Drug delivery strategies for Alzheimer's disease treatment

被引:82
作者
Di Stefano, Antonio [1 ]
Iannitelli, Antonio [1 ]
Laserra, Sara [1 ]
Sozio, Piera [1 ]
机构
[1] Univ G DAnnunzio, Sch Pharm, Dept Drug Sci, I-66100 Chieti, Italy
关键词
Alzheimer's disease; drug delivery devices; drug delivery systems; pharmaceutical formulations; therapeutic strategies; TRANSDERMAL RIVASTIGMINE PATCH; CENTRAL-NERVOUS-SYSTEM; BLOOD-BRAIN-BARRIER; GROWTH-FACTOR-I; DOUBLE-BLIND; EXTENDED-RELEASE; NASAL CAVITY; CHOLINESTERASE-INHIBITORS; POSTMENOPAUSAL WOMEN; IMMEDIATE-RELEASE;
D O I
10.1517/17425247.2011.561311
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Current Alzheimer's disease (AD) therapy is based on the administration of the drugs donepezil, galantamine, rivastigmine and memantine. Until disease-modifying therapies become available, further research is needed to develop new drug delivery strategies to ensure ease of administration and treatment persistence. Areas covered: In addition to the conventional oral formulations, a variety of drug delivery strategies applied to the treatment of AD are reviewed in this paper, with a focus on strategies leading to simplified dosage regimens and to providing new pharmacological tools. Alternatives include extended release, orally disintegrating or sublingual formulations, intranasal or short- and long-acting intramuscular or transdermal forms, and nanotechnology-based delivery systems. Expert opinion: The advent of new research on molecular mechanisms of AD pathogenesis has outlined new strategies for therapeutic intervention; these include the stimulation of alpha-secretase cleavage, the inhibition of gamma-secretase activity, the use of non-steroidal anti-inflammatory drugs, neuroprotection based on antioxidant therapy, the use of estrogens, NO synthetase inhibitors, and natural agents such as polyphenols. Unfortunately, these compounds might not help patients with end stage AD, but might hopefully slow or stop the disease process in its early stage. Nanotechnologies may prove to be a promising contribution in future AD drug delivery strategies, in particular drug carrier nano- or microsystems, which can limit the side effects of anti-Alzheimer drugs.
引用
收藏
页码:581 / 603
页数:23
相关论文
共 173 条
[21]   Transdermal delivery of treatment for Alzheimer's disease [J].
Chan, Agnes L. F. ;
Chien, Yie W. ;
Lin, Shun Jin .
DRUGS & AGING, 2008, 25 (09) :761-775
[22]   BIOLOGIC EFFECTS OF TRANSDERMAL ESTRADIOL [J].
CHETKOWSKI, RJ ;
MELDRUM, DR ;
STEINGOLD, KA ;
RANDLE, D ;
LU, JK ;
EGGENA, P ;
HERSHMAN, JM ;
ALKJAERSIG, NK ;
FLETCHER, AP ;
JUDD, HL .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (25) :1615-1620
[23]   Direct nose-brain transport of benzoylecgonine following intranasal administration in rats [J].
Chow, HHS ;
Anavy, N ;
Villalobos, A .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (11) :1729-1735
[24]  
Chow HHS, 1999, J PHARM SCI, V88, P754
[25]   Oxidative stress and Alzheimer disease [J].
Christen, Y .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2000, 71 (02) :621S-629S
[26]   Alzheimer disease: Current concepts and emerging diagnostic and therapeutic strategies [J].
Clark, CM ;
Karlawish, JHT .
ANNALS OF INTERNAL MEDICINE, 2003, 138 (05) :400-410
[27]   A systematic review of the associations between dose regimens and medication compliance [J].
Claxton, AJ ;
Cramer, J ;
Pierce, C .
CLINICAL THERAPEUTICS, 2001, 23 (08) :1296-1310
[28]  
*CLINICALTRIALS GO, COMP 23 MG DON SUST
[29]  
*CLINICALTRIALS GO, EFF RIV PATCH ACT DA
[30]  
*CLINICALTRIALS GO, SAF SWITCH DON RIV P