Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.ajps.2017.09.001
Title: Intranasal administration of carbamazepine-loaded carboxymethyl chitosan nanoparticles for drug delivery to the brain
Authors: Liu, S. 
Yang, S. 
Ho, P.C. 
Keywords: Blood-brain barrier
Carbamazepine
Chitosan
Nanoparticles
Nasal drug delivery
Pharmacokinetics
Issue Date: 2018
Publisher: Shenyang Pharmaceutical University
Citation: Liu, S., Yang, S., Ho, P.C. (2018). Intranasal administration of carbamazepine-loaded carboxymethyl chitosan nanoparticles for drug delivery to the brain. Asian Journal of Pharmaceutical Sciences 13 (1) : 72-81. ScholarBank@NUS Repository. https://doi.org/10.1016/j.ajps.2017.09.001
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Epilepsy is considered as a common and diverse set of chronic neurological disorders and its symptoms can be controlled by antiepileptic drugs (AEDs). The presence of p-glycoprotein and multi-drug resistance transporters in the blood-brain barrier could prevent the entry of AEDs into the brain, causing drug resistant epilepsy. To overcome this problem, we propose using carboxymethyl chitosan nanoparticles as a carrier to deliver carbamazepine (CBZ) intra-nasally with the purpose to bypass the blood-brain barrier thus to enhance the brain drug concentration and the treatment efficacy. Results so far indicate that the developed CBZ-NPs have small particle size (218.76 ± 2.41 nm) with high drug loading (around 35%) and high entrapment efficiency (around 80%). The in vitro release profiles of CBZ from the NPs are in accordance with the Korsmeyer-peppas model. The in vivo results show that both encapsulation of CBZ in nanoparticles and the nasal route determined the enhancement of the drug bioavailability and brain targeting characteristics. © 2018 Shenyang Pharmaceutical University
Source Title: Asian Journal of Pharmaceutical Sciences
URI: https://scholarbank.nus.edu.sg/handle/10635/212127
ISSN: 18180876
DOI: 10.1016/j.ajps.2017.09.001
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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