1227 Lipopolysaccharide Release from Dental Casting Alloys
S.K. NELSON, J. WATAHA, P. LOCKWOOD, and B. BLACKBURN, Medical College of Georgia, Augusta, USA

Lipolysaccharide (LPS) is known to adhere to dental casting alloys, but its release from alloys has not been measured.  Objective:  To measure LPS released passively from dental casting alloys over time, and during subsequent ultrasonic treatment.  Methods:  Four alloys (2 high noble (HN) and 2 noble (N); 1cm diameter x 1mm thick; n=3) were polished, cleaned and disinfected, then exposed to LPS (E. coli, 100 mg/mL) for 24h.  Specimens were transferred into l mL phosphate buffered saline (PBS) for 24h, transferred to new PBS for 48h, then 96h.  Alloys were then placed into 1.0 mL of PBS and ultrasonically (Ult/Son) treated  for 10 min.  LPS concentrations (pg/mL) were assessed at each time interval and after Ult/Son treatment using the Limulus Amebocyte Lysate assay. PBS solution served as the control.  Results:  LPS release was significantly greater than controls (* in table, ANOVA/Tukey, a=0.05) for all alloys at 24h, but release was lower at other times (48, 96h). LPS release after Ult/Son treatment was significantly
LPS (pg/mL) (SD) 24h 48h 96h PBS Control Ult/Son Treatment
AuPt (HN) 870 (140)* a 39 (21) 24 (13) 22 (15) 60 (40) a
AuPd (HN) 440 (130) * b 130 (22) * 58 (33) 25 (13) 170 (70)* b
PdCuGa (N) 940 (160) * a 26 (13) 25  (13) 27 (13) 19 (13) a
PdAg (N) 410 (250) * b 70 (40) * 60 (27)* 23 (14) 140 (70)* b
greater than controls for the AuPd and PdAg alloys (*).  Alloy type significantly influenced LPS release at 24h and after Ult/Son treatment (a,b in table, ANOVA/Tukey). Conclusions: In this in vitro system, LPS release was dependent on the alloy type, and was greatest in the first 24h. (Support: Metalor and MCG Biocompatibility Prog.)

Seq #121 - Casting Alloys I
3:45 PM-5:00 PM, Thursday, 7 March 2002 San Diego Convention Center Exhibit Hall C

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