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<ArticleSet><Article><Journal><PublisherName>Isfahan University of Medical Sciences</PublisherName><JournalTitle>Dental Research Journal</JournalTitle><Issn>1735-3327</Issn><Volume>4</Volume><Issue>1</Issue><PubDate PubStatus="epublish"><Year>2008</Year><Month>01</Month><Day>20</Day></PubDate></Journal><ArticleTitle>Antibacterial Substantivity of Three Concentrations of Doxycycline on Bovine Root Dentin Infections: an In Vitro Study</ArticleTitle><FirstPage>49</FirstPage><LastPage>49</LastPage><AuthorList><Author><FirstName>Z.</FirstName><LastName>Mohammadi</LastName><Affiliation>. mohammadi_zahed@yahoo.com</Affiliation></Author><Author><FirstName>A. R.</FirstName><LastName>Farhad</LastName></Author><Author><FirstName>F.</FirstName><LastName>Ezoddini Ardakani</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2010</Year><Month>11</Month><Day>06</Day></PubDate></History><Abstract>Introduction&#13;
The aim of this in vitro study was to compare the antimicrobial activity and substan-tivity of three concentrations of doxycycline on bovine root dentin infections.&#13;
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Methods and Materials&#13;
Seventy dentin tubes prepared from intact bovine incisors were infected in vitro for 14 days with Enterococcus faecalis. The specimens were divided into five groups accord-ing to the used intracanal irrigation as follows: Group1: l00mg/ml of doxycycline hydrochloride so-lution (DHS) (n=20); Group 2: 50mg/ml of DHS (n=20); Group 3: 10mg/ml of DHS (n=20); Group 4: positive control (infected dentin tubes) (n=10); and Group 5: sterile saline (negative control) (n=10). Dentin chips were removed from the canals with sequential sterile low - speed round burs with increasing diameters of ISO sizes: 025, 027, 029, 031, and 033 at experi-mental times of 0, 7, 14, 21, and 28 days. After culturing, the numbers of colony-forming units (CFUs) were counted. Data were analyzed using analysis of variance and covariance with repeated measures (ANOVA) to indicate differences between the experimental groups and the positive control. One-way ANOVA (Tukey's method) was used to indicate differ-ences within each layer.&#13;
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Results&#13;
The numbers of CFUs in all three experimental groups were minimum in first cultures, and the obtained results were significantly different from each other at any time period (P</Abstract></Article></ArticleSet>
