Synthesis and Characterization of Fatty Acid Grafted Chitosan Polymeric Micelles for Improved Gene Delivery of VGF to the Brain through Intranasal Route

• Published in: Biomedicines Vol. 10; no. 2; p. 493
• Main Authors: Lamptey, Richard Nii Lante, Gothwal, Avinash, Trivedi, Riddhi, Arora, Sanjay, Singh, Jagdish
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 19.02.2022; MDPI
• Subjects: Alzheimer's disease; Astrocytes; Blood-brain barrier; Brain research; Chitosan; chitosan grafted micelles; Ethanol; Fatty acids; Fourier transforms; Gene transfer; Growth factors; Hemodialysis; intranasal; Intranasal administration; Intravenous administration; Mannose; Micelles; Nanoparticles; Nervous system; NMR; Nuclear magnetic resonance; Oleic acid; Peptides; polymer; Polymers; synthesis; transfection; Zeta potential; Canada; United States > US; polymer; synthesis; targeted gene delivery; blood–brain barrier; chitosan grafted micelles; transfection; intranasal; polyplex
• ISSN: 2227-9059; 2227-9059
• DOI: 10.3390/biomedicines10020493

Multifunctional fatty acid grafted polymeric micelles are an effective and promising approach for drug and gene delivery to the brain. An alternative approach to bypass the blood–brain barrier is administration through intranasal route. Multifunctional fatty acid grafted polymeric micelles were prepared and characterized for pVGF delivery to the brain. In vitro pVGF expression was analyzed in bEnd.3 cells, primary astrocytes, and neurons. Comparative in-vivo pVGF expression was analyzed to evaluate the effective route of administration between intranasal and intravenous. Biocompatible, multifunctional polymeric micelles were prepared, having an average size of 200 nm, and cationic zeta potential. Modified polymers were found to be hemo- and cyto-compatible. When transfected with the different modified chitosan formulations, significantly (p < 0.05) higher VGF expression was observed in primary astrocytes and neurons using the mannose, Tat peptide, and oleic acid grafted chitosan polymer. Compared to intravenous administration, intranasal administration of pVGF in polyplex formulation led to significantly (p < 0.05) higher pVGF expression. Developed multifunctional polymeric micelles were an effective pVGF delivery platform to the brain. Mannose and Tat ligand tagging improved the pVGF delivery to the brain.