Peptide drug modifications to enhance bioavailability and blood-brain barrier permeability

被引:179
作者
Witt, KA [1 ]
Gillespie, TJ [1 ]
Huber, JD [1 ]
Egleton, RD [1 ]
Davis, TP [1 ]
机构
[1] Univ Arizona, Coll Med, Dept Pharmacol, Tucson, AZ 85724 USA
关键词
D O I
10.1016/S0196-9781(01)00537-X
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 have the potential to be potent pharmaceutical agents for the treatment of many central nervous system derived maladies. Unfortunately peptides are generally water-soluble compounds that will not enter the central nervous system, via passive diffusion. due to the existence of the blood-brain barrier. Peptides can also undergo metabolic deactivation by peptidases, thus further reducing their therapeutic benefits. In targeting peptides to the central nervous system consideration must be focused both on increasing bioavailability and enhancing brain uptake. To date multiple strategies have been examined with this focus. However, each strategy comes with its own complications and considerations. In this review we assess the strengths and weaknesses of many of the methods currently being examined to enhance peptide entry into the central nervous system. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:2329 / 2343
页数:15
相关论文
共 202 条
[1]  
Abbruscato TJ, 1997, J NEUROCHEM, V69, P1236
[2]  
Abbruscato TJ, 1996, J PHARMACOL EXP THER, V276, P1049
[3]  
Adam A, 2001, CAN J CARDIOL, V17, p11A
[4]   ELECTRICAL CHARGE - ITS ROLE IN THE PATHOGENESIS AND PREVENTION OF EXPERIMENTAL MEMBRANOUS NEPHROPATHY IN THE RABBIT [J].
ADLER, SG ;
WANG, H ;
WARD, HJ ;
COHEN, AH ;
BORDER, WA .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (03) :487-499
[5]   A quantitative evaluation of the permeability of the blood brain barrier of portacaval shunted bats [J].
Alexander, B ;
Li, X ;
Benjamin, IS ;
Segal, MB ;
Sherwood, R ;
Preston, JE .
METABOLIC BRAIN DISEASE, 2000, 15 (02) :93-103
[6]   MEMBRANE-BOUND PITUITARY METALLOENDOPEPTIDASE - APPARENT IDENTITY TO ENKEPHALINASE [J].
ALMENOFF, J ;
WILK, S ;
ORLOWSKI, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1981, 102 (01) :206-214
[7]   Omapatrilat, a dual angiotensin-converting enzyme and neutral endopeptidase inhibitor, prevents fatty streak deposit in apolipoprotein E-deficient mice [J].
Arnal, JF ;
Castano, C ;
Maupas, E ;
Mugniot, A ;
Darblade, B ;
Gourdy, P ;
Michel, JB ;
Bayard, F .
ATHEROSCLEROSIS, 2001, 155 (02) :291-295
[8]   ABSORPTION CHARACTERISTICS OF CHEMICALLY MODIFIED-INSULIN DERIVATIVES WITH VARIOUS FATTY-ACIDS IN THE SMALL AND LARGE-INTESTINE [J].
ASADA, H ;
DOUEN, T ;
WAKI, M ;
ADACHI, S ;
FUJITA, T ;
YAMAMATO, A ;
MURANISHI, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (06) :682-687
[9]  
AUDUS KL, 1992, BRAIN UPTAKE DRUGS I, P1
[10]   Acyloxyalkoxy-based cyclic prodrugs of opioid peptides: Evaluation of the chemical and enzymatic stability as well as their transport properties across Caco-2 cell monolayers [J].
Bak, A ;
Gudmundsson, OS ;
Friis, GJ ;
Siahaan, TJ ;
Borchardt, RT .
PHARMACEUTICAL RESEARCH, 1999, 16 (01) :24-29