Author:
Yin Wencui,Al-Wabli Reem I.,Attwa Mohamed W.,Rahman A. F. M. Motiur,Kadi Adnan A.
Abstract
AbstractSimvastatin (SV) is a hypolipidemic agent, and it is the 2nd most widely prescribed lipid-lowering drug. Here, the detection and characterization of SV and its metabolites was studied in selected organs/tissues (lung, liver, brain, heart and kidney) and biological samples (blood, urine and feces) of rats. MALDI Orbitrap MS was used as a high-resolution mass analyzer. 2,5-Dihydroxybenzoic acid (DHB) and 1,5-diaminonaphthalene (DAN) were used as matrices. Several sample loading methods onto the MALDI plate were attempted and dried droplet method was found to be superior. Two different cell disruption methods, pulverization and homogenization, were also evaluated for the optimum sensitivity in MALDI. Pulverization allowed the detection of more metabolites in all organs except the liver, where homogenization led to the detection of more metabolites. Altogether, 13 metabolites were detected, and one metabolite tentatively identified as a reduced product is being reported for the first time. SV and its metabolites were distributed to all the tissues studied except the brain. Overall, the results implied that the pulverized samples were more uniform and larger in surface area, resulting in their more efficient and complete extraction during sample preparation. As shown in the present study, MALDI Orbitrap MS is a useful tool to study drug and metabolite detection and characterization.
Funder
Deanship of Scientific Research at the King Saud University
Publisher
Springer Science and Business Media LLC
Reference38 articles.
1. Paul, A. Drug distribution. in Introduction to Basics of Pharmacology and Toxicology: Volume 1: General and Molecular Pharmacology: Principles of Drug Action (eds Raj, G. M. & Raveendran, R.) 89–98 (Springer, Singapore, 2019).
2. Marko-Varga, G. et al. Drug localization in different lung cancer phenotypes by MALDI mass spectrometry imaging. J. Proteomics 74, 982–992 (2011).
3. Gillette, J. R. The importance of tissue distribution in pharmacokinetics. J. Pharmacokinet. Biopharm. 1, 497–520. https://doi.org/10.1007/BF01059788 (1973).
4. Lanao, J. M. & Fraile, M. A. Drug tissue distribution: Study methods and therapeutic implications. Curr. Pharm. Des. 11, 3829–3845. https://doi.org/10.2174/138161205774580679 (2005).
5. Baca, Q. J. & Golan. D. E. Pharmaconinetics. in Principles of Pharmacology: The pathophysiologic basis of drug therapy, 4th edn (eds Golan. D. E. et al.) 27–42 (Wolters Kluwer, 2017).
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献