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1.
J Oral Rehabil ; 36(5): 362-7, 2009 May.
Article in English | MEDLINE | ID: mdl-19210680

ABSTRACT

This study was conducted to evaluate the effect of polyphosphoric acid (PPA) treatment on bone regeneration around titanium (Ti) implants in vivo. Adsorption of PPA by Ti was achieved by immersing Ti implants (2 mm in diameter, 4 mm in length) in different concentrations of PPA solution (0, 1 and 10 wt%) for 24 h at 37 degrees C after proper Ti surface cleaning. The treated Ti implants were implanted on 8-week-old-male rat (n = 30) tibiae. Two or four weeks after implantation, all animals were deeply anaesthetized and underwent perfusion fixation. Ten specimens in each condition were further immersed in the same fixative for 1 week and eventually embedded in polyester resin. Afterwards, undecalcified sections were ground to a thickness of approximately 70 microm parallel to the long axis of the implant. The sections were stained with basic fuchsine and methylene blue and then examined by light microscopy. For quantitative evaluation of bone regeneration around the implants, the bone-implant contact ratio (BICR) was determined. Polyphosphoric acid treatment of the Ti implant surface significantly enhanced direct bone contact to the Ti surface. Especially, the BICRs of the 1 wt% PPA-treated Ti implants were significantly higher than those of the control untreated Ti implants, both 2 and 4 weeks after implantation. At 4 weeks, 10 wt% PPA-treated implants also significantly increased the BICR as compared to that of the untreated Ti implants. These results suggest that PPA treatment promotes osteoconductivity of Ti in vivo.


Subject(s)
Bone Regeneration/drug effects , Implants, Experimental , Phosphoric Acids/pharmacology , Polymers/pharmacology , Titanium , Animals , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical/methods , Male , Osseointegration/drug effects , Rats , Rats, Wistar , Tibia/anatomy & histology , Tibia/drug effects , Tibia/surgery
2.
Mutat Res ; 446(2): 149-54, 1999 Dec 13.
Article in English | MEDLINE | ID: mdl-10635336

ABSTRACT

We administered mitomycin C (0.5 mg/kg) intraperitoneally to hyperthermic-treated mice and examined the effect of hyperthermia on micronucleus induction. Hyperthermia enhanced micronucleus induction. The timing of chemical administration relative to the start of hyperthermic treatment (37 degrees C ambient temperature) influenced micronucleus frequency, and the effect was greatest 2 h after the start of hyperthermic treatment. But the hyperthermic treatment did not change the time course of micronucleus induction. In addition, we investigated the effect of hyperthermia on micronucleus induction by chemicals with different modes of action, i.e., alkylating agents (mitomycin C at 0.1-0.5 mg/kg, cyclophosphamide at 1.25-10 mg/kg), a spindle poison (colchicine at 0.05-1.0 mg/kg), and an antimetabolite (5-fluorouracil at 2.5-50 mg/kg). Hyperthermia enhanced only the clastogenicity of alkylating agents.


Subject(s)
Cell Nucleus/genetics , Fever/genetics , Mutagens/toxicity , Alkylating Agents/toxicity , Animals , Antimetabolites/toxicity , Colchicine/toxicity , Cross-Linking Reagents/toxicity , Cyclophosphamide/toxicity , Fluorouracil/toxicity , Hyperthermia, Induced , Male , Mice , Mice, Inbred Strains , Micronucleus Tests , Mitomycin/toxicity , Time Factors
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