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1.
J Pharm Biomed Anal ; 162: 112-116, 2019 Jan 05.
Artigo em Inglês | MEDLINE | ID: mdl-30236818

RESUMO

New unknown impurity at m/z 421.15 was observed during the accelerated stability analysis (40 °C/75% relative humidity) in the multi-component tablets of amlodipine besylate by reversed-phase ultra-high performance liquid chromatography-mass spectrometry (UHPLC-MS). UHPLC-MS and nuclear magnetic resonance (NMR) techniques were employed to identify and fully characterize the degradation compound. The degradation product was unambiguously identified as 3-ethyl 5-methyl 4-(2-chlorophenyl)-6-methyl-2-(morpholin-2-yl)-1,4-dihydropyridine-3,5-dicarboxylate and mechanism of its formation was proposed. It was confirmed that the degradation product was formed by the reaction of amlodipine with formaldehyde originating from the excipients present in the dosage form.


Assuntos
Anlodipino/química , Contaminação de Medicamentos , Química Farmacêutica/métodos , Cromatografia Líquida de Alta Pressão , Cromatografia de Fase Reversa , Combinação de Medicamentos , Estabilidade de Medicamentos , Excipientes/química , Formaldeído/química , Hidroclorotiazida/química , Espectroscopia de Ressonância Magnética , Estrutura Molecular , Espectrometria de Massas por Ionização por Electrospray , Fatores de Tempo , Valsartana/química
2.
J Lipid Res ; 58(8): 1579-1590, 2017 08.
Artigo em Inglês | MEDLINE | ID: mdl-28576934

RESUMO

Cholesteryl esters of ω-(O-acyl)-hydroxy FAs (Chl-ωOAHFAs) were identified for the first time in vernix caseosa and characterized using chromatography and MS. Chl-ωOAHFAs were isolated using adsorption chromatography on silica gel and magnesium hydroxide. Their general structure was established using high-resolution and tandem MS of intact lipids, and products of their transesterification and derivatizations. Individual molecular species were characterized using nonaqueous reversed-phase HPLC coupled to atmospheric pressure chemical ionization. The analytes were detected as protonated molecules, and their structures were elucidated in the negative ion mode using controlled thermal decomposition and data-dependent fragmentation. About three hundred molecular species of Chl-ωOAHFAs were identified in this way. The most abundant Chl-ωOAHFAs contained 32:1 ω-hydroxy FA (ω-HFA) and 14:0, 15:0, 16:0, 16:1, and 18:1 FAs. The double bond in the 32:1 ω-HFA was in the n-7 and n-9 positions. Chl-ωOAHFAs are estimated to account for approximately 1-2% of vernix caseosa lipids.


Assuntos
Ésteres do Colesterol/metabolismo , Ácidos Graxos/química , Ácidos Graxos/metabolismo , Verniz Caseoso/metabolismo , Humanos , Recém-Nascido
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