Magnetic activated carbon particles as stimuli-responsive vehicles for methotrexate
Metadatos
Mostrar el registro completo del ítemAutor
Lirio Piñar, Juan Antonio; Lázaro Callejón, Marina; Iglesias Salto, Guillermo Ramón; Romacho, Tania; Delgado Mora, Ángel Vicente; García García, Gracia; Ahualli Yapur, Silvia AlejandraEditorial
Royal Society of Chemistry
Fecha
2025-02-25Referencia bibliográfica
Mater. Adv., 2025, Advance Magnetic activated carbon particles as stimuli-responsive vehicles for methotrexate [DOI: 10.1039/d4ma01037j]
Patrocinador
Grant TED2021- 131855BI00/AEI/10.13039/501100011033/Unión Europea Next Generation EU/PRTR; PID2023-151881OB-I00 MICIU/AEI/ 10.13039/501100011033/and FEDER; Ramón y Cajal RYC2022-035807Resumen
This study investigates porous activated carbon (AC) particles as drug delivery vehicles for methotrexate (MTX). To enhance functionality, magnetic nanoparticles are embedded in AC imparting superparamagnetic properties (MAC composites), making them suitable for controlled transport and localization, as well as for facilitating their response to external fields. The composites are further functionalized with branched low molecular weight polyethyleneimine (PEI) to confer them a positive charge. After characterizing size, composition, and magnetic hysteresis, their potential as MTX carriers is assessed. Electrophoretic mobility and infrared data confirm the presence of magnetite, polymer, and drug molecules. Photothermal therapy (PTT) tests reveal that MAC–PEI particles produce up to 180 W g−1 of specific absorption rate (SAR) under infrared laser radiation. Due to its anisotropy, rotating magnetic fields (RMF) induce particle rotation, offering another external stimulus. Biocompatibility studies with human skin M1 fibroblasts confirm no significant cytotoxicity at concentrations below 700 μg mL−1. The particles adsorb over 80% of MTX from 0.6 mM solutions, with release evaluated at pH 5.8 under PTT and RMF stimuli. Both methods significantly enhance MTX release, achieving twice the drug release compared to passive conditions, demonstrating the particles’ high potential as active vehicles for targeted MTX delivery.