Narang P K, Crouthamel W G, Carliner N H, Fisher M L
Clin Pharmacol Ther. 1978 Dec;24(6):654-62. doi: 10.1002/cpt1978246654.
It has been shown that the antiarrhythmic and toxic effects of lidocaine may be in part dependent on its two active metabolites, monoethylglycylxylidide (MEGX) and glycylxylidide (GX). Presently available gas liquid chromatographic analytic methods require long and tedious steps or sophisticated equipment such as gas liquid chromatography-mass spectrometry. The assay method reported here with the use of high-performance liquid chromatography is rapid and allows accurate, precise determination of lidocaine, MEGX, and GX in biologic fluids. On the 3 patients studied extensively with the use of this assay, one patient had MEGX concentrations almost twice those of lidocaine. At 83% lidocaine potency, the contribution of MEGX in this patient was about 1.5 times that of lidocaine. The second patient studied on two consecutive days had a 20% increase in serum lidocaine concentration and an equivalent decrease in MEGX concentration on the second day. In the third patient lidocaine was stopped with a resulting half-life of 3.8 hr, which is consistent with previously reported values for patients on long-term lidocaine infusion. Urinary excretion of lidocaine and its metabolites is in agreement with previous work. These data suggest that much information still remains to be learned about the active metabolites of lidocaine as well as of lidocaine.
已表明利多卡因的抗心律失常作用和毒性作用可能部分取决于其两种活性代谢产物,单乙基甘氨酰二甲苯酰胺(MEGX)和甘氨酰二甲苯酰胺(GX)。目前可用的气液色谱分析方法需要冗长繁琐的步骤或精密设备,如气液色谱 - 质谱联用仪。本文报道的使用高效液相色谱的测定方法快速,且能准确、精确地测定生物体液中的利多卡因、MEGX和GX。对3例患者使用该测定方法进行广泛研究,其中1例患者的MEGX浓度几乎是利多卡因浓度的两倍。在利多卡因效力为83%时,该患者体内MEGX的作用约为利多卡因的1.5倍。对第2例患者连续两天进行研究,其血清利多卡因浓度在第二天升高了20%,而MEGX浓度相应降低。第3例患者停用利多卡因后,其半衰期为3.8小时,这与先前报道的长期输注利多卡因患者的值一致。利多卡因及其代谢产物的尿排泄情况与先前的研究结果相符。这些数据表明,关于利多卡因及其活性代谢产物仍有许多信息有待了解。