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艾滋病患者中克拉霉素和齐多夫定的药代动力学

Pharmacokinetics of clarithromycin and zidovudine in patients with AIDS.

作者信息

Vance E, Watson-Bitar M, Gustavson L, Kazanjian P

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

Antimicrob Agents Chemother. 1995 Jun;39(6):1355-60. doi: 10.1128/AAC.39.6.1355.

Abstract

The interrelationships between the pharmacokinetics of zidovudine alone and of zidovudine plus clarithromycin were evaluated with 18 volunteers with AIDS who had no infection with Mycobacterium avium complex or clinical evidence of gastroenteritis. Patients received 200 mg of zidovudine orally every 8 h on days 1 to 4 and 1,000 mg of clarithromycin every 12 h, given 2 h apart from zidovudine, on days 2 to 4. Concentrations of zidovudine in plasma were measured at steady state both prior to (phase 1, day 1) and during (phase 2, day 4) administration of clarithromycin. Levels of clarithromycin were measured at steady state on day 4. The maximum concentrations of zidovudine in plasma were significantly different in phases 1 and 2 (616.6 and 949.0 ng/ml, respectively), as were the times to the maximum concentrations of zidovudine (2.1 and 1.0 h, respectively). However, the minimum concentrations in plasma and the areas under the concentration-time curves from 0 to 6 h did not differ on days 1 and 4. There is no significant impact on the overall bioavailability of zidovudine from the addition of clarithromycin in patients with AIDS. Clarithromycin may increase the rate of zidovudine absorption, but this is unlikely to have clinical relevance.

摘要

在18名未感染鸟分枝杆菌复合体且无肠胃炎临床证据的艾滋病志愿者中,评估了齐多夫定单独用药以及齐多夫定与克拉霉素联合用药时的药代动力学相互关系。患者在第1至4天每8小时口服200毫克齐多夫定,在第2至4天每12小时口服1000毫克克拉霉素,与齐多夫定间隔2小时给药。在克拉霉素给药前(第1阶段,第1天)和给药期间(第2阶段,第4天),均在稳态下测定血浆中的齐多夫定浓度。在第4天测定克拉霉素的稳态水平。第1阶段和第2阶段血浆中齐多夫定的最大浓度有显著差异(分别为616.6和949.0纳克/毫升),达到齐多夫定最大浓度的时间也有显著差异(分别为2.1和1.0小时)。然而,第1天和第4天血浆中的最低浓度以及0至6小时浓度-时间曲线下的面积并无差异。在艾滋病患者中,添加克拉霉素对齐多夫定的总体生物利用度没有显著影响。克拉霉素可能会提高齐多夫定的吸收速率,但这在临床上不太可能具有相关性。

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