Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

CiteULike is a free service for managing and discovering scholarly references - click here to get started.

Sign In to gain access to subscriptions and/or personal tools.
Critical Reviews in Oral Biology & Medicine
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Levine, M. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
4(3):279-286 (1993)     Crit Rev Oral Biol Med
© 1993 SAGE Publications

Development of Artificial Salivas

Michael J. Levine

Dept. of Oral Biology and Dental Research Institute, School of Dental Medicine, 109 Foster Hall, State University of New York at Buffalo, Buffalo, NY 14214

Salivary research is at a critical crossroads regarding the clinical application of basic knowledge. Studies by numerous salivary researchers over the last 5 years using advanced technologies (e.g., protein chemistry, molecular biology, and biophysics) have demonstrated that the structural requirements for salivary function are quite complex. Nevertheless, several patterns or principles have evolved. First, the majority if not all salivary molecules are multifunctional. Second, the conformation of a molecule is an important factor in biological activity. Third, many molecules have overlapping functions (e.g., mucins and amylase interact with viridans streptococci; statherin and proline-rich proteins are involved in mineralization). Thus, saliva has "built-in" compensatory or redundant properties. Nevertheless, it must be determined which molecule is more potent or effective with respect to a particular function. Fourth, salivary molecules may be "amphifunctional". In other words, the different functions of a single molecule may be protective or potentially harmful depending on the intraoral site of action. Examples of amphifunctional molecules are amylase and statherin. Fifth, functional relationships may exist between different salivary components. The principles mentioned above can provide experimental strategies for the design and synthesis of a first generation of salivary substitutes that can be topically applied to oral surfaces. These molecules should be used to combat microbial mediated diseases and occlusal disharmony in subjects with normal salivary flow as well as those with xerostomia. In general, these substitutes should be long-lasting, biocompatible, biodegradable, and provide specific protective qualities that can be targeted to selected intraoral sites. Subsequent research endeavors will focus on the design and subsequent engineering of a second generation of artificial salivas comprised of molecules with enhanced as well as multiple functions. Examples of these strategies are provided.

Key Words: saliva • xerostomia • saliva substitute.

Critical Reviews in Oral Biology & Medicine, Vol. 4, No. 3, 279-286 (1993)
DOI: 10.1177/10454411930040030401


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
J Biomater ApplHome page
H. Bilhan, T. Bilgin, A.F. Cakir, B. Yuksel, and J.A. Von Fraunhofer
The Effect of Mucine, IgA, Urea, and Lysozyme on the Corrosion Behavior of Various Non-precious Dental Alloys and Pure Titanium in Artificial Saliva
J Biomater Appl, November 1, 2007; 22(3): 197 - 221.
[Abstract] [PDF]


Home page
CROBMHome page
A. Vissink, F.R. Burlage, F.K.L. Spijkervet, J. Jansma, and R.P. Coppes
PREVENTION AND TREATMENT OF THE CONSEQUENCES OF HEAD AND NECK RADIOTHERAPY
Critical Reviews in Oral Biology & Medicine, May 1, 2003; 14(3): 213 - 225.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
J. D. Rogers, R. J. Palmer Jr., P. E. Kolenbrander, and F. A. Scannapieco
Role of Streptococcus gordonii Amylase-Binding Protein A in Adhesion to Hydroxyapatite, Starch Metabolism, and Biofilm Formation
Infect. Immun., November 1, 2001; 69(11): 7046 - 7056.
[Abstract] [Full Text] [PDF]


Home page
JDRHome page
J.D. Rudney, K.L. Hickey, and Z. Ji
Cumulative Correlations of Lysozyme, Lactoferrin, Peroxidase, S-IgA, Amylase, and Total Protein Concentrations with Adherence of Oral Viridans Streptococci to Microplates Coated with Human Saliva
Journal of Dental Research, March 1, 1999; 78(3): 759 - 768.
[Abstract] [PDF]


Home page
JDRHome page
I. Iontcheva, F.G. Oppenheim, and R.F. Troxler
Human Salivary Mucin MG1 Selectively Forms Heterotypic Complexes with Amylase, Proline-rich Proteins, Statherin, and Histatins
Journal of Dental Research, March 1, 1997; 76(3): 734 - 743.
[Abstract] [PDF]


Home page
CROBMHome page
J.D. Rudney
Does Variability in Salivary Protein Concentrations Influence Oral Microbial Ecology and Oral Health?
Critical Reviews in Oral Biology & Medicine, January 1, 1995; 6(4): 343 - 367.
[Abstract] [Full Text] [PDF]


Home page
JDRHome page
J.L. Jensen, T. Xu, M.S. Lamkin, P. Brodin, H. Aars, T. Berg, and E. Oppenheim
Physiological Regulation of the Secretion of Histatins and Statherins in Human Parotid Saliva
Journal of Dental Research, December 1, 1994; 73(12): 1811 - 1817.
[Abstract] [PDF]


Home page
CROBMHome page
F. A. Scannapieco
Saliva-Bacterium Interactions in Oral Microbial Ecology
Critical Reviews in Oral Biology & Medicine, January 1, 1994; 5(3): 203 - 248.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Prakobphol, F. Xu, V. M. Hoang, T. Larsson, J. Bergstrom, I. Johansson, L. Frangsmyr, U. Holmskov, H. Leffler, C. Nilsson, et al.
Salivary Agglutinin, Which Binds Streptococcus mutans and Helicobacter pylori, Is the Lung Scavenger Receptor Cysteine-rich Protein gp-340
J. Biol. Chem., December 15, 2000; 275(51): 39860 - 39866.
[Abstract] [Full Text] [PDF]