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Validation of a Static Franz Diffusion Cell System for In Vitro Permeation Studies

机译:静态Franz扩散池系统用于体外渗透研究的验证

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摘要

Over the years, in vitro Franz diffusion experiments have evolved into one of the most important methods for researching transdermal drug administration. Unfortunately, this type of testing often yields permeation data that suffer from poor reproducibility. Moreover, this feature frequently occurs when synthetic membranes are used as barriers, in which case biological tissue-associated variability has been removed as an artefact of total variation. The objective of the current study was to evaluate the influence of a full-validation protocol on the performance of a tailor-made array of Franz diffusion cells (GlaxoSmithKline, Harlow, UK) available in our laboratory. To this end, ibuprofen was used as a model hydrophobic drug while synthetic membranes were used as barriers. The parameters investigated included Franz cell dimensions, stirring conditions, membrane type, membrane treatment, temperature regulation and sampling frequency. It was determined that validation dramatically reduced derived data variability as the coefficient of variation for steady-state ibuprofen permeation from a gel formulation was reduced from 25.7% to 5.3% (n = 6). Thus, validation and refinement of the protocol combined with improved operator training can greatly enhance reproducibility in Franz cell experimentation.
机译:多年来,体外Franz扩散实验已发展成为研究经皮给药的最重要方法之一。不幸的是,这种类型的测试通常会产生渗透性较差的渗透数据。此外,当使用合成膜作为屏障时,经常会出现此特征,在这种情况下,与生物组织相关的变异性已作为总变异的伪影而被消除。本研究的目的是评估我们实验室中可用的完全验证方案对定制的Franz扩散池阵列(GlaxoSmithKline,Harlow,英国)的性能的影响。为此,布洛芬用作模型疏水性药物,而合成膜用作屏障。研究的参数包括Franz池尺寸,搅拌条件,膜类型,膜处理,温度调节和采样频率。已确定,由于从凝胶制剂中稳态布洛芬渗透的变异系数从25.7%降至5.3%(n = 6),因此验证极大地降低了衍生数据的可变性。因此,方案的验证和完善与改进的操作员培训相结合,可以大大提高Franz细胞实验的可重复性。

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