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氟氯西林在新生儿中的蛋白结合情况。

Protein binding of flucloxacillin in neonates.

作者信息

Pullen Joyce, Stolk Leo M L, Degraeuwe Pieter L J, van Tiel Frank H, Neef Cees, Zimmermann Luc J I

机构信息

Department of Clinical Pharmacy and Toxicology, Division of Neonatology, University Hospital of Maastricht, Maastricht, The Netherlands.

出版信息

Ther Drug Monit. 2007 Jun;29(3):279-83. doi: 10.1097/FTD.0b013e318063e30f.

Abstract

The isoxazolyl penicillins, including flucloxacillin, have the highest levels of plasma protein binding among the semisynthetic penicillins. Because only the free fraction of the penicillin is pharmacologically active, it would be useful to measure both protein-bound and free flucloxacillin to determine its protein binding. Until now, flucloxacillin protein binding in newborn infants has been investigated in only two studies with relatively small populations. In the present study, flucloxacillin protein binding was investigated in 56 (preterm) infants aged 3 to 87 days (gestational age, 25-41 weeks). Surplus plasma samples from routine gentamicin assays of each infant were collected and combined to obtain a sufficiently large sample for analysis. Free flucloxacillin was separated from protein-bound flucloxacillin using ultrafiltration. Reversed-phase high-performance liquid chromatography with ultraviolet detection was used to measure free flucloxacillin concentrations in ultrafiltrate and total flucloxacillin concentrations in pooled plasma. Flucloxacillin protein binding was 74.5% +/- 13.1% (mean +/- standard deviation) with a high variability among the infants (34.3% to 89.7%). High Pearson correlations were found between protein binding and the covariates-plasma albumin concentration (r = 0.804, P < 0.001, n = 18) and plasma creatinine concentration (r = -0.601, P < 0.001, n = 45). Statistically significant but less striking correlations were found between protein binding and gestational age, postconceptional age, body weight, and triglyceride concentration. Because of the high variability of protein binding among infants, it is difficult to devise a flucloxacillin dosage regimen effective for all infants. Individualized dosing, based on free flucloxacillin concentrations, might help to optimize treatment of late-onset neonatal sepsis, but practical obstacles will probably prevent analysis of free flucloxacillin concentrations in newborn infants on a routine basis.

摘要

异恶唑基青霉素,包括氟氯西林,在半合成青霉素中具有最高水平的血浆蛋白结合率。由于只有青霉素的游离部分具有药理活性,因此测量结合蛋白的氟氯西林和游离氟氯西林以确定其蛋白结合情况将很有用。到目前为止,仅在两项针对相对较小群体的研究中对新生儿的氟氯西林蛋白结合情况进行了调查。在本研究中,对56名年龄在3至87天(胎龄25 - 41周)的(早产)婴儿进行了氟氯西林蛋白结合情况的调查。收集每个婴儿常规庆大霉素检测剩余的血浆样本并合并,以获得足够大的样本用于分析。使用超滤将游离氟氯西林与结合蛋白的氟氯西林分离。采用带紫外检测的反相高效液相色谱法测量超滤液中游离氟氯西林浓度和合并血浆中总氟氯西林浓度。氟氯西林蛋白结合率为74.5%±13.1%(平均值±标准差),婴儿之间存在高度变异性(34.3%至89.7%)。发现蛋白结合与协变量——血浆白蛋白浓度(r = 0.804,P < 0.001,n = 18)和血浆肌酐浓度(r = -0.601,P < 0.001,n = 45)之间存在高度皮尔逊相关性。还发现蛋白结合与胎龄、孕龄、体重和甘油三酯浓度之间存在统计学显著但不太明显的相关性。由于婴儿之间蛋白结合的高度变异性,很难设计出对所有婴儿都有效的氟氯西林给药方案。基于游离氟氯西林浓度的个体化给药可能有助于优化迟发性新生儿败血症的治疗,但实际障碍可能会阻止常规分析新生儿的游离氟氯西林浓度。

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