• Nenhum resultado encontrado

Conclusions

No documento Cátia Sofia Dias Oliveira (páginas 119-127)

CHAPTER III. Tubular fibrous scaffold functionalized with tropoelastin as a small-diameter vascular

3.6 Conclusions

We have successfully developed a biofunctional eTF scaffold for vascular applications with appropriate uniaxial tensile properties within the same range of those of native blood vessels. By tailoring the surface functionality, different interactions between the biofunctional substrate and endothelial cells can be achieved. Indeed, exposing tropoelastin -COOH groups to cells seemed to influence the endothelial cells behaviour towards enhancing its viability and activity. Otherwise, exposing its -NH2 groups stimulated endothelial cells to produce higher amounts of protein. After 7 days of culture, a confluent endothelial cell monolayer was present on the eTF scaffolds surface which promoted a rapid endothelialization. This study suggests that by combining the fibrous and porous structure, and the mechanical properties obtained from eTF scaffolds with biochemical cues provided by tropoelastin, it is possible to design a biofunctional and bioactive tubular scaffold as a valid alternative to functional engineered vascular grafts.

3.7 References

[1] D.G. Seifu, A. Purnama, K. Mequanint, D. Mantovani, Small-diameter vascular tissue engineering, Nat. Rev. Cardiol. 10 (2013) 410–421.

[2] A. D. Michaels and K. Chatterjee, Angioplasty Versus Bypass Surgery for Coronary Artery Disease, Circulation. 106 (2002) 176–178.

[3] R.Y. Kannan, H.J. Salacinski, P.E. Butler, G. Hamilton, A.M. Seifalian, Current status of prosthetic bypass grafts: A review, J. Biomed. Mater. Res. - Part B Appl. Biomater. 74 (2005) 570–581.

[4] R. Langer, J.P. Vacanti, Tissue Engineering, Science. 260 (1993) 920–926.

[5] N. L’Heureux, N. Dusserre, G. Konig, B. Victor, P. Keire, T.N. Wight, N.A.F. Chronos, A.E.

Kyles, C.R. Gregory, G. Hoyt, R.C. Robbins, T.N. McAllister, Human tissue-engineered blood vessels for adult arterial revascularization, Nat. Med. 12 (2006) 361–365.

[6] S.L.M. Dahl, A.P. Kypson, J.H. Lawson, J.L. Blum, J.T. Strader, Y. Li, R.J. Manson, W.E.

Tente, L. DiBernardo, M.T. Hensley, R. Carter, T.P. Williams, H.L. Prichard, M.S. Dey, K.G.

Begelman, L.E. Niklason, Readily available tissue-engineered vascular grafts., Sci. Transl.

Med. 3 (2011) 68–79.

[7] D. Seliktar, R.A. Black, R.P. Vito, R.M. Nerem, Dynamic Mechanical Conditioning of Collagen-Gel Blood Vessel Constructs Induces Remodeling In Vitro, Ann. Biomed. Eng. 28 (2000) 351–362.

[8] L. Soletti, Y. Hong, J. Guan, J.J. Stankus, M.S. El-kurdi, A bilayered elastomeric scaffold for tissue engineering of small diameter vascular grafts, Acta Biomater. 6 (2010) 110–122.

[9] S. Jin, J. Liu, S. Heang, S. Soker, A. Atala, J.J. Yoo, Development of a composite vascular scaffolding system that withstands physiological vascular conditions, Biomaterials. 29 (2008) 2891–2898.

[10] B. Nottelet, E. Pektok, D. Mandracchia, J.C. Tille, B. Walpoth, R. Gurny, M. Möller, Factorial design optimization and in vivo feasibility of poly(ε-caprolactone)-micro- and nanofiber-based small diameter vascular grafts, J. Biomed. Mater. Res. - Part A. 89 (2009) 865–875.

[11] M. Stekelenburg, D. Ph, M.C.M. Rutten, D. Ph, L.H.E.H. Snoeckx, D. Ph, F.P.T. Baaijens, D. Ph, Dynamic Straining Combined with Fibrin Gel Cell Seeding Improves Strength of Tissue-Engineered Small-Diameter Vascular Grafts, Tissue Eng. - Part A. 15 (2009) 1081–

1089.

[12] A. Karimi, M. Navidbakhsh, A. Shojaei, S. Faghihi, Measurement of the uniaxial mechanical properties of healthy and atherosclerotic human coronary arteries, Mater. Sci. Eng. C. 33 (2013) 2550–2554.

[13] A. Tajaddini, D.L. Kilpatrick, P. Schoenhagen, E.M. Tuzcu, M. Lieber, D.G. Vince, D.L.

Kilpatrick, P. Schoenhagen, M. Tuzcu, M. Lieber, D.G. Vince, Impact of age and hyperglycemia on the mechanical behavior of intact human coronary arteries : an ex vivo intravascular ultrasound study, Am. J. Physiol. Hear. Circ. Physiol. 44195 (2005) 250–

255.

[14] D.A. Vorp, B.J. Schiro, M.P. Ehrlich, T.S. Juvonen, M.A. Ergin, B.P. Griffith, Effect of Aneurysm on the Tensile Strength and Biomechanical Behavior of the Ascending Thoracic

Aorta, Ann. Thorac. Surg. 75 (2003) 1210–1214.

[15] A. Martins, J. V Araújo, R.L. Reis, N.M. Neves, Electrospun nanostructured scaffolds for tissue engineering applications, Nanomedicine (Lond). 2 (2007) 929–942.

[16] A. Martins, R.L. Reis, N.M. Neves, Electrospinning: processing technique for tissue engineering scaffolding, Int. Mater. Rev. 53 (2008) 257–274.

[17] T.-H. Nguyen, B.-T. Lee, The effect of cross-linking on the microstructure, mechanical properties and biocompatibility of electrospun polycaprolactone–gelatin/PLGA–

gelatin/PLGA–chitosan hybrid composite, Sci. Technol. Adv. Mater. 13 (2012) 35002.

[18] Y.M. Ju, J.S. Choi, A. Atala, J.J. Yoo, S.J. Lee, Bilayered scaffold for engineering cellularized blood vessels, Biomaterials. 31 (2010) 4313–4321.

[19] C.M. Vaz, S. van Tuijl, C.V.C. Bouten, F.P.T. Baaijens, Design of scaffolds for blood vessel tissue engineering using a multi-layering electrospinning technique, Acta Biomater. 1 (2005) 575–582.

[20] S.G. Wise, M.J. Byrom, A. Waterhouse, P.G. Bannon, M.K.C. Ng, A.S. Weiss, A multilayered synthetic human elastin / polycaprolactone hybrid vascular graft with tailored mechanical properties, Acta Biomater. 7 (2011) 295–303.

[21] E. Pektok, B. Nottelet, J.-C. Tille, R. Gurny, A. Kalangos, M. Moeller, B.H. Walpoth, Degradation and Healing Characteristics of Small-Diameter Poly ( epsilon-Caprolactone ) Vascular Grafts in the Rat Systemic, Circulation. 118 (2008) 2563–2570.

[22] S. de Valence, J.C. Tille, D. Mugnai, W. Mrowczynski, R. Gurny, M. Möller, B.H. Walpoth, Long term performance of polycaprolactone vascular grafts in a rat abdominal aorta replacement model, Biomaterials. 33 (2012) 38–47.

[23] P.C. Caracciolo, M.I. Rial-Hermida, F. Montini-Ballarin, G.A. Abraham, A. Concheiro, C.

Alvarez-Lorenzo, Surface-modified bioresorbable electrospun scaffolds for improving hemocompatibility of vascular grafts, Mater. Sci. Eng. C. 75 (2017) 1115–1127.

[24] G.C. Yeo, A. Kondyurin, E. Kosobrodova, S. Weiss, M.M.M. Bilek, A sterilizable ,

Soc. Interface. 14 (2017).

[25] S.M. Mithieux, S.G. Wise, A.S. Weiss, Tropoelastin — A multifaceted naturally smart material, Adv. Drug Deliv. Rev. 65 (2013) 421–428.

[26] L.M. Maurer, B.R. Tomasini-johansson, D.F. Mosher, Emerging roles of fibronectin in thrombosis, Thromb. Res. 125 (2010) 287–291.

[27] S.P. Vyas, B. Vaidya, Targeted delivery of thrombolytic agents: role of integrin receptors, Expert Opin. Drug Deliv. 6 (2009) 499–508.

[28] S.G. Wise, H. Liu, A. Kondyurin, M.J. Byrom, P.G. Bannon, G.A. Edwards, A.S. Weiss, S.

Bao, M.M. Bilek, Plasma Ion Activated Expanded Polytetrafluoroethylene Vascular Grafts with a Covalently Immobilized Recombinant Human Tropoelastin Coating Reducing Neointimal Hyperplasia, ACS Biomater. Sci. Eng. 2 (2016) 1286–1297.

[29] A. Waterhouse, Y. Yin, S.G. Wise, D. V. Bax, D.R. McKenzie, M.M.M. Bilek, A.S. Weiss, M.K.C. Ng, The immobilization of recombinant human tropoelastin on metals using a plasma-activated coating to improve the biocompatibility of coronary stents, Biomaterials.

31 (2010) 8332–8340.

[30] P.E. Tyllianakis, S.E. Kakabakos, G.P. Evangelatos, Colorimetric Determination of Reactive Primary Amino Groups of Macro- and Microsolid Supports, Appl. Biochem. Biotechnol. 38 (1993) 15–25.

[31] N.A. Hotaling, K. Bharti, H. Kriel, C.G. Simon, DiameterJ: A Validated Open Source Nanofiber Diameter Measurement Tool, Biomaterials. 61 (2015) 327–338.

[32] S.L. Martin, B. Vrhovski, A.S. Weiss, Total synthesis and expression in Escherichia coli of a gene encoding human tropoelastin, Gene. 154 (1995) 159–166.

[33] A. Abdal-hay, A. Memic, K.H. Hussein, Y. Seul, M. Fouad, F.F. Al-jassir, H. Woo, Y. Morsi, Rapid fabrication of highly porous and biocompatible composite textile tubular scaffold for vascular tissue engineering, Eur. Polym. J. 96 (2017) 27–43.

[34] M. Neufurth, X. Wang, E. Tolba, B. Dorweiler, Modular Small Diameter Vascular Grafts with Bioactive Functionalities, PLoS One. 10 (2015) 1–24.

[35] M. Richard, R. Black, C. Kielty, PCL – PU composite vascular scaffold production for vascular tissue engineering : Attachment , proliferation and bioactivity of human vascular endothelial cells, Biomaterials. 27 (2006) 3608–3616.

[36] F. Han, X. Jia, D. Dai, X. Yang, J. Zhao, Y. Zhao, Y. Fan, X. Yuan, Performance of a multilayered small-diameter vascular scaffold dual-loaded with VEGF and PDGF, Biomaterials. 34 (2013) 7302–7313.

[37] D. V. Bax, A. Kondyurin, A. Waterhouse, D.R. McKenzie, A.S. Weiss, M.M.M. Bilek, Surface plasma modification and tropoelastin coating of a polyurethane co-polymer for enhanced cell attachment and reduced thrombogenicity, Biomaterials. 35 (2014) 6797–6809.

[38] M. Ahmed, H. Ghanbari, B.G. Cousins, G. Hamilton, A.M. Seifalian, Small calibre polyhedral oligomeric silsesquioxane nanocomposite cardiovascular grafts: Influence of porosity on the structure, haemocompatibility and mechanical properties, Acta Biomater. 7 (2011) 3857–

3867.

[39] N. Monteiro, A. Martins, R. Pires, S. Faria, N.A. Fonseca, J. Moreira, R.L. Reis, N.M. Neves, Immobilization of bioactive factor-loaded liposomes on the surface of electrospun nanofibers targeting tissue engineering, Biomater. Sci. 2 (2014) 1195–1209.

[40] C. Oliveira, A.R. Costa-pinto, R.L. Reis, A. Martins, N.M. Neves, Biofunctional Nanofibrous Substrate Comprising Immobilized 2 Antibodies and Selective Binding of Autologous Growth Factors, Biomacromolecules. 15 (2014) 2196–205.

[41] L.A. Bosworth, W. Hu, Y. Shi, S.H. Cartmell, Enhancing Biocompatibility without Compromising Material Properties : An Optimised NaOH Treatment for Electrospun Polycaprolactone Fibres, J. Nanomater. 2019 (2019) 1–11.

[42] S.J.P. Mcinnes, T.J. Macdonald, I.P. Parkin, T. Nann, N.H. Voelcker, Electrospun Composites of Polycaprolactone and Porous Silicon Nanoparticles for the Tunable Delivery of Small Therapeutic Molecules, Nanomaterials. 8 (2018) 1–12.

[43] D. Cho, S. Lee, M.W. Frey, Characterizing zeta potential of functional nanofibers in a microfluidic device, J. Colloid Interface Sci. 372 (2012) 252–260.

[44] K. Cai, M. Frant, G. Hildebrand, K. Liefeith, K.D. Jandt, Surface functionalized titanium thin films : Zeta-potential , protein adsorption and cell proliferation, Colloids Surfaces B Interfaces. 50 (2006) 1–8.

[45] H. Chen, J. Huang, J. Yu, S. Liu, P. Gu, Electrospun chitosan-graft-poly (-caprolactone)/poly (-caprolactone) cationic nanofibrous mats as potential scaffolds for skin tissue engineering, Int. J. Biol. Macromol. 48 (2011) 13–19.

[46] B. Vrhovski, A.S. Weiss, Biochemistry of tropoelastin, Eur. J. Biochem. 8 (1998) 1–18.

[47] D. V Bax, U.R. Rodgers, M.M.M. Bilek, A.S. Weiss, Cell Adhesion to Tropoelastin Is Mediated via the C-terminal GRKRK Motif and Integrin αvβ3, J. Biol. Chem. 284 (2009) 28616–

28623.

[48] D. V Bax, Y. Wang, Z. Li, P.K.M. Maitz, D.R. Mckenzie, M.M.M. Bilek, A.S. Weiss, Binding of the cell adhesive protein tropoelastin to PTFE through plasma immersion ion implantation treatment, Biomaterials. 32 (2011) 5100–5111.

[49] M.A. Hiob, S.G. Wise, A. Kondyurin, A. Waterhouse, M.M. Bilek, M.K.C. Ng, A.S. Weiss, The use of plasma-activated covalent attachment of early domains of tropoelastin to enhance vascular compatibility of surfaces, Biomaterials. 34 (2013) 7584–7591.

[50] Y. Yin, S.G. Wise, N.J. Nosworthy, A. Waterhouse, D. V Bax, H. Youssef, M.J. Byrom, M.M.M.

Bilek, D.R. Mckenzie, A.S. Weiss, M.K.C. Ng, Covalent immobilisation of tropoelastin on a plasma deposited interface for enhancement of endothelialisation on metal surfaces, Biomaterials. 30 (2009) 1675–1681.

[51] S. Landau, A.A. Szklanny, G.C. Yeo, Y. Shandalov, E. Kosobrodova, A.S. Weiss, S.

Levenberg, Tropoelastin coated PLLA-PLGA scaffolds promote vascular network formation, Biomaterials. 122 (2017) 72–82.

CHAPTER IV.

General Conclusions and Future Work

No documento Cátia Sofia Dias Oliveira (páginas 119-127)

Documentos relacionados