Multiple parameter cytotoxicity index on dental alloys and pure metals

被引:83
作者
Hornez, JC [1 ]
Lefèvre, A
Joly, D
Hildebrand, HF
机构
[1] Fac Med Lille, UPRES EA 1049, Grp Rech Biomat, F-59045 Lille, France
[2] Sterngold CLAL, F-75003 Paris, France
来源
BIOMOLECULAR ENGINEERING | 2002年 / 19卷 / 2-6期
关键词
dental alloys; palladium; proliferation; viability; inflammation; cytotoxicity index;
D O I
10.1016/S1389-0344(02)00017-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Palladium (Pd) is a metal frequently used for dental alloys. In order to elucidate controversial options about Pd concerning its biological performances, our study consists in the evaluation of commercial and experimental PFM and C&B precious and semiprecious dental alloys. This investigation was also designated to the establishment of a cytotoxicity index (CI) such as it was described for hemocompatibility testing. The following materials were tested: 36 commercial alloys (Au-, Pd- and Ag-base), 14 experimental alloys (Pd-base established by an experience plan) and pure metals (Ag, Au, Cu, Ni, Cr, In, Sri, Pt, Ti, Zn). The cells culture experiments were carried out with epithelial L132 cells and NIH 3T3 fibroblasts. In vitro cell viability tests show that Pt, Sri, In, Ti, Au and Pd have no cytotoxic effect; Cr, Cu and Ag are toxic, Ni, Zn, and Co are highly toxic. An identical ranking was found with the inflammatory and proliferation tests. Toxic and highly toxic metals induced slight or strong prosthetic dental restoration morphological alterations after 3-days cultures and mostly cell death after 6-days cultures. These effects are dependent on the leakage of the element into the culture medium as revealed by ICP. The addition of Au gives benefit to Pd-Ag alloys, but does not produce any major effect on Pd-Cu alloys. This qualitative ranking can quantitatively be confirmed by cytocompatibility testing after application of a Cl. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:103 / 117
页数:15
相关论文
共 21 条
[1]  
ANKE M, 1980, THESIS KARL MARX U L, P3
[2]  
[Anonymous], 1991, TRACE ELEMENTS HLTH
[3]   EFFECTS OF NICKEL HYDROXYCARBONATE ON ALVEOLAR MACROPHAGE FUNCTIONS [J].
ARSALANE, K ;
AERTS, C ;
WALLAERT, B ;
VOISIN, C ;
HILDEBRAND, HF .
JOURNAL OF APPLIED TOXICOLOGY, 1992, 12 (04) :285-290
[4]   TISSUE ACCUMULATION OF NICKEL RELEASED DUE TO ELECTROCHEMICAL CORROSION OF NON-PRECIOUS DENTAL CASTING ALLOYS [J].
BERGMAN, M ;
BERGMAN, B ;
SOREMARK, R .
JOURNAL OF ORAL REHABILITATION, 1980, 7 (04) :325-330
[5]  
BLACK J, 1988, NATO ASI SERIES A, V158, P83
[6]  
BROWN SS, 1983, CHEM TOXICOLOGY CLIN
[7]   AMALGAM PIGMENTATION (AMALGAM TATTOO) OF THE ORAL-MUCOSA - CLINICOPATHOLOGIC STUDY OF 268 CASES [J].
BUCHNER, A ;
HANSEN, LS .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1980, 49 (02) :139-147
[8]  
BUNDY KJ, 1994, CRIT REV BIOMED ENG, V22, P139
[9]   FOLLOW-UP-STUDY OF PATIENTS WITH CONTACT-DERMATITIS CAUSED BY CHROMATES, NICKEL, AND COBALT [J].
DOOMSGOOSSENS, A ;
CEUTERICK, A ;
VANMAELE, N ;
DEGREEF, H .
DERMATOLOGICA, 1980, 160 (04) :249-260
[10]  
FRAZIER ME, 1979, TRACE METALS HLTH DI, P71