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      https://www.riss.kr/link?id=A102592322

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      다국어 초록 (Multilingual Abstract)

      Recently gene delivery has been designed newly using bioactive biomaterial and applied in the various field by many researchers. In this study, we proposed a new gene delivery system which has the capability of targeting effect in the specific tissue ...

      Recently gene delivery has been designed newly using bioactive biomaterial and applied in the various field by many researchers. In this study, we proposed a new gene delivery system which has the capability of targeting effect in the specific tissue and remarkably enhanced transfection efficiency. We investigated 1H-NMR spectroscopy, particle size analyzer and gel retardation to confirm the correct preparation of gene delivery. Also, we identified the hemo-compatibility of gene delivery by hemolysis assay, non-cytotoxicity by MTT test and transfection efficiency. The uptake mechanism of the gene carrier was confirmed using inhibitor agent such as sodium azide, indomethacin, quercetin, colchicine, and chloropromazine. As a results, it was identified that gene carrier prepared by in this study entered in the cell by the microtubule-dependent, energy-dependent and clathrin-mediated endocytosis pathway.

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      목차 (Table of Contents)

      • Abstract
      • 1. INTRODUCTION
      • 2. MATERIALS AND METHODS
      • 3. RESULTS AND DISCUSSION
      • 4. CONCLUSION
      • Abstract
      • 1. INTRODUCTION
      • 2. MATERIALS AND METHODS
      • 3. RESULTS AND DISCUSSION
      • 4. CONCLUSION
      • REFERENCES
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      참고문헌 (Reference)

      1 Gardlik, R., "Vectors and delivery systems in gene therapy" 11 : RA110-RA121, 2005

      2 Kim, S. H., "VEGF siRNA delivery system using arginine-grafted bioreducible poly" 6 : 718-726, 2009

      3 Deshpande, D., "Target specific optimization of cationic lipidbased systems for pulmonary gene therapy" 15 : 1340-1347, 1998

      4 Nam, J. P., "Target gene delivery from targeting ligand conjugated chitosan-PEI copolymer for cancer therapy" 135 : 153-161, 2016

      5 Kay, M. A., "State-of-the-art gene-based therapies: The road ahead" 12 : 316-328, 2011

      6 Rejman, J., "Sizedependent internalization of particles via the pathways of clathrinand caveolae-mediated endocytosis" 377 : 159-169, 2004

      7 Christensen, L. V., "Reducible poly(amido ethylenimine)s designed for triggered intracellular gene delivery" 17 : 1233-1240, 2006

      8 Wang, X., "Reducible chimeric polypeptide consisting of octa-D-arginine and tetra-L-histidine peptides as an efficient gene delivery vector" 10 : 4669-4690, 2015

      9 Guo, X., "Recent advances in nonviral vectors for gene delivery" 45 : 971-979, 2012

      10 Lee, M., "Polyethylene glycol-conjugated copolymers for plasmid DNA delivery" 22 : 1-10, 2005

      1 Gardlik, R., "Vectors and delivery systems in gene therapy" 11 : RA110-RA121, 2005

      2 Kim, S. H., "VEGF siRNA delivery system using arginine-grafted bioreducible poly" 6 : 718-726, 2009

      3 Deshpande, D., "Target specific optimization of cationic lipidbased systems for pulmonary gene therapy" 15 : 1340-1347, 1998

      4 Nam, J. P., "Target gene delivery from targeting ligand conjugated chitosan-PEI copolymer for cancer therapy" 135 : 153-161, 2016

      5 Kay, M. A., "State-of-the-art gene-based therapies: The road ahead" 12 : 316-328, 2011

      6 Rejman, J., "Sizedependent internalization of particles via the pathways of clathrinand caveolae-mediated endocytosis" 377 : 159-169, 2004

      7 Christensen, L. V., "Reducible poly(amido ethylenimine)s designed for triggered intracellular gene delivery" 17 : 1233-1240, 2006

      8 Wang, X., "Reducible chimeric polypeptide consisting of octa-D-arginine and tetra-L-histidine peptides as an efficient gene delivery vector" 10 : 4669-4690, 2015

      9 Guo, X., "Recent advances in nonviral vectors for gene delivery" 45 : 971-979, 2012

      10 Lee, M., "Polyethylene glycol-conjugated copolymers for plasmid DNA delivery" 22 : 1-10, 2005

      11 Brus, C., "Physicochemical and biological characterization of polyethylenimine-graft-poly(ethylene glycol) block copolymers as a delivery system for oligonucleotides and ribozymes" 15 : 677-684, 2004

      12 Wadhwa, M. S., "Peptide-mediated gene delivery: Influence of peptide structure on gene expression" 8 : 81-88, 1997

      13 Hyvonen, Z., "Novel cationic amphiphilic 1,4-dihydropyridine derivatives for DNA delivery" 1509 : 451-466, 2000

      14 Ou, M., "Novel biodegradable poly(disulfide amine)s for gene delivery with high efficiency and low cytotoxicity" 19 : 626-633, 2008

      15 Chang, C. W., "Non-ionic amphiphilic biodegradable PEG-PLGA-PEG copolymer enhances gene delivery efficiency in rat skeletal muscle" 118 : 245-253, 2007

      16 Wang, L. H., "Mis-assembly of clathrin lattices on endosomes reveals a regulatory switch for coated pit formation" 123 : 1107-1117, 1993

      17 Templeton, N. S., "Improved DNA: Liposome complexes for increased systemic delivery and gene expression" 15 : 647-652, 1997

      18 Kaouass, M., "Histonefection:Novel and potent non-viral gene delivery" 113 : 245-254, 2006

      19 Balicki, D., "Histone H2A-mediated transient cytokine gene delivery induces efficient antitumor responses in murine neuroblastoma" 97 : 11500-11504, 2000

      20 Niidome, T., "Gene transfer into hepatoma cells mediated by galactose-modified alpha-helical peptides" 21 : 1811-1819, 2000

      21 Schnitzer, J. E., "Filipin-sensitive caveolae-mediated transport in endothelium: Reduced transcytosis, scavenger endocytosis, and capillary permeability of select macromolecules" 127 : 1217-1232, 1994

      22 Dangoria, N. S., "Extracellular simian virus 40 induces an ERK/MAP kinase-independent signalling pathway that activates primary response genes and promotes virus entry" 77 : 2173-2182, 1996

      23 Kim, J. B., "Enhanced transfection of primary cortical cultures using arginine-grafted PAMAM dendrimer, PAMAM-Arg" 114 : 110-117, 2006

      24 Choi, J. S., "Enhanced transfection efficiency of PAMAM dendrimer by surface modification with L-arginine" 99 : 445-456, 2004

      25 Kim, W. J., "Efficient siRNA delivery with non-viral polymeric vehicles" 26 : 657-666, 2009

      26 Tanaka, K., "Disulfide crosslinked stearoyl carrier peptides containing arginine and histidine enhance siRNA uptake and gene silencing" 398 : 219-224, 2010

      27 Kichler, A., "Cationic amphipathic histidine-rich peptides for gene delivery" 1758 : 301-307, 2006

      28 Nam, H. Y., "Biodegradable PAMAM ester for enhanced transfection efficiency with low cytotoxicity" 30 : 665-673, 2009

      29 Futaki, S., "Arginine-rich peptides. An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery" 276 : 5836-5840, 2001

      30 Kim, T. I., "Arginine-grafted bioreducible poly(disulfide amine) for gene delivery systems" 30 : 658-664, 2009

      31 Kamimura, K., "Advances in gene delivery systems" 25 : 293-306, 2011

      32 Fischer, D., "A novel non-viral vector for DNA delivery based on low molecular weight, branched polyethylenimine: effect of molecular weight on transfection efficiency and cytotoxicity" 16 : 1273-1279, 1999

      33 Ou, M., "A family of bioreducible poly(disulfide amine)s for gene delivery" 30 : 5804-5814, 2009

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 재인증평가 신청대상 (재인증)
      2019-01-01 평가 등재학술지 유지 (계속평가) KCI등재
      2016-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2015-12-01 평가 등재후보로 하락 (기타) KCI등재후보
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-08-28 학술지명변경 한글명 : 한국생물공학회지 -> KSBB Journal
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      KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.37 0.37 0.38
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.37 0.36 0.662 0.02
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