2006
DOI: 10.1002/jbm.b.30490
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Synthesis and performance of amphiphilic copolymers for blood cell separation

Abstract: Three types of amphiphilic copolymers using n-butylmethacrylate (BMA) as a hydrophobic monomer, and each of N,N'-dimethylacrylamide (DMA), N-acryloylmorpholine (AMO), and N-vinylpyrrolidone (VP) as hydrophilic comonomers were synthesized for coating filters used to remove leukocytes. The influence of the amphiphilic property of the resulting filters, which were composed of nonwoven fabrics coated with the above copolymers, on leukocyte removal and platelet permeation through the filters from whole blood was in… Show more

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Cited by 10 publications
(13 citation statements)
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“…These observations indicate together with the saltatory motion seen by cells moving over PNAM covered surfaces (see Supporting Information movie 2) that adhesions seem to be less stable allowing spreading only to a limited extent. The cells growth and ongoing divisions in close proximity to or on PNAM covered areas (see Supporting Information movie 1) indicate that the polymer, albeit acting as a temporary barrier to cell adhesion, is not toxic for the cells, which is in line with previous reports of limited toxicity for NAM containing copolymers . It is also worth highlighting that although the PNAM does contain unreacted monomer (∼12%)—acrylate monomers are generally toxic—the monomer appears to have little effect on cell viability, although a more in‐depth cytotoxicity study is required to elucidate NAM effects on cells.…”
Section: Resultssupporting
confidence: 80%
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“…These observations indicate together with the saltatory motion seen by cells moving over PNAM covered surfaces (see Supporting Information movie 2) that adhesions seem to be less stable allowing spreading only to a limited extent. The cells growth and ongoing divisions in close proximity to or on PNAM covered areas (see Supporting Information movie 1) indicate that the polymer, albeit acting as a temporary barrier to cell adhesion, is not toxic for the cells, which is in line with previous reports of limited toxicity for NAM containing copolymers . It is also worth highlighting that although the PNAM does contain unreacted monomer (∼12%)—acrylate monomers are generally toxic—the monomer appears to have little effect on cell viability, although a more in‐depth cytotoxicity study is required to elucidate NAM effects on cells.…”
Section: Resultssupporting
confidence: 80%
“…The cells growth and ongoing divisions in close proximity to or on PNAM covered areas (see Supporting Information movie 1) indicate that the polymer, albeit acting as a temporary barrier to cell adhesion, is not toxic for the cells, which is in line with previous reports of limited toxicity for NAM containing copolymers. 16,17 It is also worth highlighting that although the PNAM does contain unreacted monomer (12%)-acrylate monomers are generally toxic-the monomer appears to have little effect on cell viability, although a more in-depth cytotoxicity study is required to elucidate NAM effects on cells. Interestingly, polyacrylates frequently have varying degrees of unreacted monomer, which are not indicated as having an effect in cell adhesion studies.…”
Section: Cellular Response and Migrationmentioning
confidence: 99%
“…In the present study with 32-sheet stacks of the filter coated with DB40, a (55 6 10)% platelet permeation ratio and a 3.23 6 0.45 logarithmic reduction of leukocytes were observed as in Table III, although DB40-coated filter showed a 79% platelet permeation ratio and a 1.2 logarithmic reduction of leukocytes in the previous simplified system with four-sheet stacks of the coated filter. 16 The increase in the number of stacked sheets thus proved to improve the logarithmic reduction of leukocytes remarkably, but lowered the platelet permeation to some extent. This implies that BMA units in DB40 may be slightly too hydrophobic for the platelet permeation.…”
Section: Discussionmentioning
confidence: 97%
“…16 They were immersed in a copolymer solution (3, 5, or 10 wt % in EtOH) in a glass vial. The vial was placed in an ultrasonic generator to degas the filters for 30 min.…”
Section: Preparation Of Coated Filters For Blood Cell Separationmentioning
confidence: 99%
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