PNIPAAM modified mesoporous hydroxyapatite for sustained osteogenic drug release and promoting cell attachment
Materials Science and Engineering: C, ISSN: 0928-4931, Vol: 62, Page: 888-896
2016
- 35Citations
- 37Captures
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Metrics Details
- Citations35
- Citation Indexes35
- 35
- CrossRef10
- Captures37
- Readers37
- 37
Article Description
This work presented a sustained release system of simvastatin (SIM) based on the mesoporous hydroxyapatite (MHA) capped with poly(N-isopropylacrylamide) (PNIPAAM). The MHA was prepared by using cetyltrimethylammonium bromide (CTAB) as a template and the modified PNIPAAM layer on the surface of MHA was fabricated through surface-initiated atom transfer radical polymerization (SI-ATRP). The SIM loaded MHA-PNIPAAM showed a sustained release of SIM at 37 °C over 16 days. The bone marrow mesenchymal stem cell (BMSC) proliferation was assessed by cell counting kit-8 (CCK-8) assay, and the osteogenic differentiation was evaluated by alkaline phosphatase (ALP) activity and Alizarin Red staining. The release profile showed that the release of SIM from MHA-SIM-PNIPAAM lasted 16 days and the cumulative amount of released SIM was almost seven-fold than MHA-SIM. Besides, SIM loaded MHA-PNIPAAM exhibited better performance on cell proliferation, ALP activity, and calcium deposition than pure MHA due to the sustained release of SIM. The quantity of ALP in MHA-SIM-PNIPAAM group was more than two fold than pure MHA group at 7 days. Compared to pure MHA, better BMSC attachment on PNIPAAM modified MHA was observed using fluorescent microscopy, indicating the better biocompatibility of MHA-PNIPAAM.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0928493116300121; http://dx.doi.org/10.1016/j.msec.2016.01.012; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84959449220&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/26952496; https://linkinghub.elsevier.com/retrieve/pii/S0928493116300121; https://dx.doi.org/10.1016/j.msec.2016.01.012
Elsevier BV
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