2019
DOI: 10.1038/s41428-018-0164-1
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Surface-functionalization of isotactic polypropylene via dip-coating with a methacrylate-based terpolymer containing perfluoroalkyl groups and poly(ethylene glycol)

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Cited by 10 publications
(11 citation statements)
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“…Immobilization of horseradish peroxidase on AuNPsimmobilized substrate 40 AuNPs-immobilized substrates were washed three times with Milli-Q water and immersed in 2 mL of Milli-Q water containing 5 mM N-hydroxysuccinimide and 10 mM water-soluble carbodiimide and shaken for 30 min at 25 C. The substrates were immersed in phosphate buffer (0.1 M, pH 7.4, 2 mL) containing 0.3 mg mL À1 horseradish peroxidase (HRP) and 0.15 M NaCl and shaken for 2 h at 25 C. The substrates were washed three times with phosphate buffer (0.1 M, pH 7.4) containing 0.05 vol% Tween-20 and 0.15 M NaCl, and then washed twice with Milli-Q water. The enzymatic activity of HRP on the substrate surface was measured with a mixture of 0.1 mL phosphate buffer and a 0.9 mL ELISA-POD substrate kit containing 2,2 0 -azinobis[3-ethylbenzothiazoline-6-sulfonic acid]diammonium salt (ABTS) (Nakarai Tesque, Kyoto, Japan).…”
Section: Ft-ir Measurementsmentioning
confidence: 99%
“…Immobilization of horseradish peroxidase on AuNPsimmobilized substrate 40 AuNPs-immobilized substrates were washed three times with Milli-Q water and immersed in 2 mL of Milli-Q water containing 5 mM N-hydroxysuccinimide and 10 mM water-soluble carbodiimide and shaken for 30 min at 25 C. The substrates were immersed in phosphate buffer (0.1 M, pH 7.4, 2 mL) containing 0.3 mg mL À1 horseradish peroxidase (HRP) and 0.15 M NaCl and shaken for 2 h at 25 C. The substrates were washed three times with phosphate buffer (0.1 M, pH 7.4) containing 0.05 vol% Tween-20 and 0.15 M NaCl, and then washed twice with Milli-Q water. The enzymatic activity of HRP on the substrate surface was measured with a mixture of 0.1 mL phosphate buffer and a 0.9 mL ELISA-POD substrate kit containing 2,2 0 -azinobis[3-ethylbenzothiazoline-6-sulfonic acid]diammonium salt (ABTS) (Nakarai Tesque, Kyoto, Japan).…”
Section: Ft-ir Measurementsmentioning
confidence: 99%
“…Many bioinert polymers have thus far been developed as a coating material that leads to the durability, efficacy, and safety of various articles such as ship bottoms and food packaging. In particular, poly­(ethylene oxide) (PEO), , zwitterionic polymers, , and their derivatives , have been widely used in biorelated fields. Recently, a possible mechanism for how such polymers including poly­(vinyl ether) derivatives and poly­(2-methoxyethyl acrylate) exhibit such excellent anti-biofouling properties has been proposed on the basis of the interfacial aggregation states and dynamics in water.…”
mentioning
confidence: 99%
“…Since most bioinert polymers are hydrophilic or water-soluble, they need to be firmly anchored to solid substrates to avoid their elution into the water phase when they are used to construct the device surface. A typical method for achieving this is the covalent grafting of polymer chains onto the solid based on surface-initiated polymerization or polymer reactions using specific functional groups. ,, Another technique based on the chemical/physical adsorption using appropriate units introduced into a chain has also been reported. , Elsewhere, the surface segregation of functional units exhibiting bioinertness in a matrix polymer has been applied to construct the bioinert water interface. , A simple surface functionalization method with a nonsolvent has also been developed …”
mentioning
confidence: 99%
“…This occurs because of the surface segregation of the hydrophobic moieties in the polymer to minimize the surface energy. [46][47][48][49][50] We previously reported that the surface segregation of PEG moieties during dip-coating with a PEGylated copolymer can be controlled using a perfluoroalkylated surfactant (surfactant 1). 51 In the present study, we aimed to functionalize cellulose paper surfaces by a simple dip-coating procedure using a PEGylated copolymer and surfactant 1.…”
mentioning
confidence: 99%
“…Coating with a functional polymer solution is a simple and versatile approach to functionalizing material surfaces and does not require any specific apparatus. In general, any hydrophilic moieties are likely to be buried in the bulk phase of the polymer when it is used as a coating solution. This occurs because of the surface segregation of the hydrophobic moieties in the polymer to minimize the surface energy. We previously reported that the surface segregation of PEG moieties during dip-coating with a PEGylated copolymer can be controlled using a perfluoroalkylated surfactant (surfactant 1) …”
mentioning
confidence: 99%