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Volumn 16, Issue 24, 2000, Pages 9604-9608

Self-assembled monolayers of alkanethiolates presenting mannitol groups are inert to protein adsorption and cell attachment

Author keywords

[No Author keywords available]

Indexed keywords

ADSORPTION; INTERFACES (MATERIALS); MONOLAYERS; OLIGOMERS; POLYETHYLENE GLYCOLS; PROTEINS; SPECTROSCOPIC ANALYSIS;

EID: 0034317224     PISSN: 07437463     EISSN: None     Source Type: Journal    
DOI: 10.1021/la0004653     Document Type: Article
Times cited : (417)

References (34)
  • 6
    • 0347800805 scopus 로고    scopus 로고
    • Chemistry and biological applications of polyethylene glycol
    • (b) Mrksich, M.; Whitesides, G. M. Chemistry and Biological Applications of Polyethylene Glycol. Am. Chem. Soc. Symp. Ser. 1997, 680, 361-373.
    • (1997) Am. Chem. Soc. Symp. Ser. , vol.680 , pp. 361-373
    • Mrksich, M.1    Whitesides, G.M.2
  • 10
    • 0033964689 scopus 로고    scopus 로고
    • Patterned alkylsiloxanes on hydroxylated substrates have been widely used to pattern cells. It remains unclear whether cells are confined by regions of substrate that are truly inert or rendered inert by the adsorption of protein. For examples, see (a) Jo, S.; Park, K. Biomaterials 2000, 21, 605-616.
    • (2000) Biomaterials , vol.21 , pp. 605-616
    • Jo, S.1    Park, K.2
  • 21
    • 0343352885 scopus 로고    scopus 로고
    • note
    • 2 in ethanolic solutions of alkanethiol (2 mM) for 9 h. The SAMs were rinsed with ethanol and dried with nitrogen before use.
  • 24
    • 0342917703 scopus 로고    scopus 로고
    • note
    • All SPR experiments were performed on a BIAcore 1000 instrument. Monolayer substrates were glued into plastic BIACore cassettes with a two-part epoxy (Devcon). Phosphate-buffered saline (PBS; 10 mM phosphate, 150 mM sodium chloride, pH 7.6) was degassed under vacuum, and all protein solutions were filtered through 0.45-μm filters before use.
  • 25
    • 0342917702 scopus 로고    scopus 로고
    • note
    • Albino 3T3-Swiss fibroblasts (American Type Culture Collector) were harvested from culture dishes with trypsin-EDTA, washed, and resuspended in DMEM supplemented with 10% fetal bovine serum. The suspended cells were added to wells (10 000/ well) containing patterned monolayer substrates immersed in DMEM supplemented with serum. Serum-supplemented medium was exchanged with fresh medium after 12 h and then every 5 days. Cell cultures were maintained at 37 °C and photographed daily with a Hamamatsu CCD camera through a Zeiss axiovert phase-contrast microscope (5 × magnification).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.