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      Controlled Release of Naringin in GelMA-Incorporated Rutile Nanorod Films to Regulate Osteogenic Differentiation of Mesenchymal Stem Cells

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          Abstract

          Naringin, a Chinese herbal medicine, has been demonstrated to concentration-dependently promote osteogenic differentiation of mesenchymal stem cells (MSCs). However, it remains a challenge to load naringin on coatings for osteogenesis and further control the release kinetics. Here, we demonstrated that the release behavior of naringin on rutile nanorod films could be controlled by either mixing naringin with gelatin methacryloyl (GelMA) before spinning onto the films or soaking the obtained GelMA-incorporated films with the naringin solution to achieve the distinct degradation-type release and diffusion-type release, respectively. We further revealed that the naringin-loaded coatings facilitated adhesion, proliferation and late differentiation, and mineralization of MSCs. Our findings provided a novel strategy to engineer the coatings with controlled release of naringin and emphasized the bioactivity of naringin for the osteogenic differentiation of MSCs.

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          Most cited references30

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          Engineering biocompatible implant surfaces

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            Biodegradable Gelatin Methacryloyl Microneedles for Transdermal Drug Delivery

            Biocompatible and bioresponsive microneedles (MNs) are emerging technology platforms for sustained drug release with a potential to be a key player in transdermal delivery of therapeutics. In this paper, we report an innovative biodegradable MNs patch for the sustained delivery of drugs using a polymer patch which can adjust delivery rates based on its crosslinking degree. Gelatin methacryloyl (GelMA) was used as the base for engineering biodegradable MNs. The anticancer drug Doxorubicin (DOX) was loaded into GelMA MNs using the one molding step. The GelMA MNs could efficiently penetrate the stratum corneum layer of a mouse cadaver skin. Mechanical properties and drug release behavior of the GelMA MNs could be adjusted by tuning the degree of crosslinking. We have tested the efficacy of the DOX released from the GelMA MNs and demonstrated the anticancer efficacy of the released drugs against melanoma cell line A375. Since GelMA is versatile material in engineering tissue scaffolds, we expect that the GelMA MNs could be used as a platform for the delivery of various therapeutics.
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              Gelatin methacrylate scaffold for bone tissue engineering: The influence of polymer concentration

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                06 November 2019
                19 November 2019
                : 4
                : 21
                : 19350-19357
                Affiliations
                []The Affiliated Stomatologic Hospital, School of Medicine, Zhejiang University , Hangzhou 310003, Zhejiang Province, China
                []Department of Stomatology, The Affiliated Ningbo First Hospital, Zhejiang University , Ningbo 315010, Zhejiang Province, China
                [§ ]Hangzhou Dental Hospital , Hangzhou 310006, Zhejiang Province, China
                []School of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University , Hangzhou 310027, Zhejiang Province, China
                Author notes
                [* ]E-mail: whmwhm@ 123456zju.edu.cn (H.W.).
                [* ]E-mail: yumengfei@ 123456zju.edu.cn (M.Y.).
                [* ]E-mail: lingqingdong@ 123456zju.edu.cn (L.D.).
                Article
                10.1021/acsomega.9b02751
                6868884
                31763559
                aa346ae2-0c46-4ad3-b664-bd6a5d30754f
                Copyright © 2019 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 26 August 2019
                : 30 October 2019
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                Custom metadata
                ao9b02751
                ao9b02751

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