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一种用于估算游离卡铂血浆浓度-时间曲线下面积的单样本分析方法。

A single-sample assay for the estimation of the area under the free carboplatin plasma concentration versus time curve.

作者信息

Ghazal-Aswad S, Calvert A H, Newell D R

机构信息

Cancer Research Unit, Medical School, University of Newcastle upon Tyne, UK.

出版信息

Cancer Chemother Pharmacol. 1996;37(5):429-34. doi: 10.1007/s002800050408.

Abstract

The aim of this study was to develop and validate a simple and rapid method for the estimation of the area under the free carboplatin plasma concentration versus time curve (AUC). The relationship between the carboplatin AUC and the total plasma platinum (Pt) concentration 24 h after treatment was studied using data from 49 patients treated with 20-1600 mg/m2 carboplatin as a 60-100 min infusion (median 60 min). The relationship was confirmed by the in vitro incubation of carboplatin in human plasma and prospectively validated in 13 ovarian cancer patients. Free carboplatin was separated by ultrafiltration (MW cut off 30,000), and free and total Pt measured by atomic absorption spectrophotometry. There was a linear relationship in vivo between the 24 h (median 24.4; range 16.3-27.3 h) total plasma Pt concentration (microM) and free carboplatin AUC (mg/ml.min): AUC=(24 h Pt+0.3)/0.82 (r2=0.93, AUC median 5.8 (0.13-28)mg/ml.min, 24h Pt median 4.4 (0.1-23) microM). A similar relationship was observed in vitro [AUC =(24h Pt +0.1)/0.93 (r2=0.98, AUC median 7.9 (2.0-17) mg/ml.min, 24 h Pt median 7.1 (1.8-15) microM)]. The relationship derived from the in vivo data gave an unbiased and reasonably accurate estimate of the measured carboplatin AUC in 13 patients (AUC =5.1-8.7 mg/ml.min, GFR=59-129 ml/min, infusion time 30-45 min, 24 h sampling time 22.9-24.5 h), giving a percentage mean error of -4.2% and root mean squared percentage error of 11.5%. These results show that the analysis of a single blood sample taken 24 h after carboplatin administration can be used to produce an unbiased and reasonably accurate measure of the free carboplatin AUC. Unlike published limited sampling strategies, this method is not complicated by the need to accurately control the duration of the carboplatin infusion or the time at which the sample is taken.

摘要

本研究的目的是开发并验证一种简单快速的方法,用于估算卡铂游离血药浓度-时间曲线下面积(AUC)。利用49例接受20 - 1600mg/m²卡铂静脉滴注60 - 100分钟(中位数60分钟)治疗患者的数据,研究了卡铂AUC与治疗后24小时总血浆铂(Pt)浓度之间的关系。通过卡铂在人血浆中的体外孵育对该关系进行了确认,并在13例卵巢癌患者中进行了前瞻性验证。通过超滤(截留分子量30,000)分离游离卡铂,并用原子吸收分光光度法测定游离和总Pt。体内24小时(中位数24.4;范围16.3 - 27.3小时)总血浆Pt浓度(微摩尔)与游离卡铂AUC(毫克/毫升·分钟)之间存在线性关系:AUC =(24小时Pt + 0.3)/0.82(r² = 0.93,AUC中位数5.8(0.13 - 28)毫克/毫升·分钟,24小时Pt中位数4.4(0.1 - 23)微摩尔)。体外也观察到类似关系[AUC =(24小时Pt + 0.1)/0.93(r² = 0.98,AUC中位数7.9(2.0 - 17)毫克/毫升·分钟,24小时Pt中位数7.1(1.8 - 15)微摩尔)]。从体内数据得出的关系对13例患者(AUC = 5.1 - 8.7毫克/毫升·分钟,肾小球滤过率(GFR)= 59 - 129毫升/分钟,输注时间30 - 45分钟,24小时采样时间22.9 - 24.5小时)测得的卡铂AUC给出了无偏且合理准确的估计,平均误差百分比为 - 4.2%,均方根百分比误差为11.5%。这些结果表明,在卡铂给药后24小时采集的单个血样分析可用于对游离卡铂AUC进行无偏且合理准确的测量。与已发表的有限采样策略不同,该方法不受精确控制卡铂输注持续时间或采样时间的需求的影响。

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