Major Topics in Quantitative Microradiography of Enamel and Dentin: R Parameter, Mineral Distribution Visualization, and Hyper-Remineralization

1997 ◽  
Vol 11 (4) ◽  
pp. 403-414 ◽  
Author(s):  
J. Arends ◽  
J.L. Ruben ◽  
D. Inaba
Keyword(s):  
Mineral Content ◽  
Dissolution Kinetics ◽  
Lesion Length ◽  
Computer Assisted ◽  
Average Amount ◽  
Mineral Distribution ◽  
Loss Parameter ◽  
Mineral Loss

Three aspects of quantitative transverse microradiography are described and discussed: (1) the average mineral loss parameter of enamel or dentin lesions (R) in vol%; (2) mineral distribution visualization of lesions by means of a computer-assisted videodensitometric (CAV) method; and (3) the microradiography of hyper-remineralized lesions. "R", defined as the average amount of mineral lost (or gained) in a lesion per unit lesion length, is a useful parameter in dental caries. The results show that, in vitro, R is about constant over the demineralization period for enamel and dentin. This was found even for quite different dissolution kinetics. R is strongly reduced by the presence of small amounts of fluoride in the demineralizing system. R of dentin lesions is smaller than for enamel lesions. We conclude that the mineral loss value (ΔZ) and the lesion depth (ld) are in general dependent parameters during in vitro or in situ studies on enamel or dentin. During lesion formation, mineral loss from the lesion and acid penetration in the tissue are obviously linked. This is possible only if the mineral content in the lesion does not change very much after passage of the lesion front. The CAV method presented is illustrated for enamel lesions formed in vitro and in situ.

In Situ Models, Physico-Chemical Aspects

1994 ◽  
Vol 8 (2) ◽  
pp. 125-133 ◽  
Author(s):  
J.M. Ten Cate
Keyword(s):  
Single Point ◽  
Limiting Factor ◽  
Model Parameters ◽  
Laboratory Findings ◽  
Physiological Processes ◽  
Physico Chemical ◽  
Crystallite Surface ◽  
Mineral Loss

In situ (intra-oral) caries models are used for two purposes. First, they provide information about oral physiological processes. Such information helps to detail our knowledge of the oral ecosystem and to verify conclusions from in vitro experiments. Second, in situ models are utilized to test preventive agents in the phase between laboratory testing and clinical trials. Most investigations involving enamel inserts have been aimed at testing new dentifrices. The experimental designs of such studies usually do not allow one to draw conclusions on physico-chemical processes, e.g., because of single point measurements. Studies of model parameters (lesion type, lesion severity, and de/remineralization in time) constitute only a minority of the research reports. The most striking observation obtained with in situ models has been the significant differences in de/remineralization observed among individuals and, more importantly, within one individual during different time periods and between different sites in the same mouth (for review, see ten Cate et al., 1992). Regardless of this, some general findings can be inferred: During in situ demineralization, up to 62 vol%μm/day may be removed from enamel. For dentin specimens, this value may be as high as 89 vol%μm/day. For remineralization, during fluoride dentifrice treatment, a median deposition rate of 0.7%/day (for lesions with integrated mineral loss values between 2000 and 4000 vol%μm) is found. The rate of deposition seems to be correlated with the extent of the pre-formedlesion. This suggests that the number of sites (crystallite surface) available for calcium phosphate precipitation is an important parameter. However, the rate at which mineral ions are supplied (by saliva) could also be a limiting factor, as is shown in a theoretical analysis of mass-balance of enamel constituents. The few studies that have monitored caries development in time reveal that mineral loss (and also lesion progression in depth) from enamel in situ is linear in time. This is in contrast to results from laboratory findings.

scholarly journals Effect of starch on the cariogenic potential of sucrose

2005 ◽  
Vol 94 (1) ◽  
pp. 44-50 ◽  
Author(s):  
Cecilia C. C. Ribeiro ◽  
Cínthia P. M. Tabchoury ◽  
Altair A. Del Bel Cury ◽  
Livia M. A. Tenuta ◽  
Pedro L. Rosalen ◽  
...  
Keyword(s):  
Animal Studies ◽  
Amylase Activity ◽  
Negative Control ◽  
Cross Sectional ◽  
Dental Biofilm ◽  
Enamel Demineralization ◽  
Two Phases ◽  
Mineral Loss

Sincein vitroand animal studies suggest that the combination of starch with sucrose may be more cariogenic than sucrose alone, the study assessedin situthe effects of this association appliedin vitroon the acidogenicity, biochemical and microbiological composition of dental biofilm, as well as on enamel demineralization. During two phases of 14 d each, fifteen volunteers wore palatal appliances containing blocks of human deciduous enamel, which were extra-orally submitted to four groups of treatments: water (negative control, T1); 2 % starch (T2); 10 % sucrose (T3); and 2 % starch+10 % sucrose (T4). The solutions were dripped onto the blocks eight times per day. The biofilm formed on the blocks was analysed with regard to amylase activity, acidogenicity, and biochemical and microbiological composition. Demineralization was determined on enamel by cross-sectional microhardness. The greatest mineral loss was observed for the association starch+sucrose (P<0·05). Also, this association resulted in the highest lactobacillus count in the biofilm formed (P<0·05). In conclusion, the findings suggest that a small amount of added starch increases the cariogenic potential of sucrose.

Comparison of Solution- and Gel-prepared Enamel Lesions-an in vitro pH-cycling Study

1988 ◽  
Vol 67 (8) ◽  
pp. 1122-1125 ◽  
Author(s):  
F.A. Damato ◽  
R. Strang ◽  
K.W. Stephen
Keyword(s):  
Mineral Content ◽  
Ph Cycling ◽  
Subsequent Behavior ◽  
Group D ◽  
Mineral Loss

A variety of methods has been employed to produce artificial caries-like enamel lesions. The aim of this paper was to use a pH-cycling regime to compare the de-/remineralization behavior of lesions prepared by two methods. Lesions were produced by use of either an acidified undialyzed gelatin system or a buffered solution. Enamel sections, each containing four lesions, were allocated to four groups (A, B, C, D) and subjected to a daily ph-cycling regime of 16-hour demineralization and eight-hour remineralization. Groups A & B contained gelatin-prepared lesions, whereas Groups C & D contained solution-prepared lesions. To the remineralizing solutions used in Groups B & D, 2 ppm fluoride was added. The mineral content in the lesions was assessed, by means of microradiography/microdensitometry, at baseline and at intervals for six weeks. The lesions in all four groups exhibited net demineralization. In terms of the total mineral lost from the lesion (the Δz parameter), the demineralization rates of the solution-prepared lesions were significantly greater than those of the corresponding gelatin-prepared lesions. All sections in the non-fluoride groups showed subsurface demineralization in initially sound enamel, whereas only one section in the fluoride groups showed an area of mineral loss. Laminations in the mineral content profiles were apparent only in Group D. The results of this study indicate that the method of lesion preparation affects the subsequent behavior of lesions when exposed to de- and remineralizing protocols.

Synergistic Inhibition of Enamel Demineralization by Peptide 8DSS and Fluoride

2016 ◽  
Vol 50 (1) ◽  
pp. 32-39 ◽  
Author(s):  
Yang Yang ◽  
Xueping Lv ◽  
Wenyuan Shi ◽  
Xuedong Zhou ◽  
Jiyao Li ◽  
...  
Keyword(s):  
Mineral Content ◽  
Positive Control ◽  
Negative Control ◽  
Fluoride Uptake ◽  
Beneficial Effects ◽  
Enamel Demineralization ◽  
Demineralized Enamel ◽  
Ph Cycling ◽  
Mineral Loss

The biomimetic peptide 8DSS has shown beneficial effects in promoting remineralization of demineralized enamel in vitro. Here we examined the ability of 8DSS alone and in combination with fluoride to inhibit enamel demineralization during pH-cycling mimicking intraoral conditions. Enamel blocks were subjected to 9 days of pH-cycling in the presence of 1,000 ppm NaF (positive control), distilled-deionized water (DDW; negative control), 25 μM 8DSS alone, 25 μM 8DSS with 500 ppm NaF (8DSS-FL) or 25 μM 8DSS with 1,000 ppm NaF (8DSS-FH) twice daily for 1 min each time. The blocks were analyzed in terms of surface microhardness (SMH), fluoride uptake and mineral content. The 8DSS-treated blocks showed significantly lower mineral loss, shallower lesions and higher SMH than the DDW-treated blocks. No significant differences were observed between the blocks treated with 8DSS alone or fluoride alone. The blocks treated with 8DSS alone or DDW showed similar amounts of fluoride uptake, which was the lowest of all the treatment groups. The blocks treated with 8DSS-FL or 8DSS-FH did not differ significantly, and both groups showed significantly greater SMH and fluoride uptake as well as significantly lower mineral loss and shallower lesions than the NaF-treated blocks. Mineral content was significantly higher in the 8DSS-treated blocks than in the DDW-treated blocks from the surface layer (10 µm) to the lesion depth (110 µm), and it was significantly higher in the blocks treated with 8DSS-FL or 8DSS-FH than in the NaF-treated blocks from 10 to 90 µm. These findings illustrate the potential of 8DSS for inhibiting enamel demineralization and for enhancing the anticaries effect of NaF.

scholarly journals Different Protocols to Produce Artificial Dentine Carious Lesions in vitro and in situ: Hardness and Mineral Content Correlation

2013 ◽  
Vol 47 (2) ◽  
pp. 162-170 ◽  
Author(s):  
B.M. Moron ◽  
L.P. Comar ◽  
A. Wiegand ◽  
W. Buchalla ◽  
H. Yu ◽  
...  
Keyword(s):  
Mineral Content ◽  
Carious Lesions

Demineralization and Remineralization Evaluation Techniques

1992 ◽  
Vol 71 (3_suppl) ◽  
pp. 924-928 ◽  
Author(s):  
J. Arends ◽  
J.J. ten Bosch
Keyword(s):  
Light Scattering ◽  
Mineral Content ◽  
Polarized Light ◽  
Cross Sectional ◽  
Main Emphasis ◽  
Measuring Techniques ◽  
Mineral Loss ◽  
Mineral Changes

This paper compares the experimental techniques utilized to assess the de- or remineralization of enamel or dentin in intra-oral studies. In in situ studies, it is important for one to know how much mineral has been lost or gained, and where the loss or gain occurred. The main emphasis in this paper is on techniques suitable for direct or indirect mineral quantification. The measuring techniques considered are microradiography, iodine absorptiometry, various microhardness tests, polarized light, light-scattering, iodide permeability, and wet chemical analysis. The various techniques are compared concerning suitability for the determination of mineral content in vol% (or wt%), mineral changes in vol% μm (or kg.m–2), and mineral distributions. Furthermore, sample preparation, the importance of protein penetration, nominal mineral loss range, the estimated mineral loss threshold, and the applicability to dentin are compared and considered. It is concluded that, although more than ten techniques are available for the measurement of changes after de- or remineralization in situ, transverse microradiography is the most practical technique for the direct and quantitative measurement of mineral content, mineral changes, and mineral distributions. Cross-sectional microhardness testing and light-scattering are also practical indirect techniques for quantitative mineral loss (or gain) determinations in intra-oral studies.

Application of Transverse Microradiography for Measurement of Mineral Loss by Acid Erosion

1997 ◽  
Vol 11 (4) ◽  
pp. 420-425 ◽  
Author(s):  
A.F. Hall ◽  
J.P. Sadler ◽  
R. Strang ◽  
E. De Josselin De Jong ◽  
R.H. Foye ◽  
...  
Keyword(s):  
Penetration Depth ◽  
Mineral Content ◽  
Orthophosphoric Acid ◽  
Correlation Coefficients ◽  
Maximum Depth ◽  
Depth Of Penetration ◽  
Acceptable Method ◽  
Mineral Loss ◽  
Detection And Quantification

This paper describes a novel application of transverse microradiography for the detection and quantification of mineral loss due to acid erosion in thin tooth sections. Sixty-four specimens were randomly divided into eight equal-sized groups and exposed to an orthophosphoric-acid-based erosive fluid (pH = 3) for 0, 0.25, 0.5, 1, 2, 5, 12, or 24 hrs. We made microdensitometric scans separately across both enamel and dentin to derive data for the total mineral loss and the minimum mineral content within the eroded area. We then analyzed specimens using a profilometer to determine (1) the area above a plot of penetration depth against distance and (2) the maximum depth of penetration. Correlation coefficients for comparisons between microradiographic and profilometric data for both enamel and dentin specimens varied between 0.87 and 0.96. Two-sample t tests demonstrated that the microradiographic technique could detect early erosion, i.e., discriminate between erosion times of less than 1 hr. It was concluded that this application of transverse microradiography was a useful and acceptable method for the measurement of early mineral loss in vitro, occurring as a result of acid erosion.

Correlated Studies of Cellular Interactions Using TEM, Freeze Etching, and SEM

1974 ◽  
Vol 32 ◽  
pp. 320-321
Author(s):  
J. P. Revel
Keyword(s):  
Developmental Stages ◽  
Three Dimensional ◽  
Cell Movement ◽  
Cellular Interactions ◽  
Serial Sections ◽  
Cell Sheets ◽  
Freeze Etching ◽  
Early Developmental

Movement of individual cells or of cell sheets and complex patterns of folding play a prominent role in the early developmental stages of the embryo. Our understanding of these processes is based on three- dimensional reconstructions laboriously prepared from serial sections, and from autoradiographic and other studies. Many concepts have also evolved from extrapolation of investigations of cell movement carried out in vitro. The scanning electron microscope now allows us to examine some of these events in situ. It is possible to prepare dissections of embryos and even of tissues of adult animals which reveal existing relationships between various structures more readily than used to be possible vithout an SEM.

In vitro and in vivo polysaccharides assembly: ultrastructural and cytochemical study of growing plant cell wall components.

1978 ◽  
Vol 36 (2) ◽  
pp. 434-435
Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland
Keyword(s):  
Cell Wall ◽  
Self Assembly ◽  
Plant Cell Wall ◽  
Higher Plants ◽  
Three Dimensional ◽  
Cytochemical Study ◽  
Wall Components

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.

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