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Biomedical subjects

J Ruben

Publications and source records attributed to J Ruben.

At least 55 records · Page 3Linked to original sources
PubMed1990

Relative cariostatic effects of KOH-soluble and KOH-insoluble fluoride in situ.

The relative cariostatic effects of fluoride as fluorapatite, CaF2, loosely-bound fluoride, or KOH-soluble fluoride are debated. The present study was carried out to investigate this further in an intra-oral caries model. Pairs of premolars extracted for orthodontic reasons were used. Enamel from one tooth of each pair was used as control (untreated). Two slabs were cut from the enamel of the other contralateral premolar. These slabs were treated with 2% NaF for 24 h. One slab was then treated with 1 mol/L KOH twice for 24 h for removal of all loosely-bound fluoride. The slabs treated with 2% NaF and then with 1 mol/L KOH would contain the KOH-insoluble fluoride. Those treated with only 2% NaF would, in addition, contain KOH-soluble fluoride. Each slab, control, KOH-insoluble F, and KOH-soluble and insoluble F was mounted on different upper removable appliances. The slabs were covered with orthodontic banding material, thus allowing space for plaque accumulation. Five individuals wore the appliance in three separate four-week periods. The slabs were analyzed by quantitative microradiography. The average mineral loss (delta Z) was 1680 +/- 1000 vol% x microns in the control teeth, 620 +/- 76 vol% x microns in the KOH-soluble and -insoluble F teeth, and 2167 +/- 1278 vol% x microns in the KOH-insoluble F teeth. The average lesion depths were 90 +/- 41 microns in the control teeth, 35.3 +/- 5.5 microns in the KOH-soluble F teeth, and 88 +/- 35 microns in the KOH-insoluble F teeth. It was concluded that only KOH-soluble fluoride reduced mineral loss and lesion depths significantly, compared with the untreated teeth.

Calcium Fluoride↗
PubMed1990

Effect of fluoride release from a fluoride-containing composite resin on secondary caries: an in vitro study.

The effect of fluoride, released from a fluoride-containing composite resin, on secondary caries was investigated by quantitative microradiography. In all teeth investigated, less demineralization was found near the composite resin than was found at a distance of a few millimeters from the material after an acid attack. The presence of the fluoride-releasing composite resin reduced the lesion depth measured after an acid attack by about 35%. Therefore, in vivo, a reduction of recurrent caries may be expected around fluoride-containing composite resins.

Adult↗
PubMed1989

Influence of glutardialdehyde on dentin demineralization in vitro and in vivo.

In this paper the results are presented on the action of glutardialdehyde (GDA) on the in vitro demineralization of human dentin and on the in vivo demineralization of dentin using the Ogaard orthodontic banding system. The results show that a 2 min application of a 2% GDA solution at pH = 3.6 reduces dentin demineralization in vitro and in vivo substantially. Microradiography shows a percentage reduction of lesion depth and mineral loss in vitro of 20 and 36%, respectively. After 2 wk in vivo demineralization the same percentage reductions are 60 and 44%, respectively. The mechanism of action of GDA on dentin is not certain yet. Presumably the in vitro action is due to surface cross-linking of the dentin matrix causing reduced Ca and phosphate transport out of the dentin. In vivo an additional effect may be a rather short term influence of GDA on plaque or on plaque accumulation. The results of this paper indicate that glutardialdehyde is an interesting agent to consider in the reduction of root caries.

Aldehydes↗
PubMed1989

Dentine caries in vivo. Combined scanning electron microscopic and microradiographic investigation.

Dentine subjected to an in vivo demineralization challenge by plaque looses substantial amounts of mineral and is expected to change its ultrastructure. Results are presented of a combined microradiography and scanning electron microscopy (SEM) study on in vivo demineralized human dentine. The tissue was first demineralized in vivo under plaque for 3 weeks and subsequently analyzed by microradiography and SEM. In 6 participants dentine was positioned in a full prosthesis just under M2 in such a way that the outer surface of the tissue was 1.5 mm lower than the surface of the prosthesis; plaque accumulation takes place in the recessed area. A special technique allows SEM observations (at a given distance from the outer surface) on broken thin sections of demineralized dentine with a mineral content determined by microradiography. The results show that the ultrastructure of the dentine changes during severe demineralization. The main ultrastructural features are, however, still largely intact, even if half of the mineral originally present has been lost. In dentine with a mineral content of about 25 vol%, the dentinal tubules are enlarged by about 30%. In vivo demineralized dentine looses mineral in substantial amounts both from intertubular and from peritubular regions.

Adolescent↗
PubMed1989

Remineralization of bovine dentine in vitro. The influence of the F content in solution on mineral distribution.

In this paper remineralization of bovine dentine is reported. After demineralization of the dentine in an acidic gel system creating lesions of about 180 microns depth, the tissue was remineralized in a 1.5 mM Ca and 0.9 mM phosphate containing solution at pH 7 and 37 degrees C for 8 or 21 days. The F content in the remineralization solution was 0.02, 2, or 10 ppm as NaF. Samples were analyzed by means of microradiography and scanning electron microscopy. The results show that remineralization (without F added in solution) causes a decrease in mineral loss and in lesion depth. With 2 or 10 ppm in solution, however, a substantial mineral accumulation in the lesion, but particularly on the original dentine surface, was observed. During 3 weeks of remineralization, mineral accumulations of 67 and 70 vol% of mineral for 2 and 10 ppm F in solution, respectively, were found near the original outer surface, with the sound dentine mineral value being 48 vol%. The combined microradiography and scanning electron microscopy data show that the mineral accumulated is for a major part deposited on the dentine tissue and partly inside. The latter deposition occurred both inside the tubules as well as in the intertubular areas. Inside the tubules dense precipitates were observed. Because several differences exist between bovine and human dentine, an extrapolation to the human in vivo situation is speculative. The results indicate that the presence of fluoride in the parts per million range is important for dentine remineralization efficacy and that the outer surface area in dentine can be 'overremineralized'.

Animals↗
PubMed1988

Corneal fistulas and their management.

We reviewed three representative cases of chronic corneal fistula formation and provide a systematic approach to the assessment and therapeutic alternatives for this problem. In two of our patients, the fistula was managed surgically. The third patient developed endophthalmitis, which resulted in loss of light perception. Chronic corneal fistulization is a rare clinical entity resulting from malapposition of corneal tissue after traumatic, surgical, or infectious perforation. Fistulas may result in prolonged or recurrent hypotony, peripheral anterior synechia formation, or endophthalmitis. Accurate assessment of the risks associated with corneal fistula formation takes into account the type of fistula, its location in the cornea, and the condition of the ocular adnexae. We reviewed the risk factors that will determine the urgency and type of therapy used.

Aged↗
PubMed1988

Microradiographic study of demineralization of shark enamel in a human caries model.

The aim of the present study was to compare the resistance of fluoroapatite (shark enamel) and hydroxyapatite (human enamel) against a high caries challenge in a human in vivo model. Two samples of shark enamel and human enamel were each placed in removable appliances in six children and carried for 1 month and a plaque retentive device was placed over each enamel sample. The results showed that the mean total mineral loss (delta Z) was 1680 vol% micron in human enamel and 965 vol% micron in shark enamel. The corresponding mean values for lesion depth were 90 micron and 36 micron, respectively. It is concluded that even shark enamel containing 30,000 ppm F has a limited resistance against caries attacks.

Adolescent↗
PubMedDate not supplied

In vitro remineralization of in vivo and in vitro formed enamel lesions.

Thin sections of natural white spot enamel lesions (WS) and of artificial in vitro lesions (VL) were remineralized simultaneously in vitro. The sections, clamped in a PMMA holder, were microradiographed at baseline and after remineralization in a calcium- and phosphate-containing solution (pH = 7.0; 1 ppm F) after 2 and 4 weeks. All data were analyzed with respect to baseline. The results show that the lesion depth values did not change significantly during 2 and 4 weeks of remineralization. The mineral accumulation (change in DeltaZ), however, was substantial and significant in WS and VL. In WS the change in mineral accumulation was roughly proportional to the amount of mineral at baseline. The WS accumulated more than two times the amount of mineral than VL in the same periods of remineralization. After 4 weeks of remineralization the maximum mineral value Vmax in the surface layer of the WS was nearly up to the sound enamel level thick approximate87 vol%. This study shows that the technique and calculation procedure described make this single section method attractive for longitudinal demineralization-remineralization studies in vitro or in situ. Both WS and VL samples obviously remineralized in vitro similarly with respect to the baseline. Furthermore, this in vitro work indicates that remineralization inhibitors present in saliva, and previously penetrated into the enamel tissue, do not influence remineralization later on.

Absorptiometry, Photon↗
PubMedDate not supplied

The effect of window width on the demineralization of human dentine and enamel.

When lesion formation in dental enamel or dentine is studied in vitro, a well-defined area of the material, a 'window', is exposed to the demineralization medium. In the present experiments, we report the effect of window width on lesion formation in enamel and dentine. Rectangular windows, longest dimension always 5 mm and shortest dimension varying from 0.5 to 5 mm, were exposed to demineralization media. Lesions in dentine were formed by placing the specimens in an acidified unstirred 6% carboxymethyl cellulose (CMC) gel, an unstirred 0.5% CMC gel, a mildly stirred 0.5% CMC gel, or in a mildly stirred demineralization solution. Lesions in enamel were formed only in an unstirred acidified 6% CMC gel. pH in the demineralization media was 5.0 in all experiments. The microradiographic technique was used to assess lesion depth and mineral loss (vol% x microm) of lesions formed. Lesions formed in the unstirred gels were deeper, and there was a larger mineral loss, the narrower the window. There was no effect of window size on lesions formed in stirred systems. These effects can be explained by the strong dependence of concentration gradient in stirred gels just outside the exposed window on the window size. The phenomenon found here in vitro may at least partly explain why secondary caries may lead to localized, but relatively deep, lesions.

Carboxymethylcellulose Sodium↗
PubMedDate not supplied

The remineralization of EDTA-treated human dentine.

The remineralization of whole human dentine treated with a neutral EDTA solution was investigated: the treatment periods were 15, 30 and 120 min. From the literature it is known that EDTA removes noncollagenous proteins (NCPs) from dentine powders. In order to extract more phosphoproteins from dentine lesions, in part of this work samples were also treated with 1 M NaCl or 4 M guanidine chloride solutions. All the dentine samples after the treatments mentioned were immersed subsequently in a remineralizing solution without fluoride for 2 weeks and microradiographed. To investigate the effects of fluoride, samples treated with EDTA for 120 min were also remineralized with 2 ppm fluoride in solution. The results presented show that: (1) Measurable remineralization did not occur when fluoride was free in the remineralizing solution. Because remineralization occurred neither at the lesion front nor in the nonmineral part of the surface-softened tissue, presumably the NCPs (inhibitors) of underlying dentine diffused into the tissue during the remineralization period. (2) 2 ppm fluoride caused remineralization at the lesion front. In this case we assume fluoride either acted as nucleating agent or overcame the NCP effects at the lesion front.

Analysis of Variance↗