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Enhancing the intestinal absorption of poorly water-soluble weak-acidic compound by controlling local pH

机译:通过控制局部pH值来增强水溶性差的弱酸性化合物的肠道吸收

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Recently, the number of poorly water-soluble drug candidates has increased and has hindered the rapid improvement of new drugs with low intestinal absorption; however, the intestinal absorption of pH-dependent poorly water-soluble compounds is expected to be markedly improved by changing the pH in the vicinity of the absorption site. The aim of this study is to clarify the effect of local pH change in the intestinal tract by magnesium oxide on the intestinal absorption of hydrochlorothiazide, a model poorly water-soluble weak-acid compound. The application of hydrochlorothiazide granule containing magnesium oxide to the rat intestinal loop increased the pH in the vicinity of the dosing site to more than 8.5 for 90min without any mucosal damage. As a result, absorption of hydrochlorothiazide increased by the addition of magnesium oxide to the granule. Intraintestinal administration of a suspension prepared from hydrochlorothiazide granules with magnesium oxide increased the intestinal absorption and the AUC value was 3-fold higher than that without magnesium oxide. To further increase the intestinal absorption of hydrochlorothiazide, we prepared granules containing magnesium oxide and chitosan as a mucoadhesive and tight junction opening material. Chitosan showed a marked increase of intestinal absorption, and the AUC value after the administration of suspensions of chitosan granules was more than 5-fold higher than that of granules containing hydrochlorothiazide alone, respectively. In summary, it has been clarified that the intestinal absorption of weak-acidic poorly water-soluble compound can be enhanced by increasing local pH, mucoadhesion and opening tight junction.
机译:最近,水溶性差的候选药物的数量增加了,并且阻碍了肠道吸收低的新药的快速改进。但是,通过改变吸收部位附近的pH值,可望显着改善pH依赖性水溶性差的化合物的肠吸收。这项研究的目的是弄清氧化镁在肠道中局部pH值变化对水溶性弱酸模型氢氯噻嗪的肠道吸收的影响。将含氧化镁的氢氯噻嗪颗粒应用于大鼠肠环,可在90分钟内将给药部位附近的pH值提高至8.5以上,而不会对粘膜造成任何损害。结果,通过向颗粒中加入氧化镁增加了氢氯噻嗪的吸收。由氢氯噻嗪颗粒制成的混悬液与氧化镁的肠内给药可增加肠道吸收,AUC值比无氧化镁高3倍。为了进一步增加氢氯噻嗪的肠道吸收,我们制备了含有氧化镁和壳聚糖作为粘膜粘附和紧密连接开口材料的颗粒。壳聚糖显示出肠道吸收的显着增加,并且给予壳聚糖颗粒悬浮液后的AUC值分别比仅含氢氯噻嗪的颗粒高出5倍以上。总之,已经阐明,通过增加局部pH,粘膜粘附和打开紧密连接可以增强弱酸性难溶于水的化合物的肠吸收。

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