Rikako Miyamoto, H. Inoue, Kenta Ohashi, H. Shibata, Meguro Takashi, Fukuyama Shigeo, K. Hashimoto
{"title":"EVALUATION OF THE CELL CYTOTOXICITY OF β-TRICALCIUM PHOSPHATE DOPED WITH VANADIUM IONS","authors":"Rikako Miyamoto, H. Inoue, Kenta Ohashi, H. Shibata, Meguro Takashi, Fukuyama Shigeo, K. Hashimoto","doi":"10.3363/PRB.26.113","DOIUrl":null,"url":null,"abstract":"Tricalcium phosphate doped with a small amount of both V(III) and V(V) ions (V-β-TCPV) was successfully prepared using a solid-state reaction, and its in vitro cell cytotoxicity was investigated using V79 cells. We found that the V(III) ion was substituted for a Ca ion at the Ca(5) site located in the β-Ca3(PO4)2 (β-TCP) crystal structure and that the V(V) ion was substituted for a P ion in the PO4 group of the β-TCP crystal structure. The cell cytotoxicity of the V-β-TCPVs increased gradually with increasing amounts of vanadium ion doping. The β-TCP doped with 1.0 mol% vanadium ions showed low toxicity. V-β-TCPVs doped with a small amount of vanadium ions are expected to be significant new implant biomaterials. (Received June 14, 2012; Accepted June 20, 2012)","PeriodicalId":20022,"journal":{"name":"Phosphorus Research Bulletin","volume":"89 1","pages":"113-116"},"PeriodicalIF":0.0000,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phosphorus Research Bulletin","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3363/PRB.26.113","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Tricalcium phosphate doped with a small amount of both V(III) and V(V) ions (V-β-TCPV) was successfully prepared using a solid-state reaction, and its in vitro cell cytotoxicity was investigated using V79 cells. We found that the V(III) ion was substituted for a Ca ion at the Ca(5) site located in the β-Ca3(PO4)2 (β-TCP) crystal structure and that the V(V) ion was substituted for a P ion in the PO4 group of the β-TCP crystal structure. The cell cytotoxicity of the V-β-TCPVs increased gradually with increasing amounts of vanadium ion doping. The β-TCP doped with 1.0 mol% vanadium ions showed low toxicity. V-β-TCPVs doped with a small amount of vanadium ions are expected to be significant new implant biomaterials. (Received June 14, 2012; Accepted June 20, 2012)