Hemocompatibility of β-Cyclodextrin-Modified (Methacryloyloxy)ethyl Phosphorylcholine Coated Magnetic Nanoparticles

被引:7
|
作者
Li, Shuhui [1 ]
Sharaf, Mehdi Ghaffari [1 ]
Rowe, Elyn M. [2 ]
Serrano, Katherine [2 ]
Devine, Dana V. [2 ]
Unsworth, Larry D. [1 ]
机构
[1] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 1H9, Canada
[2] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6T 1Z7, Canada
基金
加拿大健康研究院;
关键词
polymer-coated magnetic nanoparticles; cyclodextrin; protein adsorption; uremic toxin; COMPLEMENT ACTIVATION; PROTEIN ADSORPTION; GOLD NANOPARTICLE; BLOOD-PLASMA; ALBUMIN; BINDING; SURFACE; MEMBRANES; CORONA; IDENTIFICATION;
D O I
10.3390/biom13081165
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adsorbing toxins from the blood to augment membrane-based hemodialysis is an active area of research. Films composed of beta-cyclodextrin-co-(methacryloyloxy)ethyl phosphorylcholine (p(PM fiCD-co-MPC)) with various monomer ratios were formed on magnetic nanoparticles and characterized. Surface chemistry effects on protein denaturation were evaluated and indicated that unmodified magnetic nanoparticles greatly perturbed the structure of proteins compared to coated particles. Plasma clotting assays were conducted to investigate the stability of plasma in the presence of particles, where a 2:2 monomer ratio yielded the best results for a given total surface area of particles. Total protein adsorption results revealed that modified surfaces exhibited reduced protein adsorption compared to bare particles, and pure MPC showed the lowest adsorption. Immunoblot results showed that fibrinogen, ff1-antitrypsin, vitronectin, prekallikrein, antithrombin, albumin, and C3 correlated with film composition. Hemocompatibility testing with whole blood illustrated that the 1:3 ratio of CD to MPC had a negative impact on platelets, as evidenced by the increased activation, reduced response to an agonist, and reduced platelet count. Other formulations had statistically significant effects on platelet activation, but no formulation yielded apparent adverse effects on hemostasis. For the first time, p(PM fiCD-co-MPC)-coated MNP were synthesized and their general hemocompatibility assessed.
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页数:21
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