Plasma vigabatrin enantiomer ratios in adults and children.

Clinical and experimental neurology Pub Date : 1993-01-01
L Nagarajan, T Schramm, D B Appleton, C J Burke, M J Eadie
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Abstract

The new anticonvulsant vigabatrin (gamma-vinyl-gamma-aminobutyric acid) is normally supplied as a racemate, but its anticonvulsant effect is thought to reside in its [S]-enantiomer only. The plasma concentration ratio of the [R] to [S] enantiomers appears to remain constant across the vigabatrin dosage interval in adult volunteers, and in the present study this has also proved to be the case in 12 chronically treated adult epileptic patients. However, in 8 epileptic children chronically treated with other anticonvulsants and given add-on vigabatrin therapy because of failure to control seizures, plasma [R]:[S]-vigabatrin ratios changed across the drug dosage interval, the [R]-vigabatrin levels tending to be relatively higher soon after intake, and to fall more rapidly than the [S]-vigabatrin concentrations over the next few hours (mean half-lives 2.52 +/- SD 0.49 and 6.53 +/- SD 6.62 hours). The reason for the shorter half-life of [R]-vigabatrin in children remains to be elucidated, but it appears that measurement of racemic vigabatrin plasma concentrations in children, though not in adults, may lead to somewhat misleading conclusions as regards the amount of the circulating anticonvulsant [S]-vigabatrin.

成人和儿童血浆维他汀对映体比率。
新的抗惊厥药维加巴林(γ -乙烯基- γ -氨基丁酸)通常以外消旋体形式供应,但其抗惊厥作用被认为仅存在于其[S]-对映体中。在成人志愿者中,[R]与[S]对映体的血浆浓度比似乎在整个维加巴林剂量间隔内保持不变,在本研究中,12名长期治疗的成人癫痫患者也证明了这一点。然而,在8例长期服用其他抗惊厥药物并因控制癫痫发作失败而加用维加巴林治疗的癫痫患儿中,血浆[R]:[S]-维加巴林比值在药物剂量间隔内发生变化,[R]-维加巴林水平在摄入后不久趋于相对较高,并且在接下来的几个小时内比[S]-维加巴林浓度下降得更快(平均半衰期为2.52 +/- SD 0.49和6.53 +/- SD 6.62小时)。[R]-vigabatrin在儿童中的半衰期较短的原因仍有待阐明,但似乎在儿童中测量外消旋维加巴特林的血浆浓度,而不是在成人中,可能会导致一些关于循环抗惊厥药[S]-维加巴特林的量的误导性结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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