Transformations in pharmaceutical research and development, driven by innovations in multidimensional mass spectrometry-based technologies

被引:40
作者
Hoke, SH
Morand, KL
Greis, KD
Baker, TR
Harbol, KL
Dobson, RLM
机构
[1] Procter & Gamble Co, Hlth Care Res Ctr, Mason, OH 45040 USA
[2] Procter & Gamble Pharmaceut, Hlth Care Res Ctr, Mason, OH 45040 USA
[3] Procter & Gamble Pharmaceut, Woods Corners Res Facil, Norwich, NY 13815 USA
关键词
mixture analysis; mass spectrometry; liquid chromatography; gas chromatography; pharmaceuticals;
D O I
10.1016/S1387-3806(01)00499-7
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
In the pharmaceutical industry, there is a tremendous need for qualitative and quantitative analysis of target analytes such as peptides, proteins, drugs, metabolites, biomarkers, impurities, and degradation products in various mixtures including synthetic reactions, in vitro cultures, biological fluids, drug substances, finished products. and many others. To provide adequate specificity for analysis in these complex mixtures, multidimensional analytical techniques are required. Mass spectrometry plays a central role in many of these multidimensional approaches to mixture analysis because it provides an unparalleled combination of sensitivity and specificity that is useful for both molecular identification and quantitative applications. Recent innovations in mass spectrometry and industrial implementation of these advances have transformed many aspects of pharmaceutical research and development. Data that were previously unattainable, or were not collected due to exorbitant cost or time constraints, can now be obtained using mass spectrometry-based technologies. The impact of these innovations has been most dramatically felt in early stages of discovery, as more data are available to make critical decisions. such as selecting compounds for advancement to costly preclinical and clinical trials. New MS technologies have also accelerated the progression of drug candidates through development and toward regulatory approval. Here, five major categories of pharmaceutical applications of mass spectrometry are reviewed. They are new chemical entity characterization, biomacromolecule characterization, bioanalytical quantitation, metabolite identification, and impurity and degradation product identification. A brief historical perspective and evolution of technologies for each application area are presented. Those discussions are followed with a description of the current strategies for implementation of the tremendous capabilities of the state-of-the-art approaches, along with representative applications. In addition, emerging technologies for each application area are presented to indicate the future directions of instrumentation for mixture analysis in the pharmaceutical industry. (C) 2001 Elsevier Science B.V.
引用
收藏
页码:135 / 196
页数:62
相关论文
共 361 条
[41]   PROTEIN LADDER SEQUENCING [J].
CHAIT, BT ;
WANG, R ;
BEAVIS, RC ;
KENT, SBH .
SCIENCE, 1993, 262 (5130) :89-92
[42]   Microfabricated polymer devices for automated sample delivery of peptides for analysis by electrospray ionization tandem mass spectrometry [J].
Chan, JH ;
Timperman, AT ;
Qin, D ;
Aebersold, R .
ANALYTICAL CHEMISTRY, 1999, 71 (20) :4437-4444
[43]   Direct profiling of proteins in biological tissue sections by MALDI mass spectrometry [J].
Chaurand, P ;
Stoeckli, M ;
Caprioli, RM .
ANALYTICAL CHEMISTRY, 1999, 71 (23) :5263-5270
[44]   Peptide and protein identification by matrix-assisted laser desorption ionization (MALDI) and MALDI-post-source decay time-of-flight mass spectrometry [J].
Chaurand, P ;
Luetzenkirchen, F ;
Spengler, B .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1999, 10 (02) :91-103
[45]   The solid-phase combinatorial synthesis of beta-thioketones [J].
Chen, CX ;
Randall, LAA ;
Miller, RB ;
Jones, AD ;
Kurth, MJ .
TETRAHEDRON, 1997, 53 (19) :6595-6609
[46]   Unfolding and disassembly of the chaperonin GroEL occurs via a tetradecameric intermediate with a folded equatorial domain [J].
Chen, JW ;
Smith, DL .
BIOCHEMISTRY, 2000, 39 (15) :4250-4258
[47]   Analysis of coptisine, berberine and palmatine in adulterated Chinese medicine by capillary electrophoresis-electrospray ion trap mass spectrometry [J].
Chen, YR ;
Wen, KC ;
Her, GR .
JOURNAL OF CHROMATOGRAPHY A, 2000, 866 (02) :273-280
[48]  
Cheng YF, 2001, RAPID COMMUN MASS SP, V15, P141, DOI 10.1002/1097-0231(20010130)15:2<141::AID-RCM201>3.0.CO
[49]  
2-I
[50]   Role of accurate mass measurement (±10 ppm) in protein identification strategies employing MS or MS MS and database searching [J].
Clauser, KR ;
Baker, P ;
Burlingame, AL .
ANALYTICAL CHEMISTRY, 1999, 71 (14) :2871-2882