journal article·2023-04-14

Investigation of hemocompatibility and physicochemical properties of acellular caprine pericardium for biomedical applications

Thirumalai Deepak, Anju R. Babu

Journal of Materials Research· Volume 38· Issue 7
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Abstract

In this study, the combination of sodium dodecyl sulfate (SDS) and Triton X-100 was used to investigate the hemocompatibility and physicochemical properties of the native and decellularized caprine pericardium (DCP). Histology and infrared spectroscopy were used to characterize the DCP. The DCP was sterilized with ethanol and antibiotics, and the detergent’s residual cytotoxicity was investigated. The native pericardium and DCP were then tested for hemocompatibility and in vitro enzyme biodegradability. The histology shows no cell nuclei with intact matrix, while infrared spectroscopy shows identical peaks in DCP and native pericardium and antibiotic treatment only make DCP completely sterile. The SDS and Triton X-100 detergents are cytotoxic, and the cytotoxicity was significantly reduced by the addition of washing steps. According to the hemocompatibility study, the hemolytic indices of native and DCP are 2% and 5%. DCP showed higher degradation resistance with the trypsin enzyme than with the collagenase. Thus the scaffold created from this xenogeneic model has promising qualities that are useful for tissue engineering applications.Graphical abstract
Source: expertdata · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Tissue Engineering and Regenerative Medicine · Electrospun Nanofibers in Biomedical Applications · Xenotransplantation and immune response

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (40)

Show source-provided references
1. L. Jin, H. He, F. Yang, L. Xu, G. Guo, Y. Wang, Tough pNAGA hydrogel hybridized porcine pericardium for the pre-mounted TAVI valve with improved anti-tearing properties and hemocompatibility. Biomed. Mater. 15(6), 065013 (2020)10.1088/1748-605X/aba239 ↗
2. H. P. Felgueiras, J. C. Antunes, M. C. L. Martins, and M. A. Barbosa: in Pept. Proteins as Biomater. Tissue Regen. Repair (Elsevier, 2018), pp. 1–27.10.1016/B978-0-08-100803-4.00001-2 ↗
3. E.A. Grebenik, E.R. Gafarova, L.P. Istranov, E.V. Istranova, X. Ma, J. Xu, W. Guo, A. Atala, P.S. Timashev, Mammalian pericardium-based bioprosthetic materials in xenotransplantation and tissue engineering. Biotechnol. J. 15(8), 1900334 (2020)10.1002/biot.201900334 ↗
4. T. Yu, W. Yang, W. Zhuang, Y. Tian, Q. Kong, X. Chen, G. Li, Y. Wang, A bioprosthetic heart valve cross-linked by a non-glutaraldehyde reagent with improved biocompatibility, endothelialization, anti-coagulation and anti-calcification properties. J. Mater. Chem. B 9(19), 4031 (2021)10.1039/D1TB00409C ↗
5. A. Badria, P. Koutsoukos, S. Korossis, D. Mavrilas, The effect of heparin hydrogel embedding on glutaraldehyde fixed bovine pericardial tissues: Mechanical behavior and anticalcification potential. J. Mater. Sci. Mater. Med. 29(11), 175 (2018)10.1007/s10856-018-6184-8 ↗
6. S. Bose, S.F. Robertson, A. Bandyopadhyay, Surface modification of biomaterials and biomedical devices using additive manufacturing. Acta Biomater. 66, 6 (2018)10.1016/j.actbio.2017.11.003 ↗
7. G. Campion, K. Hershberger, A. Whelan, J. Conroy, C. Lally, B.P. Murphy, A biomechanical and microstructural analysis of bovine and porcine pericardium for use in bioprosthetic heart valves. Struct. Hear. 5(5), 486 (2021)10.1080/24748706.2021.1938317 ↗
8. K. Pinet, K.A. Mclaughlin, Mechanisms of physiological tissue remodeling in animals : Manipulating tissue, organ, and organism morphology. Dev. Biol. 451(2), 134 (2019)10.1016/j.ydbio.2019.04.001 ↗
9. T. Deepak, A.R. Babu, A review of current approaches for decellularization, sterilization, and hemocompatibility testing on xenogeneic pericardium. Mater. Today Commun. 33, 104478 (2022)10.1016/j.mtcomm.2022.104478 ↗
10. H. Zhuang, J.P. Zheng, H. Gao, K. De Yao, In vitro biodegradation and biocompatibility of gelatin/montmorillonite-chitosan intercalated nanocomposite. J. Mater. Sci. Mater. Med. 18(5), 951 (2007)10.1007/s10856-006-0093-y ↗
11. L. Xu, J.W. Bauer, C.A. Siedlecki, Proteins, platelets, and blood coagulation at biomaterial interfaces. Colloids Surf. B 124(717), 49 (2014)10.1016/j.colsurfb.2014.09.040 ↗
12. C. Fidalgo, L. Iop, M. Sciro, M. Harder, D. Mavrilas, S. Korossis, A. Bagno, G. Palù, P. Aguiari, G. Gerosa, A sterilization method for decellularized xenogeneic cardiovascular scaffolds. Acta Biomater. 67, 282 (2018)10.1016/j.actbio.2017.11.035 ↗
13. A.L. Woerman, G. Tamgüney, Body-first Parkinson’s disease and variant Creutzfeldt-Jakob disease—Similar or different? Neurobiol. Dis. 164, 105625 (2022)10.1016/j.nbd.2022.105625 ↗
14. H. Singh, S.D. Purohit, R. Bhaskar, I. Yadav, S. Bhushan, M.K. Gupta, N.C. Mishra, Curcumin in decellularized goat small intestine submucosa for wound healing and skin tissue engineering. J. Biomed. Mater. Res. Part B 110(1), 210 (2022)10.1002/jbm.b.34903 ↗
15. I. Banerjee, D. Mishra, T. Das, S. Maiti, T.K. Maiti, Caprine (goat) collagen: A potential biomaterial for skin tissue engineering. J. Biomater. Sci. Polym. Ed. 23(1–4), 355 (2012)10.1163/092050610X551943 ↗
16. T. Agarwal, T.K. Maiti, S.K. Ghosh, Decellularized caprine liver-derived biomimetic and pro-angiogenic scaffolds for liver tissue engineering. Mater. Sci. Eng. C 98, 939 (2019)10.1016/j.msec.2019.01.037 ↗
17. M. Todesco, S.J. Imran, T.M. Fortunato, D. Sandrin, G. Borile, F. Romanato, M. Casarin, G. Giuggioli, F. Conte, M. Marchesan, G. Gerosa, A. Bagno, A new detergent for the effective decellularization of bovine and porcine pericardia. Biomimetics 7(3), 104 (2022)10.3390/biomimetics7030104 ↗
18. S. Rallapalli, A.M. Liman, S. Guhathakurta, Hemocompatibility and surface properties of bovine pericardial patches: effects of gamma sterilization. Curr. Med. Res. Pract. 6(6), 224 (2016)10.1016/j.cmrp.2016.10.001 ↗
19. J. Mohr, M. Germain, M. Winters, S. Fraser, A. Duong, A. Garibaldi, N. Simunovic, D. Alsop, D. Dao, R. Bessemer, O.R. Ayeni, Disinfection of human musculoskeletal allografts in tissue banking: a systematic review. Cell Tissue Bank. 17(4), 573 (2016)10.1007/s10561-016-9584-3 ↗
20. E.P. Commission, European Pharmacopoeia 5.0, 2.6 -Biological Tests; 2.6.1 Sterility.
21. M. Jastrzebska, J. Zalewska-Rejdak, I. Mróz, B. Barwinski, R. Wrzalik, A. Kocot, J. Nozynski, Atomic force microscopy and FT-IR spectroscopy investigations of human heart valves. Gen. Physiol. Biophys. 25(3), 231 (2006)
22. S. Zouhair, E. Dal Sasso, S.R. Tuladhar, C. Fidalgo, L. Vedovelli, A. Filippi, G. Borile, A. Bagno, M. Marchesan, G. De Rossi, D. Gregori, W.F. Wolkers, F. Romanato, S. Korossis, G. Gerosa, L. Iop, A comprehensive comparison of bovine and porcine decellularized pericardia: new insights for surgical applications. Biomolecules 10(3), 371 (2020)10.3390/biom10030371 ↗
23. A.A. Shitole, P.S. Giram, P.W. Raut, P.P. Rade, A.P. Khandwekar, N. Sharma, B. Garnaik, Clopidogrel eluting electrospun polyurethane/polyethylene glycol thromboresistant, hemocompatible nanofibrous scaffolds. J. Biomater. Appl. 33(10), 1327 (2019)10.1177/0885328219832984 ↗
24. C. Nojiri, T. Okano, H.A. Jacobs, K.D. Park, S.F. Mohammad, D.B. Olsen, S.W. Kim, Blood compatibility of PEO grafted polyurethane and HEMA/styrene block copolymer surfaces. J. Biomed. Mater. Res. 24(9), 1151 (1990)10.1002/jbm.820240903 ↗
25. I. Firkowska-Boden, X. Zhang, K.D. Jandt, Controlling Protein Adsorption through Nanostructured Polymeric Surfaces. Adv. Healthc. Mater. 7(1), 1 (2018)10.11648/j.am.20180701.11 ↗
26. Y. Lei, L. Deng, Y. Tang, Q. Ning, X. Lan, Y. Wang, Hybrid pericardium with VEGF-loaded hyaluronic acid hydrogel coating to improve the biological properties of bioprosthetic heart valves. Macromol. Biosci. 19(6), 1 (2019)10.1002/mabi.201800390 ↗
27. S.A. Ghodbane, M.G. Dunn, Physical and mechanical properties of cross-linked type I collagen scaffolds derived from bovine, porcine, and ovine tendons. J. Biomed. Mater. Res. Part A 104(11), 2685 (2016)10.1002/jbm.a.35813 ↗
28. A.S. Braga-Vilela, E.R. Pimentel, S. Marangoni, M.H. Toyama, B. De Campos Vidal, Extracellular matrix of porcine pericardium: Biochemistry and collagen architecture. J. Membr. Biol. 221(1), 15 (2008)10.1007/s00232-007-9081-5 ↗
29. Y. Zhang, T. Iwata, K. Nam, T. Kimura, P. Wu, N. Nakamura, Y. Hashimoto, A. Kishida, Water absorption by decellularized dermis. Heliyon 4(4), e00600 (2018)10.1016/j.heliyon.2018.e00600 ↗
30. H. Park, X. Guo, J.S. Temenoff, Y. Tabata, A.I. Caplan, F.K. Kasper, A.G. Mikos, Effect of swelling ratio of injectable hydrogel composites on chondrogenic differentiation of encapsulated rabbit marrow mesenchymal stem cells in vitro. Biomacromolecules 10(3), 541 (2009)10.1021/bm801197m ↗
31. N. Bölgen, Y.Z. Menceloğlu, K. Acatay, I. Vargel, E. Pişkin, In vitro and in vivo degradation of non-woven materials made of poly(epsilon-caprolactone) nanofibers prepared by electrospinning under different conditions. J. Biomater. Sci. Polym. Ed. 16(12), 1537 (2005)10.1163/156856205774576655 ↗
32. J.J. Plantner, A. Smine, T.A. Quinn, Matrix metalloproteinases and metalloproteinase inhibitors in human interphotoreceptor matrix and vitreous. Curr. Eye Res. 17(2), 132 (1998)10.1076/ceyr.17.2.132.5610 ↗
33. H.C. Liang, Y. Chang, C.K. Hsu, M.H. Lee, H.W. Sung, Effects of crosslinking degree of an acellular biological tissue on its tissue regeneration pattern. Biomaterials 25(17), 3541 (2004)10.1016/j.biomaterials.2003.09.109 ↗
34. M. van Deemter, R. Kuijer, H. Harm Pas, R. Jacoba van der Worp, J.M.M. Hooymans, L.I. Los, Trypsin-mediated enzymatic degradation of type II collagen in the human vitreous. Mol. Vis. 19, 1591 (2013)
35. O. Bim-Junior, Y. Alania, F.S. Tabatabaei, R. Frem, A.K. Bedran-Russo, P.N. Lisboa-Filho, Biomimetic growth of metal-organic frameworks for the stabilization of the dentin matrix and control of collagenolysis. Langmuir 38(4), 1600 (2022)10.1021/acs.langmuir.1c03073 ↗
36. H.-W. Sung, H.-L. Hsu, C.-S. Hsu, Effects of various chemical sterilization methods on the crosslinking and enzymatic degradation characteristics of an epoxy-fixed biological tissue. J. Biomed. Mater. Res. 37(3), 376 (1997)10.1002/(SICI)1097-4636(19971205)37:3<376::AID-JBM8>3.0.CO;2-I ↗
37. Z.Z. Liu, M.L. Wong, L.G. Griffiths, Effect of bovine pericardial extracellular matrix scaffold niche on seeded human mesenchymal stem cell function. Sci. Rep. 6(1), 37089 (2016)10.1038/srep37089 ↗
38. H.-Y. Liu, L. Du, Y.-T. Zhao, W.-Q. Tian, In vitro hemocompatibility and cytotoxicity evaluation of halloysite nanotubes for biomedical application. J. Nanomater. 2015, 1 (2015)
39. M. Weber, H. Steinle, S. Golombek, L. Hann, C. Schlensak, H. P. Wendel, and M. Avci-Adali: Blood-Contacting Biomaterials: In Vitro Evaluation of the Hemocompatibility. Front. Bioeng. Biotechnol. 6, 12 (2018).10.3389/fbioe.2018.00099 ↗
40. M. Kimicata, J.D. Allbritton-King, J. Navarro, M. Santoro, T. Inoue, N. Hibino, J.P. Fisher, Assessment of decellularized pericardial extracellular matrix and poly(propylene fumarate) biohybrid for small-diameter vascular graft applications. Acta Biomater. 110, 68 (2020)10.1016/j.actbio.2020.04.013 ↗