From production of peptides in milligram amounts for research to multi-tons quantities for drugs of the future

被引:156
作者
Bruckdorfer, T
Marder, O
Albericio, F
机构
[1] IRIS Biotech GmbH, D-95615 Marktredwitz, Germany
[2] Luxembourg Ind Pamol Ltd, IL-61000 Tel Aviv, Israel
[3] Univ Barcelona, Barcelone Biomed Res Inst, E-08028 Barcelona, Spain
关键词
synthetic peptides; T-20; fuzeon; bulk production; HCTU; solid-phase; coupling reagents;
D O I
10.2174/1389201043489620
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peptides are key to modern drug discovery. This article reviews the requirements for bulk production of peptides and how it affects research and production of smaller scales. Peptides, as modern drugs, are currently produced in millions in mg-scale for research purpose, in order to better understand the function of biological systems. Some newly discovered sequences form the basis of modern drugs and are now produced in multi-tons. The most popular example is the T-20 peptide (Fuzeon), which is the first peptide produced at such scale by a combination of solid phase and solution phase methodologies. This particular peptide sequence has the ability to dock on the surface of the HIV virus and block the virus from entering into a human blood cell, helping patient life conditions. A multi-ton scale production was made necessary based on the high number of patients, the socio-economical importance of the disease and the strong support by governmental institutions such as the FDA. Fuzeon is the first peptide-based drug that is produced in multi-tons on solid support. This had revolutionary effects on the whole peptide synthesis techniques in general including the production of the starting materials. It also had a positive impact on the cost-effectiveness of peptides for research, as the standard technique for producing peptides in research quantities is solid phase chemistry. The decrease of the cost of all starting materials will lead to an increase of the number of produced peptides, which will certainly bring new interesting and effective sequences to be used as novel drugs.
引用
收藏
页码:29 / 43
页数:15
相关论文
共 35 条
[21]   Peptides as drugs: Is there a market? [J].
Loffet, A .
JOURNAL OF PEPTIDE SCIENCE, 2002, 8 (01) :1-7
[22]  
Madder A, 1999, EUR J ORG CHEM, V1999, P2787
[23]  
MADER C, 1998, 25 EUR PEPT S BUD
[24]  
MADER C, 2002, EUR PEPT S MONTP
[25]  
Marder O, 2002, CHIM OGGI, V20, P37
[26]   The aspartimide problem in Fmoc-based SPPS. Part I [J].
Mergler, M ;
Dick, F ;
Sax, B ;
Weiler, P ;
Vorherr, T .
JOURNAL OF PEPTIDE SCIENCE, 2003, 9 (01) :36-46
[27]   The aspartimide problem in Fmoc-based SPPS.: Part II [J].
Mergler, M ;
Dick, F ;
Sax, B ;
Stähelin, C ;
Vorherr, T .
JOURNAL OF PEPTIDE SCIENCE, 2003, 9 (08) :518-526
[28]   SOLID PHASE PEPTIDE SYNTHESIS .1. SYNTHESIS OF A TETRAPEPTIDE [J].
MERRIFIELD, RB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (14) :2149-&
[29]  
MUTT V, 1992, PEPTIDES
[30]  
RYDER M, 2002, MANUFACTURING CH MAR, P42