References
- Mondal, D., S. J. Dixon, K. Mequanint, and A. S. Rizkalla. 2017. Mechanically-competent and cytocompatible polycaprolactone-borophosphosilicate hybrid biomaterials. J. Mech. Behav. Biomed. Mater. 75:180–189. doi:https://doi.org/10.1016/j.jmbbm.2017.07.010
- Lenas, P., M. Moos, and F. P. Luyten. 2009. Developmental engineering: a new paradigm for the design and manufacturing of cell-based products. Part I: from three-dimensional cell growth to biomimetics of in vivo development. Tissue Eng. B Rev. 15:381–394. doi:https://doi.org/10.1089/ten.TEB.2008.0575
- Sheehy, E. J., D. J. Kelly, and F. J. O'Brien. 2019. Biomaterial-based endochondral bone regeneration: a shift from traditional tissue engineering paradigms to developmentally inspired strategies. Mater Today Bio. 3:100009. doi:https://doi.org/10.1016/j.mtbio.2019.100009
- Jain, N., and V. Vogel. 2018. Spatial confinement downsizes the inflammatory response of macrophages. Nat. Mater. 17:1134–1144. doi:https://doi.org/10.1038/s41563-018-0190-6
- El-Habashy, S. E., H. M. Eltaher, A. Gaballah, E. I. Zaki, R. A. Mehanna, and A. H. El-Kamel. 2021. Hybrid bioactive hydroxyapatite/polycaprolactone nanoparticles for enhanced osteogenesis. Mater. Sci. Eng. C Mater. Biol. Appl. 119:111599. doi:https://doi.org/10.1016/j.msec.2020.111599
- Zupančič, Š., S. Baumgartner, Z. Lavrič, M. Petelin, and J. Kristl. 2015. Local delivery of resveratrol using polycaprolactone nanofibers for treatment of periodontal disease. J. Drug Delivery Sci. Technol. 30:408–416. doi:https://doi.org/10.1016/j.jddst.2015.07.009
- Sivakanthan, S., S. Rajendran, A. Gamage, T. Madhujith, and S. Mani. 2020. Antioxidant, and antimicrobial applications of biopolymers: a review. Food Res. Int. 136:109327.
- Tou, J. C. 2015. Resveratrol supplementation affects bone acquisition and osteoporosis: pre-clinical evidence toward translational diet therapy. Biochim. Biophys. Acta. 1852:1186–1194. doi:https://doi.org/10.1016/j.bbadis.2014.10.003
- Sebe, I., B. Kállai-Szabó, I. Oldal, L. Zsidai, and R. Zelkó. 2020. Development of laboratory-scale high-speed rotary devices for a potential pharmaceutical microfibre drug delivery platform. Int. J. Pharm. 588:119740. doi:https://doi.org/10.1016/j.ijpharm.2020.119740
- Machado-Paula, M. M., M. A. F. Corat, M. Lancellotti, G. Mi, F. R. Marciano, M. L. Vega, A. A. Hidalgo, T. J. Webster, and A. O. Lobo. 2020. A comparison between electrospinning and rotary-jet spinning to produce PCL fibers with low bacteria colonization. Mater. Sci. Eng. C Mater. Biol. Appl. 111:110706. doi:https://doi.org/10.1016/j.msec.2020.110706
- Yao, D., L. Huang, J. Ke, M. Zhang, Q. Xiao, and X. Zhu. 2020. Bone metabolism regulation: implications for the treatment of bone diseases. Biomed. Pharmacother. 129:110494. doi:https://doi.org/10.1016/j.biopha.2020.110494
- Webster, T. J., and E. S. Ahn. 2007. Nanostructured biomaterials for tissue engineering bone. Adv. Biochem. Eng. Biotechnol. 103:275–308. doi:https://doi.org/10.1007/10_021
- Rho, J. Y., L. Kuhn-Spearing, and P. Zioupos. 1998. Mechanical properties and the hierarchical structure of bone. Med. Eng. Phys. 20:92–102. doi:https://doi.org/10.1016/S1350-4533(98)00007-1
- Henkel, J., M. A. Woodruff, D. R. Epari, R. Steck, V. Glatt, I. C. Dickinson, P. F. Choong, M. A. Schuetz, and D. W. Hutmacher. 2013. Bone regeneration based on tissue engineering conceptions – a 21st century perspective. Bone Res. 1:216–248. doi:https://doi.org/10.4248/BR201303002
- Kong, C. H., C. Steffi, Z. Shi, and W. Wang. 2018. Development of mesoporous bioactive glass nanoparticles and its use in bone tissue engineering. J. Biomed. Mater. Res. B Appl. Biomater. 106:2878–2887. doi:https://doi.org/10.1002/jbm.b.34143
- Yan, Y., H. Chen, H. Zhang, C. Guo, K. Yang, K. Chen, R. Cheng, N. Qian, N. Sandler, Y. S. Zhang, H. Shen, J. Qi, W. Cui, and L. Deng. 2019. Vascularized 3D printed scaffolds for promoting bone regeneration. Biomaterials 190–191:97–110. doi:https://doi.org/10.1016/j.biomaterials.2018.10.033
- Baker, R. M., L. F. Tseng, M. T. Iannolo, M. E. Oest, and J. H. Henderson. 2016. Self-deploying shape memory polymer scaffolds for grafting and stabilizing complex bone defects: a mouse femoral segmental defect study. Biomaterials 76:388–398. doi:https://doi.org/10.1016/j.biomaterials.2015.10.064
- Hassan, K. S. 2009. Autogenous bone graft combined with polylactic polyglycolic acid polymer for treatment of dehiscence around immediate dental implants. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 108:e19–e25. doi:https://doi.org/10.1016/j.tripleo.2009.07.023
- Dwivedi, R., S. Kumar, R. Pandey, A. Mahajan, D. Nandana, D. S. Katti, and D. Mehrotra. 2020. Polycaprolactone as biomaterial for bone scaffolds: review of literature. J. Oral Biol. Craniofac. Res. 10:381–388. doi:https://doi.org/10.1016/j.jobcr.2019.10.003
- Mondal, D., M. Griffith, and S. S. Venkatraman. 2016. Polycaprolactone-based biomaterials for tissue engineering and drug delivery: current scenario and challenges. Int. J. Polym. Mater. Polym. Biomater. 65:255–265. doi:https://doi.org/10.1080/00914037.2015.1103241
- Vastano, B. C., Y. Chen, N. Zhu, C. T. Ho, Z. Zhou, and R. T. Rosen. 2000. Isolation and identification of stilbenes in two varieties of Polygonum cuspidatum. J. Agric. Food Chem. 48:253–256. doi:https://doi.org/10.1021/jf9909196
- Kristl, J., K. Teskac, C. Caddeo, Z. Abramović, and M. Sentjurc. 2009. Improvements of cellular stress response on resveratrol in liposomes. Eur. J. Pharm. Biopharm. 73:253–259. doi:https://doi.org/10.1016/j.ejpb.2009.06.006
- Amri, A., J. C. Chaumeil, S. Sfar, and C. Charrueau. 2012. Administration of resveratrol: what formulation solutions to bioavailability limitations? J. Control Release. 158:182–193. doi:https://doi.org/10.1016/j.jconrel.2011.09.083
- Li, L., M. Yu, Y. Li, Q. Li, H. Yang, M. Zheng, Y. Han, D. Lu, S. Lu, and L. Gui. 2021. Synergistic anti-inflammatory and osteogenic n-HA/resveratrol/chitosan composite microspheres for osteoporotic bone regeneration. Bioact. Mater. 6:1255–1266. doi:https://doi.org/10.1016/j.bioactmat.2020.10.018
- Hao, Y., M. Wu, and J. Wang. 2020. Fibroblast growth factor-2 ameliorates tumor necrosis factor-alpha-induced osteogenic damage of human bone mesenchymal stem cells by improving oxidative phosphorylation. Mol. Cell. Probes. 52:101538. doi:https://doi.org/10.1016/j.mcp.2020.101538
- Tseng, P. C., S. M. Hou, R. J. Chen, H. W. Peng, C. F. Hsieh, M. L. Kuo, and M. L. Yen. 2011. Resveratrol promotes osteogenesis of human mesenchymal stem cells by upregulating RUNX2 gene expression via the SIRT1/FOXO3A axis. J. Bone Miner. Res. 26:2552–2563. doi:https://doi.org/10.1002/jbmr.460
- Peng, H., H. Xiong, J. Li, M. Xie, Y. Liu, C. Bai, and L. Chen. 2010. Vanillin cross-linked chitosan microspheres for controlled release of resveratrol. Food Chem. 121:23–28. doi:https://doi.org/10.1016/j.foodchem.2009.11.085
- Frozza, R. L., A. Bernardi, K. Paese, J. B. Hoppe, T. da Silva, A. M. Battastini, A. R. Pohlmann, S. S. Guterres, and C. Salbego. 2010. Characterization of trans-resveratrol-loaded lipid-core nanocapsules and tissue distribution studies in rats. J. Biomed. Nanotechnol. 6:694–703. doi:https://doi.org/10.1166/jbn.2010.1161
- Wu, R., Y. Li, M. Shen, X. Yang, L. Zhang, X. Ke, G. Yang, C. Gao, Z. Gou, and S. Xu. 2021. Bone tissue regeneration: the role of finely tuned pore architecture of bioactive scaffolds before clinical translation. Bioact. Mater. 6:1242–1254. doi:https://doi.org/10.1016/j.bioactmat.2020.11.003
- Zadpoor, A. A. 2015. Bone tissue regeneration: the role of scaffold geometry. Biomater. Sci. 3:231–245. doi:https://doi.org/10.1039/c4bm00291a
- Dhandapani, R., P. D. Krishnan, A. Zennifer, V. Kannan, A. Manigandan, M. R. Arul, D. Jaiswal, A. Subramanian, S. G. Kumbar, and S. Sethuraman. 2020. Additive manufacturing of biodegradable porous orthopaedic screw. Bioact. Mater. 5:458–467. doi:https://doi.org/10.1016/j.bioactmat.2020.03.009
- Arastouei, M., M. Khodaei, S. M. Atyabi, and M. J. Nodoushan. 2020. Poly lactic acid-akermanite composite scaffolds prepared by fused filament fabrication for bone tissue engineering. J. Mater. Res. Tech. 9:14540–14548. doi:https://doi.org/10.1016/j.jmrt.2020.10.036
- Turnbull, G., J. Clarke, F. Picard, P. Riches, L. Jia, F. Han, B. Li, and W. Shu. 2018. 3D bioactive composite scaffolds for bone tissue engineering. Bioact. Mater. 3:278–314. doi:https://doi.org/10.1016/j.bioactmat.2017.10.001
- de Andrade Pinto, S. A., F. J. de Nadai Dias, G. Brasil Camargo Cardoso, A. R. Dos Santos Junior, A. A. de Aro, D. S. Pino, D. H. Meneghetti, R. P. Vitti, G. M. T. Dos Santos, and C. A. de Carvalho Zavaglia. 2021. Polycaprolactone/beta-tricalcium phosphate scaffolds obtained via rotary jet-spinning: in vitro and in vivo evaluation. Cells Tissues Organs. 1–15. doi:https://doi.org/10.1159/000511570
- Cardoso, G. B., A. B. Machado-Silva, M. Sabino, A. R. Santos, Jr, and C. A. Zavaglia. 2014. Novel hybrid membrane of chitosan/poly (ε-caprolactone) for tissue engineering. Biomatter 4:e29508. doi:https://doi.org/10.4161/biom.29508
- Ardi, A., A. Fauzi, A. Rajak, and K. Khairurrijal. 2021. The effect of rotational speed of rotary forcespinning to the morphology of polyvinylpyrrolidone (PVP) fibers with garlic extract. Mater. Today Proc. 44:3403–1016. doi:https://doi.org/10.1016/j.matpr.2020.11.1024
- Munir, M. M., A. Fauzi, A. Y. Nuryantini, Nursuhud, E. Sofiari, and K. Khairurrijal 2015. Optimization of solvent system and polymer concentration for synthesis of polyvinyl alcohol (PVA) fiber using rotary forcespinning technique. Adv. Mater. Res. 1123:20–23. doi:https://doi.org/10.4028/www.scientific.net/AMR.1123.20
- Zahra, F., A. Fauzi, M. M. Munir, and K. Khairurrijal. 2019. Synthesis and characterization of rotary forcespun polyvinylpyrrolidone fibers loaded by garlic (Allium sativum) extract. IOP Conf. Ser: Mater. Sci. Eng. 515:012005. doi:https://doi.org/10.1088/1757-899X/515/1/012005
- Priyanto, A., D. Hapidin, T. Suciati, and K. Khairurrijal. 2022. Current developments on rotary forcespun nanofibers and prospects for edible applications. Food Eng. Rev. 1–27. doi:https://doi.org/10.1007/s12393-021-09304-w
- Zupančič, Š., Z. Lavrič, and J. Kristl. 2015. Stability and solubility of trans-resveratrol are strongly influenced by pH and temperature. Eur. J. Pharm. Biopharm. 93:196–204. doi:https://doi.org/10.1016/j.ejpb.2015.04.002
- Kolouchová-Hanzlı́ková, I., K. Melzoch, V. Filip, and J. Šmidrkal. 2004. Rapid method for resveratrol determination by HPLC with electrochemical and UV detections in wines. Food Chem. 87:151–158. doi:https://doi.org/10.1016/j.foodchem.2004.01.028
- Saquib, U., T. T. Kelley, S. K. Panguluri, D. Liu, R. Savai, M. S. Baig, and S. C. Schurer. 2018. Polypharmacology or promiscuity? Structural interactions of resveratrol with its bandwagon of targets. Front. Pharmacol. 9:1201.
- Bartnikowski, M., T. R. Dargaville, S. Ivanovski, and D. W. Hutmacher. 2019. Degradation mechanisms of polycaprolactone in the context of chemistry, geometry, and environment. Progress Polymer Sci. 96:1–20. doi:https://doi.org/10.1016/j.progpolymsci.2019.05.004
- Yang, C., X. Gao, M. R. Younis, N. T. Blum, S. Lei, D. Zhang, Y. Luo, P. Huang, and J. Lin. 2021. Non-invasive monitoring of in vivo bone regeneration based on alkaline phosphatase-responsive scaffolds. Chem. Eng. J. 408:127959. doi:https://doi.org/10.1016/j.cej.2020.127959
- Summerlin, N., E. Soo, S. Thakur, Z. Qu, S. Jambhrunkar, and A. Popat. 2015. Resveratrol nanoformulations: challenges and opportunities. Int. J. Pharm. 479:282–290. doi:https://doi.org/10.1016/j.ijpharm.2015.01.003