Hydrophilic/Hydrophobic Janus Nanofibers Containing Compound K for Cartilage Regeneration

References

• Bhosale AM, Richardson JB. Articular cartilage: structure, injuries and review of management. Br Med Bull. 2008;87(1):77–95. doi:10.1093/bmb/ldn025
   PubMed Web of Science ®Google Scholar
• Bedi A, Feeley BT, Williams RJ. Management of articular cartilage defects of the knee. J Bone Jt Surg. 2010;92(4):994–1009. doi:10.2106/JBJS.I.00895
   PubMedGoogle Scholar
• Wieland HA, Michaelis M, Kirschbaum BJ, et al. Osteoarthritis-an untreatable disease? Nat Rev Drug Discov. 2005;4(4):331–344. doi:10.1038/nrd1693
   PubMed Web of Science ®Google Scholar
• Armiento AR, Stoddart MJ, Alini M, et al. Biomaterials for articular cartilage tissue engineering: learning from biology. Acta Biomater. 2018;65:1–20. doi:10.1016/j.actbio.2017.11.021
   PubMed Web of Science ®Google Scholar
• Makris EA, Gomoll AH, Malizos KN, et al. Repair and tissue engineering techniques for articular cartilage. Nat Rev Rheumatol. 2015;11(1):21–34. doi:10.1038/nrrheum.2014.157
   PubMed Web of Science ®Google Scholar
• Rana D, Ratheesh G, Ramakrishna S, et al. Ch 13. Nanofiber Composites in Cartilage Tissue Engineering, Nanofiber Composite for Biomedical Applications. Woodhead Publishing; 2017:325–344.
   Google Scholar
• Chen W, Chen S, Morsi Y, et al. Superabsorbent 3D scaffold based on electrospun nanofibers for cartilage tissue engineering. ACS Appl Mater Interfaces. 2016;8(37):24415–24425. doi:10.1021/acsami.6b06825
   PubMed Web of Science ®Google Scholar
• Li WJ, Jiang YJ, Tuan RS. Cell-nanofiber-based cartilage tissue engineering using improved cell seeding, growth factor, and bioreactor technologies. Tissue Eng Part A. 2018;14(5):639–648. doi:10.1089/tea.2007.0136
   Google Scholar
• Chen W, Xu Y, Liu Y, et al. Three-dimensional printed electrospun fiber-based scaffold for cartilage regeneration. Mater Des. 2019;179:107886. doi:10.1016/j.matdes.2019.107886
   Web of Science ®Google Scholar
• Raja IS, Lee SH, Kang MS, et al. The predominant factor influencing cellular behavior on electrospun nanofibrous scaffolds: wettability or surface morphology? Mater Des. 2022;216:110580. doi:10.1016/j.matdes.2022.110580
   Web of Science ®Google Scholar
• Ahmadian E, Eftekhari A, Janas D, et al. Nanofiber scaffolds based on extracellular matrix for articular cartilage engineering: a perspective. Nanotheranostics. 2023;7(1):61–69. doi:10.7150/ntno.78611
   PubMedGoogle Scholar
• Wade RJ, Burdick JA. Advances in nanofibrous scaffolds for biomedical applications: from electrospinning to self-assembly. Nano Today. 2014;9(6):722–742. doi:10.1016/j.nantod.2014.10.002
   Web of Science ®Google Scholar
• Vasita R, Katti DS. Nanofibers and their applications in tissue engineering. Int J Nanomed. 2006;1(1):15–30. doi:10.2147/nano.2006.1.1.15
   PubMed Web of Science ®Google Scholar
• Son HY, Ryu JH, Lee H, et al. Silver‐polydopamine hybrid coatings of electrospun poly(vinyl alcohol) nanofibers. Macromol Mater Eng. 2013;298(5):547–554. doi:10.1002/mame.201200231
   Web of Science ®Google Scholar
• Venugopal J, Low S, Choon AT, et al. Interaction of cells and nanofiber scaffolds in tissue engineering. J Biomed Mater Res B. 2008;84(1):34–48. doi:10.1002/jbm.b.30841
   Google Scholar
• Chen JP, Su CH. Surface modification of electrospun PLLA nanofibers by plasma treatment and cationized gelatin immobilization for cartilage tissue engineering. Acta Biomater. 2011;7(1):234–243. doi:10.1016/j.actbio.2010.08.015
   PubMed Web of Science ®Google Scholar
• Lu Y, Huang J, Yu G, et al. Coaxial electrospun fibers: applications in drug delivery and tissue engineering. Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2016;8(5):654–677. doi:10.1002/wnan.1391
   PubMed Web of Science ®Google Scholar
• Buzgo M, Jakubova R, Mickova A, et al. Time-regulated drug delivery system based on coaxially incorporated platelet α-granules for biomedical use. Nanomedicine. 2013;8(7):1137–1154. doi:10.2217/nnm.12.140
   PubMed Web of Science ®Google Scholar
• Mondal D, Griffith M, Venkatraman SS. Polycaprolactone-based biomaterials for tissue engineering and drug delivery: current scenario and challenges. Int J Polym Mater Polym Biomater. 2016;65(5):255–265. doi:10.1080/00914037.2015.1103241
   Web of Science ®Google Scholar
• Suwantong O. Biomedical applications of electrospun polycaprolactone fiber mats. Polym Adv Technol. 2016;27(10):1264–1273. doi:10.1002/pat.3876
   Web of Science ®Google Scholar
• Janmohammadi M, Nourbakhsh MS. Electrospun polycaprolactone scaffolds for tissue engineering: a review. Int J Polym Mater Polym Biomater. 2019;68(9):527–539. doi:10.1080/00914037.2018.1466139
   Web of Science ®Google Scholar
• Girao AF, Semitela A, Ramalho G, et al. Mimicking nature: fabrication of 3D anisotropic electrospun polycaprolactone scaffolds for cartilage tissue engineering applications. Comp B Eng. 2018;154:99–107. doi:10.1016/j.compositesb.2018.08.001
   Web of Science ®Google Scholar
• Son HY, Ryu JH, Lee H, et al. Bioinspired templating synthesis of metal–polymer hybrid nanostructures within 3D electrospun nanofibers. ACS Appl Mater Interfaces. 2013;5(13):6381–6390. doi:10.1021/am401550p
   PubMed Web of Science ®Google Scholar
• Gupta N, Rao SK, Jaison D, et al. Kaempferol loaded albumin nanoparticles and dexamethasone encapsulation into electrospun polycaprolactone fibrous mat-concurrent release for cartilage regeneration. J Drug Deliv Sci Technol. 2021;64:102666. doi:10.1016/j.jddst.2021.102666
   Web of Science ®Google Scholar
• Asadian M, Onyshchenko I, Thiry D, et al. Thiolation of polycaprolactone (PCL) nanofibers by inductively coupled plasma (ICP) polymerization: physical, chemical and biological properties. Appl Surf Sci. 2019;479:942–952. doi:10.1016/j.apsusc.2019.02.178
   Web of Science ®Google Scholar
• Zhang YZ, Venugopal J, Huang ZM, et al. Characterization of the surface biocompatibility of the electrospun PCL-collagen nanofibers using fibroblasts. Biomacromolecules. 2005;6(5):2583–2589. doi:10.1021/bm050314k
   PubMed Web of Science ®Google Scholar
• Yaseri R, Fadaie M, Mirzaei E, et al. Ebrahiminezhad, Surface modification of polycaprolactone nanofibers through hydrolysis and aminolysis: a comparative study on structural characteristics, mechanical properties, and cellular performance, Sci. Rep. 2023;13(1):9434.
   Google Scholar
• Lo HY, Kuo HT, Huang YY. Application of polycaprolactone as an anti‐adhesion biomaterial film. Artif Organs. 2010;34(8):648–653. doi:10.1111/j.1525-1594.2009.00949.x
   PubMed Web of Science ®Google Scholar
• Chen CH, Chen SH, Shalumon KT, et al. Prevention of peritendinous adhesions with electrospun polyethylene glycol/polycaprolactone nanofibrous membranes. Colloids Surf B. 2015;133:221–230. doi:10.1016/j.colsurfb.2015.06.012
   PubMed Web of Science ®Google Scholar
• Martins A, Pinho ED, Faria S, et al. Surface modification of electrospun polycaprolactone nanofiber meshes by plasma treatment to enhance biological performance. Small. 2009;5(10):1195–1206. doi:10.1002/smll.200801648
   PubMed Web of Science ®Google Scholar
• Yew CHT, Azari P, Choi JR, et al. Electrospun polycaprolactone nanofibers as a reaction membrane for lateral flow assay. Polymers. 2018;10(12):1387. doi:10.3390/polym10121387
   PubMed Web of Science ®Google Scholar
• Rashtchian M, Hivechi A, Bahrami SH, et al. Fabricating alginate/poly (caprolactone) nanofibers with enhanced bio-mechanical properties via cellulose nanocrystal incorporation. Carbohydr Polym. 2020;233:115873. doi:10.1016/j.carbpol.2020.115873
   PubMed Web of Science ®Google Scholar
• Liu Y, Tian K, Hao J, et al. Biomimetic poly(glycerol sebacate)/polycaprolactone blend scaffolds for cartilage tissue engineering. J Mater Sci Mater Med. 2019;30(5):53. doi:10.1007/s10856-019-6257-3
   PubMed Web of Science ®Google Scholar
• Sharifi F, Irani S, Azadegan G, et al. Co-electrospun gelatin-chondroitin sulfate/polycaprolactone nanofibrous scaffolds for cartilage tissue engineering. Bioact Carbohydr Diet Fibre. 2020;22:100215. doi:10.1016/j.bcdf.2020.100215
   Google Scholar
• Shirehjini LM, Sharifi F, Shojaei S, et al. Poly-caprolactone nanofibrous coated with sol-gel alginate/mesenchymal stem cells for cartilage tissue engineering. J Drug Deliv Sci and Technol. 2022;74:103488. doi:10.1016/j.jddst.2022.103488
   Web of Science ®Google Scholar
• Piai JF, da Silva MA, Martins A, et al. Chondroitin sulfate immobilization at the surface of electrospun nanofiber meshes for cartilage tissue regeneration approaches. Appl Surf Sci. 2017;403:112–125. doi:10.1016/j.apsusc.2016.12.135
   Web of Science ®Google Scholar
• Lee P, Tran K, Chang W, et al. Influence of chondroitin sulfate and hyaluronic acid presence in nanofibers and its alignment on the bone marrow stromal cells: cartilage regeneration. J Biomed Nanotechnol. 2014;10(8):1469–1479. doi:10.1166/jbn.2014.1831
   PubMed Web of Science ®Google Scholar
• Kabirkoohian A, Bakhshi H, Irani S, et al. Chemical immobilization of carboxymethyl chitosan on polycaprolactone nanofibers as osteochondral scaffolds. Appl Biochem Biotechnol. 2023;195(6):3888–3899. doi:10.1007/s12010-022-03916-6
   PubMed Web of Science ®Google Scholar
• Yang XD, Yang YY, Ouyang DS, et al. A review of biotransformation and pharmacology of ginsenoside compound K. Fitoterapia. 2015;100:208–220. doi:10.1016/j.fitote.2014.11.019
   PubMed Web of Science ®Google Scholar
• Liu T, Zhu L, Wang L. A narrative review of the pharmacology of ginsenoside compound K. Ann Transl Med. 2022;10(4):234. doi:10.21037/atm-22-501
   PubMed Web of Science ®Google Scholar
• Yang JH, Shin HH, Kim D, et al. Adhesive ginsenoside compound K patches for cartilage tissue regeneration. Regen Biomater. 2023;10:rbad077.
   PubMed Web of Science ®Google Scholar
• Sophia Fox AJ, Bedi A, Rodeo SA. The basic science of articular cartilage: structure, composition, and function. Sports Health. 2009;1(6):461–468. doi:10.1177/1941738109350438
   PubMedGoogle Scholar
• Park D, Yoon M. Compound K, a novel ginsenoside metabolite, inhibits adipocyte differentiation in 3T3-L1 cells: involvement of angiogenesis and MMPs. Biochem Biophys Res Commun. 2012;422(2):263–267. doi:10.1016/j.bbrc.2012.04.142
   PubMed Web of Science ®Google Scholar
• Ryu JH, Messersmith PB, Lee H. Polydopamine surface chemistry: a decade of discovery. ACS Appl Mater Interfaces. 2018;10(9):7523–7540. doi:10.1021/acsami.7b19865
   PubMed Web of Science ®Google Scholar
• Choi SM, Jung HW, Ryu JH, et al. Effect of polydopamine and fluoride ion coating on dental enamel remineralization: an in vitro study. BMC Oral Health. 2023;23(1):526. doi:10.1186/s12903-023-03221-6
   PubMed Web of Science ®Google Scholar
• Kim S, Gim T, Jeong Y, et al. Facile construction of robust multilayered PEG films on polydopamine-coated solid substrates for marine antifouling applications. ACS Appl Mater Interfaces. 2017;10(9):7626–7631. doi:10.1021/acsami.7b07199
   PubMed Web of Science ®Google Scholar
• Nasibova A. Generation of nanoparticles in biological systems and their application prospects. Adv Biol Earth Sci. 2023;8(2):140–146.
   Google Scholar
• Ramazanli VN. Effect of pH and temperature on the synthesis of silver nanoparticles extracted from olive leaf. Adv Biol Earth Sci. 2021;6(2):169–173.
   Google Scholar
• Ahmadov IS, Bandaliyeva AA, Nasibova AN, et al. The synthesis of the silver nanodrugs in the medicinal plant Baikal skullcap (Scutellaria baicalensis Georgi) and their antioxidant, antibacterial activity. Adv Biol Earth Sci. 2020;5(2):103–118.
   Google Scholar
• Kang SI, Shin HH, Yoon G, et al. Double-layer adhesives for preventing anastomotic leakage and reducing post-surgical adhesion. Mater Today Bio. 2023;23:100806. doi:10.1016/j.mtbio.2023.100806
   PubMedGoogle Scholar
• Shin HH, Ryu JH. Bio-inspired self-healing, shear-thinning, and adhesive gallic acid-conjugated chitosan/carbon black composite hydrogels as suture support materials. Biomimetics. 2023;8(7):54. doi:10.3390/biomimetics8070542
   PubMed Web of Science ®Google Scholar
• Kwon HJ, Shin HH, Hyun DH, et al. Carbon black-containing self-healing adhesive hydrogels for endoscopic tattooing. Sci Rep. 2023;13(1):1880. doi:10.1038/s41598-023-28113-1
   PubMed Web of Science ®Google Scholar
• Ju J, Jin S, Kim S, et al. Addressing the shortcomings of polyphenol-derived adhesives: achievement of long shelf life for effective hemostasis. ACS Appl Mater Interfaces. 2022;14(22):25115–25125. doi:10.1021/acsami.2c03930
   PubMed Web of Science ®Google Scholar
• Sanandiya ND, Lee S, Rho S, et al. Tunichrome-inspired pyrogallol functionalized chitosan for tissue adhesion and hemostasis. Carbohydr Polym. 2019;208:77–85. doi:10.1016/j.carbpol.2018.12.017
   PubMed Web of Science ®Google Scholar
• Zeng W, Cheng N-M, Liang X, et al. Electrospun polycaprolactone nanofibrous membranes loaded with baicalin for antibacterial wound dressing.Sci Rep. 2022;12(1):10900. doi:10.1038/s41598-022-13141-0
   PubMed Web of Science ®Google Scholar
• Wang D, Jang J, Kim K, et al. “Tree to bone”: lignin/polycaprolactone nanofibers for hydroxyapatite biomineralization. Biomacromolecules. 2019;20(7):2684–2693. doi:10.1021/acs.biomac.9b00451
   PubMed Web of Science ®Google Scholar
• Song J, Baek IJ, Chun CH, et al. Dysregulation of the NUDT7-PGAM1 axis is responsible for chondrocyte death during osteoarthritis pathogenesis. Nat Commun. 2018;9(1):3427. doi:10.1038/s41467-018-05787-0
   PubMedGoogle Scholar
• Park S, Oh J, Kim YI, et al. Suppression of ABCD2 dysregulates lipid metabolism via dysregulation of miR-141:ACSL4 in human osteoarthritis. Cell Biochem Funct. 2018;36(7):366–376. doi:10.1002/cbf.3356
   PubMed Web of Science ®Google Scholar
• Park S, Baek IJ, Ryu JH, et al. PPARα− ACOT12 axis is responsible for maintaining cartilage homeostasis through modulating de novo lipogenesis. Nat Commun. 2022;13(1):3. doi:10.1038/s41467-021-27738-y
   PubMed Web of Science ®Google Scholar
• Chen Y, Xu W, Shafiq M, et al. Injectable nanofiber microspheres modified with metal phenolic networks for effective osteoarthritis treatment. Acta Biomater. 2023;157:593–608. doi:10.1016/j.actbio.2022.11.040
   PubMed Web of Science ®Google Scholar
• Morgan M, Humphries M, Bass M. Synergistic control of cell adhesion by integrins and syndecans. Nat Rev Mol Cell Biol. 2007;8(12):957–969. doi:10.1038/nrm2289
   PubMed Web of Science ®Google Scholar
• Stienstra R, Mandard S, Patsouris D, et al. Peroxisome proliferator-activated receptor alpha protects against obesity-induced hepatic inflammation. Endocrinology. 2007;148:2753–2763.
   PubMed Web of Science ®Google Scholar
• Zhou JL, Liu SQ, Qiu B, et al. The protective effect of sodium hyaluronate on the cartilage of rabbit osteoarthritis by inhibiting peroxisome proliferator-activated receptor gamma messenger RNA expression. Yonsei Med J. 2009;50(6):832–837. doi:10.3349/ymj.2009.50.6.832
   PubMed Web of Science ®Google Scholar
• Culley KL, Dragomir CL, Chang J, et al. Mouse models of osteoarthritis: surgical model of posttraumatic osteoarthritis induced by destabilization of the medial meniscus. Methods Mol Biol. 2015;1226:143–173.
   PubMedGoogle Scholar
• Ciliberti FK, Aubonnet R, Ramos J, et al. Novel strategies for cartilage assessment, interplay between bone and muscles. Eur J Transl Myol. 2023;33:67–68.
   Google Scholar
• Lin C, Liu L, Zeng C, et al. Activation of mTORC1 in subchondral bone preosteoblasts promotes osteoarthritis by stimulating bone sclerosis and secretion of CXCL12. Bone Res. 2019;7(1):5. doi:10.1038/s41413-018-0041-8
   PubMedGoogle Scholar