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分析柔红霉素及其代谢产物柔红霉素醇在血浆和尿液中的浓度,应用于评价急性髓系白血病患者的总清除率、肾清除率和代谢清除率。

Analysis of daunorubicin and its metabolite daunorubicinol in plasma and urine with application in the evaluation of total, renal and metabolic formation clearances in patients with acute myeloid leukemia.

机构信息

Department of Clinical, Toxicological and Bromatological Analyses, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, Brazil.

Department of Internal Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, SP, Brazil.

出版信息

J Pharm Biomed Anal. 2020 Nov 30;191:113576. doi: 10.1016/j.jpba.2020.113576. Epub 2020 Aug 26.

Abstract

This report presents improved analysis methods of daunorubicin (DAUN) and its metabolite daunorubicinol (DAUNOL) in small volumes of plasma, as total and unbound concentrations, as well as in urine. This study also presents the pharmacokinetics of DAUN and DAUNOL in patients (n = 12) diagnosed with acute myeloid leukemia treated with intravenous DAUN (60 mg/m/day, for three days). Serial blood and urine samples were collected up to 144 h after the beginning of the first infusion. The analytical methods presented no significant matrix effect. The linear ranges were 0.1-1000 ng/mL in plasma, 0.05-40 ng/mL in ultrafiltrate and 0.5-3000 ng/ml in urine. The precision and accuracy presented coefficients of variation and standard errors lower than 15 % in the three matrices. The methods allowed for the quantification of samples up to 144 h after the beginning of the first infusion. Unbound fractions for DAUN and DAUNOL were 23.91 % (17.33-32.99) and 29.23 % (25.84-33.07), respectively. The fraction recovered in urine was 4.40 % (3.87-5.03) for DAUN and 7.91 % (6.86-9.19) for DAUNOL. Total 292.96 L/h (261.74-327.90), renal 13.01 L/h (11.44-14.88), and hepatic 280.26 L/h (248.40-317.91) clearances of DAUN, as well as the DAUNOL formation clearance 23.41 L/h (19.09-28.97), were evaluated.

摘要

本报告介绍了一种改进的方法,用于分析小体积血浆中的柔红霉素(DAUN)及其代谢产物柔红霉素醇(DAUNOL),包括总浓度和游离浓度,以及尿液中的浓度。本研究还介绍了 12 例急性髓细胞白血病患者(n = 12)静脉注射柔红霉素(60 mg/m/天,连续 3 天)后的药代动力学参数。在第一次输注开始后 144 小时内采集了连续的血样和尿样。所提出的分析方法无显著基质效应。在血浆、超滤液和尿液中的线性范围分别为 0.1-1000ng/mL、0.05-40ng/mL 和 0.5-3000ng/ml。在这三种基质中,精密度和准确度的变异系数和标准误差均低于 15%。该方法可定量分析第一次输注开始后 144 小时内的样本。DAUN 和 DAUNOL 的游离分数分别为 23.91%(17.33-32.99)和 29.23%(25.84-33.07)。DAUN 在尿液中的回收率为 4.40%(3.87-5.03),DAUNOL 为 7.91%(6.86-9.19)。DAUN 的总清除率为 292.96 L/h(261.74-327.90)、肾清除率为 13.01 L/h(11.44-14.88)、肝清除率为 280.26 L/h(248.40-317.91),以及 DAUNOL 的生成清除率为 23.41 L/h(19.09-28.97)。

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