Lignocellulosic Membranes Grafted with N-Vinylcaprolactam Using Radiation Chemistry: Load and Release Capacity of Vancomycin

Author:

Rentería-Urquiza Maite1ORCID,Flores-Rojas Guadalupe Gabriel123ORCID,Gómez-Lázaro Belén2,López-Saucedo Felipe24ORCID,Vera-Graziano Ricardo3ORCID,Mendizabal Eduardo1ORCID,Bucio Emilio2ORCID

Affiliation:

1. Departamento de Química, Centro Universitario de Ciencias Exactas e Ingenierías, Universidad de Guadalajara, Blvd. M. García Barragán #1451, Guadalajara 44430, Mexico

2. Departamento de Química de Radiaciones y Radioquímica, Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, Mexico City 04510, Mexico

3. Instituto de Investigaciones en Materiales, Universidad Nacional Autónoma de México, Mexico City 04510, Mexico

4. Facultad de Ciencias, Campus El Cerrillo Piedras Blancas, Universidad Autónoma del Estado de México, Carretera Toluca-Ixtlahuaca Km 15.5, Toluca 50200, Mexico

Abstract

Radiation chemistry presents a unique avenue for developing innovative polymeric materials with desirable properties, eliminating the need for chemical initiators, which can be potentially detrimental, especially in sensitive sectors like medicine. In this investigation, we employed a radiation-induced graft polymerization process with N-vinylcaprolactam (NVCL) to modify lignocellulosic membranes derived from Agave salmiana, commonly known as maguey. The membranes underwent thorough characterization employing diverse techniques, including contact angle measurement, degree of swelling, scanning electron microscopy (SEM), atomic force microscopy (AFM), Fourier-transform infrared-attenuated total reflectance spectroscopy (FTIR-ATR), nuclear magnetic resonance (CP-MAS 13C-NMR), X-ray photoelectron spectroscopy (XPS), and uniaxial tensile mechanical tests. The membranes’ ability to load and release an antimicrobial glycopeptide drug was assessed, revealing significant enhancements in both drug loading and sustained release. The grafting of PNVCL contributed to prolonged sustained release by decreasing the drug release rate at temperatures above the LCST. The release profiles were analyzed using the Higuchi, Peppas–Sahlin, and Korsmeyer–Peppas models, suggesting a Fickian transport mechanism as indicated by the Korsmeyer–Peppas model.

Funder

Universidad de Guadalajara

Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México

Support Program for Technological Research and Innovation Projects

National Council of Science and Technology

CONAHCyT postdoctoral fellowship

Publisher

MDPI AG

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