Journal Articles

Polymeric Systems Incorporating Plant Viral Nanoparticles for Tailored Release of Therapeutics

January 20, 2013

Polymeric Systems Incorporating Plant Viral Nanoparticles for Tailored Release of Therapeutics. Advanced Healthcare Materials. January 20, 2013. Honarbakhsh S, Guenther RH, Willoughby JA, Lommel SA (Plants for Human Health Institute and DHMRI, NC Research Campus), Pourdeyhimi B.  The Nonwovens Institute, North Carolina State University, 2401 Research Drive, Raleigh, North Carolina, 27695 USA.

Abstract

Therapeutic polylactide (PLA) nanofibrous matrices are fabricated by incorporating plant viral nanoparticles (PVNs) infused with fluorescent agents ethidium bromide (EtBr) and rhodamine (Rho), and cancer therapeutic doxorubicin (Dox). The native virus, Red clover necrotic mosaic virus (RCNMV), reversibly opens and closes upon exposure to the appropriate environmental stimuli. Infusing RCNMV with small molecules allows the incorporation of PVN(Active) into fibrous matrices via two methods: direct processing by in situ electrospinning of a polymer and PVNs solution or immersion of the matrix into a viral nanoparticle solution. Five organic solvents commonly in-use for electrospinning are evaluated for potential negative impact on RCNMV stability. In addition, leakage of rhodamine from the corresponding PVN(Rho) upon solvent exposure is determined. Incorporation of the PVN into the matrices are evaluated via transmission electron, scanning electron and fluorescent microscopies. Finally, the percent cumulative release of doxorubicin from both PLA nanofibers and PLA and polyethylene oxide (PEO) hybrid nanofibers demonstrate tailored release due to the incorporation of PVN(Dox) as compared to the control nanofibers with free Dox. Preliminary kinetic analysis results suggest a two-phase release profile with the first phase following a hindered Fickian transport mechanism for the release of Dox for the polymer-embedded PVNs. In contrast, the nanofiber matrices that incorporate PVNs through the immersion processing method followed a pseudo-first order kinetic transport mechanism.

Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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