1992
DOI: 10.1016/0142-9612(92)90022-g
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ESCA investigation of low-temperature ammonia plasma-treated polyethylene substrate for immobilization of protein

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Cited by 46 publications
(23 citation statements)
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“…39,40 It has been found that the substrates with the amine and amide groups promote attachment of cells in the culture. 26,34,[41][42][43][44][45][46] This may result from the selective adsorption and immobilization of proteins on the scaffold surface 27,42,47 and/or the direct interaction of cells with the amine or amide groups. 43 Polyhydroxyacids such as polyglycolide, polylactides, and their copolymers have extensively been investigated as candidate materials for tissue engineered scaffolds.…”
Section: Discussionmentioning
confidence: 99%
“…39,40 It has been found that the substrates with the amine and amide groups promote attachment of cells in the culture. 26,34,[41][42][43][44][45][46] This may result from the selective adsorption and immobilization of proteins on the scaffold surface 27,42,47 and/or the direct interaction of cells with the amine or amide groups. 43 Polyhydroxyacids such as polyglycolide, polylactides, and their copolymers have extensively been investigated as candidate materials for tissue engineered scaffolds.…”
Section: Discussionmentioning
confidence: 99%
“…Often, the primary amino (-NH 2 ) groups serve as binding sites for spacer molecules 3 Present address: Novellus Systems, Inc., 3011 N. 1st St, San Jose, CA 95134, USA. 4 Author to whom any correspondence should be addressed.…”
Section: Introductionmentioning
confidence: 99%
“…Traditionally, low pressure plasmas sustained in N 2 or N-containing gases such as NH 3 are used for such functionalization. Hayat et al [4] used ammonia radio frequency (rf) discharges at 75 mTorr and 10 W to modify polyethylene (PE) surfaces with -NH 2 groups to subsequently immobilize proteins. They found that surface modification occurs rapidly within 1 min of treatment, increasing -NH 2 coverage from 0% up to 7%.…”
Section: Introductionmentioning
confidence: 99%
“…The binding energy (E B ) scale was fixed by the assignment of E B ϭ 285.0 eV to the OCH 2 O carbon (1s) peak. On the basis of this reference peak (called C1 in the figures) and according to previous studies, [41][42][43] the carbon chemical shifts for different oxygen-containing groups were C2 (ϾCOOO from hydroxyl, hydroperoxide, ether, or alkyl ester, ⌬E B ϭ 1.5 eV), C3 (ϾCAO from carbonyl or amide, ⌬E B ϭ 3.0 eV), and C4 (OCOOO from carboxyl or the corresponding ester, ⌬E B ϭ 4.2 eV). The areas of the different peaks were computed graphically from the spectra and were corrected with Scofields relative cross sections: 44 /C(1s)/ ϭ 1.00, /O(1s)/ ϭ 2.93, and /N(1s)/ ϭ 1.68.…”
Section: Escamentioning
confidence: 99%