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基于 LC-MS/MS 的灌胃给予高良姜胶囊后犬血浆中天麻素、对羟基苯甲醇、对羟基苯甲醇 B、C、E 的优化及灵敏药代动力学定量方法研究

An Optimized and Sensitive Pharmacokinetic Quantitative Method of Investigating Gastrodin, Parishin, and Parishin B, C and E in Beagle Dog Plasma using LC-MS/MS after Intragastric Administration of Tall Gastrodia Capsules.

机构信息

Key laboratory of Beijing for identification and safety evaluation of Chinese medicine, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, No. 16, Nanxiaojie, Dongzhimennei, Beijing 100700, China.

出版信息

Molecules. 2017 Nov 10;22(11):1938. doi: 10.3390/molecules22111938.

Abstract

Blume, called Tianma in China, has been widely used to treat headaches, convulsions and epilepsy for thousands of years. In the present study, a series of optimizations were employed to develop a rapid, sensitive, and reliable high-performance liquid chromatography-triple quadrupole mass spectrometry method, which was then used for the simultaneous determination of gastrodin, parishin, parishin B, parishin C and parishin E in beagle dog plasma after intragastric administration of tall capsules (Tianma brand). The chromatographic separation was achieved on a C column with gradient elution by using a mixture of 0.4% formic acid aqueous solution and acetonitrile as the mobile phase at a flow rate of 0.15 mL/min. A tandem mass spectrometric detection was conducted using multiple-reaction monitoring (MRM) via electrospray ionization (ESI) source in negative ionization mode. Samples were pre-treated by a single-step protein precipitation with methanol, and bergenin was used as internal standard (IS). Under the optimized conditions, the lower limit of quantification (LLOQ) was 0.10 ng/mL for gastrodin, 0.40 ng/mL for parishin B, 0.02 ng/mL for parishin E and 0.20 ng/mL for parishin and parishin C, all of which previously were the highest levels of sensitivity. The methods were optimized for selectivity, calibration curves, accuracy and precision. Extraction recoveries, matrix effects and stability were within acceptable ranges. Pharmacokinetic parameters of the tested substances were also quantitatively determined. Finally, a possible metabolic pathway was induced based on correlations obtained from quantitative and qualitative data analysis in vivo.

摘要

天麻在中国被称为“天马”,几千年来一直被广泛用于治疗头痛、抽搐和癫痫。在本研究中,采用了一系列优化方法,开发了一种快速、灵敏、可靠的高效液相色谱-三重四极杆质谱联用方法,用于同时测定灌胃给予天麻胶囊(天马牌)后比格犬血浆中天麻素、对羟基苯甲醇、对羟基苯甲醇 B、对羟基苯甲醇 C 和对羟基苯甲醇 E 的含量。采用 C 柱,以 0.4%甲酸水溶液和乙腈为流动相,梯度洗脱,流速为 0.15 mL/min,实现了色谱分离。采用电喷雾电离(ESI)源,在负离子模式下,采用多反应监测(MRM)进行串联质谱检测。样品采用甲醇一步蛋白沉淀法预处理,以没食子酸为内标(IS)。在优化条件下,天麻素、对羟基苯甲醇 B、对羟基苯甲醇 E 和对羟基苯甲醇 C 的定量下限(LLOQ)分别为 0.10、0.40、0.02 和 0.20ng/mL,均为先前的最高灵敏度水平。对选择性、校准曲线、准确度和精密度进行了方法优化。提取回收率、基质效应和稳定性均在可接受范围内。还定量测定了受试物质的药代动力学参数。最后,根据体内定量和定性数据分析得出的相关性,推断出可能的代谢途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ab7/6150220/b8388b184c74/molecules-22-01938-g001.jpg

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