Biphasic composite of calcium phosphate-based mesoporous silica as a novel bone drug delivery system
Autor: | Rafał Sądej, Gavin Walker, Adrian Szewczyk, Adrianna Skwira, Magdalena Prokopowicz |
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Rok vydání: | 2019 |
Předmět: |
Calcium Phosphates
Cell Survival Simulated body fluid Pharmaceutical Science chemistry.chemical_element 02 engineering and technology Calcium 010402 general chemistry 01 natural sciences Mineralization (biology) Apatite Cell Line Hydroxyapatite Drug Delivery Systems Adsorption medicine Humans neoplasms Drug Implants Osteoblasts Osteoblast Mesoporous silica Silicon Dioxide 021001 nanoscience & nanotechnology digestive system diseases 0104 chemical sciences medicine.anatomical_structure chemistry Doxycycline visual_art Drug delivery visual_art.visual_art_medium Original Article Powders 0210 nano-technology Porosity Nuclear chemistry |
Zdroj: | Drug Delivery and Translational Research |
ISSN: | 2190-3948 2190-393X |
Popis: | We reported the new biphasic composites of calcium phosphate and mesoporous silica material (CaP@MSi) in the form of powders and pellets as a potential bone drug delivery system for doxycycline hydrochloride (DOX). The CaP@MSi powders were synthesized by cationic surfactant-templating method. The effects of 10, 20, and 30% CaP content in the CaP@MSi powders on the molecular surface structure, the cytotoxicity against osteoblast cells in vitro, and the mineralization potential in simulated body fluid were investigated. The CaP@MSi characterized by the highest mineralization potential (30% CaP content) were used for DOX adsorption and pelletization process. The CaP which precipitated in the CaP@MSi composites was characterized as calcium-deficient with the Ca:P molar ratio between 1.0 and 1.2. The cytotoxicity assays demonstrated that the CaP content in MSi increases osteoblasts viability indicating the CaP@MSi (30% CaP content) as the most biocompatible. The combination of CaP and MSi was an effective strategy to improve the mineralization potential of parent material. Upon immersion in simulated body fluid, the CaP of composite converted into the bone-like apatite. The obtained pellets preserved the mineralization potential of CaP@MSi and provided the prolonged 5-day DOX release. The obtained biphasic CaP@MSi composites seem to have an application potential as bone-specific drug delivery system. Electronic supplementary material The online version of this article (10.1007/s13346-019-00686-3) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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