| Literature DB >> 28558188 |
Sha Lin1, Xiangmei Liu1, Lei Tan1, Zhenduo Cui2, Xianjin Yang2, Kelvin W K Yeung3, Haobo Pan4, Shuilin Wu1,2.
Abstract
Sustained drug release plays a critical role in targeting the therapy of local diseases such as bacterial infections. In the present work, porous iron-carboxylate metal-organic framework [MOF-53(Fe)] nanoparticles (NPs) were designed to entrap the vancomycin (Van) drugs. This system exhibited excellent chemical stability under acidic conditions (pH 7.4, 6.5, and 5.5) and much higher drug-loading capability because of the high porosity and large surface area of MOF NPs. The results showed that the drug-loading ratio of Van could reach 20 wt % and that the antibacterial ratio of the MOF-53(Fe)/Van system against Staphylococcus aureus could reach up to 90%. In addition, this MOF-53(Fe)/Van system exhibited excellent biocompatibility because of its chemical stability and sustained release of iron ions. Hence, these porous MOF NPs are a promising bioplatform not only for local therapy of bacterial infections but also for other biomedical therapies for tissue regeneration.Entities:
Keywords: MOF; antibacterial; biocompatibility; drug delivery; osteogenic differentiation
Mesh:
Substances:
Year: 2017 PMID: 28558188 DOI: 10.1021/acsami.7b04810
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229