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      KCI등재 SCOPUS SCIE

      Synthesis and Characterization of Magnetic Nanoparticles and Its Application in Lipase Immobilization

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      https://www.riss.kr/link?id=A103920113

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      다국어 초록 (Multilingual Abstract)

      We demonstrate herein the synthesis and modification of magnetic nanoparticles and its use in the immobilization of the lipase. Magnetic Fe3O4 nanoparticles (MNPs) were prepared by simple co-precipitation method in aqueous medium and then subsequently modified with tetraethyl orthosilicate (TEOS) and 3- aminopropyl triethylenesilane (APTES). Silanization magnetic nanoparticles (SMNP) and amino magnetic nanomicrosphere (AMNP) were synthesized successfully. The morphology, structure, magnetic property and chemical composition of the synthetic MNP and its derivatives were characterized using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) analysis, X-ray diffraction, superconducting quantum interference device (SQUID) and thermogravimetric analyses (TGA). All of these three nanoparticles exhibited good crystallization performance, apparent superparamagnetism, and the saturation magnetization of MNP, SMNP, AMNP were 47.9 emu/g, 33.0 emu/g and 19.5 emu/g, respectively. The amino content was 5.66%. The AMNP was used to immobilize lipase, and the maximum adsorption capacity of the protein was 26.3 mg/g. The maximum maintained activity (88 percent) was achieved while the amount of immobilized lipase was 23.7 mg g−1. Immobilization of enzyme on the magnetic nanoparticles can facilitate the isolation of reaction products from reaction mixture and thus lowers the cost of enzyme application.
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      We demonstrate herein the synthesis and modification of magnetic nanoparticles and its use in the immobilization of the lipase. Magnetic Fe3O4 nanoparticles (MNPs) were prepared by simple co-precipitation method in aqueous medium and then subsequently...

      We demonstrate herein the synthesis and modification of magnetic nanoparticles and its use in the immobilization of the lipase. Magnetic Fe3O4 nanoparticles (MNPs) were prepared by simple co-precipitation method in aqueous medium and then subsequently modified with tetraethyl orthosilicate (TEOS) and 3- aminopropyl triethylenesilane (APTES). Silanization magnetic nanoparticles (SMNP) and amino magnetic nanomicrosphere (AMNP) were synthesized successfully. The morphology, structure, magnetic property and chemical composition of the synthetic MNP and its derivatives were characterized using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) analysis, X-ray diffraction, superconducting quantum interference device (SQUID) and thermogravimetric analyses (TGA). All of these three nanoparticles exhibited good crystallization performance, apparent superparamagnetism, and the saturation magnetization of MNP, SMNP, AMNP were 47.9 emu/g, 33.0 emu/g and 19.5 emu/g, respectively. The amino content was 5.66%. The AMNP was used to immobilize lipase, and the maximum adsorption capacity of the protein was 26.3 mg/g. The maximum maintained activity (88 percent) was achieved while the amount of immobilized lipase was 23.7 mg g−1. Immobilization of enzyme on the magnetic nanoparticles can facilitate the isolation of reaction products from reaction mixture and thus lowers the cost of enzyme application.

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      참고문헌 (Reference)

      1 Jang, J. H., 94 : 148-, 2010

      2 Park, J. O., 256 : 6945-, 2010

      3 Park, H. J., 83 : 198-, 2011

      4 Dios, A. S., 666 : 1-, 2010

      5 Qi, H., 82 : 498-, 2011

      6 Sung, Y. J., 43 : 432-, 2013

      7 Xuan, J., 84 : 32-, 2012

      8 Li, J., 11 : 10187-, 2011

      9 Sayin, S., 33 : 2433-, 2013

      10 Klostergaard, J., 73 : 33-, 2012

      1 Jang, J. H., 94 : 148-, 2010

      2 Park, J. O., 256 : 6945-, 2010

      3 Park, H. J., 83 : 198-, 2011

      4 Dios, A. S., 666 : 1-, 2010

      5 Qi, H., 82 : 498-, 2011

      6 Sung, Y. J., 43 : 432-, 2013

      7 Xuan, J., 84 : 32-, 2012

      8 Li, J., 11 : 10187-, 2011

      9 Sayin, S., 33 : 2433-, 2013

      10 Klostergaard, J., 73 : 33-, 2012

      11 Hua, M. Y., 32 : 516-, 2011

      12 Mahapatra, A., 39 : 5443-, 2013

      13 Girginova, S., 345 : 234-, 2010

      14 Anirudhan, T. S., 107 : 1-, 2013

      15 Tran, D. T., 158 : 112-, 2012

      16 Jiang, Y. Y., 58 : 103-, 2009

      17 Liao, H. D., 82 : 600-, 2010

      18 Gokhale, A. A., 90 : 76-, 2013

      19 Mahmood, I., 73 : 72-, 2013

      20 Liang, H. F., 124 : 964-, 2010

      21 Liu, X., 56 : 142-, 2011

      22 Li, Z. L., 43 : 230-, 2012

      23 Shao, T. J., 44 : 789-, 2004

      24 Dong, H. W., 35 : 376-, 2004

      25 Schultz, N., 132 : 202-, 2007

      26 Kuo, C. H., 87 : 2538-, 2012

      27 Cui, Y. J., 150 : 171-, 2010

      28 Bradford, M. M., 72 : 248-, 1976

      29 Hatzinikolaou, D. G., 88 : 53-, 1999

      30 Gong, J. L., "R. Q. Biosens. Bioelectron. 2007" 22 : 1501-, 2007

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      유사연구자 (20) 활용도상위20명

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2008-01-01 평가 SCI 등재 (기타) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-07-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.58 0.11 0.38
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.28 0.23 0.213 0.04
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