首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >Jejunal and ileal absorption of oxprenolol in man: influence of nutrients and digestive secretions on jejunal absorption and systemic availability.
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Jejunal and ileal absorption of oxprenolol in man: influence of nutrients and digestive secretions on jejunal absorption and systemic availability.

机译:氯丁诺尔在人的空肠和回肠吸收:营养物质和消化分泌物对空肠吸收和全身利用率的影响。

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摘要

1 Study I evaluated the absorption of oxprenolol in the ileum, compared to jejunum, in healthy volunteers by an intestinal perfusion technique. Around 80 mg of drug were delivered as a saline solution directly in the small bowel. 2 Samples taken 30 cm distally to the site of perfusion showed that 63% of perfused oxprenolol was absorbed in the jejunum and 48% in the ileum; the differences were significant. 3 The plasma concentration-time profiles were similar for the two perfusions. The AUC and Cmax values of free and conjugated oxprenolol for the jejunal perfusion were significantly lower than those of ileum. They showed large but consistent intersubject variations in the two treatments. 4 Study II investigated, using the same technique, the influence of nutrients and digestive secretions on jejunal absorption and systemic availability of this drug. A saline (in treatments A and B) or a nutrient (in treatment C) solution containing oxprenolol was perfused into the jejunum below a balloon either inflated (A) or deflated (B and C). 5 The disappearance rate of oxprenolol from the jejunum was unaffected by endogenous secretions. The mean amount of drug absorbed along a 30-cm jejunal segment accounted for 52 (A) and 57% (B) of the total amount perfused. The intestinal absorption rate was markedly increased in the presence of nutrients (mean amount absorbed 96% for C). 6 The change in the rate of disappearance from the intestine had no effect on the systemic availability of oxprenolol (mean AUC values 8740, 8250 and 8020 nmol l-1 h for A, B and C, respectively) or its elimination from plasma.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1研究通过肠灌注技术评估了健康志愿者与空肠相比,回肠中羟丙诺醇的吸收。直接以盐溶液形式将约80 mg的药物以盐溶液形式输送到小肠中。 2在距灌注部位30 cm处采集的样本显示,灌注的oxprenolol在空肠中吸收了63%,在回肠中吸收了48%。差异很大。 3两种灌注的血浆浓度-时间曲线相似。空肠灌注的游离和共轭奥普萘洛的AUC和Cmax值显着低于回肠。他们在两种治疗中表现出较大但一致的受试者间差异。 4研究II使用相同的技术研究了营养物质和消化分泌物对该药物的空肠吸收和全身利用率的影响。将含有氧戊诺洛尔的盐水(在处理A和B中)或营养液(在处理C中)灌注到膨胀(A)或放气(B和C)的球囊下方的空肠中。 5空肠中奥曲洛诺的消失率不受内源性分泌物的影响。空肠段30 cm吸收的平均药物量占灌注总量的52(A)和57%(B)。在有营养的情况下,肠道吸收率显着提高(C的平均吸收量为96%)。 6肠道消失速率的变化对氧丁烯醇的全身利用率(A,B和C的平均AUC值分别为8740、8250和8020 nmol l-1 h)或从血浆中清除没有影响。(截短为250字的摘要)

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