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      Chitosan sponges as tissue engineering scaffolds for bone formation

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      https://www.riss.kr/link?id=A76262612

      • 저자

        Seol, Yang-Jo (Departments of Periodontology, College of Dentistry, Seoul National University, Departments of Periodontology, Samsung Medical Center, Sungkyunkwan university School of Medicine) ;  Lee, Jue-Yeon (College of Pharmacy, Ewha Womans University) ;  Park, Yoon-Jeong (Department of Craniomaxillofacial Reconstructive Science, College of Dentistry, Seoul National University) ;  Lee, Yong-Moo (Departments of Periodontology, College of Dentistry, Seoul National University) ;  Young-Ku (Departments of Periodontology, College of Dentistry, Seoul National University) ;  Rhyu, In-Chul (Departments of Periodontology, College of Dentistry, Seoul National University) ;  Lee, Seung-jin (College of Pharmacy, Ewha Womans University) ;  Han, Soo-Boo (Departments of Periodontology, College of Dentistry, Seoul National University) ;  Chung, Chong-Pyoung (Departments of Periodontology, College of Dentistry, Seoul National University)

      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2004

      • 작성언어

        English

      • KDC

        518

      • 자료형태

        학술저널

      • 수록면

        95-99(5쪽)

      • 제공처
      • 중단사유

        ※ 저작자의 요청에 따라 해당 논문은 원문이 제공되지 않습니다.

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      다국어 초록 (Multilingual Abstract)

      Rat calvarial osteoblasts were grown in porous chitosan sponges fabricated by freeze drying. The prepared chitosan sponges had a porous structure with a 100-200 ㎛ pore diameter, which allowed cell proliferation. Cell density, alkaline phosphatase ac...

      Rat calvarial osteoblasts were grown in porous chitosan sponges fabricated by freeze drying. The prepared chitosan sponges had a porous structure with a 100-200 ㎛ pore diameter, which allowed cell proliferation. Cell density, alkaline phosphatase activity and calcium deposition were monitored for up to 56 d culture. Cell numbers were 4×10^(6)(day 1), 11×10^(6)(day 28) and 12×10^(6)(day 56) per g sponge. Calcium depositions were 9 (day 1), 40 (day 28) and 48 (day 56) ㎍ per sponge. Histological results corroborated that bone formation within the sponges had occurred. These results show that chitotsan sponges can be used as effective scaffolding materials for tissue engineered bone formation in vitro.

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      목차 (Table of Contents)

      • Abstract
      • Introduction
      • Materials and methods
      • Materials
      • Fabrication of chitosan sponge
      • Abstract
      • Introduction
      • Materials and methods
      • Materials
      • Fabrication of chitosan sponge
      • Cell seeding into the sponges and culture in vitro
      • Osteoblastic cell proliferation
      • Measurement of alkaline phosphatase activity
      • Matrix mineralization analysis
      • Histological examination of cell-sponge constructs in vitro culture
      • Statistical analysis
      • Results and discussion
      • Chitosan sponge fabrication
      • Osteoblast proliferation in the sponges
      • Osteoblastic differentiation
      • Histological observation
      • Conclusions
      • Acknowledgement
      • References
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