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International Journal of Bioprinting 3D-printed EVs for nasal septal defects

new hope for the reconstruction of nasal septal cartilage? downstream small RNA profiling, functional modulation of
Curr Stem Cell Res Ther. 2020;15:144-54. microtia chondrocytes and tissue-engineered ear cartilage
doi: 10.2174/1574888X14666191212160757 regeneration. J Nanobiotechnol. 2022;20:164.
doi: 10.1186/s12951-022-01352-6
7. Rajzer I, Stręk P, Wiatr M, et al. Biomaterials in the
reconstruction of nasal septum perforation. Ann Otol Rhinol 18. Han B, Fang W, Yang Z, et al. Enhancement of chondrogenic
Laryngol. 2021;130:731-7. markers by exosomes derived from cultured human synovial
doi: 10.1177/0003489420970589 fluid-derived cells: a comparative analysis of 2D and 3D
8. Wu N, Liu J, Ma W, et al. Degradable calcium deficient conditions. Biomedicines. 2023;11:3145.
hydroxyapatite/poly(lactic-glycolic acid copolymer) bilayer doi: 10.3390/biomedicines11123145
scaffold through integral molding 3D printing for bone 19. Li Q, Yu H, Zhao F, et al. 3D printing of microenvironment-
defect repair. Biofabrication. 2021;13(2). specific bioinspired and exosome-reinforced hydrogel
doi: 10.1088/1758-5090/abcb48 scaffolds for efficient cartilage and subchondral bone
9. Cao Y, Sang S, An Y, Xiang C, Li Y, Zhen Y. Progress of regeneration. Adv Sci (Weinh). 2023;10:e2303650.
3D printing techniques for nasal cartilage regeneration. doi: 10.1002/advs.202303650
Aesthetic Plast Surg. 2022;46:947-64. 20. Chen J, Zhou D, Nie Z, et al. A scalable coaxial bioprinting
doi: 10.1007/s00266-021-02472-4 technology for mesenchymal stem cell microfiber fabrication
10. Acevedo Rua L, Mumme M, Manferdini C, et al. Engineered and high extracellular vesicle yield. Biofabrication. 2021;14(1).
nasal cartilage for the repair of osteoarthritic knee cartilage doi: 10.1088/1758-5090/ac3b90
defects. Sci Transl Med. 2021;13:eaaz4499. 21. Xu F, Dawson C, Lamb M, et al. Hydrogels for tissue
doi: 10.1126/scitranslmed.aaz4499 engineering: addressing key design needs toward clinical
11. He L, He T, Xing J, et al. Bone marrow mesenchymal stem translation. Front Bioeng Biotechnol. 2022;10:849831.
cell-derived exosomes protect cartilage damage and relieve doi: 10.3389/fbioe.2022.849831
knee osteoarthritis pain in a rat model of osteoarthritis. 22. Xing H, Zhang Z, Mao Q, et al. Injectable exosome-
Stem Cell Res Ther. 2020;11:276. functionalized extracellular matrix hydrogel for metabolism
doi: 10.1186/s13287-020-01781-w balance and pyroptosis regulation in intervertebral disc
12. Xu H, Xu B. BMSC-derived exosomes ameliorate degeneration. J Nanobiotechnol. 2021;19:264.
osteoarthritis by inhibiting pyroptosis of cartilage via doi: 10.1186/s12951-021-00991-5
delivering miR-326 targeting HDAC3 and STAT1//NF-κB 23. Gao F, Xu Z, Liang Q, et al. Osteochondral regeneration with
p65 to chondrocytes. In: Yokota S, ed. Mediators Inflamm. 3D-printed biodegradable high-strength supramolecular
2021:1-26. polymer reinforced-gelatin hydrogel scaffolds. Adv Sci
doi: 10.1155/2021/9972805 (Weinh). 2019;6:1900867.
13. Ha DH, Kim H-K, Lee J, et al. Mesenchymal stem/stromal doi: 10.1002/advs.201900867
cell-derived exosomes for immunomodulatory therapeutics 24. Zhang Y, Li D, Liu Y, et al. 3D-bioprinted anisotropic
and skin regeneration. Cells. 2020;9:1157. bicellular living hydrogels boost osteochondral regeneration
doi: 10.3390/cells9051157 via reconstruction of cartilage-bone interface. Innovation
14. Tienda-Vázquez MA, Hanel JM, Márquez-Arteaga EM, et al. (Camb). 2024;5:100542.
Exosomes: a promising strategy for repair, regeneration and doi: 10.1016/j.xinn.2023.100542
treatment of skin disorders. Cells. 2023;12:1625. 25. Gnatowski P, Gwizdała K, Kurdyn A, Skorek A, Augustin
doi: 10.3390/cells12121625 E, Kucińska-Lipka J. Investigation on filaments for 3D
15. Zhao H, Zhao Z, Li D, Wang X, Dai D, Fu H. Effect study printing of nasal septum cartilage implant. Materials (Basel).
of exosomes derived from platelet-rich plasma in the 2023;16:3534.
treatment of knee cartilage defects in rats. J Orthop Surg Res. doi: 10.3390/ma16093534
2023;18:160. 26. Göttel B, Lucas H, Syrowatka F, et al. In situ gelling
doi: 10.1186/s13018-023-03576-0 amphotericin B nanofibers: a new option for the treatment
16. Yan Z, Yin H, Wu J, et al. Engineering exosomes by three- of Keratomycosis. Front Bioeng Biotechnol. 2020;
dimensional porous scaffold culture of human umbilical 8:600384.
cord mesenchymal stem cells promote osteochondral repair. doi: 10.3389/fbioe.2020.600384
Materials Today Bio. 2023;19:100549. 27. Niu L, Feng C, Shen C, Wang B, Zhang X. PLGA/PLCA
doi: 10.1016/j.mtbio.2023.100549
casting and PLGA/PDPA electrospinning bilayer film for
17. Chen J, Huang T, Liu R, Wang C, Jiang H, Sun H. Congenital prevention of postoperative adhesion. J Biomed Mater Res.
microtia patients: the genetically engineered exosomes 2019;107:2030-2039.
released from porous gelatin methacryloyl hydrogel for doi: 10.1002/jbm.b.34294

Volume 10 Issue 6 (2024) 191 doi: 10.36922/ijb.4118