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蛋白质结合作为非甾体抗炎药临床药代动力学特性的主要决定因素。

Protein binding as a primary determinant of the clinical pharmacokinetic properties of non-steroidal anti-inflammatory drugs.

作者信息

Lin J H, Cocchetto D M, Duggan D E

出版信息

Clin Pharmacokinet. 1987 Jun;12(6):402-32. doi: 10.2165/00003088-198712060-00002.

Abstract

The ability of a wide variety of anionic, cationic, and neutral drugs to bind in a reversible manner to plasma proteins has long been recognised. Non-steroidal anti-inflammatory drugs (NSAIDs) are distinguished as a class by the high degree to which they bind to plasma protein. Plasma protein binding properties are primary determinants of the pharmacokinetic properties of the NSAIDs. Theoretical relationships are reviewed in order to define quantitatively the impact of plasma protein binding on clearance, half-life, apparent volume of distribution, and the duration and intensity of pharmacological effect. The quantitative relationships governing competitive displacement binding interactions are also presented. Experimental methods for in vitro and in vivo determination of the degree of plasma protein binding are discussed. The more common in vitro methods are equilibrium dialysis and ultrafiltration. Methods for characterising the degree of plasma protein binding in vivo consist of either measuring the concentration of drug at equilibrium in an implanted semipermeable vessel or measuring the relative drug concentrations in two body spaces with different protein content. Emphasis is given to the comparative advantages and disadvantages of experimental application of the various in vitro and in vivo methods. Plasma protein binding is discussed as a determinant of the trans-synovial transport of NSAIDs. Trans-synovial transport of NSAIDs appears to be a diffusional process. Limited data in humans receiving ibuprofen, indomethacin, aspirin, carprofen, alclofenac, or diclofenac suggest that clearance of each of these NSAIDs from the synovium is slower than clearance from plasma. The clinical data relevant to the relationship between plasma NSAID concentration and various measures of anti-inflammatory effect are reviewed. A positive correlation between plasma NSAID concentration and anti-inflammatory effect has been observed in only one study on naproxen and one study on piroxicam. In several other studies, the lack of concentration-response correlations is generally attributed to the relatively subjective, quantitatively inexact methods used to assess anti-inflammatory effect and analgesia in arthritic patients, as well as the substantial interpatient variabilities in the fraction of unbound NSAID and the unbound plasma NSAID concentration. In view of the generally poor correlation between concentration and therapeutic response, routine therapeutic monitoring of total plasma NSAID concentration is not recommended as a means of titrating individual dosages to the desired effect in each patient.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

长期以来,人们一直认识到多种阴离子、阳离子和中性药物能够以可逆方式与血浆蛋白结合。非甾体抗炎药(NSAIDs)作为一类药物的特点是它们与血浆蛋白的结合程度很高。血浆蛋白结合特性是NSAIDs药代动力学特性的主要决定因素。本文回顾了理论关系,以便定量确定血浆蛋白结合对清除率、半衰期、表观分布容积以及药理作用的持续时间和强度的影响。还介绍了控制竞争性置换结合相互作用的定量关系。讨论了体外和体内测定血浆蛋白结合程度的实验方法。较常见的体外方法是平衡透析和超滤。体内表征血浆蛋白结合程度的方法包括测量植入的半透膜容器中药物平衡时的浓度,或测量两个蛋白质含量不同的身体空间中的相对药物浓度。重点介绍了各种体外和体内方法在实验应用中的比较优缺点。讨论了血浆蛋白结合作为NSAIDs跨滑膜转运的决定因素。NSAIDs的跨滑膜转运似乎是一个扩散过程。在接受布洛芬、吲哚美辛、阿司匹林、卡洛芬、阿氯芬酸或双氯芬酸的人类中,有限的数据表明,这些NSAIDs从滑膜中的清除比从血浆中的清除要慢。回顾了与血浆NSAID浓度和各种抗炎作用指标之间关系相关的临床数据。仅在一项关于萘普生的研究和一项关于吡罗昔康的研究中观察到血浆NSAID浓度与抗炎作用之间存在正相关。在其他几项研究中,缺乏浓度-反应相关性通常归因于用于评估关节炎患者抗炎作用和镇痛作用的相对主观、定量不准确的方法,以及未结合NSAID分数和未结合血浆NSAID浓度在患者之间的巨大变异性。鉴于浓度与治疗反应之间普遍存在较差的相关性,不建议将常规监测血浆NSAID总浓度作为在每个患者中调整个体剂量以达到预期效果的手段。(摘要截短为400字)

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