RECOMBINANT-DNA-DERIVED INSULIN ANALOGS AS POTENTIALLY USEFUL THERAPEUTIC AGENTS

被引:22
作者
BRISTOW, AF
机构
[1] Division of Endocrinology, National Institute for Biological Standards and Control, Potters Bar, Herts. EN6 3QG, Blanche Lane, South Mimms
关键词
D O I
10.1016/0167-7799(93)90018-5
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
Whilst insulin is a spectacularly successful drug for the management of diabetes mellitus, it remains difficult to mimic the physiological pattern of insulin secretion, even using the various quick-acting and insoluble formulations that are available. The introduction of recombinant-DNA technology to the manufacture of therapeutic insulin has made the rational design and production of insulin analogues with altered pharmacokinetic and pharmacological properties possible. Such analogues include 'monomeric' insulins, which do not form the insulin-zinc hexamer in solution and are absorbed more rapidly from the injection site, and long-acting insulins, which are absorbed very slowly at physiological pH. Many of these analogues are being tested clinically, and it is possible that the next generation of insulin therapy will be various combinations of rationally designed insulin analogues produced by industrial biotechnology.
引用
收藏
页码:301 / 305
页数:5
相关论文
共 21 条
[1]   MONOMERIC INSULINS OBTAINED BY PROTEIN ENGINEERING AND THEIR MEDICAL IMPLICATIONS [J].
BRANGE, J ;
RIBEL, U ;
HANSEN, JF ;
DODSON, G ;
HANSEN, MT ;
HAVELUND, S ;
MELBERG, SG ;
NORRIS, F ;
NORRIS, K ;
SNEL, L ;
SORENSEN, AR ;
VOIGT, HO .
NATURE, 1988, 333 (6174) :679-682
[2]   MONOMERIC INSULINS AND THEIR EXPERIMENTAL AND CLINICAL IMPLICATIONS [J].
BRANGE, J ;
OWENS, DR ;
KANG, S ;
VOLUND, A .
DIABETES CARE, 1990, 13 (09) :923-954
[3]   SUPERACTIVE INSULINS [J].
BURKE, GT ;
HU, SQ ;
OHTA, N ;
SCHWARTZ, GP ;
ZONG, L ;
KATSOYANNIS, PG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 173 (03) :982-987
[4]   DOUBLE-BLIND CROSSOVER COMPARISON OF HUMAN AND PORCINE INSULINS IN PATIENTS REPORTING LACK OF HYPOGLYCEMIA AWARENESS [J].
COLAGIURI, S ;
MILLER, JJ ;
PETOCZ, P .
LANCET, 1992, 339 (8807) :1432-1435
[5]   NORMAL INSULIN-SECRETION - THE GOAL OF ARTIFICIAL INSULIN DELIVERY SYSTEMS [J].
EATON, RP ;
ALLEN, RC ;
SCHADE, DS ;
STANDEFER, JC .
DIABETES CARE, 1980, 3 (02) :270-273
[6]  
FRANK BH, 1982, PEPTIDES SYNTHESIS S, P729
[7]   BIOSYNTHETIC HUMAN PROINSULIN - REVIEW OF CHEMISTRY, INVITRO AND INVIVO RECEPTOR-BINDING, ANIMAL AND HUMAN PHARMACOLOGY STUDIES, AND CLINICAL-TRIAL EXPERIENCE [J].
GALLOWAY, JA ;
HOOPER, SA ;
SPRADLIN, CT ;
HOWEY, DC ;
FRANK, BH ;
BOWSHER, RR ;
ANDERSON, JH .
DIABETES CARE, 1992, 15 (05) :666-692
[8]  
HEATH WF, 1992, J BIOL CHEM, V267, P419
[9]   NOVOSOL BASAL - PHARMACOKINETICS OF A NOVEL SOLUBLE LONG-ACTING INSULIN ANALOG [J].
JORGENSEN, S ;
VAAG, A ;
LANGKJAER, L ;
HOUGAARD, P ;
MARKUSSEN, J .
BRITISH MEDICAL JOURNAL, 1989, 299 (6696) :415-419
[10]   COMPARISON OF SUBCUTANEOUS SOLUBLE HUMAN INSULIN AND INSULIN ANALOGS (ASPB9,GLUB27-ASPB10-ASPB28) ON MEAL-RELATED PLASMA-GLUCOSE EXCURSIONS IN TYPE-I DIABETIC SUBJECTS [J].
KANG, S ;
CREAGH, FM ;
PETERS, JR ;
BRANGE, J ;
VOLUND, A ;
OWENS, DR .
DIABETES CARE, 1991, 14 (07) :571-577