评估粘蛋白对 BCS 2 类基本药物过饱和度和渗透性的影响

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL Journal of pharmaceutical sciences Pub Date : 2024-11-01 DOI:10.1016/j.xphs.2024.08.016
Tania Ng, Dawen Kou
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引用次数: 0

摘要

本研究评估了在 pH 值偏移的 2 阶段模型中,粘蛋白对 BCS 第 2 类碱性药物的过饱和及渗透的影响。粘蛋白对 DoS 和通量的影响(如果有的话)似乎是针对特定化合物的,可能与其 pKa 和电离状态有关。总体而言,在测试条件下,粘蛋白对三种模型化合物的过饱和度和渗透性的影响从适度到极小不等。使用 MacroFLUX 的 pH 值偏移模型能够监测胃和肠道溶解情况,并同时评估肠道粘蛋白对过饱和度和通量的影响。
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Evaluation of the impact of mucin on supersaturation and permeation of BCS class 2 basic drugs
This study evaluated the impact of mucin on supersaturation and permeation of BCS Class 2 basic drugs in a pH-shift, 2-stage model using three model compounds, dipyridamole, ricobendazole, and Compound A. The three compounds showed various degrees of supersaturation (DoS) in Stage 2 and modest to no increases in flux with the presence of mucin in the dissolution media. Mucin's impact on DoS and flux, if any, appeared to be compound specific and possibly related to its pKa and ionization state. Overall, the increases in supersaturation and permeation due to mucin ranged from modest to minimal for the three model compounds under the conditions tested. The pH-shift model using MacroFLUX was able to monitor gastric and intestinal dissolution and simultaneously assess the effect of intestinal mucin on supersaturation and flux.
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来源期刊
CiteScore
7.30
自引率
13.20%
发文量
367
审稿时长
33 days
期刊介绍: The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.
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