DOI QR코드

DOI QR Code

Surface Immobilization of $(1{\to}3)(1{\to}6)-{\beta}-glucan$ onto Biodegradable Polymer for Tissue Regeneration

조직 재생을 위한 Poly (D, L-lactide-co-glycolide) 표면에 $(1{\to}3)(1{\to}6)-{\beta}-glucan$ 고정에 대한 세포 점착 및 성장 효과

  • Lee, S.G. (Dept. of Biomedical Engineering, Inje Univ.) ;
  • Lee, J.B. (Dept. of Biomedical Engineering, Inje Univ.) ;
  • Yu, S.M. (Dept. of Biomedical Engineering, Inje Univ.) ;
  • Park, J.C. (Dept. Medical Eng., Collage of Med., Yonsei Univ.) ;
  • Choi, J.B. (Dept. Mechanical Systems Eng., Hansung Univ.) ;
  • Kim, J.K. (Dept. of Biomedical Engineering, Inje Univ.)
  • 이상길 (인제대학교 의용공학과) ;
  • 이정복 (인제대학교 의용공학과) ;
  • 유성미 (인제대학교 의용공학과) ;
  • 박종철 (연세의과대학 의학공학교실) ;
  • 최재봉 (한성대학 기계시스템공학과) ;
  • 김정구 (인제대학교 의용공학과)
  • Published : 2006.10.31

Abstract

We examined the effects of ${\beta}$-glucan-reinforced PLGA film and scaffold on HDFs (human dermal fibroblast) attachment and proliferation. The PLGA films were prepared by simple solvent-casting method. The prepared films were grafted with $(1{\to}3)(1{\to}6)-{\beta}-glucan$ in various ratios after plasma treatment on surface. The surface of the film was characterized by contact angle measurement, scanning electron microscope (SEM), and Fourier-transform infrared spectrophotometer (FT-IR). The amount of $(1{\to}3)(1{\to}6)-{\beta}-glucan$ in the prepared film was indirectly determined by phenol-sulfuric acid method. The HDFs (Human dermal fibroblasts) were used to evaluate the cell attachment and proliferation on PLGA specimens before and after plasma/${\beta}-glucan$ treatment. The result showed that the plasma treated groups exhibited more mont of ${\beta}-glucan$ might be grafted than the non plasma treated groups. Cell attachment was significantly enhanced in the plasma/${\beta}-glucan$ grafted group after 4 hours incubation (p<0.05) due to the improved hydrophilicity and cytoactivity effect of the ${\beta}-glucan$. The cell proliferation of plasma/${\beta}-glucan$ (2mg/ml) grafted group was the highest rate among the groups (p<0.05).

Keywords

References

  1. B.L. Seal, T.C. Otero, A. Panitch, 'Polymeric biomaterials for tissue and organ regeneration,' Mater Sci. and Eng., vol. 34, pp.147-230, 2001 https://doi.org/10.1016/S0927-796X(01)00035-3
  2. Khang GS, Lee Sj, Jeon JH, Lee HB., 'Interaction of fibroblast cell onto physicochemically treated PLGA surfaces,' Polymer (Korea), vol.24, pp.869-876, 2000
  3. Ting-Wu Q. Zhi-Ming Y, Ze-Zhi W, Hui-Qi Xie, Jian Q, ShaoXi Cai, 'Adhesion strength of hyman tenocytes to exracellualr matrix component-modified poly (D,L-lactide-co-glycolide acid) substrates,' Biomater, vol.26, pp.6635-6642, 2005 https://doi.org/10.1016/j.biomaterials.2005.04.023
  4. Ming-Hua H, Da-MIng W, Hsyue-Jen H, Hwa-Chang L, TzuYang H, Juin-Yih L, 'Lein- Tuan H Preparation and characterization of RGD-immobilized chitosan scaffolds,' Biomater, vol.26, pp.3197-3206, 2005 https://doi.org/10.1016/j.biomaterials.2004.08.032
  5. J.J. Yoon, S.H. song, D.S. Lee, T.G. Park, 'Immobilization of cell adhesive RGD peptide onto the surface of highly porous biodegradable polymer scaffolds fabricated by a gas foaming/salt leaching method,' Biomater, vol. 25, pp.5613-5620, 2004 https://doi.org/10.1016/j.biomaterials.2004.01.014
  6. M. Ramchandani, D. Robinson, 'In vitro and in vivo release of ciprofloxacin from PLGA 50:50 implants,' J. Controlled Release, voI.54,pp.167-175,1998 https://doi.org/10.1016/S0168-3659(97)00113-2
  7. Gao J, Niklason L, Langer R, 'Surface hydrolysis of Poly(glycolic acid) mechs increase the seeding density of vascular smooth muscle cells,' J. Biomed. Mater. Res., vol.42, pp.417-424, 1999
  8. Chavan M, Suzuki T, Recowicz M, Lennarz W., 'Genetic, biochemical, and morphological evidence for the involvement of N-glycosylation in biosynthesis of the cell wall beta 1,6-glucan of Saccharomyces cerevisiae,' in Proc. Natl. Acad. Sci., USA, 2003, vol.100, pp.15381-15386
  9. Sang Bong Lee, Hyun Wook Jeon, Young Woo Lee, et al., 'Bio-artificial skin composed of gelatin and (1$\rightarrow$3)(1$\rightarrow$6)-$\beta$-glucan,' Biomater, vol.24, pp.2503-2511, 2003 https://doi.org/10.1016/S0142-9612(03)00003-6
  10. Delatte S.J, Evans J, Hebra A, Adamson W, 'Othersen HB, Tagge EP. Effectiveness of beta-gluecan collagen for treatment of partialthickness burn in children,' J. Pediatr. Surg., vol.36, pp.113-118, 2001 https://doi.org/10.1053/jpsu.2001.20024
  11. Kernodle DS, Gates H, Kaiser AB, 'Prophylactic anti-infective activity of poly-[1-6]-beta-D-glucopyranosyl-[1-3]-beta-Dglucopyranose glucan in a guinea pig model of staphylococcal wound infection,' Antimicrob Agents Chemother, vol.42, pp.545-549,1998
  12. Kaiser AB, Kernodle DS., 'Synergism between poly-(1-6)-beta-Dglucopyranosyl-[1-3]-beta-D-glucopyranose glucan and cefazolin in prophylaxis of staphylococcal wound infection,' Antimicrob Agents Chemother, vol.42, pp.2449-2451, 1998
  13. A. Mueller, J. Raptis, P.J. Rice, J.H. Kalbfleisch, R.D. Stout, H.E. Ensley, W. Browder, D.L. Williams, 'Modulation of Endotoxin- and Enterotoxin-Induced Cytokine Release by In Vivo Treatment with beta-(1,6)-Branched beta-(1,3)-Glucan,' Glycobiology, vol.10, pp.339-346, 2000 https://doi.org/10.1093/glycob/10.4.339
  14. P. Kougias, D. Wei, P.J. Rice, H.E. Ensely, J Kalbfleiseh, D.L. Williams, I.W. Browder, ' The influence of glucan polymer structure and solution conformation on binding to (1$\rightarrow$3)-betaD-glucan receptors in a human monocyte-like cell line,' Infect. Immun., vol.69, pp.3933, 2001 https://doi.org/10.1128/IAI.69.6.3933-3938.2001
  15. Son HJ, Bae HC, Kim HJ, Lee DH, Han DW, Park JC., 'Effect of beta-glucan on proliferation and migration of fibroblasts,' Current Appli. Phy., vol.5, pp.468-471, 2005 https://doi.org/10.1016/j.cap.2005.01.011