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Author:

Zhou, Xuan (Zhou, Xuan.) | Kong, Ming (Kong, Ming.) | Cheng, Xiaojie (Cheng, Xiaojie.) | Li, Jingjing (Li, Jingjing.) | Li, Jing (Li, Jing.) | Chen, Xiguang (Chen, Xiguang.)

Indexed by:

EI Scopus SCIE PubMed

Abstract:

The aim was to investigate the potential of chitosan microspheres (CMs) with different acetylation using as a chemoembolic agent. Chitosan microspheres (CMs) were prepared via water-in-oil (W/O) emulsification cross-linking method, and acetylated chitosan microspheres (ACMs) were obtained by acetylation of CMs. Next, we characterized the morphology, size, composition and degrees of deacetylation using scanning electron microscopy (TEM), dynamic laser light scattering (DLS), and Fourier transform infrared spectrometer (FTIR). All microspheres had smooth surfaces and good mechanical flexibility, and all could pass through a 5F catheter. The swelling rate (SR) of CMs decreased significantly with the increase of pH (4.0-10.0) but ACMs did not change under the same conditions. Protein absorption assays suggested that albumin was more greatly adsorbed on CMs than on ACMs. Furthermore, CMs caused more blood clots than ACMs. ACMs caused hemolysis less than CMs (<5% of the time). Data indicated that ACMs had more hemocompatibility. Cytotoxicity tests indicated that ACMs initially had less cell attached proliferation but increased with incubation. In contrast, the relative growth rate of mouse embryo fibroblasts (MEFs) on CMs decreased gradually. The results suggested that ACMs could stimulate the growth of MEFs, and CMs were not cytotoxic to MEFs. Thus, ACMs were more biocompatible with greater potential to be used as chemoembolic material. (C) 2014 Published by Elsevier B.V.

Keyword:

Thrombogenicity Hemocompatibility Cytotoxicity Microspheres Chitosan Hemolysis

Author Community:

  • [ 1 ] [Zhou, Xuan]Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
  • [ 2 ] [Kong, Ming]Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
  • [ 3 ] [Cheng, Xiaojie]Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
  • [ 4 ] [Li, Jingjing]Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
  • [ 5 ] [Li, Jing]Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
  • [ 6 ] [Chen, Xiguang]Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
  • [ 7 ] [Zhou, Xuan]Chinese Acad Sci, Key Lab Nanobio Interface Res, Suzhou Key Lab Nanotheranost, Div Nanobiomed,Suzhou Inst Nanotech & Nanobion, Suzhou 215123, Peoples R China
  • [ 8 ] [Li, Jingjing]Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100022, Peoples R China

Reprint Author's Address:

  • [Chen, Xiguang]Ocean Univ China, Coll Marine Life Sci, 5 Yushan Rd, Qingdao 266003, Peoples R China

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Source :

COLLOIDS AND SURFACES B-BIOINTERFACES

ISSN: 0927-7765

Year: 2014

Volume: 123

Page: 387-394

5 . 8 0 0

JCR@2022

ESI Discipline: BIOLOGY & BIOCHEMISTRY;

ESI HC Threshold:285

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count: 36

SCOPUS Cited Count: 35

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 3

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