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19种吩噻嗪类药物的正负离子质谱分析及快速净化

Positive- and negative-ion mass spectrometry and rapid clean-up of 19 phenothiazines.

作者信息

Ishikawa Y, Suzuki O, Hattori H

机构信息

Department of Pharmacy, Hamamatsu University School of Medicine, Japan.

出版信息

Forensic Sci Int. 1990 Feb;44(2-3):93-105. doi: 10.1016/0379-0738(90)90239-u.

Abstract

Positive-ion electron impact (PIEI), positive-ion chemical ionization (PICI) and negative-ion chemical ionization (NICI) mass spectra of 19 phenothiazines are presented. In the PIEI mode, peaks due to M, M minus side chain (M - R1), M - R1 + H, and side chain itself (R1) appeared for most compounds. The M - R1 and R1 ions were very useful for drug screening. In the PICI mode, most spectra showed base or intense peaks due to M + H, and small peaks due to M + C2H5; peaks due to M - R1 + 2H and R1 also appeared in many compounds. In the NICI mode, fragmentation modes were different in different compound groups; molecular or [M - H]- quasi-molecular anions appeared in many compounds with aliphatic side chains. Anions at m/z 98 and 115 were characteristic for compounds with (N-methylpiperazinyl)propyl side chains. Selected ion monitoring in the PIEI mode generally gave much higher sensitivity than in the PICI and NICI modes. Phenothiazines present in urine or plasma could be rapidly isolated by use of Sep-Pak C18 cartridges. Thirteen of 19 phenothiazines could be detected by HP-17 wide-bore capillary gas chromatography with satisfactory separation from impurities in their underivatized forms.

摘要

本文给出了19种吩噻嗪类药物的正离子电子轰击(PIEI)、正离子化学电离(PICI)和负离子化学电离(NICI)质谱。在PIEI模式下,大多数化合物出现了归因于M、M减去侧链(M - R1)、M - R1 + H以及侧链本身(R1)的峰。M - R1和R1离子对药物筛选非常有用。在PICI模式下,大多数质谱显示出归因于M + H的基峰或强峰,以及归因于M + C2H5的小峰;许多化合物中还出现了归因于M - R1 + 2H和R1的峰。在NICI模式下,不同化合物组的裂解模式不同;许多带有脂肪族侧链的化合物中出现了分子或[M - H]-准分子阴离子。对于带有(N - 甲基哌嗪基)丙基侧链的化合物,m/z 98和115处的阴离子具有特征性。PIEI模式下的选择离子监测通常比PICI和NICI模式具有更高的灵敏度。尿液或血浆中存在的吩噻嗪类药物可通过使用Sep - Pak C18柱快速分离。19种吩噻嗪类药物中的13种可通过HP - 17大口径毛细管气相色谱法检测,其未衍生化形式与杂质能得到令人满意的分离。

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