Quantitative analysis of polypeptide pharmaceuticals by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

被引:9
作者
Amini, Ahmad [1 ,2 ]
Nilsson, Elin [3 ]
机构
[1] MPA, SE-75103 Uppsala, Sweden
[2] Uppsala Univ, Biomed Ctr, Div Analyt Pharmaceut Chem, SE-75103 Uppsala, Sweden
[3] Uppsala Univ, Dept Med Sci Clin Chem, SE-75185 Uppsala, Sweden
关键词
calcitonin; human insulin; MALDI-TOF-MS; quantification; injection solution and suspension;
D O I
10.1016/j.jpba.2007.10.028
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An accurate method based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) has been developed for quantitative analysis of calcitonin and insulin in different commercially available pharmaceutical products. Tryptic peptides derived from these polypeptides were chemically modified at their C-terminal lysine-residues with 2-methoxy-4,5-dihydro-imidazole (light tagging) as standard and deuterated 2-methoxy-4,5-dihydro-imidazole (heavy tagging) as internal standard (IS). The heavy modified tryptic peptides (4D-Lys tag), differed by four atomic mass units from the corresponding light labelled counterparts (4H-Lys tag). The normalized peak areas (the ratio between the light and heavy tagged peptides) were used to construct a standard curve to determine the concentration of the analytes. The concentrations of calcitonin and insulin content of the analyzed pharmaceutical products were accurately determined, and less than 5% error was obtained between the present method and the manufacturer specified values. It was also found that the cysteine residues in CSNLSTCVLGK from tryptic calcitonin were converted to lanthionine by the loss of one sulfhydryl group during the labelling procedure. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:411 / 417
页数:7
相关论文
共 33 条
[1]   Analysis of calcitonin and its analogues by capillary zone electrophoresis and matrix-assisted laser-desorption ionization time-of-flight mass spectrometry [J].
Amini, A ;
Olofsson, IM .
JOURNAL OF SEPARATION SCIENCE, 2004, 27 (09) :675-685
[2]  
BOHAK Z, 1964, J BIOL CHEM, V239, P2878
[3]   CHEMICAL-STABILITY OF INSULIN .1. HYDROLYTIC DEGRADATION DURING STORAGE OF PHARMACEUTICAL PREPARATIONS [J].
BRANGE, J ;
LANGKJAER, L ;
HAVELUND, S ;
VOLUND, A .
PHARMACEUTICAL RESEARCH, 1992, 9 (06) :715-726
[4]   INFLUENCE OF CYSTEINE TO CYSTEIC ACID OXIDATION ON THE COLLISION-ACTIVATED DECOMPOSITION OF PROTONATED PEPTIDES - EVIDENCE FOR INTRAIONIC INTERACTIONS [J].
BURLET, O ;
YANG, CY ;
GASKELL, SJ .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1992, 3 (04) :337-344
[5]   Characterization of the covalent binding of thiostrepton to a thiostrepton-induced protein from Streptomyces lividans [J].
Chiu, ML ;
Folcher, M ;
Griffin, P ;
Holt, T ;
Klatt, T ;
Thompson, CJ .
BIOCHEMISTRY, 1996, 35 (07) :2332-2341
[6]   Accelerated on-column lysine derivatization and cysteine methylation by imidazole reaction in a deuterated environment for enhanced product ion analysis [J].
Cindric, M ;
Cepo, T ;
Skrlin, A ;
Vuletic, M ;
Bindila, L .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2006, 20 (04) :694-702
[7]   Mass spectrometry-based glycoproteomic approach involving lysine derivatization for structural characterization of recombinant human erythropoietin [J].
Cindric, Mario ;
Bindila, Laura ;
Cepo, Tina ;
Peter-Katalinic, Jasna .
JOURNAL OF PROTEOME RESEARCH, 2006, 5 (11) :3066-3076
[8]   Influence of matrix solution conditions on the MALDI-MS analysis of peptides and proteins [J].
Cohen, SL ;
Chait, BT .
ANALYTICAL CHEMISTRY, 1996, 68 (01) :31-37
[9]   FORMATION OF LYSINOALANINE DURING TREATMENT OF WOOL WITH ALKALI [J].
CORFIELD, MC ;
WOOD, C ;
ROBSON, A ;
WILLIAMS, MJ ;
WOODHOUSE, JM .
BIOCHEMICAL JOURNAL, 1967, 103 (02) :C15-+
[10]   Cyclization of N-terminal S-carbamoylmethylcysteine causing loss of 17 Da from peptides and extra peaks in peptide maps [J].
Geoghegan, KF ;
Hoth, LR ;
Tan, DH ;
Borzillerl, KA ;
Withka, JM ;
Boyd, JG .
JOURNAL OF PROTEOME RESEARCH, 2002, 1 (02) :181-187