Selective and quantitative detection of influenza virus proteins in commercial vaccines using two-dimensional high-performance liquid chromatography and fluorescence detection

被引:58
作者
Garcia-Canas, Virginia [1 ]
Lorbetskie, Barry [1 ]
Bertrand, Diane [1 ]
Cyr, Terry D. [1 ]
Girard, Michel [1 ]
机构
[1] Hlth Canada, Biol Res Ctr, Ottawa, ON K1A 0L2, Canada
关键词
D O I
10.1021/ac0621120
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, we report on the applicability of two-dimensional high-performance liquid chromatography (2D-HPLC) for the comprehensive characterization of inactivated influenza vaccine proteins. This novel procedure features minimal sample treatment and combines the on-line coupling of size exclusion HPLC to reversed-phase HPLC. A comparative analysis of commercial vaccines from three different manufacturers showed the method to be highly selective by providing characteristic reproducible chromatographic profiles for each vaccine. In addition, the method provided enhanced sensitivity for most constituents as a result of the use of native fluorescence detection in the reversed-phase HPLC step. The limits of detection (at a signal-to-noise ratio of > 3) for hemagglutinin (HA) antigens were 105 and 172 ng/mL for influenza A/New Caledonia/20/99 and B/Jiangsu/10/2003 strains, respectively. The potential of this 2D-HPLC procedure in terms of quantitative antigen analysis was assessed by determination of the HA content of commercial vaccines. Results provided very good correlation with nominal HA values. The reproducibility (RSD) of the whole procedure was also evaluated and was found to be better than 2 and 3% for calculated antigen concentrations expressed as micrograms of HA per milliliter in commercial vaccines for samples of the same lot (n = 5) or different lots (n = 3), respectively. In addition, it allowed the selective detection of several influenza constituents including nucleoproteins from type A and B viruses and the highly hydrophobic matrix protein 1 from both virus strains.
引用
收藏
页码:3164 / 3172
页数:9
相关论文
共 24 条
[1]   Combined results from solution studies on intact influenza virus M1 protein and from a new crystal form of its N-terminal domain show that M1 is an elongated monomer [J].
Arzt, S ;
Baudin, F ;
Barge, A ;
Timmins, P ;
Burmeister, WP ;
Ruigrok, RWH .
VIROLOGY, 2001, 279 (02) :439-446
[2]   ISOLATION OF INFLUENZA VIRAL-PROTEINS BY SIZE-EXCLUSION AND ION-EXCHANGE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY - THE INFLUENCE OF CONDITIONS ON SEPARATION [J].
CALAM, DH ;
DAVIDSON, J .
JOURNAL OF CHROMATOGRAPHY, 1984, 296 (JUL) :285-292
[3]  
Dellepiane N, 2000, B WORLD HEALTH ORGAN, V78, P155
[4]   Rapid and selective characterization of influenza virus constituents in monovalent and multivalent preparations using non-porous reversed-phase high performance liquid chromatography columns [J].
Garcia-Canas, Virginia ;
Lorbetskie, Barry ;
Girard, Michel .
JOURNAL OF CHROMATOGRAPHY A, 2006, 1123 (02) :225-232
[5]   CONCEPTS AND COMPARISONS IN MULTIDIMENSIONAL SEPARATION [J].
GIDDINGS, JC .
JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY & CHROMATOGRAPHY COMMUNICATIONS, 1987, 10 (05) :319-323
[6]  
GIRARD M, UNPUB J CHROMATOGR A
[7]   Transformations in pharmaceutical research and development, driven by innovations in multidimensional mass spectrometry-based technologies [J].
Hoke, SH ;
Morand, KL ;
Greis, KD ;
Baker, TR ;
Harbol, KL ;
Dobson, RLM .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2001, 212 (1-3) :135-196
[8]   Influenza: Lessons from past pandemics, warnings from current incidents [J].
Horimoto, T ;
Kawaoka, Y .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (08) :591-600
[9]   Haemagglutinin quantification and identification of influenza A&B strains propagated in PER.C6® cells:: A novel RP-HPLC method [J].
Kapteyn, JC ;
Saidi, MD ;
Dijkstra, R ;
Kars, C ;
Tjon, JCMSK ;
Weverling, GJ ;
de Vocht, ML ;
Kompier, R ;
van Montfort, BA ;
Guichoux, JY ;
Goudsmit, J ;
Lagerwerf, FM .
VACCINE, 2006, 24 (16) :3137-3144
[10]   Antigenic surveillance of the influenza virus by mass spectrometry [J].
Kiselar, JG ;
Downard, KM .
BIOCHEMISTRY, 1999, 38 (43) :14185-14191