Protein crystals for the delivery of biopharmaceuticals

被引:26
作者
Basu, SK [1 ]
Govardhan, CP [1 ]
Jung, CW [1 ]
Margolin, AL [1 ]
机构
[1] Altus Biol Inc, Cambridge, MA 02139 USA
关键词
biopharmaceuticals; controlled release; drug delivery; high dose protein delivery; parenteral products; protein crystals; stability;
D O I
10.1517/14712598.4.3.301
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The year 2002 marked the 20th anniversary of the first successful product of modern biotechnology, the regulatory approval of recombinant insulin for biopharmaceutical applications. Insulin is also the first crystalline protein to be approved for therapeutic use. Over the past two decades, almost 150 biopharmaceuticals have gained marketing authorisation; however, insulin remains the only crystalline protein on the market. Significant research and development efforts have focused on the engineering of protein molecules, efficacy testing, model development, and protein production and characterisation. These advances have dramatically boosted the therapeutic applications of proteins, which now include treatments against acute conditions, such as cancer, cardiovascular disease and viral disease, and chronic conditions, such as diabetes, growth hormone deficiency, haemophilia, arthritis, psoriasis and Crohn's disease. Despite these successes, many challenges normally associated with biopharmaceuticals, such as poor stability and limited delivery options, remain. Protein crystals have shown significant benefits in the delivery of biopharmaceuticals to achieve high concentration, low viscosity formulation and controlled release protein delivery. This review will discuss challenges related to the broader utilisation of protein crystals in biopharmaceutical applications, as well as recent advances and valuable new directions that protein crystallisation-based technologies present.
引用
收藏
页码:301 / 317
页数:17
相关论文
共 100 条
[1]  
ALTUS BIOL INC, 2003, Patent No. 6541606
[2]  
ALTUS BIOL INC, 1999, Patent No. 9955310
[3]  
ALTUS BIOL INC, 2002, Patent No. 02072636
[4]   QUANTITATIVE STUDIES OF THE STRUCTURE OF PROTEINS IN SOLUTION BY FOURIER-TRANSFORM INFRARED-SPECTROSCOPY [J].
ARRONDO, JLR ;
MUGA, A ;
CASTRESANA, J ;
GONI, FM .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1993, 59 (01) :23-56
[5]   EFFECT OF INTRAVENOUS ADMINISTRATION OF CRYSTALLINE PANCREATIC DESOXYRIBONUCLEASE IN PATIENTS WITH GOUT [J].
AYVAZIAN, JH ;
AYVAZIAN, LF .
NEW ENGLAND JOURNAL OF MEDICINE, 1960, 263 (20) :999-1002
[6]   How to determine diffusion coefficients in planar phospholipid systems by confocal fluorescence correlation spectroscopy [J].
Benda, A ;
Benes, M ;
Marecek, V ;
Lhotsky, A ;
Hermens, WT ;
Hof, M .
LANGMUIR, 2003, 19 (10) :4120-4126
[7]   Hybrid insulin cocrystals for controlled release delivery [J].
Brader, ML ;
Sukumar, M ;
Pekar, AH ;
McClellan, DS ;
Chance, RE ;
Flora, DB ;
Cox, AL ;
Irwin, L ;
Myers, SR .
NATURE BIOTECHNOLOGY, 2002, 20 (08) :800-804
[8]   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
[9]   Insulin analogs with improved pharmacokinetic profiles [J].
Brange, J ;
Volund, A .
ADVANCED DRUG DELIVERY REVIEWS, 1999, 35 (2-3) :307-335
[10]  
Brange J, 1987, GALENICS INSULIN PHY