Dual-Action Gemcitabine Delivery: Chitosan–Magnetite–Zeolite Capsules for Targeted Cancer Therapy and Antibacterial Defense
Yuly Andrea Guarín-González,
Gerardo Cabello-Guzmán,
José Reyes-Gasga,
Yanko Moreno-Navarro,
Luis Vergara-González,
Antonia Martin-Martín,
Rodrigo López-Muñoz,
Galo Cárdenas-Triviño,
Luis F. Barraza
Affiliations
Yuly Andrea Guarín-González
Laboratorio Térmico de Nano y Macromateriales, Edificio de Procesos Sustentables, Departamento de Ingeniería en Maderas, Universidad del Bío-Bío, Concepción 4081112, Chile
Gerardo Cabello-Guzmán
Facultad de Ciencias, Departamento de Biología y Química, Universidad del Bío-Bío, Chillán 3780000, Chile
José Reyes-Gasga
Instituto de Física, Departamento de Materia Condensada, Universidad Autónoma de México, Coyoacán 04510, Mexico
Yanko Moreno-Navarro
Facultad de Ciencias, Departamento de Química, Universidad de la Serena, La Serena 1720170, Chile
Luis Vergara-González
Departamento de Ciencias Biológicas y Químicas, Facultad de Medicina y Ciencia, Universidad San Sebastián, Campus Las Tres Pascualas, Lientur 1457, Concepción 4060000, Chile
Antonia Martin-Martín
Instituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, Valdivia 5090000, Chile
Rodrigo López-Muñoz
Instituto de Farmacología y Morfofisiología, Facultad de Ciencias Veterinarias, Universidad Austral de Chile, Valdivia 5090000, Chile
Galo Cárdenas-Triviño
Laboratorio Térmico de Nano y Macromateriales, Edificio de Procesos Sustentables, Departamento de Ingeniería en Maderas, Universidad del Bío-Bío, Concepción 4081112, Chile
Luis F. Barraza
Departamento de Ciencias Biológicas y Químicas, Facultad de Medicina y Ciencia, Universidad San Sebastián, General Lagos 1163, Valdivia 5090000, Chile
Cancer and infectious diseases are two of the world’s major public health problems. Gemcitabine (GEM) is an effective chemotherapeutic agent against several types of cancer. In this study, we developed macrocapsules incorporating GEM into a chitosan matrix blended with magnetite and zeolite by ionic gelation. Physicochemical characterization was performed using HRTEM-ED, XRD, FESEM–EDS, FT-IR, TGA, encapsulation efficiency (%E.E.), and release profiles at pHs 7.4 and 5.0. Cell viability tests against A549 and H1299 cell lines, and microbiological properties against staphylococcal strains were performed. Our results revealed the successful production of hemispherical capsules with an average diameter of 1.22 mm, a rough surface, and characteristic FT-IR material interaction bands. The macrocapsules showed a high GEM encapsulation efficiency of over 86% and controlled release over 24 h. Cell viability assays revealed that similar cytotoxic effects to free GEM were achieved with a 45-fold lower GEM concentration, suggesting reduced dosing requirements and potentially fewer side effects. Additionally, the macrocapsules demonstrated potent antimicrobial activity, reducing Staphylococcus epidermidis growth by over 90%. These results highlight the macrocapsules dual role as a chemotherapeutic and antimicrobial agent, offering a promising strategy for treating lung cancer in patients at risk of infectious diseases or who are immunosuppressed.