Significant delivery of tacrine into the brain using magnetic chitosan microparticles for treating Alzheimer's disease

被引:50
|
作者
Wilson, Barnabas [1 ]
Samanta, Malay Kumar [1 ]
Santhi, Kumaraswamy
Kumar, Kokilampal Perumal Sampath [1 ]
Ramasamy, Muthu [2 ]
Suresh, Bhojraj [1 ]
机构
[1] JSS Coll Pharm, Dept Pharmaceut, Ootacamund 643001, Tamil Nadu, India
[2] Delhi Inst Pharmaceut Sci & Res, New Delhi 110017, India
关键词
Alzheimer's disease; Tacrine; Magnetic chitosan microparticles; Targeted drug delivery; ALBUMIN MICROSPHERES; DRUG; NANOPARTICLES; PREVALENCE; ADRIAMYCIN; CARRIERS; RELEASE; SODIUM;
D O I
10.1016/j.jneumeth.2008.10.036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is a progressive degenerative disorder of the brain characterized by a slow, progressive decline in cognitive function and behavior. As the disease advances, persons have a tough time with daily tasks like using the phone, cooking, handling money or driving the car. AD affects 15 million people worldwide and it has been estimated that AD affects 4.5 million Americans. Tacrine is a reversible cholinesterase inhibitor used for treating mild to moderate AD. In the present study, an attempt was made to target the anti-Alzheimer's drug tacrine in the brain by using magnetic chitosan microparticles. The magnetic chitosan micro particles were prepared by emulsion cross-linking. The formulated microparticles were characterized for process yield, drug loading capacity, particle size, in vitro release, release kinetics and magnetite content. The particle size was analyzed by scanning electron microscope. The magnetite content of the microparticles was determined by atomic absorption spectroscopy. For animal testing, the microparticles were injected intravenously after keeping a suitable magnet at the target region. The concentrations of tacrine at the target and non-target organs were analyzed by HPLC. The magnetic chitosan microparticles significantly increased the concentration of tacrine in the brain in comparison with the free drug. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:427 / 433
页数:7
相关论文
共 50 条
  • [21] Long-term tacrine treatment in Alzheimer's disease
    Farre, M
    Roset, PN
    LANCET, 1996, 348 (9035): : 1181 - 1182
  • [22] Maximizing function in Alzheimer's disease: What role for tacrine?
    Smucker, WD
    AMERICAN FAMILY PHYSICIAN, 1996, 54 (02) : 645 - 652
  • [24] Penetration of tacrine into cerebrospinal fluid in patients with Alzheimer's disease
    Grothe, DR
    Piscitelli, SC
    Dukoff, R
    Fullerton, T
    Sunderland, T
    Molchan, SE
    JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1998, 18 (01) : 78 - 81
  • [25] Development, optimisation and evaluation of chitosan nanoparticles of alendronate against Alzheimer's disease in intracerebroventricular streptozotocin model for brain delivery
    Zameer, Saima
    Ali, Javed
    Vohora, Divya
    Najmi, Abul Kalam
    Akhtar, Mohd
    JOURNAL OF DRUG TARGETING, 2021, 29 (02) : 199 - 216
  • [26] Metabolic brain mapping in Alzheimer's disease using proton magnetic resonance spectroscopy
    Lazeyras, F
    Charles, HC
    Tupler, LA
    Erickson, R
    Boyko, OB
    Krishnan, KRR
    PSYCHIATRY RESEARCH-NEUROIMAGING, 1998, 82 (02) : 95 - 106
  • [27] Topical drug delivery using chitosan nano- and microparticles
    Sezer, Ali Demir
    Cevher, Erdal
    EXPERT OPINION ON DRUG DELIVERY, 2012, 9 (09) : 1129 - 1146
  • [28] Superhydrophilic Nanostructured Microparticles for Enhanced Phosphoprotein Enrichment from Alzheimer's Disease Brain
    Shang, Danyi
    Song, Yongyang
    Cui, Yun
    Chen, Cheng
    Xu, Feifei
    Zhu, Congcong
    Dong, Xuefang
    Chen, Yifan
    Wang, Shutao
    Li, Xiuling
    Liang, Xinmiao
    ACS NANO, 2025, 19 (08) : 8118 - 8130
  • [29] Treating apathy in Alzheimer's disease
    Boyle, PA
    Malloy, PF
    DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2004, 17 (1-2) : 91 - 99
  • [30] Brain proton magnetic resonance spectroscopy in Alzheimer's disease
    Xie, HG
    Cheng, LQ
    Wang, LM
    Cai, YQ
    NEUROBIOLOGY OF AGING, 2002, 23 (01) : S482 - S482