Controlled and customizable baculovirus NOS3 gene delivery using PVA-based hydrogel systems

Nitric oxide synthase 3 (NOS3) eluting polyvinyl alcohol-based hydrogels have a large potential in medical applications and device coatings. NOS3 promotes nitric oxide and nitrate production and can effectively be delivered using insect cell viruses, termed baculoviruses. Nitric oxide is known for regulating cell proliferation, promoting blood vessel vasodilation, and inhibiting bacterial growth. The polyvinyl alcohol (PVA)-based hydrogels investigated here sustained baculovirus elution from five to 25 days, depending on the hydrogel composition. The quantity of viable baculovirus loaded significantly declined with each freeze-thaw from one to four (15.3 +/- 2.9% vs. 0.9 +/- 0.5%, respectively). The addition of gelatin to the hydrogels protected baculovirus viability during the freeze-thaw cycles, resulting in a loading capacity of 94.6 +/- 1.2% with sustained elution over 23 days. Adding chitosan, PEG-8000, and gelatin to the hydrogels altered the properties of the hydrogel, including swelling, blood coagulation, and antimicrobial effects, beneficial for different therapeutic applications. Passive absorption of the baculovirus into PVA hydrogels exhibited the highest baculovirus loading (96.4 +/- 0.6%) with elution over 25 days. The baculovirus-eluting hydrogels were hemocompatible and non-cytotoxic, with no cell proliferation or viability reduction after incubation. This PVA delivery system provides a method for high loading and sustained release of baculoviruses, sustaining nitric oxide gene delivery. This proof of concept has clinical applications as a medical device or stent coating by delivering therapeutic genes, improving blood compatibility, preventing thrombosis, and preventing infection.

Automated summary

This study investigates the release of nitric oxide synthase 3 (NOS3) using polyvinyl alcohol-based hydrogels, with a focus on the effects of different compositions on the hydrogel properties. Gelatin is found to protect the viability of the loaded baculovirus, while the addition of chitosan, PEG-8000, and gelatin alters the properties of the hydrogel for different therapeutic applications. Passive absorption of the baculovirus into the hydrogel exhibits the highest loading capacity. Overall, this PVA delivery system demonstrates its potential for high loading and sustained release of baculoviruses, with various clinical applications.