West China Journal of Stomatology

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The Development andin vitroRelease Rate Determination of Controlled-release Delivery Gutta-percha Point Containing Metronidazole Compound

WANG Duo*,WANG Zhuping,GAOJing,et al.   

  1. *Department ofOralMedicine,College ofStomatology,the DentistrySchool ofShandong University,Jinan250012,China
  • Received:2003-10-25 Revised:2003-10-25 Online:2003-10-20 Published:2003-10-20

Abstract:

Objective To prepare the controlled-release delivery gutta-percha points containing metronidazole compound (CDGMC) and to determine its release ratein vitro.Methods The drug points were made by using compound drugs and gutta- percha as a carrier, and CDGMCwere prepared followed by enveloping a release membrane outward. The best formulawas select- ed according to the release parameters of the drugs extracted in the release experimentsin vitro. The CDGMCwere placed into the extracted teeth after root canals were routinely prepared. The non-drug CDGMC was used as the control. The absorbency of the drugs in normal saline (37℃,pH7.4) was determined timely. The percentage of release and cumulated release of the drugswere calculated according to the concentrations of drugs in medium.Results Thein vitroexperiments showed that this system con- tained 1 880μg ofmetronidazole and 267μg of ciprofloxacin. The experiments in healthy single root canal showed thatthe drug re- lease amounts around the perioapical areawere metronidazole 88·54μg/ml and ciprofloxacin 9·05μg/ml in 10 days.Conclusion  CDGMC can continuously release effective drug concentrations more than 10 days and could be considered as an ideal method for clinical application.

Key words: metronidazole, ciprofloxacin, controlled-release delivery system