Suppr超能文献

一种测定血浆中亚硝基脲的新方法:用于测定福莫司汀动力学的高效液相色谱法。

A new method for the measurement of nitrosoureas in plasma: an h.p.l.c. procedure for the measurement of fotemustine kinetics.

作者信息

Gordon B H, Richards R P, Hiley M P, Gray A J, Ings R M, Campbell D B

机构信息

Servier Research and Development Ltd., Fulmer Hall, Slough, UK.

出版信息

Xenobiotica. 1989 Mar;19(3):329-39. doi: 10.3109/00498258909042277.

Abstract
  1. An analytical method for a novel nitrosourea, fotemustine, has been developed using solid-phase extraction and h.p.l.c. with u.v. detection. As part of the development, different methods for stabilising fotemustine after sample collection have been investigated. The method has been successfully applied to pharmacokinetic studies in monkeys and man. 2. Providing plasma was separated immediately from blood and frozen within 3 min of collection, negligible degradation of fotemustine occurred. The samples could then be stored at -20 degrees C in the dark for up to six days particularly if thawing prior to analysis was accelerated using a 50 degrees C water-bath so that it was complete within 3 min. Equivalent results were also obtained with samples stabilised with 0.1 M citric acid immediately after the preparation of plasma. 3. The analytical method showed good precision with a within-day variation ranging between +/- 10.7% at the lowest concentration investigated (0.1 micrograms ml-1) to 2.0% at 50.0 micrograms ml-1. The accuracy of measurement was from 108.9% to 97.6% at 0.1 and 50.0 micrograms ml-1 respectively and the response was linear up to 50 micrograms ml-1. The minimum level of quantitation was 20 ng ml-1. 4. After a single intravenous bolus dose of [14C]fotemustine (100 mg m-2) to Cynomolgus monkeys, intact drug levels rapidly declined (t1/2 12.6 +/- 0.5 min) although the half-life of radioactivity (approx 100 h) was much longer. The plasma clearance of fotemustine was 225 +/- 63 ml min-1 with a volume of distribution based on area of 4.1 +/- 1.2 litres. 5. As with monkey, plasma levels of intact fotemustine in a patient given [14C]-drug as a 1 h constant rate intravenous infusion (approx. 100 mg m-2), declined rapidly but with a half-life of 23.2 min. Again, the half-life for total radioactivity was considerably longer (30.8 h). The plasma clearance was 1426 ml min-1 and the volume of distribution based on area was 47.71.
摘要
  1. 已开发出一种用于新型亚硝基脲福莫司汀的分析方法,该方法采用固相萃取和配有紫外检测的高效液相色谱法。作为方法开发的一部分,研究了样品采集后稳定福莫司汀的不同方法。该方法已成功应用于猴子和人类的药代动力学研究。2. 如果血浆在采集后3分钟内立即从血液中分离并冷冻,福莫司汀的降解可忽略不计。然后样品可在-20℃黑暗中保存长达6天,特别是如果在分析前使用50℃水浴加速解冻,使其在3分钟内完成解冻。血浆制备后立即用0.1M柠檬酸稳定的样品也得到了相同的结果。3. 该分析方法具有良好的精密度,日内变异在最低研究浓度(0.1微克/毫升)时为±10.7%,在50.0微克/毫升时为2.0%。在0.1和50.0微克/毫升时测量的准确度分别为108.9%至97.6%,响应在高达50微克/毫升时呈线性。最低定量水平为20纳克/毫升。4. 向食蟹猴单次静脉推注[14C]福莫司汀(100毫克/平方米)后,完整药物水平迅速下降(半衰期12.6±0.5分钟),尽管放射性的半衰期(约100小时)长得多。福莫司汀的血浆清除率为225±63毫升/分钟,基于面积的分布容积为4.1±1.2升。5. 与猴子一样,一名患者以1小时恒速静脉输注(约100毫克/平方米)给予[14C]药物后,完整福莫司汀的血浆水平迅速下降,但半衰期为23.2分钟。同样,总放射性的半衰期长得多(30.8小时)。血浆清除率为1426毫升/分钟,基于面积的分布容积为47.71。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验