首页> 外文期刊>British Journal of Clinical Pharmacology >Pharmacokinetics of two formulations of omeprazole administered through a gastrostomy tube in patients with severe neurodevelopmental problems.
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Pharmacokinetics of two formulations of omeprazole administered through a gastrostomy tube in patients with severe neurodevelopmental problems.

机译:通过胃造口管给药的两种奥美拉唑制剂在严重神经发育问题患者中的药代动力学。

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AIMS: Omeprazole is often administered through a gastrostomy tube as either (i) a Multiple Unit Pellet System (MUPS(R)) tablet disintegrated in water (MUPS(R) formulation), or (ii) a suspension in 8.4% sodium bicarbonate (suspension formulation). This bioavailability study evaluates this practice in tube-fed patients with severe neurodevelopmental problems. METHODS: Nonblinded, two-phase cross-over trial. RESULTS: In seven of 10 patients, bioavailability was higher for the suspension formulation than for the MUPS(R) formulation. Median (90% confidence interval) area under the plasma concentration-time curve ratio (MUPS(R) over suspension) was 0.5 (0.06-2.37). CONCLUSIONS: In this population, omeprazole MUPS(R) formulation has no apparent advantage over the more easily administered suspension formulation.
机译:目的:奥美拉唑通常通过胃造口管给药,方法是(i)在水中崩解的多单位药丸系统(MUPS®制剂),或者(ii)8.4%碳酸氢钠的混悬液(悬浮液配方)。这项生物利用度研究对患有严重神经发育问题的管饲患者进行了评估。方法:无盲,两阶段交叉试验。结果:在10名患者中,有7名患者的悬浮液制剂的生物利用度高于MUPS(R)制剂。血浆浓度-时间曲线比率(悬浮液上的)的中值(90%置信区间)面积为0.5(0.06-2.37)。结论:在该人群中,奥美拉唑MUPS(R)制剂与较易于给药的混悬剂相比没有明显的优势。

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