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壳聚糖与Ⅰ型胶原制备组织工程复合支架材料的扫描电镜研究 被引量:17

Micro-structure of Composite Tissue Engineering Scaffold of Chitosan and TypeⅠ Collagen with Scanning Electron Microscope
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摘要 【目的】通过扫描电镜观察壳聚糖和Ⅰ型胶原在不同温度下以不同比例制备成冻干状组织工程复合支架材料的微观结构,以获得最佳浓度、比例、温度匹配组合,制备理想的组织工程复合支架材料。【方法】在-5℃、-20℃和-80℃将不同浓度的壳聚糖、Ⅰ型胶原以及它们不同比例的混合液冷冻12h后冻干24h,扫描电镜观察不同材料表面和内部的微观结构,并计算其平均孔径和孔隙率。【结果】壳聚糖、Ⅰ型胶原以及它们的混合液冻干后都形成白色海绵状固体,冷冻温度越低冻干后材料的孔径越小,孔隙率越低;材料的浓度越高冻干后孔径越小,孔隙率越低;壳聚糖-Ⅰ型胶原混合液中壳聚糖含量越高,材料冻干后孔径越小,孔隙率越低。【结论】壳聚糖-Ⅰ型胶原复合支架的孔径和溶液浓度、二者配比以及冻干前的冷冻温度密切相关。 [Objective] To observe the various microstructures of frozen drying forms of tissue engineering scaffold, which was made of chitosan and type Ⅰ collagen with their various proportions, concentrations, and under different temperatures by scanning electron microscope (SEM). To obtain the ideal combinant tissue engineering scaffold. [Methods] Different concentration of chitosan, type Ⅰ collagen and the mixed liquor of them in different proportions were frozen firstly for 12 h at -5, -20, and -80 ℃, respectively, then were frozen dried for 24 h, at last, the microstructure of the new materials were observed by scanning electron microscope, and the average pore diameters and interval porosities were calculated. [Results] Platinum sponge solid were formed after chitosan, type Ⅰ collagen and the mixed liquor of them were frozen drying. And the lower temperature materials were frozen before drying, the smaller pore diameter and lower interval porosity they had. The higher concentration of materials and higher proportion of chitosan in mixed liquor were, the smaller pore diameter and lower interval porosity they had. [Conclusion] The pore diameters of chitosan-type Ⅰ collagen composite scaffold are closely related with the concentration, proportion of materials and the freezing temperature before drying.
出处 《中山大学学报(医学科学版)》 CAS CSCD 北大核心 2006年第5期557-561,共5页 Journal of Sun Yat-Sen University:Medical Sciences
基金 广东省科技计划项目(2004B31201003)
关键词 壳聚糖 Ⅰ型胶原 复合支架 扫描电镜 chitosan type Ⅰ collagen composite scaffold scanning electron microscope
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参考文献10

  • 1RAO S B,SHARMA C P.Use of chitosan as a biomaterial:studies on its safety and hemostatic potential[J].J Biomed Mater Res,1997,34(1):21-28. 被引量:1
  • 2WAHL D A,CZERNUSZKA J T.Collagenhydroxyapatite composites for hard tissue repair[J].Eur Cell Mater,2006,28(11):43-56. 被引量:1
  • 3LEE J Y,KIM K H,SHIN S Y,et al.Enhanced bone formation by transforming growth factor-beta1-releasing collagen/chitosan microgranules[J].J Biomed Mater Res A,2006,76(3):530-539. 被引量:1
  • 4ZHANG Y,CHENG X,WANG J,et al.Novel chitosan/collagen scaffold containing transforming growth factor-beta1 DNA for periodontal tissue engineering[J].Biochem Biophys Res Commun,2006,344(1):362-369. 被引量:1
  • 5ZHANG R,MA P X.Poly (alpha-hydroxyl acids)/hydroxyapatite porous composites for bone-tissue engineering I preparation and morphology[J].J Biomed Mater Res,1999,44 (4):446-455. 被引量:1
  • 6曾春,蔡道章,全大萍,布丽斯,卢华定,李晓峰,史德海.TGF-β1壳聚糖缓释微球的制备和体外检测[J].中山大学学报(医学科学版),2005,26(3):347-350. 被引量:18
  • 7冉炜,郭冰,李轶,王迎军,葛建华.可降解骨组织工程支架材料修复兔下颌骨缺损的实验研究[J].中山大学学报(医学科学版),2004,25(B06):18-20. 被引量:4
  • 8BRAYE F,HAUTIER A,BOUEZ C,et al.Skin substitutes reconstructed in the laboratory:application in burn treatment[J].Pathol Biol (Paris),2005,53(10):613-617. 被引量:1
  • 9SHIN S Y,PARK H N,KIM K H,et al.Biological evaluation of chitosan nanofiber membrane for guided bone regeneration[J].J Periodontol,2005,76 (10):1778-1784. 被引量:1
  • 10ZKINIC G,SENEL S,AKINCIBAY H,et al.Effect of chitosan on a periodontal pathogen porphyromonas gingivalis[J].Int J Pharm,2002,235(1-2):121-127. 被引量:1

二级参考文献19

  • 1郑有华,任材年,陈小华.珊瑚人工骨和自体骨髓复合移植修复兔下颌骨缺损实验[J].中山医科大学学报,1995,16(4):40-43. 被引量:5
  • 2Barry F, Boynton RE, Liu B, et al. Chondrogenic differentiation of mesenchymal stem cells from bone marrow:differentiation-dependent gene expression of matrix components[J]. Exp Cell Res, 2001, 268(2): 189-200. 被引量:1
  • 3Song SU, Hong YJ, Oh IS, et al. Regeneration of hyaline articular cartilage with irradiated transforming growth factor beta1-producing fibroblasts[J]. Tissue Eng,2004, 10(5-6): 665-72. 被引量:1
  • 4Moulharat N, Lesur C, Thomas M, et al. Effects of transforming growth factor-beta on aggrecanase production and proteoglycan degradation by human chondrocytes in vitro[J]. Osteoarthritis Cartilage, 2004, 12(4): 296-305. 被引量:1
  • 5Kim SE, Park JH, Cho YW, et al. Porous chitosan scaffold containing microspheres loaded with transforming growth factor-β1: implications for cartilage tissue engineering[J]. J Controll Release, 2003, 91(3): 365-74. 被引量:1
  • 6ao JS, Liu HF, Yin YJ, et al. The properties of chitosan-gelatin membranes and scaffolds modified with hyaluronic acid by different methods[J]. Biomaterials,2003, 24(9): 1621-9. 被引量:1
  • 7Nettles DL, Elder SH, Gilbert JA. Potential use of chitosan as a cell scaffold material for cartilage tissue engineering[J]. Tissue Eng, 2002, 8(6): 1009-16. 被引量:1
  • 8Subramanian A, Lin HY, Vu D, et al. Synthesis and evaluation of scaffolds prepared from chitosan fibers for potential use in cartilage tissue engineering[J]. Biomed Sci Instrum, 2004, 40:117-22. 被引量:1
  • 9Ozbas TS, Akbuga J, Aral C. Controlled release of interleukin-2 from chitosan microspheres[J]. J Pharm Sci,2002, 91(5): 1245-51. 被引量:1
  • 10Sinha VR, Singla AK, Wadhawan S, et al. Chitosan microspheres as a potential carrier for drugs [J]. Int J Pharm, 2004, 274(1-2): 1-33. 被引量:1

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