Effect of nanotubes and apatite on growth factor release from PLLA scaffolds
2010; Wiley; Volume: 5; Issue: 6 Linguagem: Inglês
10.1002/term.339
ISSN1932-7005
AutoresMeike van der Zande, X. Frank Walboomers, Beatriz Olalde, M. J. Jurado, J.I. Álava, Otto C. Boerman, John A. Jansen,
Tópico(s)Graphene and Nanomaterials Applications
ResumoJournal of Tissue Engineering and Regenerative MedicineVolume 5, Issue 6 p. 476-482 Research Article Effect of nanotubes and apatite on growth factor release from PLLA scaffolds Meike van der Zande, Meike van der Zande Department of Biomaterials, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The NetherlandsSearch for more papers by this authorX. Frank Walboomers, X. Frank Walboomers Department of Biomaterials, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The NetherlandsSearch for more papers by this authorBeatriz Olalde, Beatriz Olalde INASMET Foundation, Materials Research Centre, San Sebastian, SpainSearch for more papers by this authorMaria J. Jurado, Maria J. Jurado INASMET Foundation, Materials Research Centre, San Sebastian, SpainSearch for more papers by this authorJ. Iñaki Álava, J. Iñaki Álava INASMET Foundation, Materials Research Centre, San Sebastian, SpainSearch for more papers by this authorOtto C. Boerman, Otto C. Boerman Department of Nuclear Medicine, Radboud University Nijmegen Medical Centre, Nijmegen, The NetherlandsSearch for more papers by this authorJohn A. Jansen, Corresponding Author John A. Jansen [email protected] Department of Biomaterials, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The NetherlandsRadboud University Nijmegen Medical Centre, Department of Biomaterials 309, PO Box 9101, 6500 HB Nijmegen, The Netherlands.Search for more papers by this author Meike van der Zande, Meike van der Zande Department of Biomaterials, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The NetherlandsSearch for more papers by this authorX. Frank Walboomers, X. Frank Walboomers Department of Biomaterials, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The NetherlandsSearch for more papers by this authorBeatriz Olalde, Beatriz Olalde INASMET Foundation, Materials Research Centre, San Sebastian, SpainSearch for more papers by this authorMaria J. Jurado, Maria J. Jurado INASMET Foundation, Materials Research Centre, San Sebastian, SpainSearch for more papers by this authorJ. Iñaki Álava, J. Iñaki Álava INASMET Foundation, Materials Research Centre, San Sebastian, SpainSearch for more papers by this authorOtto C. Boerman, Otto C. Boerman Department of Nuclear Medicine, Radboud University Nijmegen Medical Centre, Nijmegen, The NetherlandsSearch for more papers by this authorJohn A. Jansen, Corresponding Author John A. Jansen [email protected] Department of Biomaterials, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The NetherlandsRadboud University Nijmegen Medical Centre, Department of Biomaterials 309, PO Box 9101, 6500 HB Nijmegen, The Netherlands.Search for more papers by this author First published: 08 September 2010 https://doi.org/10.1002/term.339Citations: 8Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Abstract There is an evident clinical need for artificial bone restorative materials. In this respect, novel composites based on poly(L-lactic acid) (PLLA) have been described. The bone response of such polymer-based composites is usually improved by the addition of bone morphogenetic protein-2 (BMP-2). However, released BMP-2 is cleared almost immediately from the site of implantation by diffusion, whereas a prolonged retention of BMP-2 onto the scaffold has been suggested to be more favourable. Besides the ability to improve the mechanical strength and osteoconductivity of polymeric scaffolds, both carbon nanotubes (CNTs) and microhydroxyapatite (µHA) have been described to facilitate such retention of BMP-2 when incorporated into a composite scaffold. Therefore, in the current study, radiolabelled BMP-2 was loaded onto plain PLLA and composite PLLA–CNT–µHA scaffolds. Subsequently, the scaffolds were implanted subcutaneously for 5 weeks in rats and BMP-2 release was measured. Release started with an initial phase of quick release, followed by a gradual release of BMP-2. Both scaffold types comprised the same in vivo release properties for BMP-2. The bioactivity of the BMP-2 remained unaltered. It can be concluded that incorporated CNTs and µHA did not affect BMP-2 release from composite scaffold materials. Copyright © 2010 John Wiley & Sons, Ltd. References Abarrategi A, Gutierrez MC, Moreno-Vicente C, et al. 2008; Multiwall carbon nanotube scaffolds for tissue engineering purposes. Biomaterials 29(1): 94–102. Akman AC, Tigli RS, Gümüsderelioglu MS, et al. 2009; bFGF-loaded HA–Chitosan: a promising scaffold for periodontal tissue engineering. J Biomed Mater Res A 92A: 953–962. Anderson JM, Shive MS. 1997; Biodegradation and biocompatibility of PLA and PLGA microspheres. Adv Drug Deliv Rev 28(1): 5–24. Armentano I, Dottori M, Puglia D, et al. 2008; Effects of carbon nanotubes (CNTs) on the processing and in vitro degradation of poly(DL-lactide-co-glycolide)/CNT films. J Mater Sci Mater Med 19(6): 2377–2387. Cai D, Doughty CA, Potocky TB, et al. 2007; Carbon nanotube-mediated delivery of nucleic acids does not result in non-specific activation of B lymphocytes. Nanotechnology 18: 1–10. Chang PC, Liu BY, Liu CM, et al. 2007; Bone tissue engineering withnovel rhBMP2–PLLA composite scaffolds. J Biomed Mater Res A 81A(4): 771–780. Chen RJ, Bangsaruntip S, Drouvalakis KA, et al. 2003; Noncovalent functionalization of carbon nanotubes for highly specific electronic biosensors. Proc Natl Acad Sci USA 100(9): 4984–4989. Cui D, Tian F, Ozkan CS, et al. 2005; Effect of single wall carbon nanotubes on human HEK293 cells. Toxicol Lett 155(1): 73–85. Devin JE, Attawia MA, Laurencin CT. 1996; Three-dimensional degradable porous polymer–ceramic matrices for use in bone repair. J Biomater Sci Polym Ed 7(8): 661–669. Ding L, Stilwell J, Zhang T, et al. 2005; Molecular characterization of the cytotoxic mechanism of multiwall carbon nanotubes and nano-onions on human skin fibroblast. Nano Lett 5(12): 2448–2464. Feng JT, Sui JH, Cai W, et al. 2008; Microstructure and mechanical properties of carboxylated carbon nanotubes/poly(L-lactic acid) composite. J Compos Mater 42(16): 1587–1595. Fraker PJ, Speck JC. 1978; Protein and cell-membrane iodinations with a sparingly soluble chloramide, 1,3,4,6-tetrachloro-3A,6A-diphenylglycoluril. Biochem Biophys Res Commun 80(4): 849–857. Fu YC, Nie H, Ho ML, et al. 2008; Optimized bone regeneration based on sustained release from three-dimensional fibrous PLGA/HAp composite scaffolds loaded with BMP-2. Biotechnol Bioeng 99(4): 996–1006. Harrison BS, Atala A. 2007; Carbon nanotube applications for tissue engineering. Biomaterials 28(2): 344–353. Helland A, Wick P, Koehler A, et al. 2008; Reviewing the environmental and human health knowledge base of carbon nanotubes. Cien Saude Colet 13(2): 441–452. Huang YX, Ren J, Chen C, et al. 2008; Preparation and properties of poly(lactide-co-glycolide) (PLGA)/nano-hydroxyapatite (NHA) scaffolds by thermally induced phase separation and rabbit MSCs culture on scaffolds. J Biomater Appl 22(5): 409–432. Huczko A, Lange H. 2001; Carbon nanotubes: experimental evidence for a null risk of skin irritation and allergy. Fullerene Sci Technol 9(2): 247–250. Jarcho M, Kay JF, Gumaer KI, et al. 1977; Tissue, cellular and subcellular events at a bone–ceramic hydroxy-apatite interface. J Bioeng 1(2): 79–92. Keller S, Nickel J, Zhang JL, et al. 2004; Molecular recognition of BMP-2 and BMP receptor IA. Nat Struct Mol Biol 11(5): 481–488. Kim K, Fisher JP. 2007; Nanoparticle technology in bone tissue engineering. J Drug Target 15(4): 241–252. Kim SS, Park MS, Jeon O, et al. 2006; Poly(lactide-co-glycolide)/hydroxyapatite composite scaffolds for bone tissue engineering. Biomaterials 27(8): 1399–1409. Miki T, Masaka K, Imai Y, et al. 2000; Experience with freeze-dried PGLA/HA/rhBMP-2 as a bone graft substitute. J Craniomaxillofac Surg 28(5): 294–299. Moon SI, Jin F, Lee C, et al. 2005; Novel carbon nanotube/poly(L-lactic acid) nanocomposites; their modulus, thermal stability, and electrical conductivity. Macromol Sympos 224: 287–295. Na K, Kim SW, Sun BK, et al. 2007; Osteogenic differentiation of rabbit mesenchymal stem cells in thermo-reversible hydrogel constructs containing hydroxyapatite and bone morphogenic protein-2 (BMP-2). Biomaterials 28(16): 2631–2637. Nie H, Soh BW, Fu YC, et al. 2008; Three-dimensional fibrous PLGA/HAp composite scaffold for BMP-2 delivery. Biotechnol Bioeng 99(1): 223–234. Niederwanger M, Urist MR. 1996; Demineralized bone matrix supplied by bone banks for a carrier of recombinant human bone morphogenetic protein (rhBMP-2): a substitute for autogeneic bone grafts. J Oral Implantol 22(3–4): 210–215. Pistner H, Bendix DR, Muhling J, et al. 1993; Poly(L-Lactide)—A long-term degradation study in vivo. 3. Anal Charact Biomater 14(4): 291–298. Ruhe PQ, Boerman OC, Russel FGM, et al. 2006; In vivo release of rhBMP-2 loaded porous calcium phosphate cement pretreated with albumin. J Mater Sci Mater Med 17(10): 919–927. Sayes CM, Liang F, Hudson JL, et al. 2006; Functionalization density dependence of single-walled carbon nanotubes cytotoxicity in vitro. Toxicol Lett 161(2): 135–142. Shi XF, Hudson JL, Spicer PP, et al. 2005; Rheological behaviour and mechanical characterization of injectable poly(propylene fumarate)/single-walled carbon nanotube composites for bone tissue engineering. Nanotechnology 16(7): 531–538. Shim M, Kam NWS, Chen RJ, et al. 2002; Functionalization of carbon nanotubes for biocompatibility and biomolecular recognition. Nano Lett 2(4): 285–288. Sitharaman B, Shi X, Walboomers XF, et al. 2008; In vivo biocompatibility of ultra-short single-walled carbon nanotube/biodegradable polymer nanocomposites for bone tissue engineering. Bone 43(2): 362–370. Sitharaman B, van der Zande M, Ananta JS, et al. 2009; Magnetic resonance imaging studies on gadonanotube reinforced biodegradable polymer nanocomposites. J Biomed Mater Res A 93: 1454–1462. Thies RS, Bauduy M, Ashton BA, et al. 1992; Recombinant human bone morphogenetic protein-2 induces osteoblastic differentiation in W-20–17 stromal cells. Endocrinology 130(3): 1318–1324. Tsai SW, Hsu FY, Chen PL. 2008; Beads of collagen–nanohydroxyapatite composites prepared by a biomimetic process and the effects of their surface texture on cellular behavior in MG63 osteoblast-like cells. Acta Biomater 4(5): 1332–1341. Usui Y, Aoki K, Narita N, et al. 2008; Carbon nanotubes with high bone-tissue compatibility and bone-formation acceleration effects. Small 4(2): 240–246. Warheit DB, Laurence BR, Reed KL, et al. 2004; Comparative pulmonary toxicity assessment of single-wall carbon nanotubes in rats. Toxicol Sci 77(1): 117–125. Zhang DH, Kandadai MA, Cech J, et al. 2006; Poly(L-lactide) (PLLA)/multiwalled carbon nanotube (MWCNT) composite: characterization and biocompatibility evaluation. J Phys Chem B 110(26): 12910–12915. Zhang RY, Ma PX. 1999; Poly(α-hydroxyl acids) hydroxyapatite porous composites for bone-tissue engineering. I. Preparation and morphology. J Biomed Mater Res 44(4): 446–455. Citing Literature Volume5, Issue6June 2011Pages 476-482 ReferencesRelatedInformation
Referência(s)