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一种使用固相萃取法通过液相色谱-串联质谱法测定大鼠体内WKYMVm肽的方法的定量与应用。

Quantification and application of a liquid chromatography-tandem mass spectrometric method for the determination of WKYMVm peptide in rat using solid-phase extraction.

作者信息

Lee Byeong Ill, Park Min-Ho, Heo Soon Chul, Park Yuri, Shin Seok-Ho, Byeon Jin-Ju, Kim Jae Ho, Shin Young G

机构信息

College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.

College of Medicine, Pusan National University, Republic of Korea.

出版信息

Biomed Chromatogr. 2018 Mar;32(3). doi: 10.1002/bmc.4107. Epub 2017 Nov 3.

Abstract

A liquid chromatographic-electrospray ionization-time-of-flight/mass spectrometric (LC-ESI-TOF/MS) method was developed and applied for the determination of WKYMVm peptide in rat plasma to support preclinical pharmacokinetics studies. The method consisted of micro-elution solid-phase extraction (SPE) for sample preparation and LC-ESI-TOF/MS in the positive ion mode for analysis. Phenanthroline (10 mg/mL) was added to rat blood immediately for plasma preparation followed by addition of trace amount of 2 m hydrogen chloride to plasma before SPE for stability of WKYMVm peptide. Then sample preparation using micro-elution SPE was performed with verapamil as an internal standard. A quadratic regression (weighted 1/concentration ), with the equation y = ax  + bx + c was used to fit calibration curves over the concentration range of 3.02-2200 ng/mL for WKYMVm peptide. The quantification run met the acceptance criteria of ±25% accuracy and precision values. For quality control samples at 15, 165 and 1820 ng/mL from the quantification experiment, the within-run and the between-run accuracy ranged from 92.5 to 123.4% with precision values ≤15.1% for WKYMVm peptide from the nominal values. This novel LC-ESI-TOF/MS method was successfully applied to evaluate the pharmacokinetics of WKYMVm peptide in rat plasma.

摘要

开发了一种液相色谱-电喷雾电离-飞行时间/质谱(LC-ESI-TOF/MS)方法,并将其应用于大鼠血浆中WKYMVm肽的测定,以支持临床前药代动力学研究。该方法包括用于样品制备的微洗脱固相萃取(SPE)和用于分析的正离子模式下的LC-ESI-TOF/MS。立即向大鼠血液中加入菲咯啉(10 mg/mL)以制备血浆,然后在SPE之前向血浆中加入痕量的2 m盐酸以保持WKYMVm肽的稳定性。然后以维拉帕米为内标,使用微洗脱SPE进行样品制备。使用二次回归(加权1/浓度),方程y = ax + bx + c,在3.02-2200 ng/mL的浓度范围内拟合WKYMVm肽的校准曲线。定量运行符合±25%准确度和精密度值的验收标准。对于定量实验中浓度为15、165和1820 ng/mL的质量控制样品,WKYMVm肽的批内和批间准确度在92.5%至123.4%之间,精密度值≤15.1%(相对于标称值)。这种新型的LC-ESI-TOF/MS方法成功应用于评估WKYMVm肽在大鼠血浆中的药代动力学。

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