大鼠血清中具有孕激素活性的孕激素-孕丁醇及其两种代谢物同时测定方法的建立

Q3 Pharmacology, Toxicology and Pharmaceutics Drug Development and Registration Pub Date : 2021-05-29 DOI:10.33380/2305-2066-2021-10-2-112-118
E. Stepanova, L. Makarenkova, S. Goryainov, T. Fedotcheva, N. Shimanovsky
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引用次数: 0

摘要

介绍。孕丁醇是一种具有孕激素活性的合成孕激素。Gestobutanoil有两种药理活性代谢物(AMOL和醋酸甲地孕酮)。这意味着需要对代谢物的动力学进行详细的研究。将地母丁醇及其代谢物(AMOL和醋酸甲地孕酮)的药动学研究结合起来是合理的。采用色谱-质谱联用技术可同时测定大鼠血清中几种分析物的含量。建立同时测定生物基质(大鼠血清)中地丁油及其两种代谢物的分析方法。材料和方法。采用GC-MS、HPLC-ESI-MS、衍生化HPLC-ESI-MS、HPLC-APCI-MS等方法测定生物基质中孕丁醇及其两种代谢物。结果和讨论。在使用GC-MS时,gestobutyoyl, AMOL和mege孕酮醋酸酯的色谱峰出现了强烈的模糊和重叠,这显然是由于物质的热性所致。采用高效液相色谱法代替气相色谱-质谱法。在C18色谱柱上采用高效液相色谱梯度洗脱分离。ESI电离并没有得到gestobutyoyl和AMOL的典型质子化离子,而且在AMOL和gestobutyoyl的光谱中观察到的它们的阳离子离子和片段离子的强烈信号,由于它们的形成条件不适合常规分析,不能保证光谱的再现性。分析物衍生生成肟和取代腙并没有得到HPLC-ESI-MS预期的反应产物。APCI可以从gestobutyoyl和AMOL的光谱中去除强烈的阳离子离子,提高了方法的可靠性。在模型大鼠血清上重现了HPLCAPCI-MS技术。建立了高效液相色谱-质谱同时测定孕丁醇、醋酸甲地孕酮和AMOL的方法。该技术在含有所有三种分析物的模型大鼠血清上进行了测试。
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Development of Simultaneous Determination Method of a Pregnan Steroid with Gestagenic Activity – Gestobutanoil and Two its Metabolites in Rat Serum
Introduction. Gestobutanoil is a synthetic pregnane steroid with gestagenic activity. Gestobutanoil has two pharmacologically active metabolites (AMOL and megestrol acetate). This implies the need for a detailed study of the kinetics of metabolites. It is rational to combine the study of the pharmacokinetics of gestobutanoil and its metabolites (AMOL and megestrol acetate). The simultaneous determination of several analytes in the rats’ serum can be carried out using chromatography-mass-spectrometry.Aim. Development of an analytical method for the simultaneous determination of gestobutanoil and two its metabolites in a biomatrix (rat serum).Materials and methods. The following methods were used to determine gestobutanoyl and two its metabolites in a biological matrix: GC-MS, HPLCESI-MS, HPLC-ESI-MS with derivatization, HPLC-APCI-MS.Results and discussion. When working with GC-MS, the chromatographic peaks of gestobutanoyl, AMOL, and megestrol acetate were strongly blurred and superimposed on each other, which is apparently due to the thermolability of the substances. The GC-MS method was abandoned in favor of HPLC. Analytes were separated by HPLC gradient elution on a C18 column. ESI ionization did not give typical protonated ions of gestobutanoyl and AMOL, and the intense signals of their cationized ions and fragment ions, which were observed in the spectra of AMOL and gestobutanoyl, could not ensure the reproducibility of the spectra, since the conditions of their formation are not suitable for routine analysis. Derivatization of analytes to form oximes and substituted hydrazones did not give the expected reaction products for HPLC-ESI-MS. APCI made it possible to remove intense cationized ions from the spectra of gestobutanoyl and AMOL and to increase the reliability of the method. The HPLCAPCI-MS technique was reproduced on model rat blood serum.Conclusion. An HPLC-MS method was developed for the simultaneous determination of gestobutanoyl, megestrol acetate, and AMOL. The technique was tested on a model rat blood serum containing all three analytes.
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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