二价和三价金属离子对氟喹诺酮类药物人工膜渗透的影响。

IF 3.4 Q2 CHEMISTRY, MEDICINAL
ADMET and DMPK Pub Date : 2022-01-01 DOI:10.5599/admet.1427
Nanami Nakatani, Kiyohiko Sugano
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引用次数: 0

摘要

本研究的目的是评估PAMPA对金属离子对氟喹诺酮类药物(FQ)生物利用度影响的可预测性。本研究采用了11种FQs和7种金属离子。PAMPA膜由10%的大豆卵磷脂(SL) -癸烷溶液组成。将含有或不含金属离子(作为氯盐添加)的MES缓冲液中的药物溶液添加到供体室中。在没有金属离子的情况下,FQ在SL-PAMPA中具有较高的渗透性(> 5 × 10-6 cm/sec),尽管FQ具有亲水性和两性离子性质。随着加/不加金属离子的PAMPA通透率越小,尿排泄量和AUC比值也越小,提示SL-PAMPA是一种适合用于评价金属离子对FQ生物利用度潜在影响的体外模型。然而,对于低溶解度的金属离子制剂(干燥的氢氧化铝凝胶和La2(CO3)3·8H2O), AUC和尿排泄的减少被高估了。在这种情况下,应同时评估金属离子制剂的溶解和FQs的渗透。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of divalent and trivalent metal ions on artificial membrane permeation of fluoroquinolones.

Effect of divalent and trivalent metal ions on artificial membrane permeation of fluoroquinolones.

Effect of divalent and trivalent metal ions on artificial membrane permeation of fluoroquinolones.

Effect of divalent and trivalent metal ions on artificial membrane permeation of fluoroquinolones.

The purpose of the present study was to evaluate the predictability of PAMPA for the effect of metal ions on the bioavailability of fluoroquinolones (FQ). Eleven FQs and seven metal ions were employed in this study. The PAMPA membrane consisted of a 10 % soybean lecithin (SL) - decane solution. A drug solution in MES buffer with or without a metal ion (added as a chloride salt) was added to the donor compartment. In the absence of metal ions, FQ showed relatively high permeability (> 5 × 10-6 cm/sec) in SL-PAMPA despite their hydrophilic and zwitterionic properties. As the PAMPA permeability ratio with/without metal ions became smaller, the urinary excretion and AUC ratios tended to be smaller, suggesting that SL-PAMPA is a suitable in vitro model to evaluate the potential effect of metal ions on the bioavailability of FQ. However, the reduction in AUC and urinary excretion was overestimated for low solubility metal ion formulations (dried aluminum hydroxide gel and La2(CO3)3・8H2O). In such cases, the dissolution of the metal ion formulations and the permeation of FQs should be simultaneously evaluated.

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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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