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Influence of drug physicochemical characteristics on in vitro transdermal absorption of hydrophobic drug nanosuspensions

机译:药物理化特性​​对疏水性药物纳米混悬剂体外透皮吸收的影响

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The purpose of this paper was to study the influence of drug physicochemical characteristics on in vitro transdermal absorption of hydrophobic drug nanosuspensions. Four drug nanosuspensions were produced by high-pressure homogenization technique, which were the same in stabilizer and similar in particle size. Differential scanning calorimetry and powder X-ray diffraction analysis showed that the crystalline state of the nanocrystals did not change. In vitro permeation study demonstrated that the drug nanosuspensions have a higher rate of permeation that ranged from 1.69- to 3.74-fold compared to drug microsuspensions. Correlation analysis between drug physicochemical properties and J(ss) revealed that log P and pKa were factors that influenced the in vitro transdermal absorption of hydrophobic drug nanosuspensions, and drugs with a log P value around 3 and a higher pKa value (when pKaH+2) would gain higher J(ss) in this paper.
机译:本文旨在研究药物理化特性​​对疏水性药物纳米混悬剂体外透皮吸收的影响。通过高压均质技术制备了四种药物纳米悬浮液,它们的稳定剂相同,粒径相似。差示扫描量热法和粉末X射线衍射分析表明,纳米晶体的晶体状态没有改变。体外渗透研究表明,与药物微悬浮液相比,药物纳米混悬液的渗透率更高,范围为1.69至3.74倍。药物理化性质与J(ss)之间的相关性分析表明,log P和pKa是影响疏水性药物纳米悬液的体外透皮吸收的因素,log P值约为3且pKa值较高(当pKa H +2)将在本文中获得更高的J(ss)。

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