Literature DB >> 29131605

Poly(ω-methoxyalkyl acrylate)s: Nonthrombogenic Polymer Family with Tunable Protein Adsorption.

Shingo Kobayashi1, Miyuki Wakui2, Yukihisa Iwata2, Masaru Tanaka1.   

Abstract

A series of polyacrylates with different n-alkyl side chain lengths (1 to 6, and 12 carbons) and a ω-methoxy terminal group (poly(ω-methoxyalkyl acrylate): PMCxA) were prepared to study their nonthrombogenicity using human platelet adhesion, micro bicinchoninic acid (micro BCA) protein assay, and enzyme-linked immunosorbent assay (ELISA) tests. In all cases, human platelet adhesion was suppressed on the PMCxA-coated substrates, and the number of human platelets adhered to the PMC3A (poly(3-methoxypropyl acrylate))-coated surface was comparable to that of commercialized nonthrombogenic coating agent poly(2-methoxyethyl acrylate) (PMEA, equal to PMC2A). The amount of protein adsorbed onto the PMCxA was investigated by micro BCA using bovine serum albumin (BSA) and human fibrinogen (hFbn), revealing that PMC3A exhibited significantly high resistance to nonspecific BSA adsorption. Additionally, the amount of hFbn adsorbed onto the PMC3A was suppressed to the same extent as PMEA. The exposure degree of platelet adhesion sites in adsorbed hFbn was evaluated using an ELISA test, and the degree on the PMCxA with three to six methylene carbons was comparable to the PMEA. The hydration water structure in the hydrated PMCxA was also characterized using differential scanning calorimetry (DSC). The amount of intermediate water, which is the hydration water molecules that moderately interact with the polymer matrix, was maximum in the PMEA with two methylene run lengths, whereas the amount decreased by increasing the number of methyelnes in the side chain. The amount of adsorbed protein increased with a decrease in the amount of intermediate water, suggesting that the protein adsorption amount is tunable by simply changing the number of methylene carbons in the side chain. The present study revealed that poly(ω-methoxyalkyl acrylate)s are useful for blood-contacting medical devices, and PMC3A is the best mode of PMCxA to apply as an antiprotein adsorption coating agent.

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Year:  2017        PMID: 29131605     DOI: 10.1021/acs.biomac.7b01247

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  4 in total

1.  Infrared Spectra and Hydrogen-Bond Configurations of Water Molecules at the Interface of Water-Insoluble Polymers under Humidified Conditions.

Authors:  Yuka Ikemoto; Yoshihisa Harada; Masaru Tanaka; Shin-Nosuke Nishimura; Daiki Murakami; Naoya Kurahashi; Taro Moriwaki; Kosuke Yamazoe; Hitoshi Washizu; Yoshiki Ishii; Hajime Torii
Journal:  J Phys Chem B       Date:  2022-05-31       Impact factor: 3.466

2.  Analysis of Interaction Between Interfacial Structure and Fibrinogen at Blood-Compatible Polymer/Water Interface.

Authors:  Tomoya Ueda; Daiki Murakami; Masaru Tanaka
Journal:  Front Chem       Date:  2018-11-08       Impact factor: 5.221

3.  Conformable microneedle pH sensors via the integration of two different siloxane polymers for mapping peripheral artery disease.

Authors:  Wonryung Lee; Seung-Hwan Jeong; Young-Woo Lim; Hyunhwan Lee; Joohyuk Kang; Hyunjae Lee; Injun Lee; Hyung-Seop Han; Shingo Kobayashi; Masaru Tanaka; Byeong-Soo Bae
Journal:  Sci Adv       Date:  2021-11-26       Impact factor: 14.136

4.  Nonthrombogenic, stretchable, active multielectrode array for electroanatomical mapping.

Authors:  Wonryung Lee; Shingo Kobayashi; Masase Nagase; Yasutoshi Jimbo; Itsuro Saito; Yusuke Inoue; Tomoyuki Yambe; Masaki Sekino; George G Malliaras; Tomoyuki Yokota; Masaru Tanaka; Takao Someya
Journal:  Sci Adv       Date:  2018-10-19       Impact factor: 14.136

  4 in total

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