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艾滋病患者血清中克林霉素的蛋白结合情况。

Protein binding of clindamycin in sera of patients with AIDS.

作者信息

Flaherty J F, Gatti G, White J, Bubp J, Borin M, Gambertoglio J G

机构信息

Division of Clinical Pharmacy, School of Pharmacy, University of California, San Francisco 94143-0622, USA.

出版信息

Antimicrob Agents Chemother. 1996 May;40(5):1134-8. doi: 10.1128/AAC.40.5.1134.

DOI:10.1128/AAC.40.5.1134
PMID:8723453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC163278/
Abstract

Patients with AIDS have altered pharmacokinetics of clindamycin compared with those of healthy control subjects. In an attempt to better understand these differences, we undertook a study of protein binding of clindamycin in sera of patients with AIDS. Fifteen patients with AIDS and 15 healthy volunteers were given a single 600-mg dose of clindamycin orally and intravenously, and serum samples were collected at three time points corresponding to high, midpoint, and low clindamycin concentrations. Protein binding was determined by ultrafiltration, and total and unbound clindamycin concentrations were measured with a gas chromatography assay. AIDS patients had alpha 1-acid glycoprotein values approximately twice those of healthy volunteers (mean +/- standard deviation, 103 +/- 27 versus 61 +/- 11 mg/dl; P = 0.001). Overall, serum protein binding levels were higher in AIDS patients (mean +/- standard deviation, 83 +/- 7 versus 78% +/- 8%; P = 0.0001), which is likely the result of increased alpha 1-acid glycoprotein levels in these patients. Total concentrations of clindamycin in plasma were significantly higher in AIDS patients at most time points studied, while unbound serum clindamycin concentrations did not differ among the groups at each sampling time after both oral and intravenous dosing. Increased protein binding may partly explain the altered pharmacokinetic disposition of clindamycin in AIDS patients; however, other factors cannot be excluded.

摘要

与健康对照受试者相比,艾滋病患者的克林霉素药代动力学发生了改变。为了更好地理解这些差异,我们对艾滋病患者血清中克林霉素的蛋白结合情况进行了一项研究。15名艾滋病患者和15名健康志愿者口服和静脉注射单次600毫克剂量的克林霉素,并在对应于克林霉素高、中、低浓度的三个时间点采集血清样本。通过超滤法测定蛋白结合情况,并用气相色谱法测定总克林霉素浓度和未结合克林霉素浓度。艾滋病患者的α1-酸性糖蛋白值约为健康志愿者的两倍(平均值±标准差,103±27对61±11毫克/分升;P = 0.001)。总体而言,艾滋病患者的血清蛋白结合水平更高(平均值±标准差,83±7对78%±8%;P = 0.0001),这可能是这些患者α1-酸性糖蛋白水平升高的结果。在大多数研究时间点,艾滋病患者血浆中克林霉素的总浓度显著更高,而口服和静脉给药后,各采样时间点各组间未结合血清克林霉素浓度无差异。蛋白结合增加可能部分解释了艾滋病患者中克林霉素药代动力学处置的改变;然而,其他因素也不能排除。

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本文引用的文献

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