JDR JDR Most Cited Articles
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Dent Res 36(1): 75-86, 1957
© 1957 International and American Associations for Dental Research

This Article
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by MANLY, R. S.
Right arrow Articles by HARGREAVES, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by MANLY, R. S.
Right arrow Articles by HARGREAVES, G.

INHIBITION OF ACID PRODUCTION OF SALIVARY SEDIMENT BY ETHERS, ESTERS, PHENOLS, AND ALCOHOLS

R. S. MANLY PH.D.1 and GLADYS HARGREAVES M.S.1

1 Tufts University School of Dental Medicine, Boston, Mass.

Studies have been made on 492 alcohols, phenols, ethers, and esters, in order to determine whether any simple organic chemicals have the capacity to reduce acid formation rate of salivary sediment. A study on monosubstituted ethers and esters or a combination of these 2 groupings indicated that these substances in themselves had no ability to effect acid formation. There were no inhibitory ethers. The one inhibitory ester may have owed its activity to the presence of unesterified alcohol or to the ability of oral enzymes to cause its hydrolysis.

There were a few alcohols or phenols which had the capacity to affect salivary sediment when tested in water solution, but the majority of substances required the presence of 10 per cent propylene glycol for their effect to be demonstrated. In a few instances it appeared that propylene glycol had a synergistic action in with the chemical but in most cases the glycol apparently acted chiefly to increase the solubility of the compound enough to allow it to be inhibitory. Most of the phenols tested at maximum concentration were not superior to phenol itself. A high percentage of inhibitory action occurred among compounds with 6 to 13 carbon atoms, 1 to 3 code units, and ring structures.

Submitted on August 23, 1955







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
IADR Journals Advances in Dental Research ®
Journal of Dental Research ® Critical Reviews (1990-2004)
Copyright © 1957 Institutional Access Guidelines