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Bio-inspired zwitterionic polymeric chelating assembly for treatment of copper-induced cytotoxicity and hemolysis.
Kuo, Shing-Yu; Chen, Pin-Chun; Huang, Kang-Ting; Huang, Chun-Jen.
Affiliation
  • Kuo SY; Department of Biomedical Sciences and Engineering, National Central University, Jhong-Li, Taoyuan 320, Taiwan.
  • Chen PC; Department of Biomedical Sciences and Engineering, National Central University, Jhong-Li, Taoyuan 320, Taiwan.
  • Huang KT; Department of Biomedical Sciences and Engineering, National Central University, Jhong-Li, Taoyuan 320, Taiwan; Department of Chemical & Materials Engineering, National Central University, Jhong-Li, Taoyuan 320, Taiwan.
  • Huang CJ; Department of Chemical & Materials Engineering, National Central University, Jhong-Li, Taoyuan 320, Taiwan; R&D Center for Membrane Technology, Chung Yuan Christian University, 200 Chung Pei Rd., Chung-Li City 32023, Taiwan; NCU-DSM Research Center, National Central University, Jhong-Li, Tao
Mater Sci Eng C Mater Biol Appl ; 129: 112367, 2021 Oct.
Article in En | MEDLINE | ID: mdl-34579886
ABSTRACT
We developed a hemocompatible, bio-inspired, multivalent, polymeric-chelating assembly based on the poly(2-methacryloyloxyethyl phosphorylcholine)-b-poly(serinyl acrylate) (PMPC-b-PserA) zwitterionic diblock copolymer. Functional PMPC-b-PserA was synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization to catch and encapsulate free copper ions (Cu2+) in a solution. PMPC with an identical polar group to phospholipids exhibits high hydrophilicity and fouling resistance against non-specific adsorption, and inertness to the metal ions. On the other hand, PserA with pendant groups of amino acids possesses a strong capability to react with Cu2+ by coordination interaction. Therefore, when PMPC-b-PserA was brought into contact with Cu2+, a hydrophobic core with multiple coordination "bridges" between polymers and Cu2+ was formed, leading to self-assembly of core-shell polymer-metal nanoparticles. As a result, free Cu2+ ions can be removed from the solution to prevent damage to cells and tissues. The synthesis and chemical structure of PMPC-b-PserA were characterized, and the formation of self-assembled polymer-Cu2+ nanoparticles and colloidal stability were analyzed. More importantly, the detoxification of PMPC-b-PserA in presence of Cu2+ with fibroblast cells was demonstrated by increased cell viability >80%. In addition, the hemolysis, which occurred due to disruption of RBC membranes by free Cu2+, was effectively suppressed by adding PMPC-b-PserA. The bio-inspired and biocompatible chelating agent of PMPC-b-PserA provides a new treatment approach to encapsulate and detoxify heavy metals in complex media for chelation therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Copper / Hemolysis Limits: Humans Language: En Journal: Mater Sci Eng C Mater Biol Appl Year: 2021 Document type: Article Affiliation country: Taiwan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Copper / Hemolysis Limits: Humans Language: En Journal: Mater Sci Eng C Mater Biol Appl Year: 2021 Document type: Article Affiliation country: Taiwan