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首页> 外文期刊>Journal of Clinical Pharmacy and Therapeutics >Rectal controlled-release morphine: plasma levels of morphine and its metabolites following the rectal administration of MST Continus 100 mg.
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Rectal controlled-release morphine: plasma levels of morphine and its metabolites following the rectal administration of MST Continus 100 mg.

机译:直肠控释吗啡:正常施用MST延续100毫克,血浆血浆及其代谢物。

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Eight patients undergoing major maxillary surgery were given sustained-release morphine (100 mg MST Continus) rectally, immediately after induction of general anaesthesia. Blood samples for assay were taken just prior to morphine administration, together with a further 11 samples over the following 24 h. Assay of the plasma for morphine, morphine-3-glucuronide and morphine-6-glucuronide was carried out using a validated high-performance liquid chromatography technique. Morphine Tmax ranged from 3 h to 12 h (median 6 h), Cmax 8.0-40.0 ng/ml and AUC0-24 90.1-429.7 ng/h/ml in subjects offering blood samples over the 24-h period. Likewise, morphine-3-glucuronide Tmax ranged from 3 h to 24 h (median 9 h), Cmax 153-370 ng/ml and AUC0-24 2776-4390 ng/h/ml. Morphine-6-glucuronide Tmax ranged from 8 h to 12 h (median 10 h), Cmax 24-59 ng/ml and AUC0-24 137-803 ng/h/ml. Morphine and morphine metabolite AUC0-24 ratios were calculated, but they did not correlate with analgesic needs. The AUC0-24 ratios were similar to those following oral and rectal dosing in other studies involving cancer patients. The wide variation of individual morphine and metabolite plasma levels, and their AUC ratios indicates considerable interpatient variability in the absorption and metabolism of rectal sustained-release morphine. This large interpatient variation may indicate that it is not suitable for acute pain, because analgesic requirements change much more rapidly than in the chronic pain situation where individual patient titration can take place.
机译:在诱导全身麻醉后立即进行持续释放的吗啡(100mg MST继续)持续释放吗啡(100mg MST延续)患者。用于测定的血液样品仅在吗啡给药之前进行,同时在以下24小时内与另外11个样品一起进行。使用验证的高效液相色谱技术进行吗啡,吗啡-3-葡糖苷和吗啡-6-葡糖醛酸等离子体的测定。吗啡Tmax范围从3小时到12小时(中位6小时),Cmax 8.0-40.0 ng / ml和Auc0-24 90.1-429.7 ng / h / ml在24小时内提供血液样品的受试者。同样,吗啡-3-葡萄糖蛋白酶Tmax从3小时到24小时(中值9小时),Cmax 153-370 ng / ml和Auc0-24 2776-4390 Ng / h / ml。吗啡-6-葡萄糖蛋白酶Tmax从8小时到12小时(中位数10小时),Cmax 24-59 ng / ml和Auc0-24 137-803 Ng / h / ml。计算吗啡和吗啡代谢物AUC0-24比率,但它们与镇痛药无关。 AUC0-24比率与涉及癌症患者的其他研究中口服和直肠给药后的比率类似。个体吗啡和代谢物血浆水平的广泛变化,以及它们的AUC比率表明直肠缓释吗啡的吸收和代谢的相当大的内部内部变异性。这种大型介入性变异可能表明它不适合急性疼痛,因为镇痛要求比在可以进行个体患者滴定的慢性疼痛情况下更快地变得更快。

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