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Ultra-Performance Liquid Chromatography Mass Spectrometry and Sensitive Bioassay Methods for Quantification of Posaconazole Plasma Concentrations after Oral Dosing

机译:口服给药后泊沙康唑血浆浓度的超高效液相色谱质谱和灵敏生物测定方法

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摘要

Posaconazole (POS) is a new antifungal agent for prevention and therapy of mycoses in immunocompromised patients. Variable POS pharmacokinetics after oral dosing may influence efficacy: a trough threshold of 0.5 μg/ml has been recently proposed. Measurement of POS plasma concentrations by complex chromatographic techniques may thus contribute to optimize prevention and management of life-threatening infections. No microbiological analytical method is available. The objective of this study was to develop and validate a new simplified ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method and a sensitive bioassay for quantification of POS over the clinical plasma concentration range. The UPLC-MS/MS equipment consisted of a triple quadrupole mass spectrometer, an electrospray ionization (ESI) source, and a C18 analytical column. The Candida albicans POS-hypersusceptible mutant (MIC of 0.002 μg/ml) Δcdr1 Δcdr2 Δflu Δmdr1 Δcan constructed by targeted deletion of multidrug efflux transporters and calcineurin genes was used for the bioassay. POS was extracted from plasma by protein precipitation with acetonitrile-methanol (75%/25%, vol/vol). Reproducible standard curves were obtained over the range 0.014 to 12 (UPLC-MS/MS) and 0.028 to 12 μg/ml (bioassay). Intra- and interrun accuracy levels were 106% ± 2% and 103% ± 4% for UPLC-MS/MS and 102% ± 8% and 104% ± 1% for bioassay, respectively. The intra- and interrun coefficients of variation were 7% ± 4% and 7% ± 3% for UPLC-MS/MS and 5% ± 3% and 4% ± 2% for bioassay, respectively. An excellent correlation between POS plasma concentrations measured by UPLC-MS/MS and bioassay was found (concordance, 0.96). In 26 hemato-oncological patients receiving oral POS, 27/69 (39%) trough plasma concentrations were lower than 0.5 μg/ml. The UPLC-MS/MS method and sensitive bioassay offer alternative tools for accurate and precise quantification of the plasma concentrations in patients receiving oral posaconazole.
机译:泊沙康唑(POS)是一种新的抗真菌药,用于预防和治疗免疫功能低下患者的真菌病。口服给药后可变的POS药代动力学可能会影响疗效:最近提出了0.5μg/ ml的谷值阈值。因此,通过复杂的色谱技术测量POS血浆浓度可能有助于优化预防和处理威胁生命的感染。没有微生物分析方法。这项研究的目的是开发和验证一种新的简化的超高效液相色谱串联质谱法(UPLC-MS / MS)和一种敏感的生物测定法,用于在临床血浆浓度范围内定量POS。 UPLC-MS / MS设备由三重四极杆质谱仪,电喷雾电离(ESI)源和C18分析柱组成。可通过靶向删除多药外排转运蛋白和钙调神经磷酸酶基因构建白色念珠菌POS超敏突变体(MIC为0.002μg/ ml)Δcdr1Δcdr2ΔfluΔmdr1Δ。通过用乙腈-甲醇(75%/ 25%,体积/体积)进行蛋白沉淀从血浆中提取POS。在0.014至12(UPLC-MS / MS)和0.028至12μg/ ml(生物测定)的范围内获得了可重现的标准曲线。 UPLC-MS / MS的批内和批内准确度分别为106%±2%和103%±4%,生物测定分别为102%±8%和104%±1%。对于UPLC-MS / MS,批内和批内变异系数分别为7%±4%和7%±3%,对于生物测定,变异系数分别为5%±3%和4%±2%。通过UPLC-MS / MS测量的POS血浆浓度与生物测定之间发现极好的相关性(一致性,0.96)。在接受口服POS的26例血液肿瘤患者中,有27/69(39%)的低谷血浆浓度低于0.5μg/ ml。 UPLC-MS / MS方法和灵敏的生物测定法为准确,准确地定量口服泊沙康唑患者的血浆浓度提供了替代工具。

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