Elucidation of differential mineralisation on native and regenerated silk matrices

Materials Science and Engineering C

Volumn 68, Issue , 2016, Pages 663-674

  Midha, Swati ^a   Tripathi, Rohit ^a   Geng, Hua ^b   Lee, Peter D ^b   Ghosh, Sourabh ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY DELHI   (India)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

Hydroxyapatite; Mineralisation; Silk fibroin; Simulated body fluid; Textile braid

Indexed keywords

AMIDES; ANIMALS; BONE; CHLORINE COMPOUNDS; DEPOSITION; HYDROXYAPATITE; NANOCOMPOSITE FILMS; NANOCOMPOSITES; NANOCRYSTALS; NUCLEATION; SPINNING (FIBERS); SURFACE ROUGHNESS; TEXTILES; WEAVING;

BOMBYX MORI SILKWORM; ELECTROSTATIC ATTRACTIONS; MINERALISATION; ORTHOPAEDIC APPLICATIONS; PREFERENTIAL GROWTH; SECONDARY CONFORMATION; SILK FIBROIN; SIMULATED BODY FLUIDS;

MINERALOGY;

ARTIFICIAL MEMBRANE; BIOMIMETIC MATERIAL; FIBROIN; NANOPARTICLE;

ANIMAL; ARTIFICIAL MEMBRANE; BOMBYX; CHEMISTRY;

ANIMALS; BIOMIMETIC MATERIALS; BOMBYX; FIBROINS; MEMBRANES, ARTIFICIAL; NANOPARTICLES;

EID: 84988260228     PISSN: 09284931     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.msec.2016.06.041     Document Type: Article

References (51)

1. [1] Iafisco, M., Palazzo, B., Ito, T., Otsuka, M., Senna, M., Delgado-Lopez, J., et al. Preparation of core-shell poly(L-lactic) acid-nanocrystalline apatite hollow microspheres for bone repairing applications. J. Mater. Sci. Mater. Med. 23 (2012), 2659–2669.
2. [2] Wang, J., Yu, F., Qu, L., Meng, X., Wen, G., Study of synthesis of nano-hydroxyapatite using a silk fibroin template. Biomed. Mater., 5, 2010, 041002.
3. [3] Gomez-Morales, J., Iafisco, M., Delgado-Lopez, J.M., Sarda, S., Drouet, C., Progress on the preparation of nanocrystalline apatites and surface characterization: overview of fundamental and applied aspects. Prog. Cryst. Growth Charact. Mater. 59 (2013), 1–46.
4. [4] Drouet, C., Apatite formation: why it may not work as planned, and how to conclusively identify apatite compounds. BioMed Res. Int., 2013, 2013.
5. [5] Park, S.H., Gil, E.S., Shi, H., Kim, H.J., Lee, K., Kaplan, D.L., Relationships between degradability of silk scaffolds and osteogenesis. Biomaterials 31 (2010), 6162–6172.
6. [6] Hu, X., Park, S.H., Gil, E.S., Xia, X.X., Weiss, A.S., Kaplan, D.L., The influence of elasticity and surface roughness on myogenic and osteogenic-differentiation of cells on silk-elastin biomaterials. Biomaterials 32 (2011), 8979–8989.
7. [7] Panilaitis, B., Altman, G.H., Chen, J., Jin, H.J., Karageorgiou, V., Kaplan, D.L., Macrophage responses to silk. Biomaterials 24 (2003), 3079–3085.
8. [8] Bhattacharjee, M., Schultz-Thater, E., Trella, E., Miot, S., Das, S., Loparic, M., et al. The role of 3D structure and protein conformation on the innate and adaptive immune responses to silk-based biomaterials. Biomaterials 34 (2013), 8161–8171.
9. [9] Melke, J., Midha, S., Ghosh, S., Ito, K., Hofmann, S., Silk fibroin as biomaterial for bone tissue engineering. Acta Biomater. 31 (2016), 1–16.
10. [10] Yang, M., He, W., Shuai, Y., Min, S., Zhu, L., Nucleation of hydroxyapatite crystals by self-assembled Bombyx mori silk fibroin. J. Polym. Sci. B Polym. Phys. 51 (2013), 742–748.
11. [11] Vetsch, J.R., Paulsen, S.J., Muller, R., Hofmann, S., Effect of fetal bovine serum on mineralisation in silk fibroin scaffolds. Acta Biomater. 13 (2015), 277–285.
12. [12] Lee, M.J., Park, J.B., Kim, H.H., Ki, C.S., Park, S.Y., Kim, H.J., et al. Surface coating of hydroxyapatite on silk nanofibre through biomineralisation using ten times concentrated simulated body fluid and the evaluation for bone regeneration. Macromol. Res. 22 (2014), 710–716.
13. [13] Kim, H.J., Kim, U.J., Kim, H.S., Li, C., Wada, M., Leisk, G.G., et al. Bone tissue engineering with premineralised silk scaffolds. Bone 42 (2008), 1226–1234.
14. [14] Perrone, G.S., Leisk, G.G., Lo, T.J., Moreau, J.E., Haas, D.S., Papenburg, B.J., et al. The use of silk-based devices for fracture fixation. Nat. Commun., 5, 2014, 3385.
15. [15] Kino, R., Ikoma, T., Monkawa, A., Yunoki, S., Munekata, M., Tanaka, J., et al. Deposition of bone-like apatite on modified silk fibroin films from simulated body fluid. J. Appl. Polym. Sci. 99 (2006), 2822–2830.
16. [16] Lin, F., Li, Y., Jin, J., Cai, Y., Wei, K., Yao, J., Deposition behavior and properties of silk fibroin scaffolds soaked in simulated body fluid. Mater. Chem. Phys. 111 (2008), 92–97.
17. [17] Radev, L., Gerganov, T., Georgiev, H., Kolev, A., Vassileva, V., Silk fibroin/calcium phosphate silicate composites: in vitro bioactivity. Int. J. Mater. Chem. 3 (2013), 8–15.
18. [18] He, X., Huang, X., Lu, Q., Bai, S., Zhu, H., Nanoscale control of silks for regular hydroxyapatite formation. Prog. Nat. Sci.: Mater. Int. 22 (2012), 115–119.
19. [19] Koebley, S.R., Thorpe, D., Pang, P., Chrisochoides, P., Greving, I., Vollrath, F., et al. Silk reconstitution disrupts fibroin self-assembly. Biomacromolecules 16 (2015), 2796–2804.
20. [20] Marelli, B., Ghezzi, C.E., Alessandrino, A., Barralet, J.E., Freddi, G., Nazhat, S.N., Silk fibroin derived polypeptide-induced biomineralisation of collagen. Biomaterials 33 (2012), 102–108.
21. [21] Dubey, P., Murab, S., Karmakar, S., Chowdhury, P.K., Ghosh, S., Modulation of self-assembly process of fibroin: an insight for regulating the conformation of silk biomaterials. Biomacromolecules 16 (2015), 3936–3944.
22. [22] Kong, X.D., Cui, F.Z., Wang, X.M., Zhang, M., Zhang, W., Silk fibroin regulated mineralisation of hydroxyapatite nanocrystals. J. Cryst. Growth 270 (2004), 197–202.
23. [23] Ghosh, S., Parker, S.T., Wang, X., Kaplan, D.L., Lewis, J.A., Direct-write assembly of microperiodic silk fibroin scaffolds for tissue engineering applications. Adv. Funct. Mater. 18 (2008), 1883–1889.
24. [24] Murab, S., Chameettachal, S., Bhattacharjee, M., Das, S., Kaplan, D.L., Ghosh, S., Matrix-embedded cytokines to simulate osteoarthritis-like cartilage microenvironments. Tissue Eng. A 19 (2013), 1733–1753.
25. [25] Kokubo, T., Kushitani, H., Sakka, S., Kitsugi, T., Yamamuro, T., Solutions able to reproduce in vivo surface-structure changes in bioactive glass-ceramic A–W. J. Biomed. Mater. Res. 24 (1990), 721–734.
26. [26] Takeuchi, A., Ohtsuki, C., Miyazaki, T., Tanaka, H., Yamazaki, M., Tanihara, M., Deposition of bone-like apatite on silk fiber in a solution that mimics extracellular fluid. J. Biomed. Mater. Res. A 65 (2003), 283–289.
27. [27] Parfitt, A.M., Bone histomorphometry: standardization of nomenclature, symbols and units (summary of proposed system). Bone 9 (1988), 67–69.
28. [28] Fyhrie, D.P., Zauel, R., Directional tortuosity as a predictor of modulus damage for vertebral cancellous bone. J. Biomech. Eng., 137, 2015, 011007.
29. [29] De Nardo, L., Bertoldi, S., Tanzi, M.C., Haugen, H.J., Farè, S., Shape memory polymer cellular solid design for medical applications. Smart Mater. Struct., 20, 2011, 035004.
30. [30] Azaroff, L.V., Elements of X-ray Crystallography. 1968, McGraw-Hill, New York.
31. [31] Cai, Y., Jin, J., Mei, D., Xia, N., Yao, J., Effect of silk sericin on assembly of hydroxyapatite nanocrystals into enamel prism-like structure. J. Mater. Chem. 19 (2009), 5751–5758.
32. [32] Ferraz, M.P., The role of dialysis and freezing on structural conformation, thermal properties and morphology of silk fibroin hydrogels. Biomatter, 4, 2014, e28536.
33. [33] Rnjak-Kovacina, J., Wray, L.S., Burke, K.A., Torregrosa, T., Golinski, J.M., Huang, W., Kaplan, D.L., Lyophilized silk sponges: a versatile biomaterial platform for soft tissue engineering. ACS Biomater. Sci. Eng. 1 (2015), 260–270.
34. [34] Zhang, W., Liao, S.S., Cui, F.Z., Hierarchical self-assembly of nano-fibrils in mineralised collagen. Chem. Mater. 15 (2003), 3221–3226.
35. [35] Ferraz, M.P., Monteiro, F.J., Manuel, C.M., Hydroxyapatite nanoparticles: a review of preparation methodologies. J. Appl. Biomater. Biomech. 2 (2004), 74–80.
36. [36] Terada, D., Yokoyama, Y., Hattori, S., Kobayashi, H., Tamada, Y., The outermost surface properties of silk fibroin films reflect ethanol-treatment conditions used in biomaterial preparation. Mater. Sci. Eng. C 58 (2016), 119–126.
37. [37] Li, Y., Cai, Y., Kong, X., Yao, J., Anisotropic growth of hydroxyapatite on the silk fibroin films. Appl. Surf. Sci. 255 (2008), 1681–1685.
38. [38] Mahamid, J., Aichmayer, B., Shimoni, E., Ziblat, R., Li, C., Siegel, S., et al. Mapping amorphous calcium phosphate transformation into crystalline mineral from the cell to the bone in zebrafish fin rays. Proc. Natl. Acad. Sci. U. S. A. 107 (2010), 6316–6321.
39. [39] Beniash, E., Metzler, R.A., Lam, R.S.K., Gilbert, P.U.P.A., Transient amorphous calcium phosphate in forming enamel. J. Struct. Biol. 166 (2009), 133–143.
40. [40] Dey, A., Bomans, P.H., Muller, F.A., Will, J., Frederik, P.M., de With, G., et al. The role of prenucleation clusters in surface-induced calcium phosphate crystallisation. Nat. Mater. 9 (2010), 1010–1014.
41. [41] Meldrum, F.C., Colfen, H., Controlling mineral morphologies and structures in biological and synthetic systems. Chem. Rev. 108 (2008), 4332–4432.
42. [42] Hunter, G.K., Interfacial aspects of biomineralisation. Curr. Opinion Solid State Mater. Sci. 1 (1996), 430–435.
43. [43] Figueroa, I.A., Novelo-Peralta, O., Flores-Morales, C., Gonzalez-Tenorio, R., Pina-Barba, M.C., Synthesis and characterization of biocompatible-nanohydroxyapatite crystals obtained by a modified sol-gel processing. Biomatter 2 (2012), 71–76.
44. [44] Qiu, Z., Cui, Y., Tao, C., Zhang, Z., Tang, P., Mao, K., et al. Mineralised collagen: rationale, current status, and clinical applications. Materials 8 (2015), 4733–4750.
45. [45] Boonrungsiman, S., Gentleman, E., Carzaniga, R., Evans, N.D., McComb, D.W., Porter, A.E., et al. The role of intracellular calcium phosphate in osteoblast-mediated bone apatite formation. PNAS 109 (2012), 14170–14175.
46. [46] Wang, J., Zhou, W., Hu, W., Zhou, L., Wang, S., Zhang, S., Collagen/silk fibroin bi-template induced biomimetic bone-like substitutes. J. Biomed. Mater. Res. A 99:A (2011), 327–334.
47. [47] Lochhead, M.J., Letellier, S.R., Vogel, V., Assessing the role of interfacial electrostatics in oriented mineral nucleation at charged organic monolayers. J. Phys. Chem. B 101 (1997), 10821–10827.
48. [48] Randolph, A.D., Larson, M.A., Theory of Particulate Processes. 1988, Elsevier.
49. [49] Rodríguez-Clemente, R., López-Macipe, a., Gómez-Morales, J., Torrent-Burgués, J., Castaño, V.M., Hydroxyapatite precipitation: a case of nucleation-aggregation-agglomeration-growth mechanism. J. Eur. Ceram. Soc. 18 (1998), 1351–1356.
50. [50] Gomez-Morales, J., Torrent-Burgues, J., Rodriguez-Clemente, R., Crystal size distribution of hydroxyapatite precipitated in a MSMPR reactor. Cryst. Res. Technol. 36 (2001), 1065–1074.
51. [51] Midha, S., Murab, S., Ghosh, S., Osteogenic signaling on silk-based matrices. Biomaterials 97 (2016), 133–153.