Gasthuys Elke, van Ovost Judith, Vande Casteele Sofie, Cosyns Sarah, Ceelen Wim, Van Bocxlaer Jan, Vermeulen An
Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.
Department of Human Structure and Repair, Laboratory of Experimental Surgery Faculty of Medicine and Health Sciences, Ghent University, Corneel Heymanslaan 10, 9000 Ghent, Belgium; Cancer Research Institute Ghent (CRIG), Corneel Heymanslaan 10, 9000 Ghent, Belgium.
J Chromatogr B Analyt Technol Biomed Life Sci. 2024 Feb 1;1233:123980. doi: 10.1016/j.jchromb.2023.123980. Epub 2024 Jan 6.
Irinotecan (CPT-11), an antineoplastic drug, is used for the treatment of colorectal and pancreatic cancer due to its topoisomerase I inhibitory activity. CPT-11 is a prodrug which is converted to its active metabolite SN-38 by carboxylesterases. SN-38 is further metabolized to its inactive metabolite SN-38 glucuronide. When evaluating the pharmacokinetic properties of CPT-11 and its metabolites, it is important to accurately assess the concentrations in both plasma as well as tumor tissues. Therefore, the aim of the current study was to develop and validate a robust and sensitive ultra-high performance liquid chromatography-tandem mass spectrometry method to quantify the concentration of CPT-11 and its metabolites (SN-38 and SN-38 glucuronide) in human plasma and peritoneal tumor tissue. The sample preparation of plasma and tumor tissue consisted of protein precipitation and enzymatic digestion/liquid-liquid extraction, respectively. Chromatographic separation was achieved with an Acquity UPLC BEH C18 column combined with a VanGuard pre-column. The mobile phases consisted of water +0.1 % formic acid (mobile phase A) and acetonitrile +0.1 % formic acid (mobile phase B). Mass analysis was performed using a Xevo TQS tandem mass spectrometer in the positive electrospray ionization mode. Method validation was successfully performed by assessing linearity, precision and accuracy, lower limit of quantification, carry over, selectivity, matrix effect and stability according to the following guidelines: "Committee for Medicinal Products for Human use, Guideline on Bioanalytical Method Validation". A cross-validation of the developed method was performed in a pilot pharmacokinetic study, demonstrating the usefulness of the current method to quantify CPT-11 and its metabolites in the different matrices.
伊立替康(CPT-11)是一种抗肿瘤药物,因其拓扑异构酶I抑制活性而用于治疗结直肠癌和胰腺癌。CPT-11是一种前体药物,可被羧酸酯酶转化为其活性代谢产物SN-38。SN-38进一步代谢为其无活性代谢产物SN-38葡糖醛酸苷。在评估CPT-11及其代谢产物的药代动力学特性时,准确评估血浆和肿瘤组织中的浓度非常重要。因此,本研究的目的是开发并验证一种稳健且灵敏的超高效液相色谱-串联质谱法,用于定量测定人血浆和腹膜肿瘤组织中CPT-11及其代谢产物(SN-38和SN-38葡糖醛酸苷)的浓度。血浆和肿瘤组织的样品制备分别包括蛋白沉淀和酶消化/液液萃取。使用Acquity UPLC BEH C18色谱柱结合VanGuard预柱进行色谱分离。流动相由水+0.1%甲酸(流动相A)和乙腈+0.1%甲酸(流动相B)组成。使用Xevo TQS串联质谱仪在正电喷雾电离模式下进行质谱分析。根据以下指南“人用药品委员会,生物分析方法验证指南”,通过评估线性、精密度和准确度、定量下限、残留、选择性、基质效应和稳定性,成功进行了方法验证。在一项初步药代动力学研究中对所开发的方法进行了交叉验证,证明了该方法在定量不同基质中CPT-11及其代谢产物方面的实用性。