acceptor compartment of 125 mL and a diffusion area of 2.5 cm2. Additionally, two different membranes were evaluated: A generic type (regenerated cellulose) and a transdermal simulation type (Strat-M®). The KTP permeation profiles demonstrated that depending on the membrane type and the vehicle used, the permeation is strongly affected. High permeation efficiencies were obtained for the gel formulation, and the opposite effect was observed for the suspension formulation. Moreover, the permeation studies using Strat-M membranes represent a reproducible methodology, which is easy to implement for pre-formulation stage or performance evaluation of semi-solid pharmaceutical products for topical or transdermal administration.
机译:这项研究旨在使用Franz扩散池的方法评估和比较酮洛芬(KTP)两种制剂的释放曲线:凝胶和常规悬浮液。第二个目的是表明该方法可以很容易地应用于半固体原型的开发,并可以在预配制阶段进行证明。在生理条件下(pH:5.6至7.4;离子强度为0.15 M;在37°C下)进行药物释放分析24小时。使用三个独立的垂直Franz池,受体室的标称体积为125 mL,扩散面积为2.5 cm 2 。此外,还评估了两种不同的膜:通用型(再生纤维素)和透皮模拟型(Strat-M ®)。 KTP渗透曲线表明,取决于膜的类型和所用的载体,渗透受到很大影响。凝胶制剂获得了高渗透效率,而悬浮液制剂则观察到相反的效果。此外,使用Strat-M膜进行的渗透研究代表了一种可重现的方法,对于局部或透皮给药的半固体药物产品的预配制阶段或性能评估,该方法易于实施。

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