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      약물전달능을 지닌 생체활성 실리카젤과 폴리카프로락톤(PCL)을 복합화한 마이크로입자의 제조

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      https://www.riss.kr/link?id=A99893253

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      다국어 초록 (Multilingual Abstract)

      Bioactive ceramic-polymer hybrid microparticles were fabricated and examined for drug delivery capability in this study. Particulated silica gel synthesized via sol-gel method was used for ceramic component, and biodegradable polycaprolactone was used as polymer matrix. Amount of silica gel particles against matrix was fixed in 30 wt% to be well dispersed in the composite, resulting in formation of microparticles. Average size of the hybrid particles synthesized was about 385 ㎛. Bioactivity of the hybrid material was confirmed by hydroxyapatite layer formed on the surface of microparticles after soaking in simulated body fluid. Tetracycline was incorporate in the hybrid microparticles to evaluate capability of drug delivery in phosphate buffered solution. Tetracycline socked in the microparticles was released slowly about 55% up to 4 weeks. From the results, the silica gel-polycaprolactone hybrid microparticles can be used for potential carrier for drug delivery and regeneration of bone.
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      Bioactive ceramic-polymer hybrid microparticles were fabricated and examined for drug delivery capability in this study. Particulated silica gel synthesized via sol-gel method was used for ceramic component, and biodegradable polycaprolactone was used...

      Bioactive ceramic-polymer hybrid microparticles were fabricated and examined for drug delivery capability in this study. Particulated silica gel synthesized via sol-gel method was used for ceramic component, and biodegradable polycaprolactone was used as polymer matrix. Amount of silica gel particles against matrix was fixed in 30 wt% to be well dispersed in the composite, resulting in formation of microparticles. Average size of the hybrid particles synthesized was about 385 ㎛. Bioactivity of the hybrid material was confirmed by hydroxyapatite layer formed on the surface of microparticles after soaking in simulated body fluid. Tetracycline was incorporate in the hybrid microparticles to evaluate capability of drug delivery in phosphate buffered solution. Tetracycline socked in the microparticles was released slowly about 55% up to 4 weeks. From the results, the silica gel-polycaprolactone hybrid microparticles can be used for potential carrier for drug delivery and regeneration of bone.

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      참고문헌 (Reference)

      1 Harris RJ, "Treatment of furcation defects with an allograft-alloplast-tetracycline composite bone graft combined with GTR: human histologic evaluation of a case report" 22 : 381-387, 2002

      2 Bonassar LJ, "Tissue engineering: the first decade and beyond" 30 : 297-303, 1998

      3 Seymour RA, "Tetracyclines in the management of periodontal diseases, A review" 22 : 22-35, 1995

      4 Vijayalakshmi U, "Synthesis and Characterization of Porous Silica Gels for Biomedical Applications. Trends Biomater" 18 : 101-105, 2005

      5 Pang L, "Surface modification of PLGA/β-TCP scaffold for bone tissue engineering: Hybridization with collagen and apatite" 201 : 9549-9557, 2007

      6 Catauro M, "Sol-gel processing of drug delivery zirconia/polycaprolactone hybrid materials" 19 : 531-540, 2008

      7 Gaetano FD, "Sol-gel processing of drug delivery materials and release kinetics" 16 : 261-265, 2005

      8 Li H, "Preparation and characterization of bioactive and biodegradable wollastonite/poly(D,L-lactic acid) composite scaffolds" 15 : 1089-1095, 2004

      9 Tampieri A, "Porous phosphate-gelatine composite as bone graft with drug delivery function" 14 : 623-627, 2003

      10 "Porous ZrO2 bone scaffold coated with hydroxyapatite with fluorapatite intermediate layer" 24 (24): 3277-3284, 200308

      1 Harris RJ, "Treatment of furcation defects with an allograft-alloplast-tetracycline composite bone graft combined with GTR: human histologic evaluation of a case report" 22 : 381-387, 2002

      2 Bonassar LJ, "Tissue engineering: the first decade and beyond" 30 : 297-303, 1998

      3 Seymour RA, "Tetracyclines in the management of periodontal diseases, A review" 22 : 22-35, 1995

      4 Vijayalakshmi U, "Synthesis and Characterization of Porous Silica Gels for Biomedical Applications. Trends Biomater" 18 : 101-105, 2005

      5 Pang L, "Surface modification of PLGA/β-TCP scaffold for bone tissue engineering: Hybridization with collagen and apatite" 201 : 9549-9557, 2007

      6 Catauro M, "Sol-gel processing of drug delivery zirconia/polycaprolactone hybrid materials" 19 : 531-540, 2008

      7 Gaetano FD, "Sol-gel processing of drug delivery materials and release kinetics" 16 : 261-265, 2005

      8 Li H, "Preparation and characterization of bioactive and biodegradable wollastonite/poly(D,L-lactic acid) composite scaffolds" 15 : 1089-1095, 2004

      9 Tampieri A, "Porous phosphate-gelatine composite as bone graft with drug delivery function" 14 : 623-627, 2003

      10 "Porous ZrO2 bone scaffold coated with hydroxyapatite with fluorapatite intermediate layer" 24 (24): 3277-3284, 200308

      11 Jones JR, "Optimising bioactive glass scaffolds for bone tissue engineering" 27 : 964-973, 2006

      12 Costa PT, "Nucleation of hydroxyapatite on silica-Gel: Experiments and thermodynamic explanation" 13 : 251-254, 1998

      13 Torres FG, "Mechanical properties and bioactivity of porous PLGA/TiO2 nanoparticle-filled composites for tissue engineering scaffolds" 67 : 1139-1147, 2007

      14 Radin S, "In vitro bioactivity and degradation behavior of silica xerogels intended as controlled release materials" 23 : 3113-3122, 2002

      15 Doyle C, "In vitro and in vivo evaluation of polyhydroxybutyrate and of polyhydroxybutyrate reinforced with hydroxyapatite" 12 : 841-847, 1991

      16 Kim HW, "Hydroxyapatite/poly(ε-caprolactone) composite coatings on hydroxyapatite porous bone scaffold for drug delivery" 25 : 1279-1287, 2004

      17 Kim HW, "Hydroxyapatite porous scaffold engineered with biological polymer hybrid coating for antibiotic Vancomycin release" 16 : 189-195, 2005

      18 Thomson RC, "Hydroxyapatite fiber reinforced poly(α-hydroxy ester) foams for bone regeneration" 19 : 1935-1943, 1998

      19 Liao SS, "Hierarchically biomimetic bone scaffold materials: nano-HA/collagen/PLA composite" 15 : 158-165, 2004

      20 Vitale-Brovarone C, "Glass-ceramic scaffolds containing silica mesophases for bone grafting and drug delivery" 20 : 809-820, 2009

      21 Jegal SH, "Functional composite nanofibers of poly(lactide-co-caprolactone) containing gelatin-apatite bone mimetic precipitate for bone regeneration" ELSEVIER SCI LTD 7 (7): 1609-1617, 2011

      22 Shor L, "Fabrication of three-dimensional polycaprolactone/hydroxyapatite tissue scaffolds and osteoblastscaffold interactions in vitro" 28 : 5291-5297, 2007

      23 Li P, "Effects of ions in aqueous media on hydroxyapatite induction by silica gel and its relevance to bioactivity of bioactive glasses and glass-ceramics" 4 : 221-229, 1993

      24 Evans GH, "Effect of various graft materials with tetracycline in localized juvenile periodontitis" 60 : 491-497, 1989

      25 Kim HW, "Development of hydroxyapatite bone scaffold for controlled drug release via poly(epsilon-caprolactone) and hydroxyapatite hybrid coatings" 70 : 240-249, 2004

      26 Shinto Y, "Calcium hydroxyapatite ceramic used as a delivery system for antibiotics" 74 : 600-604, 1992

      27 Silvio L, "Biodegradable drug delivery system for the treatment of bone infection and repair" 10 : 653-658, 1999

      28 Lee HH, "Bioactivity improvement of poly(ε-caprolactone) membrane with the addition of nanofibrous bioactive glass" 4 : 622-629, 2008

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2026 평가예정 재인증평가 신청대상 (재인증)
      2020-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2017-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2014-11-11 학회명변경 한글명 : 대한치과기재학회 -> 대한치과재료학회
      영문명 : The Korea Research Society For Dental Materials -> Korean Society For Dental Materials
      KCI등재
      2014-11-11 학술지명변경 한글명 : 대한치과기재학회지 -> 대한치과재료학회지
      외국어명 : J. Korea Res. Soc. Dent. Mater. -> Korean Journal of Dental Materials
      KCI등재
      2013-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2010-01-01 평가 등재 1차 FAIL (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2003-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2002-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.33 0.33 0.25
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.2 0.18 0.408 0.07
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