Brain targeted delivery of carmustine using chitosan coated nanoparticles via nasal route for glioblastoma treatment

• Published in: International journal of biological macromolecules Vol. 221; pp. 435 - 445
• Main Authors: Ahmad, Saeem, Khan, Iram, Pandit, Jayamanti, Emad, Nasr A., Bano, Shahnaj, Dar, Khalid Imtiyaz, Rizvi, M. Moshahid Alam, Ansari, Mohd Danish, Aqil, Mohd, Sultana, Yasmin
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 30.11.2022
• Subjects: Brain delivery; Carmustine; Chitosan; Intranasal; Nanoparticles; PLGA; Nanoparticles; PLGA; Chitosan; Brain delivery; Intranasal; Carmustine
• ISSN: 0141-8130; 1879-0003
• DOI: 10.1016/j.ijbiomac.2022.08.210

This study aims to develop chitosan-coated PLGA nanoparticles intended for nose-to-brain delivery of carmustine. Formulations were prepared by the double emulsion solvent evaporation method and optimized by using Box-Behnken Design. The optimized nanoparticles were obtained to satisfactory levels in terms of particle size, PDI, entrapment efficiency, and drug loading. In vitro drug release and ex-vivo permeation showed sustained release and enhanced permeability (approx. 2 fold) of carmustine compared to drug suspension. The AUC0-t of brain obtained with carmustine-loaded nanoparticles via nasal administration in Albino Wistar rats was 2.8 and 14.7 times that of intranasal carmustine suspension and intravenous carmustine, respectively. The MTT assay on U87 MG cell line showed a significant decrease (P < 0.05) in the IC50 value of the formulation (71.23 μg ml−1) as compared to drug suspension (90.02 μg ml−1).These findings suggest chitosan coated nanoparticles could be used to deliver carmustine via intranasal administration to treat Glioblastoma multiforme.