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估算药物在胃肠道中的溶解度。

Estimating drug solubility in the gastrointestinal tract.

作者信息

Dressman J B, Vertzoni M, Goumas K, Reppas C

机构信息

Department of Pharmaceutical Technology, Johann Wolfgang Goethe University, Frankfurt, Germany.

出版信息

Adv Drug Deliv Rev. 2007 Jul 30;59(7):591-602. doi: 10.1016/j.addr.2007.05.009. Epub 2007 May 29.

Abstract

Solubilities measured in water are not always indicative of solubilities in the gastrointestinal tract. The use of aqueous solubility to predict oral drug absorption can therefore lead to very pronounced underestimates of the oral bioavailability, particularly for drugs which are poorly soluble and lipophilic. Mechanisms responsible for enhancing the luminal solubility of such drugs are discussed. Various methods for estimating intra-lumenal solubilities are presented, with emphasis on the two most widely implemented methods: determining solubility in fluids aspirated from the human gastrointestinal tract, and determining solubility in so-called biorelevant media, composed to simulate these fluids. The ability of the biorelevant media to predict solubility in human aspirates and to predict plasma profiles is illustrated with case examples.

摘要

在水中测得的溶解度并不总是能反映在胃肠道中的溶解度。因此,使用水溶性来预测口服药物吸收可能会导致对口服生物利用度的严重低估,尤其是对于难溶性和亲脂性药物。文中讨论了提高此类药物肠腔溶解度的机制。介绍了各种估算肠腔内溶解度的方法,重点介绍了两种应用最广泛的方法:测定从人体胃肠道吸出的液体中的溶解度,以及测定在所谓的生物相关介质中的溶解度,这种介质的成分是模拟这些液体的。文中通过实例说明了生物相关介质预测人体吸出物中溶解度和预测血浆浓度曲线的能力。

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