首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >A rapid HPLC-ESI-MS/MS method for determination of β-asarone, a potential anti-epileptic agent, in plasma after oral administration of Acorus calamus extract to rats
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A rapid HPLC-ESI-MS/MS method for determination of β-asarone, a potential anti-epileptic agent, in plasma after oral administration of Acorus calamus extract to rats

机译:快速口服HPLC-ESI-MS / MS法测定大鼠腹腔注射A蒲提取物后血浆中的潜在抗癫痫药β-细辛

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摘要

β-Asarone (BAS), a phenylpropanoid from Acorus calamus Linn., has shown biological effects in the management of cognitive impairment conditions such as Alzheimer's disease. The present paper describes a selective and sensitive liquid chromatography-tandem mass spectrometric method (HPLC-MS/MS) using electrospray ionization source (ESI) for quantification of BAS in rat plasma. Briefly, the plasma samples were pre-treated using a simple solid-phase extraction method. The separation of BAS and the internal standard, caffeine, was achieved on an Agilent Zorbax XDB C18 column (50×2.1 mm i.d., 5 μm) using 0.2 mL/min isocratic mobile phase flow. The detection was performed using an Applied Biosystems Hybrid Q-Trap API 2000 mass spectrometer equipped with an ESI source operated in positive mode. Also, the developed bioanalytical method was validated as per the US FDA bioanalytical guidelines over the concentration range of 9.79-4892.50 ng/mL (r2≥0.9951) for BAS from rat plasma. The mean percentage recovery (n=3) for the low, middle and high quality control samples was 86.92±3.89, 85.30±1.09 and 87.24±4.03%, respectively. The applicability of the validated HPLC-MS/MS method was demonstrated by successful measurement of BAS from plasma following oral administration of Acorus calamus rhizome extracts to three female albino Wistar rats.
机译:β-Asarone(BAS)是来自Acorus calamus Linn。的一种苯丙烷类化合物,在认知障碍性疾病(例如阿尔茨海默氏病)的治疗中已显示出生物学作用。本文介绍了一种选择性和灵敏的液相色谱-串联质谱法(HPLC-MS / MS),使用电喷雾电离源(ESI)定量测定大鼠血浆中的BAS。简而言之,使用简单的固相萃取方法对血浆样品进行预处理。 BAS和内标咖啡因的分离是在Agilent Zorbax XDB C18色谱柱(50×2.1 mm i.d.,5μm)上进行的,流速为0.2 mL / min。使用配备有以正模式运行的ESI源的Applied Biosystems Hybrid Q-Trap API 2000质谱仪进行检测。此外,根据美国FDA的生物分析指南,已开发的生物分析方法在大鼠血浆BAS的浓度范围为9.79-4892.50 ng / mL(r2≥0.9951)时得到了验证。低,中和高质量对照样品的平均回收率(n = 3)分别为86.92±3.89、85.30±1.09和87.24±4.03%。通过对三只雌性白化病Wistar大鼠口服给予cor蒲根茎提取物,成功地测定了血浆中的BAS,证明了已验证的HPLC-MS / MS方法的适用性。

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