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1 erephthalate (PEOT/PBT) block copolymer, and polysulfone.
2 dialysis with CTA (10.91 +/- 3.65 ng/mL) and polysulfone (10.73 +/- 2.24 ng/mL) dialyzers were signif
3                                         With polysulfone as an example, we demonstrated the feasibili
4 ed phenomenon, wherein a demonstrably stable polysulfone backbone degrades rapidly in alkaline soluti
5 e addition of PVP as hydrophilic modifier to polysulfone-based membranes increases the biocompatibili
6 hese enzymes have been co-immobilized into a polysulfone/carbon nanotubes/ferrocene membrane by means
7 eters by approximately 5 A, so that a single polysulfone chain has an apparent diameter of 9-12 A in
8 Cs increased after chronic hemodialysis with polysulfone dialyzers (from 0.039+/-0.002 to 0.043+/-0.0
9 ents on hemodialysis: 28 patients started on polysulfone dialyzers and were switched to polynephron d
10 ncreased after one hemodialysis session with polysulfone dialyzers but not with polynephron dialyzers
11                     Chronic (3-month) use of polysulfone dialyzers did not significantly increase pre
12       Furthermore, chronic hemodialysis with polysulfone dialyzers increased oxidative stress in PBMC
13 p dialysis circuit with either new high-flux polysulfone dialyzers or dialyzers reprocessed once or 2
14 trate that dialysis with cellulose, CTA, and polysulfone dialyzers results in a significant increase
15 s demonstrate that reprocessing of high-flux polysulfone dialyzers with bleach increases the risk of
16 g/mL, respectively, with cellulose, CTA, and polysulfone dialyzers, and postdialysis levels were 17,8
17 , and 3790 +/- 1151% for cellulose, CTA, and polysulfone dialyzers, respectively.
18 f predialysis ratios for cellulose, CTA, and polysulfone dialyzers, respectively.
19 n polynephron dialyzers and were switched to polysulfone dialyzers.
20  cellulose, cellulose-tri-acetate (CTA), and polysulfone dialyzers.
21 o dialysis with new or reprocessed high-flux polysulfone dialyzers.
22 fficiency" cellulose (T220L) and "high-flux" polysulfone (F80B) dialyzers reprocessed with formaldehy
23  kD nominal molecular weight cut-off (MWCO), polysulfone fibers with 400 kD MWCO, and mixed cellulose
24 ous hemodialysis in 50-min intervals using a polysulfone filter (1.2 m2; mean pore size, 0.50 nm; blo
25 ound that some polymers such as PEOT/PBT and polysulfone interfere with islet function.
26 ketone, amine, hydroxyl, and aldehyde to the polysulfone main chain in excellent conversion.
27 monstrate that physical diffusion across the polysulfone membrane does not alter the carbon isotope v
28 separator consists of an asymmetric, porous, polysulfone membrane housed in a disposable chamber.
29                            Using a 3-cm-long polysulfone membrane with averaged molecular weight cuto
30                                    In vitro, polysulfone membranes released significantly more BPA in
31 ated contained either modified cellulosic or polysulfone membranes, whereas the germicides examined i
32 d the effect of dialysis with BPA-containing polysulfone or BPA-free polynephron dialyzers on BPA lev
33 as to investigate if the treatment of porous polysulfone (PPSF) with various concentrations of platel
34                      Culture on PEOT/PBT and polysulfone profoundly disturbed function of islets, and
35  polymeric dialyzer membranes, consisting of polysulfone (PS) and polyvinylpyrrolidone (PVP), were in
36 luorescens, a biofilm-forming bacterium, and polysulfone (PSF) ultrafiltration (UF) membranes to unra
37 rbonyl trichloride, on a polydopamine-coated polysulfone support.
38 A) bilayers on a polydopamine-functionalized polysulfone support.
39  abluminal membrane surface consists more of polysulfone than polyvinylpyrrolidone, and the luminal m
40 nce of helical regions in these freeze-dried polysulfones thus reflects their solution conformations
41 pin)(2)] to form the corresponding borylated polysulfones up to high concentrations with nearly const
42  Similarly, postdialysis levels with CTA and polysulfone were significantly greater (P < 0.05) than t
43 ld, iridium-catalyzed borylation of aromatic polysulfone with bis(pinacolato)diboron [B(2)(pin)(2)] t
44 ra cross-coupling reactions of the borylated polysulfones with functionalized aryl bromides allows in

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