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[慢性肾功能衰竭患者中克拉霉素的蛋白结合情况]

[Protein binding of clarithromycin in patients with chronic renal failure].

作者信息

Yago K, Kuroyama M, Motohashi S, Kumano K

机构信息

Department of Pharmacy, Kitasato University East Hospital.

出版信息

Jpn J Antibiot. 1996 Mar;49(3):256-63.

PMID:8935121
Abstract

Assessment was made on the serum protein binding of clarithromycin (CAM), a representative oral macrolide, using sera from healthy subjects (HS) and patients with chronic renal failure (CRF) applying equilibrium dialysis in vitro. The protein binding of CAM was 81.9 +/- 1.9%, 85.9 +/- 3.6%, 82.9 +/- 3.3% and 86.8 +/- 3.3% for sera from HS, from patients in conservative treatment (ND), from those receiving hemodialysis (HD) and from those with continuous ambulatory peritoneal dialysis (CAPD), respectively. There was no significant difference among these values. The protein binding of CAM was 82.9 +/- 3.3% and 68.8 +/- 3.5% for sera before and after HD, respectively. There was significant difference between these values. In the study of the protein binding in patients on HD at an albumin concentration of 0.5 mM, the protein binding of CAM for sera was found to be significantly decreased following HD as compared to that prior to HD. The addition of palmitic acid (PA), a common NEFA, to pooled sera from HS, the protein binding of CAM showed no change. These findings suggest that changes in the protein binding of CAM with HD have been possibly caused by an increase in a drug binding inhibiter other than NEFA (PA) or by an allosteric effect on the albumin binding capacity. At therapy using CAM, the possibility of enhanced pharmacological effects and increased adverse reactions of CAM due to decreased protein binding in patients on HD should be considered.

摘要

采用平衡透析法,在体外对健康受试者(HS)和慢性肾衰竭(CRF)患者的血清进行检测,评估代表性口服大环内酯类药物克拉霉素(CAM)的血清蛋白结合情况。HS、保守治疗患者(ND)、接受血液透析(HD)患者和持续非卧床腹膜透析(CAPD)患者血清中CAM的蛋白结合率分别为81.9±1.9%、85.9±3.6%、82.9±3.3%和86.8±3.3%。这些数值之间无显著差异。HD前后血清中CAM的蛋白结合率分别为82.9±3.3%和68.8±3.5%。这些数值之间存在显著差异。在对白蛋白浓度为0.5 mM的HD患者进行蛋白结合研究时,发现HD后血清中CAM的蛋白结合率较HD前显著降低。向HS混合血清中添加常见的非酯化脂肪酸(NEFA)棕榈酸(PA)后,CAM的蛋白结合率未发生变化。这些发现表明,HD导致CAM蛋白结合率变化的原因可能是除NEFA(PA)之外的药物结合抑制剂增加,或者是对白蛋白结合能力的变构效应。在使用CAM进行治疗时,应考虑HD患者因蛋白结合率降低导致CAM药理作用增强和不良反应增加的可能性。

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