Literature DB >> 27604714

Methods of Drug Delivery in Neurotrauma.

Ying Deng-Bryant1, Ryan Readnower2, Lai Yee Leung2, Frank Tortella2, Deborah Shear2.   

Abstract

The central nervous system (CNS) is protected by blood-brain barrier (BBB) and blood-cerebrospinal-fluid (CSF) barrier that limit toxic agents and most molecules from penetrating the brain and spinal cord. However, these barriers also prevent most pharmaceuticals from entering into the CNS. Drug delivery to the CNS following neurotrauma is complicated. Although studies have shown BBB permeability increases in various TBI models, it remains as the key mitigating factor for delivering drugs into the CNS. The commonly used methods for drug delivery in preclinical neurotrauma studies include intraperitoneal, subcutaneous, intravenous, and intracerebroventricular delivery. It should be noted that for a drug to be successfully translated into the clinic, it needs to be administered preclinically as it would be anticipated to be administered to patients. And this likely leads to better dose selection of the drug, as well as recognition of any possible side effects, prior to transition into a clinical trial. Additionally, novel approach that is noninvasive and yet circumvents BBB, such as drug delivery through nerve pathways innervating the nasal passages, needs to be investigated in animal models, as it may provide a viable drug delivery method for patients who sustain mild CNS injury or require chronic treatments. Therefore, the focus of this chapter is to present rationales and methods for delivering drugs by IV infusion via the jugular vein, and intranasally in preclinical studies.

Entities:  

Keywords:  Drug delivery; Intranasal; Intravenous; Neurotrauma; Traumatic brain injury

Mesh:

Substances:

Year:  2016        PMID: 27604714     DOI: 10.1007/978-1-4939-3816-2_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  Intranasal delivery of dexamethasone efficiently controls LPS-induced murine neuroinflammation.

Authors:  G Meneses; G Gevorkian; A Florentino; M A Bautista; A Espinosa; G Acero; G Díaz; A Fleury; I N Pérez Osorio; A Del Rey; G Fragoso; E Sciutto; H Besedovsky
Journal:  Clin Exp Immunol       Date:  2017-09-07       Impact factor: 4.330

2.  Achyranthes bidentata polypeptide protects dopaminergic neurons from apoptosis in Parkinson's disease models both in vitro and in vivo.

Authors:  Su Peng; Caiping Wang; Jinyu Ma; Ketao Jiang; Yuhui Jiang; Xiaosong Gu; Cheng Sun
Journal:  Br J Pharmacol       Date:  2018-01-06       Impact factor: 8.739

3.  Acute administration of catalase targeted to ICAM-1 attenuates neuropathology in experimental traumatic brain injury.

Authors:  Evan M Lutton; Roshanak Razmpour; Allison M Andrews; Lee Anne Cannella; Young-Jin Son; Vladimir V Shuvaev; Vladimir R Muzykantov; Servio H Ramirez
Journal:  Sci Rep       Date:  2017-06-19       Impact factor: 4.379

  3 in total

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