Gamma-Irradiated Bacterial Cellulose as a Three-Dimensional Scaffold for Osteogenic Differentiation of Rat Bone Marrow Stromal Cells

https://doi.org/10.22146/ijc.71823

Farah Nurlidar(1*), Mime Kobayashi(2), Ade Lestari Yunus(3), Rika Heryani(4), Muhamad Yasin Yunus(5), Tita Puspitasari(6), Darmawan Darwis(7)

(1) Center for Research and Technology of Isotopes and Radiation Application, The National Research and Innovation Agency, Jl. Lebak Bulus Raya No. 49, Jakarta Selatan 12440, Indonesia
(2) Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0192, Japan
(3) Center for Research and Technology of Isotopes and Radiation Application, The National Research and Innovation Agency, Jl. Lebak Bulus Raya No. 49, Jakarta Selatan 12440, Indonesia
(4) Center for Research and Technology of Isotopes and Radiation Application, The National Research and Innovation Agency, Jl. Lebak Bulus Raya No. 49, Jakarta Selatan 12440, Indonesia
(5) Center for Research and Technology of Isotopes and Radiation Application, The National Research and Innovation Agency, Jl. Lebak Bulus Raya No. 49, Jakarta Selatan 12440, Indonesia
(6) Center for Research and Technology of Isotopes and Radiation Application, The National Research and Innovation Agency, Jl. Lebak Bulus Raya No. 49, Jakarta Selatan 12440, Indonesia
(7) Center for Research and Technology of Isotopes and Radiation Application, The National Research and Innovation Agency, Jl. Lebak Bulus Raya No. 49, Jakarta Selatan 12440, Indonesia
(*) Corresponding Author

Abstract


The effect of gamma-irradiation on bacterial cellulose (BC) was investigated in terms of improving its properties as scaffolds for tissue engineering. BC pellicles were exposed to 25, 50, and 75 kGy gamma-ray irradiation, and X-ray diffraction analyses showed that the crystallinity of the BC decreased as stronger irradiation accelerated BC’s degradation. Fourier transform infrared spectroscopy of the irradiated BC revealed the appearance of a new peak at 1724 cm–1, indicating the formation of a new carbonyl group due to the cleavage of glycosidic linkages of the BC. Rat bone marrow stromal cells seeded on the gamma-irradiated BC incubated in an osteogenic medium for 14 days produced calcium, a late marker for osteogenic differentiation, as shown by Alizarin Red S (ARS) staining. Gamma-irradiated BC with higher irradiation doses showed intense ARS staining indicating higher calcium deposition. These findings demonstrate the feasibility of using gamma-irradiated BC as a cytocompatible 3D scaffold for bone tissue regeneration.

Keywords


bacterial cellulose; gamma-irradiation; Alizarin Red S staining; osteogenic differentiation; calcium deposition

Full Text:

Full Text PDF


References

[1] Caliari, S.R., and Burdick, J.A., 2016, A practical guide to hydrogels for cell culture, Nat. Methods, 13 (5), 405–414.

[2] Choe, G., Park, J., Park, H., and Lee, J.Y., 2018, Hydrogel biomaterials for stem cell microencapsulation, Polymers, 10 (9), 1–17.

[3] Li, X., Sun, Q., Li, Q., Kawazoe, N., and Chen, G., 2018, Functional hydrogels with tunable structures and properties for tissue engineering applications, Front. Chem., 6, 499.

[4] Torgbo, S., and Sukyai, P., 2018, Bacterial cellulose-based scaffold materials for bone tissue engineering, Appl. Mater. Today, 11, 34–49.

[5] Pang, M., Huang, Y., Meng, F., Zhuang, Y., Liu, H., Du, M., Ma, Q., Wang, Q., Chen, Z., Chen, L., Cai, T., and Cai, Y., 2020, Application of bacterial cellulose in skin and bone tissue engineering, Eur. Polym. J., 122, 109365.

[6] Hickey, R.J., and Pelling, A.E., 2019, Cellulose biomaterials for tissue engineering, Front. Bioeng. Biotechnol., 7, 45.

[7] Portela, R., Leal, C.R., Almeida, P.L., and Sobral, R.G., 2019, Bacterial cellulose: A versatile biopolymer for wound dressing applications, Microb. Biotechnol., 12 (4), 586–610.

[8] Cherng, J.H., Chou, S.C., Chen, C.L., Wang, Y.W., Chang, S.J., Fan, G.Y., Leung, F.S., and Meng, E., 2021, Bacterial cellulose as a potential bio-scaffold for effective re-epithelialization therapy, Pharmaceutics, 13 (10), 1592.

[9] Criado, P., Fraschini, C., Jamshidian, M., Salmieri, S., Safrany, A., and Lacroix, M., 2017, Gamma-irradiation of cellulose nanocrystals (CNCs): Investigation of physicochemical and antioxidant properties, Cellulose, 24 (5), 2111–2124.

[10] Gorgieva, S., and Trček, J., 2019, Bacterial cellulose: Production, modification and perspectives in biomedical applications, Nanomaterials, 9 (10), 1352.

[11] Unal, S., Arslan, S., Yilmaz, B.K., Oktar, F.N., Sengil, A.Z., and Gunduz, O., 2021, Production and characterization of bacterial cellulose scaffold and its modification with hyaluronic acid and gelatin for glioblastoma cell culture, Cellulose, 28 (1), 117–132.

[12] Bayir, E., Bilgi, E., Hames, E.E., and Sendemir, A., 2019, Production of hydroxyapatite–bacterial cellulose composite scaffolds with enhanced pore diameters for bone tissue engineering applications, Cellulose, 26 (18), 9803–9817.

[13] Popa, L., Ghica, M.V., Tudoroiu, E.E., Ionescu, D.G., and Dinu-Pîrvu, C.E., 2022, Bacterial cellulose–A remarkable polymer as a source for biomaterials tailoring, Materials, 15 (3), 1054.

[14] Nurlidar, F., and Kobayashi, M., 2019, Succinylated bacterial cellulose induce carbonated hydroxyapatite eposition in a solution mimicking body fluid, Indones. J. Chem., 19 (4), 858–864.

[15] da Silva Aquino, K.A., 2012, "Sterilization by Gamma Irradiation" in Gamma Radiation, Eds., Adrovic, F., IntechOpen, Rijeka, Croatia.

[16] Pérez Davila, S., González Rodríguez, L., Chiussi, S., Serra, J., and González, P., 2021, How to sterilize polylactic acid based medical devices?, Polymers, 13 (13), 2115.

[17] Baccaro, S., Carewska, M., Casieri, C., Cemmi, A., and Lepore, A., 2013, Structure modifications and interaction with moisture in γ-irradiated pure cellulose by thermal analysis and infrared spectroscopy, Polym. Degrad. Stab., 98 (10), 2005–2010.

[18] Bouchard, J., Méthot, M., and Jordan, B., 2006, The effects of ionizing radiation on the cellulose of woodfree paper, Cellulose, 13 (5), 601–610.

[19] Darwis, D., Khusniya, T., Hardiningsih, L., Nurlidar, F., and Winarno, H., 2012, In-vitro degradation behaviour of irradiated bacterial cellulose membrane, Atom Indones., 38 (2), 78–82.

[20] Ferro, M., Mannu, A., Panzeri, W., Theeuwen, C.H.J., and Mele, A., 2020, An integrated approach to optimizing cellulose mercerization, Polymers, 12 (7), 1559.

[21] Wojdyr, M., 2010, Fityk: A general-purpose peak fitting program, J. Appl. Crystallogr., 43 (5-1), 1126–1128.

[22] Park, S., Baker, J.O., Himmel, M.E., Parilla, P.A., and Johnson, D.K., 2010, Cellulose crystallinity index: Measurement techniques and their impact on interpreting cellulase performance, Biotechnol. Biofuels, 3 (1), 10.

[23] Wada, M., Sugiyama, J., and Okano, T., 1993, Native celluloses on the basis of two crystalline phase (Iα/Iβ) system, J. Appl. Polym. Sci., 49 (8), 1491–1496.

[24] Ju, X., Bowden, M., Brown, E.E., and Zhang, X., 2015, An improved X-ray diffraction method for cellulose crystallinity measurement, Carbohydr. Polym., 123, 476–481.

[25] Luo, H., Li, W., Yang, Z., Ao, H., Xiong, G., Zhu, Y., Tu, J., and Wan, Y., 2018, Preparation of oriented bacterial cellulose nanofibers by flowing medium-assisted biosynthesis and influence of flowing velocity, J. Polym. Eng., 38 (3), 299–305.

[26] Eo, M.Y., Fan, H., Cho, Y.J., Kim, S.M., and Lee, S.K., 2016, Cellulose membrane as a biomaterial: From hydrolysis to depolymerization with electron beam, Biomater. Res., 20 (1), 16.

[27] Liu, Y., Chen, J., Wu, X., Wang, K., Su, X., Chen, L., Zhou, H., and Xiong, X., 2015, Insights into the effects of γ-irradiation on the microstructure, thermal stability and irradiation-derived degradation components of microcrystalline cellulose (MCC), RSC Adv., 5 (43), 34353–34363.

[28] Soares, S., Camino, G., and Levchik, S., 1995, Comparative study of the thermal decomposition of pure cellulose and pulp paper, Polym. Degrad. Stab., 49 (2), 275–283.

[29] Chamchoy, K., Pakotiprapha, D., Pumirat, P., Leartsakulpanich, U., and Boonyuen, U., 2019, Application of WST-8 based colorimetric NAD(P)H detection for quantitative dehydrogenase assays, BMC Biochem., 20 (1), 4.

[30] Vadaye Kheiry, E., Parivar, K., Baharara, J., Fazly Bazzaz, B.S., and Iranbakhsh, A., 2018, The osteogenesis of bacterial cellulose scaffold loaded with fisetin, Iran. J. Basic Med. Sci., 21 (9), 965–971.

[31] Cui, H., and Sinko, P.J., 2012, The role of crystallinity on differential attachment/proliferation of osteoblasts and fibroblasts on poly (caprolactone-co-glycolide) polymeric surfaces, Front. Mater. Sci., 6 (1), 47–59.

[32] Kaivosoja, E., Barreto, G., Levón, K., Virtanen, S., Ainola, M., and Konttinen, Y.T., 2012, Chemical and physical properties of regenerative medicine materials controlling stem cell fate, Ann. Med., 44 (7), 635–650.

[33] Klecker, C., and Nair, L.S., 2017, "Matrix Chemistry Controlling Stem Cell Behavior" in Biology and Engineering of Stem Cell Niches, Eds. Vishwakarma, A., and Karp, J.M., Academic Press, Boston, US, 195–213.

[34] Fu, C., Bai, H., Zhu, J., Niu, Z., Wang, Y., Li, J., Yang, X., and Bai, Y., 2017, Enhanced cell proliferation and osteogenic differentiation in electrospun PLGA/hydroxyapatite nanofibre scaffolds incorporated with graphene oxide, PLoS One, 12 (11), e0188352.



DOI: https://doi.org/10.22146/ijc.71823

Article Metrics

Abstract views : 1848 | views : 1247


Copyright (c) 2022 Indonesian Journal of Chemistry

Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

 


Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

Web
Analytics View The Statistics of Indones. J. Chem.