Studies were conducted to gain insights into how remineralization by fluorapatite (FAP) deposition onto hydroxyapatite (HAP) crystals might influence dissolution rate behavior and acid resistance. Dissolution rate behavior of compressed pellets was studied in 0.1 M acetate buffer, pH 4.5, ionic strength 0.5, using the rotating disk method. Attempts were made to determine the dissolution rate controlling phase by addition of common ions (Ca, P, F) to the buffer solution. Preliminary studies on HAP pellets and almost pure FAP pellets showed that FAP dissolved appreciable slower than HAP under the conditions used. The specific ion effects on FAP dissolution were consistent with predictions based on the expected ionic activity product of this mineral. The dissolution rate behavior of FAP-HAP mixtures in acid without common ions present in the buffer solution were interpreted as follows. With pellets prepared from HAP crystals onto which FAP had been precipitated, the first dissolving phase was FAP even at the lowest concentration of this phase. With pellets of mechanically mixed FAP and HAP the two components dissolved relatively independently. The reduced dissolution rates of FAP mineralized HAP compared with the mechanically mixed case and particularly with pellets of pure HAP may be of clinical significance. It is suggested that deposition of fairly low levels of FAP during in vivo remineralization may significantly decrease the tendency for caries formation.

This content is only available via PDF.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.