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      이중구조 합성 폴리머 차폐막에 위한 골성 회복능 평가 = Evaluation of the Hydrophilized Asymmetric Pore Sized Polydioxanone Membrane for Guided Bone Regeneration

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      https://www.riss.kr/link?id=A99586932

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      다국어 초록 (Multilingual Abstract)

      Bone defects occur in a variety of clinical situation, and their reconstruction to provide mechanical integrity to the skeleton is a necessary step in the patient rehabilitation. Bones can regenerate themselves to repair defects up to a certain size but sometimes the suitable implant materials have to be applied to facilitate the bone repair. As a part of the effort to improve the efficiency of bone repair, we evaluated the hydrophilized asymmetric pore sized polydioxanone membrane for guided bone regeneration. The polydioxanone membrane was fabricated to have different pore size at inner (around 50 nm in diameter) and outer surface (around 50 μm in diameter) with an average 0.4 mm thickness. The cytotoxic effect of it was analyzed in vitro and the histocompatibility and guided bone regeneration effects were evaluated in vivo, respectively. The rat tibia bone defects measuring 7 mm×3 mm in size were treated with polydioxanone membrane with or without application of 10 mM LiCl or 100 μg/ml T-CAM. The defects were evaluated at 3weeks after treatment by radiography and histology. The polydioxanone membrane was relatively resilient with some cushion. It was no cytotoxic and evoked neither an immune nor an inflammatory response. It was gradually absorbed by numerous multinucleated giant cells with time and completely disappeared within 8 weeks at rat subcutaneous pouches. The application of polydioxanone membrane at rat tibia bone defects induced more effective bone repair with matured cortical plate regeneration compared to none membrane applied group. In addition, the treatment of 10 mM LiCl and 100 μg/ml T-CAM within polydioxanone membrane facilitated bony healing. These results suggest that the combined application of bioactive molecules such as 10 mM LiCl or 100 μg/ml T-CAM with hydrophilized sized polydioxanone membrane can facilitate the guided bone regeneration.
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      Bone defects occur in a variety of clinical situation, and their reconstruction to provide mechanical integrity to the skeleton is a necessary step in the patient rehabilitation. Bones can regenerate themselves to repair defects up to a certain size b...

      Bone defects occur in a variety of clinical situation, and their reconstruction to provide mechanical integrity to the skeleton is a necessary step in the patient rehabilitation. Bones can regenerate themselves to repair defects up to a certain size but sometimes the suitable implant materials have to be applied to facilitate the bone repair. As a part of the effort to improve the efficiency of bone repair, we evaluated the hydrophilized asymmetric pore sized polydioxanone membrane for guided bone regeneration. The polydioxanone membrane was fabricated to have different pore size at inner (around 50 nm in diameter) and outer surface (around 50 μm in diameter) with an average 0.4 mm thickness. The cytotoxic effect of it was analyzed in vitro and the histocompatibility and guided bone regeneration effects were evaluated in vivo, respectively. The rat tibia bone defects measuring 7 mm×3 mm in size were treated with polydioxanone membrane with or without application of 10 mM LiCl or 100 μg/ml T-CAM. The defects were evaluated at 3weeks after treatment by radiography and histology. The polydioxanone membrane was relatively resilient with some cushion. It was no cytotoxic and evoked neither an immune nor an inflammatory response. It was gradually absorbed by numerous multinucleated giant cells with time and completely disappeared within 8 weeks at rat subcutaneous pouches. The application of polydioxanone membrane at rat tibia bone defects induced more effective bone repair with matured cortical plate regeneration compared to none membrane applied group. In addition, the treatment of 10 mM LiCl and 100 μg/ml T-CAM within polydioxanone membrane facilitated bony healing. These results suggest that the combined application of bioactive molecules such as 10 mM LiCl or 100 μg/ml T-CAM with hydrophilized sized polydioxanone membrane can facilitate the guided bone regeneration.

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      참고문헌 (Reference)

      1 김준호, "새로운 비대칭 미세다공성 뼈재생유도막의 제조 및 분석" 한국생체재료학회 10 (10): 55-60, 2006

      2 M Mastrogiacomo, "Tissue engineering of bone: search for a better scaffold" 8 : 277-, 2005

      3 WL Fodor, "Tissue engineering and cell based therapies, from the bench to the clinic: the potential to replace, repair and regenerate" 13 : 102-, 2003

      4 S Nyman, "The regenerative potential of the periodontal ligament, an experimental study in the monkey" 9 : 257-, 1982

      5 A Mansukhani, "Sox2 induction by FGF and FGFR2 activating mutations inhibits Wnt signaling and osteoblast differentiation" 28 : 1065-, 2005

      6 Z Li, "Repair of mandible defect with tissue engineering bone in rabbits" 75 : 1017-, 2005

      7 HC Blair, "Recent advances in osteoclast biology and pathological bone resorption" 19 : 189-, 2004

      8 MD Kofron, "Protein- and gene-based tissue engineering in bone repair" 15 : 399-, 2004

      9 Y Zubery, "Ossification of a novel cross-linked porcine collagen barrier in guided bone regeneration in dogs" 78 : 112-, 2007

      10 AH Melcher, "On the repair potential of periodontal tissues" 47 : 256-, 1976

      1 김준호, "새로운 비대칭 미세다공성 뼈재생유도막의 제조 및 분석" 한국생체재료학회 10 (10): 55-60, 2006

      2 M Mastrogiacomo, "Tissue engineering of bone: search for a better scaffold" 8 : 277-, 2005

      3 WL Fodor, "Tissue engineering and cell based therapies, from the bench to the clinic: the potential to replace, repair and regenerate" 13 : 102-, 2003

      4 S Nyman, "The regenerative potential of the periodontal ligament, an experimental study in the monkey" 9 : 257-, 1982

      5 A Mansukhani, "Sox2 induction by FGF and FGFR2 activating mutations inhibits Wnt signaling and osteoblast differentiation" 28 : 1065-, 2005

      6 Z Li, "Repair of mandible defect with tissue engineering bone in rabbits" 75 : 1017-, 2005

      7 HC Blair, "Recent advances in osteoclast biology and pathological bone resorption" 19 : 189-, 2004

      8 MD Kofron, "Protein- and gene-based tissue engineering in bone repair" 15 : 399-, 2004

      9 Y Zubery, "Ossification of a novel cross-linked porcine collagen barrier in guided bone regeneration in dogs" 78 : 112-, 2007

      10 AH Melcher, "On the repair potential of periodontal tissues" 47 : 256-, 1976

      11 A Stavropoulos, "Oily calcium hydroxide suspension (osteoinductal) used as an adjunct to guided bone regeneration: an experimental study in rats" 18 : 761-, 2007

      12 J Gottlow, "New attachment formation as the result of controlled tissue regeneration" 11 : 494-, 1984

      13 P Cortellini, "Localized ridge augmentation using guided tissue regeneration in humans, a report of nine cases" 4 : 203-, 1993

      14 DR Hunt, "Hyaluronan supports recombinant human bone morphogenetic protein-2 induced bone reconstruction of advanced alveolar ridge defects in dogs. a pilot study" 72 : 651-, 2001

      15 T Karring, "Healing following implantation of periodontitis affected roots into bone tissue" 7 : 96-, 1980

      16 SC Park, "Fabrication and characterization of nerve growth factor-immobilized asymmetrically poroeus PDOCL/Pluronic F127 nerve guide conduit" 8 : 192-, 2011

      17 JW Park, "Effects of a cell adhesion molecule coating on the blasted surface of titanium implants on bone healing in the rabbit femur" 22 : 533-, 2007

      18 N Caplanis, "Effect of allogeneic, freeze-dried, demineralized bone matrix on guided bone regeneration in supraalveolar peri-implant defects in dogs" 12 : 634-, 1997

      19 JH Song, "Collagen-apatite nanocomposite membranes for guided bone regeneration" 83 : 248-, 2007

      20 AJ Salgado, "Bone tissue engineering: state of the art and future trends" 9 : 743-, 2004

      21 ME Aichelmann-Reidy, "Bone replacement grafts. the bone substitutes" 42 : 491-, 1998

      22 CA Vacanti, "Bone and cartilage reconstruction with tissue engineering approaches" 27 : 263-, 1994

      23 K Okazaki, "Blood-filled spaces with and without deproteinized bone grafts in guided bone regeneration, a histomorphometric study of the rabbit skull using non-resorbable membrane" 16 : 236-, 2005

      24 L Broens, "Asymmetric membrane structures as a result of phase separation phenomena" 32 : 33-, 1980

      25 JH Lee, "Anorgaic bone mineral coated with tetra-cell adhesion molecule enhances bone formation in rabbit calvarial defects" 309 : 981-, 2006

      26 KS Cho, "Alveolar bone formation at dental implant dehiscence defects following guided bone regeneration and xenogeneic freeze-dried demineralized bone matrix" 9 : 419-, 1998

      27 CM Cowan, "Adipose-derived adult stromal cells heal critical-size mouse calvarial defects" 22 : 560-, 2004

      28 I Needleman, "A systematic review of guided tissue regeneration for periodontal infrabony defects" 37 : 380-, 2002

      29 D Hutmacher, "A review of material properties of biodegradable and bioresorbable polymers and devices for GTR and GBR applications" 11 : 667-, 1996

      30 Y Taguchi, "A histological evaluation for guided bone regeneration induced by a collagenous membrane" 26 : 6158-, 2005

      31 CT Laurencin, "A highly porous three dimensional polyphosphazene polymer matrix for skeletal tissue regeneration" 30 : 133-, 1996

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      학술지등록 한글명 : 조직공학과 재생의학
      외국어명 : Tissue Engineering and Regenerative Medicine
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2013-10-01 평가 등재학술지 선정 (기타) KCI등재
      2012-01-01 평가 등재후보 1차 FAIL (기타) KCI등재후보
      2011-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2010-01-01 평가 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2008-01-01 평가 SCIE 등재 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.08 0.42 0.81
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.69 0.51 0.367 0.03
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