Engineered pH-Responsive Mesoporous Carbon Nanoparticles for Drug Delivery

In this work, two types of mesoporous carbon particles with different morphology, size and pore structure have been functionalized with a self-immolative polymer sensitive to changes in pH and tested as drug nanocarriers. It is shown that their textural properties allow significantly higher loading...

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Detalles Bibliográficos
Autores: Gisbert Garzarán, Miguel, Berkmann, Julia, Giasafaki, Dimitra, Lozano Borregón, Daniel, Spyrou, Konstantinos, Manzano García, Miguel, Steriotis, Theodore A, Duda, Georg, Schmidt-Bleek, Katharina, Charalambopoulou, Georgia, Vallet Regí, María Dulce Nombre
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/6083
Acceso en línea:https://hdl.handle.net/20.500.14352/6083
Access Level:acceso abierto
Palabra clave:615.46
546
Mesoporous Carbons
pH-responsive
self-immolative coating
drug delivery
controlled release
Materiales
Química inorgánica (Farmacia)
3312 Tecnología de Materiales
Descripción
Sumario:In this work, two types of mesoporous carbon particles with different morphology, size and pore structure have been functionalized with a self-immolative polymer sensitive to changes in pH and tested as drug nanocarriers. It is shown that their textural properties allow significantly higher loading capacity compared to typical mesoporous silica nanoparticles. In vial release experiments of a model Ru dye at pH 7.4 and 5 confirm the pH-responsiveness of the hybrid systems, showing that only small amounts of the cargo are released at physiological pH, whereas at slightly acidic pH (e.g. that of lysosomes) self-immolation takes place and a significant amount of the cargo is released. Cytotoxicity studies using human osteosarcoma cells show that the hybrid nanocarriers are not cytotoxic by themselves but induce significant cell growth inhibition when loaded with a chemotherapeutic drug such as doxorubicin. In preparation of an in vivo application, in vial responsiveness of the hybrid system to short-term pH-triggering is confirmed. The consecutive in vivo study shows no substantial cargo release over a period of 96 hours under physiological pH conditions. Short-term exposure to acidic pH releases an experimental fluorescent cargo during and continuously after the triggering period over 72 hours.