2014
DOI: 10.1080/1539445x.2013.812873
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Interaction of Polyethyleneimines with Fibrinogen and Erythrocyte Membrane

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Cited by 7 publications
(7 citation statements)
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“…To further compare the different effects of mPEG2k–PCL2k and mPEG5k–PCL2k, a rheological experiment was conducted to record the viscoelasticity changes of whole blood containing the copolymers as a function of time . The time‐dependent storage modulus ( G ′) and loss modulus ( G ″) of the whole blood/mPEG–PCL samples are shown in Figure .…”
Section: Resultsmentioning
confidence: 99%
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“…To further compare the different effects of mPEG2k–PCL2k and mPEG5k–PCL2k, a rheological experiment was conducted to record the viscoelasticity changes of whole blood containing the copolymers as a function of time . The time‐dependent storage modulus ( G ′) and loss modulus ( G ″) of the whole blood/mPEG–PCL samples are shown in Figure .…”
Section: Resultsmentioning
confidence: 99%
“…Platelet‐rich plasma (PRP) was obtained by centrifuging citrated whole blood at 100 g for 10 min, and platelet‐poor plasma (PPP) was collected by spinning the citrated whole blood at 1000 g for 10 min. The following methods refer to the previous studies …”
Section: Methodsmentioning
confidence: 99%
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“…Following procedures previously reported in literature [24,32], the amount of adsorbed proteins was determined in an indirect way by measuring the non-adsorbed proteins and subtracting this value from the initial known protein feed. For the quantification of the protein in the PBS solutions, the characteristic absorbance of the Fibrinogen proteins at 280 nm [33] was analyzed on a HP 8453 UV-Vis spectrophotometer equipped with a Peltier cell using a quartz cuvette (1 cm path length). Each coating was measured in triplicate.…”
Section: Characterization Techniques and Proceduresmentioning
confidence: 99%
“…The quantification of the adsorbed FB was done by UV/Vis spectroscopy and making use of the characteristic absorption peak of these proteins at 280 nm, due to the presence of aromatic aminoacids in their chemical structure. [24][25] The coatings were fully covered with a known amount of a PBS solution of FB. The adsorbed proteins were quantified by determining the proteins remaining in the PBS solution (not-absorbed) after 24 hours of incubation and with reference to a previously prepared calibration curve (see Figure S3 in Supporting Information).…”
Section: Evaluation Of Anti-fouling Propertiesmentioning
confidence: 99%