{"title":"Apigenin Release from Chitosan/Gelatin Membranes Promotes Osteogenic Differentiation of Adipose-Derived Mesenchymal Stem Cells","authors":"Azam Bozorgi, Mozafar Khazaei, Maryam Bozorgi, Zahra Jamalpoor","doi":"10.1007/s40846-023-00832-w","DOIUrl":null,"url":null,"abstract":"<h3 data-test=\"abstract-sub-heading\">Purpose</h3><p>Apigenin is a widespread phytochemical with beneficial effects on osteoblastic differentiation. However, short half-life and unstable chemical structure restrict apigenin application in bone tissue engineering applications. Here, we investigated the impact of apigenin-loaded chitosan/gelatin (Api. Cs/Gel) membranes on the osteogenic differentiation of human adipose-derived mesenchymal stem cells (hADMSCs).</p><h3 data-test=\"abstract-sub-heading\">Methods</h3><p>Api10. Cs/Gel and Api25. Cs/Gel membranes were fabricated using the solution casting method, followed by characterizing their physicochemical and biological properties. hADMSCs were isolated from healthy donors and characterized using flow cytometry. hADMSCs were seeded onto Api. Cs/Gel membranes and cultured under osteogenic differentiation for 7 and 21 days. The expression of osteogenic markers ALP, RUNX2, OCN, and COL1 was assessed using real-time PCR, and calcium mineralization was analyzed using the quantitative Alizarin red S staining.</p><h3 data-test=\"abstract-sub-heading\">Results</h3><p>The Api. Cs/Gel membranes were successfully fabricated, and characterization data confirmed their structural uniformity, chemical homogeneity, cross-linking, and apigenin incorporation. Membranes exhibited favorable degradation, swelling ratio, and long-term apigenin release. The membranes were non-toxic and supported hADMSCs attachment, viability, and proliferation. The expression of ALP, RUNX2, OCN, and COL1 and cellular mineralization increased on day 21, and significant overexpression was observed in hADMSCs seeded onto Apigenin-loaded membranes.</p><h3 data-test=\"abstract-sub-heading\">Conclusion</h3><p>Cs/Gel membranes provided an approving matrix for cellular interactions and apigenin inclusion, followed by a sustained release associated with enhanced osteogenic differentiation of hADMSCs and matrix mineralization.</p>","PeriodicalId":50133,"journal":{"name":"Journal of Medical and Biological Engineering","volume":"32 1","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2023-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medical and Biological Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s40846-023-00832-w","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose
Apigenin is a widespread phytochemical with beneficial effects on osteoblastic differentiation. However, short half-life and unstable chemical structure restrict apigenin application in bone tissue engineering applications. Here, we investigated the impact of apigenin-loaded chitosan/gelatin (Api. Cs/Gel) membranes on the osteogenic differentiation of human adipose-derived mesenchymal stem cells (hADMSCs).
Methods
Api10. Cs/Gel and Api25. Cs/Gel membranes were fabricated using the solution casting method, followed by characterizing their physicochemical and biological properties. hADMSCs were isolated from healthy donors and characterized using flow cytometry. hADMSCs were seeded onto Api. Cs/Gel membranes and cultured under osteogenic differentiation for 7 and 21 days. The expression of osteogenic markers ALP, RUNX2, OCN, and COL1 was assessed using real-time PCR, and calcium mineralization was analyzed using the quantitative Alizarin red S staining.
Results
The Api. Cs/Gel membranes were successfully fabricated, and characterization data confirmed their structural uniformity, chemical homogeneity, cross-linking, and apigenin incorporation. Membranes exhibited favorable degradation, swelling ratio, and long-term apigenin release. The membranes were non-toxic and supported hADMSCs attachment, viability, and proliferation. The expression of ALP, RUNX2, OCN, and COL1 and cellular mineralization increased on day 21, and significant overexpression was observed in hADMSCs seeded onto Apigenin-loaded membranes.
Conclusion
Cs/Gel membranes provided an approving matrix for cellular interactions and apigenin inclusion, followed by a sustained release associated with enhanced osteogenic differentiation of hADMSCs and matrix mineralization.
期刊介绍:
The purpose of Journal of Medical and Biological Engineering, JMBE, is committed to encouraging and providing the standard of biomedical engineering. The journal is devoted to publishing papers related to clinical engineering, biomedical signals, medical imaging, bio-informatics, tissue engineering, and so on. Other than the above articles, any contributions regarding hot issues and technological developments that help reach the purpose are also included.