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Plasma binding of disopyramide and mono-N-dealkyldisopyramide.

机译:二吡yr酰胺和单-N-脱烷基二吡yr酰胺的血浆结合。

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摘要

1 Measuring total plasma levels of disopyramide (DP) and the main metabolite mono-N-dealkyldisopyramide (MND) in patients on maintenance therapy with DP has shown concentrations of MND comparable with those of DP, with wide intersubject variations. 2 A method which permits simultaneous measurement of unbound fraction of DP and MND has been developed. 3 In healthy subjects the unbound fraction of both DP and MND was concentration dependent, i.e. increased with higher concentrations of DP or MND. 4 The plasma protein binding of DP is altered by varying concentrations of MND. Clinically relevant concentrations of MND may increase the unbound fraction of DP approximately twofold. 5 The plasma protein binding of MND is also altered by varying concentrations of DP. Variation in the concentration of DP from the lower to the upper part of the therapeutic range may cause a 1.5-fold increase in the unbound fraction of MND. 6 In the assumed therapeutic range of 6-15 mumol DP/L, the interpatient variance of unbound DP concentration might be ten-fold or even higher. The present findings indicate the need for monitoring unbound drug concentrations in any attempt to establish plasma concentration/effect relationship.
机译:1在接受DP维持治疗的患者中,测量其二吡酰胺(DP)和主要代谢物单-N-脱烷基二吡酰胺(MND)的总血浆水平,发现MND的浓度与DP相当,受试者间差异很大。 2已开发出一种方法,可以同时测量DP和MND的未结合部分。 3在健康受试者中,DP和MND的未结合部分是浓度依赖性的,即随着DP或MND浓度的增加而增加。 4 DP的血浆蛋白结合通过改变MND的浓度而改变。临床上相关浓度的MND可能会使DP的未结合部分增加大约两倍。 5 MND的血浆蛋白结合也可通过改变DP的浓度而改变。 DP浓度从治疗范围的下部到上部的变化可能导致MND的未结合部分增加1.5倍。 6在假定的6-15 mumol DP / L的治疗范围内,未结合DP浓度的患者间差异可能是10倍甚至更高。目前的发现表明,在建立血浆浓度/效应关系的任何尝试中,都需要监测未结合的药物浓度。

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