Analysis of low molecular weight compounds using MALDI- and LDI-TOF-MS: Direct detection of active pharmaceutical ingredients in different formulations

被引:13
作者
Bronzel, Joao L., Jr. [1 ]
Milagre, Cintia D. F. [1 ]
Milagre, Humberto M. S. [1 ]
机构
[1] Sao Paulo State Univ UNESP, Inst Chem, Sao Paulo, Brazil
来源
JOURNAL OF MASS SPECTROMETRY | 2017年 / 52卷 / 11期
基金
巴西圣保罗研究基金会;
关键词
forensic intelligence; ionic matrices; laser desorption ionization; pharmaceutical counterfeiting; tertiary amine dehydrogenation; MASS-SPECTROMETRY; COUNTERFEIT DRUGS; DEHYDROGENATION; MATRICES; AMINES;
D O I
10.1002/jms.3984
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is a high throughput, easy to use analytical technique. The simple sample preparation of this technique and its tolerance to the presence of contaminants are among its advantages. In contrast, depending on the matrix used, MALDI can ionize and generates ions in the low m/z range that complicate the interpretation of the spectra of low molecular weight compounds. To address this issue, one can envisage the use of tunable ionic matrices that can reduce the low m/z interferents. In this work, the ionic matrices triethylammonium -cyano-4-hydroxycinnamate and diisopropylammonium -cyano-4-hydroxycinnamate were used to directly analyze 14 pharmaceutical drugs in different formulations (coated tablets, noncoated tablets, capsules, and solutions). This methodology enabled the detection of their active compounds with minimum sample preparation, thus providing a straightforward approach for the forensic analysis of pharmaceutical drugs in the quest for detecting counterfeits. LDI-MS experiments were also performed, and the active ingredient in all of the medicines analyzed were detected. However, MALDI-MS spectra for the medicines analyzed herein showed less or no fragmentation than LDI-MS, which makes the analysis easier.
引用
收藏
页码:752 / 758
页数:7
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