Intranasal Delivery of Proteins and Peptides in the Treatment of Neurodegenerative Diseases

被引:147
作者
Meredith, M. Elizabeth [1 ,2 ,3 ]
Salameh, Therese S. [2 ,3 ]
Banks, William A. [2 ,3 ]
机构
[1] Univ Washington, Dept Pathol, Seattle, WA 98108 USA
[2] Univ Washington, Sch Med, Div Gerontol & Geriatr Med, Dept Med,VAPSHCS, 1660S Columbian Way,810A Bldg 1, Seattle, WA 98108 USA
[3] Univ Washington, Geriatr Res Educ & Clin Ctr, Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA 98108 USA
关键词
blood-brain barrier; cognition; intranasal; memory; GALANIN-LIKE PEPTIDE; BLOOD-BRAIN-BARRIER; GLUCAGON-LIKE PEPTIDE-1; CYCLASE-ACTIVATING POLYPEPTIDE; MILD COGNITIVE IMPAIRMENT; CENTRAL-NERVOUS-SYSTEM; NASAL DRUG-DELIVERY; ADENYLATE-CYCLASE; ALZHEIMERS-DISEASE; ACETYLCHOLINE-RELEASE;
D O I
10.1208/s12248-015-9719-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The blood-brain barrier (BBB) is a major impediment to the therapeutic delivery of peptides and proteins to the brain. Intranasal delivery often provides a non-invasive means to bypass the BBB. Advantages of using intranasal delivery include minimizing exposure to peripheral organs and tissues, thus reducing systemic side effects. It also allows substances that typically have rapid degradation in the blood time to exert their effect. Intranasal delivery provides the ability to target proteins and peptides to specific regions of the brain when administered with substrates like cyclodextrins. In this review, we examined the use of intranasal delivery of various proteins and peptides that have implications in the treatment of neurodegenerative diseases, focusing especially on albumin, exendin/GLP-1, GALP, insulin, leptin, and PACAP. We have described their rationale for use, distribution in the brain after intranasal injection, how intranasal administration differed from other modes of delivery, and their use in clinical trials, if applicable. Intranasal delivery of drugs, peptides, and other proteins could be very useful in the future for the prevention or treatment of brain related diseases.
引用
收藏
页码:780 / 787
页数:8
相关论文
共 73 条
[1]   Solid lipid nanoparticles as a drug delivery system for peptides and proteins [J].
Almeida, Antonio J. ;
Souto, Eliana .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :478-490
[2]   Investigation of the pathophysiological mechanisms of migraine attacks induced by pituitary adenylate cyclase-activating polypeptide-38 [J].
Amin, Faisal Mohammad ;
Hougaard, Anders ;
Schytz, Henrik W. ;
Asghar, Mohammad S. ;
Lundholm, Elisabet ;
Parvaiz, Arushma I. ;
de Koning, Patrick J. H. ;
Andersen, Malene R. ;
Larsson, Henrik B. W. ;
Fahrenkrug, Jan ;
Olesen, Jes ;
Ashina, Messoud .
BRAIN, 2014, 137 :779-794
[3]  
ARIMURA A, 1992, REGUL PEPTIDES, V37, P287
[4]   Brain uptake of the glucagon-like peptide-1 antagonist exendin(9-39) after intranasal administration [J].
Banks, WA ;
During, MJ ;
Niehoff, ML .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 309 (02) :469-475
[5]   Leptin enters the brain by a saturable system independent of insulin [J].
Banks, WA ;
Kastin, AJ ;
Huang, WT ;
Jaspan, JB ;
Maness, LM .
PEPTIDES, 1996, 17 (02) :305-311
[6]   Transport of insulin across the blood-brain barrier: Saturability at euglycemic doses of insulin [J].
Banks, WA ;
Jaspan, JB ;
Huang, WT ;
Kastin, AJ .
PEPTIDES, 1997, 18 (09) :1423-1429
[7]   Differential permeability of the blood-brain barrier to two pancreatic peptides: Insulin and amylin [J].
Banks, WA ;
Kastin, AJ .
PEPTIDES, 1998, 19 (05) :883-889
[8]   Permeability of the blood-brain barrier to albumin and insulin in the young and aged SAMP8 mouse [J].
Banks, WA ;
Farr, SA ;
Morley, JE .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2000, 55 (12) :B601-B606
[9]   Uptake and degradation of blood-borne insulin by the olfactory bulb [J].
Banks, WA ;
Kastin, AJ ;
Pan, WH .
PEPTIDES, 1999, 20 (03) :373-378
[10]   Insulin in the brain: There and back again [J].
Banks, William A. ;
Owen, Joshua B. ;
Erickson, Michelle A. .
PHARMACOLOGY & THERAPEUTICS, 2012, 136 (01) :82-93