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[S6472(头孢克洛缓释制剂)的吸收与排泄研究]

[Absorption and excretion studies of S6472 (sustained release preparations of cefaclor)].

作者信息

Tateno M, Ito M, Iida M, Yasuda M, Sonoyama T, Matsuda S

出版信息

Jpn J Antibiot. 1985 Mar;38(3):834-48.

PMID:4032715
Abstract

In order to see absorption and excretion of S6472 (sustained release preparations of cefaclor (CCL], 3 studies regarding, 1) influence of meals (single dose of 375 mg in capsule form), 2) dose response (single dose of 375 mg vs. 750 mg in granule form) and 3) continuous administration (twice-a-day administration of 750 mg in granule form for 8 days) were conducted in 15 healthy adult male volunteers using capsule and granule forms of S6472. The following is the summary of the results from the above studies: Tolerance. In the above 3 studies, none of the 15 volunteers complained of subjective abnormalities. In the clinical laboratory tests performed before the administration of S6472 and at the next day of the completion of the studies, the values from the laboratory tests were within normal range. Influence of meals. The average time for peak plasma level of CCL and decrease in the plasma level following the administration of S6472 were the fastest in the fasted volunteers, followed by the volunteers with light meals and usual meals. From this, it was confirmed that plasma levels of CCL were maintained for longer period of time in the non-fasted volunteers than in the fasted volunteers. In the volunteers who had light and usual meals, the peak plasma levels, AUC of the plasma levels and urinary recovery rate were almost the same. Influence by amount of meals was scarcely observed. Dose response. Mean serum levels and their AUC in the volunteers receiving 750 mg of S6472 were approximately twice as much as those in the volunteers receiving 375 mg of S6472, and dose response between the 2 doses was confirmed. Continuous administration. Mean serum levels and their AUC at the first dose and the 15th dose (final dose) were almost the same. In the continuous administration of S6472 for 8 days (15 doses), no accumulation of CCL in the body was observed.

摘要

为观察S6472(头孢克洛缓释制剂,CCL)的吸收和排泄情况,对15名健康成年男性志愿者进行了3项研究,分别涉及:1)进餐的影响(胶囊形式单剂量375mg);2)剂量反应(颗粒形式单剂量375mg与750mg);3)连续给药(颗粒形式750mg每日两次给药,共8天),采用了S6472的胶囊和颗粒形式。以下是上述研究结果的总结:耐受性。在上述3项研究中,15名志愿者均未主诉主观异常。在服用S6472前及研究结束次日进行的临床实验室检查中,各项检查值均在正常范围内。进餐的影响。空腹志愿者服用S6472后CCL的血浆峰值水平及血浆水平下降的平均时间最快,其次是进食清淡餐和正常餐的志愿者。由此证实,非空腹志愿者中CCL的血浆水平维持时间比空腹志愿者更长。在进食清淡餐和正常餐的志愿者中,血浆峰值水平、血浆水平的AUC及尿回收率几乎相同。几乎未观察到进餐量的影响。剂量反应。接受750mg S6472的志愿者的平均血清水平及其AUC约为接受375mg S6472志愿者的两倍,证实了两剂量之间的剂量反应关系。连续给药。首剂和第15剂(末次剂量)时的平均血清水平及其AUC几乎相同。在连续8天(15剂)给予S6472的过程中,未观察到CCL在体内的蓄积。

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