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Biomedical subjects

R M Browne

Publications and source records attributed to R M Browne.

At least 55 records · Page 3Linked to original sources

Preliminary studies on the in vivo morphogenetic properties of dentine matrix proteins.

Two fractions of isolated noncollagenous extracellular matrix proteins from dentine have been implanted into the base of exposed cavities in ferret canine teeth. After sealing the cavities, reparative dentinogenesis was assessed histologically after 14 and 28 days as compared to control cavities. Reparative dentinogenesis was enhanced in the presence of these matrix proteins with evidence of tubular dentine along the walls of the exposure and on the cavity floor demonstrating the in vivo morphogenetic properties of the dentine matrix proteins.

Animals↗

A comparison of monopolar and bipolar electrical stimuli and thermal stimuli in determining the vitality of human teeth.

The sensory threshold was determined for 50 teeth in 31 patients using constant-current stimuli of 0.1, 1.0 and 10 ms duration at 10 Hz through both monopolar and bipolar electrodes. The teeth were also tested with a cold stimulus (ethyl chloride on cotton wool), then extracted, processed and examined by light microscopy. Histologically, 38 teeth were vital and 7 non-vital. The best prediction of vitality was from ethyl chloride (80% correct) or bipolar stimuli of 10 ms duration and up to 200 microA (73% correct). The remaining 5 teeth had vital radicular pulps and necrotic tissue coronally, but a comparison between the results of monopolar and bipolar stimulation did not permit the detection of this group. There was no correlation between the electrical threshold and presence of caries, restorations, pulp stones or diffuse pulpal mineralization.

Adult↗

An in vitro study of the antibacterial and antifungal properties of an irreversible hydrocolloid impression material impregnated with disinfectant.

The difficulties associated with the disinfection of alginate (irreversible hydrocolloid) materials have resulted in the development of an irreversible hydrocolloid impression material impregnated with an antimicrobial compound, didecyldimethyl ammonium chloride. This investigation assessed the antibacterial and antifungal properties in vitro of this innovative irreversible hydrocolloid material by using the agar well technique. The microorganisms used were Pseudomonas aeruginosa, Streptococcus mutans, Streptococcus sanguis, Lactobacillus odontolyticus rodriguez, Actinomyces odontolyticus, mixed salivary organisms, and Candida albicans. The results showed an absence of activity against Pseudomonas aeruginosa. Varying degrees of antibacterial activity were exhibited against the other microorganisms. It is concluded that it is not know whether the limited antibacterial and antifungal effect demonstrated in this study is sufficient to prevent bacterial and fungal colonization of the impression surface in the mouth during clinical practice.

Actinomyces↗

An in vitro study of the antiviral properties of an alginate impression material impregnated with disinfectant.

The antiviral properties of a new alginate impression material impregnated with a disinfectant (didecyldimethyl ammonium chloride) were evaluated in vitro against herpes simplex virus type I and poliovirus type I. The material was exposed to the virus suspension for periods of up to 60 min. The impregnated alginate material showed no clinically acceptable effect against either virus, although log reductions of 1.0 and 1.7 plaque-forming units of herpes virus were obtained after exposure to the material containing the disinfectant for 5 and 60 min, respectively.

Alginates↗

Human tissue response to porous hydroxyapatite implants. A case report.

Histological examination of 2 porous hydroxyapatite implants removed from a patient showed a pattern of ossification similar to that reported in a previous animal study. New bone was laid down on the surface of the hydroxyapatite but did not progress to occupy all the pores. Although porous hydroxyapatite blocks are biocompatible and well tolerated by the tissues, they are not recommended for augmentation of the resorbed alveolar ridge where the overlying mucosa is thin and atrophic, because of the risk of mucosal dehiscence and implant exposure. They are suitable in situations where they are deeply buried in the tissues and not subjected to direct trauma.

Alveolar Ridge Augmentation↗

Pulpal response to an anhydrous glass ionomer luting cement.

This investigation was designed to study the pulpal responses to Aquacem, an anhydrous glass ionomer luting cement, and to compare the results with those previously obtained for a conventional glass ionomer luting cement, Chembond. The study was carried out according to the BSI (1980) recommendations for testing restorative materials in vivo. Aquacem caused more pulpal inflammation than the control material, Kalzinol, though by an indirect mechanism. The statistical model demonstrated a significant association between bacterial presence within the experimental cavity and pulpal inflammation. The type of restorative material has no direct association with the degree of inflammation, but the model suggests that it exerts an indirect influence via its antibacterial properties and hence its influence on microbial microleakage.

Animals↗

Epithelial cell markers and proliferating cells in odontogenic jaw cysts.

The expression of keratins, CEA, EMA, and rat liver antigen (RLA) and the presence of Ki67+ proliferating cells were studied in the epithelial linings of 50 odontogenic cysts using an indirect immunoperoxidase method on acetone-fixed frozen sections. All cysts were positive with monoclonal antibodies of broad keratin specificity (CK1, AE1-3), and between 40 and 100 per cent of epithelial cells expressed keratins 13 and 19. Keratins 7, 8, and 18 were rarely expressed although surface cells in areas of mucous metaplasia often expressed keratins 7 and 18. Expression of keratin 10/11 was related to the presence of a well-ordered epithelial lining and was detected in isolated cells in 4/32 non-keratinizing cysts and in the upper suprabasal cell layers of 17/18 keratocysts. Although CEA, EMA, and RLA were detected in the epithelium of all specimens, the pattern of expression of CEA and EMA differed between cyst types. Ki67+ proliferating cells were most prevalent in keratocyst epithelia, where they were usually found within lower suprabasal layers which were negative or weakly positive for keratins 10/11 and 13. These results indicate differences in keratin, CEA, and EMA expression between cyst types which appear to be dependent on epithelial differentiation/structure rather than cyst type or histogenesis. Although these differences may not be of diagnostic significance, the consistent expression of both keratins 13 and 19 may provide a useful marker of odontogenic epithelium in general.

Antigens, Neoplasm↗

Quantification and analysis of the glycosaminoglycans in human odontogenic cyst linings.

Glycosaminoglycans (GAG) were extracted from the connective tissue of 15 dental cysts, 2 dentigerous cysts and 7 keratocysts, and separated electrophoretically and chromatographically. Hyaluronic acid (dental, 2.38; dentigerous, 3.98; keratocyst, 3.19 micrograms uronic acid/mg lyophilized tissue) was the major GAG detected, with lesser amounts of heparin (dental, 1.70; dentigerous, 1.95; keratocyst, 1.80 micrograms uronic acid/mg lyophilized tissue) and chrondroitin-4-sulphate (dental, 1.33; dentigerous, 2.85; keratocyst, 1.37 micrograms uronic acid/mg lyophilized tissue). It is suggested that enzymic release of these GAGs allows their diffusion into the luminal fluid where they may contribute to expansile cyst growth.

Chondroitin Sulfates↗

Histochemical studies on glycosaminoglycans of odontogenic cysts.

Histochemical examination of odontogenic cyst connective tissue has demonstrated that hyaluronic acid is the predominant glycosaminoglycan present with lesser amounts of the sulphated glycosaminoglycans. Mast cells were frequently observed in the connective tissue, particularly just beneath the epithelium and may be responsible for the enhanced staining for heparin observed in this area. Local tissue metabolism and inflammation will contribute to the release of glycosaminoglycans from connective tissue into the lumenal fluid. Staining of glycosaminoglycans was generally minimal in the epithelium, although hyaluronic acid and chondroitin sulphate were detected in goblet cells. Glycosaminoglycans previously demonstrated in cyst fluids are probably derived from several sources in the cyst and will be important in its expansile growth.

Chondroitin Sulfates↗

Lactoferrin in aspirates of odontogenic cyst fluid.

The possibility that the presence of lactoferrin in aspirates of odontogenic cyst fluid might be a useful preoperative diagnostic marker for odontogenic keratocyst was investigated. Using qualitative and quantitative immunodiffusion methods fluid from 29 of 29 dental (radicular) cysts, 12 of 14 dentigerous cysts and 27 of 31 keratocysts were found to contain lactoferrin. Although some of the highest concentrations of lactoferrin were detected in fluids from keratocysts, there was no significant difference between lactoferrin concentrations among the three groups. Neutrophil elastase was detected in 20 of 24 samples tested, 22 of which also contained lactoferrin. Immunocytochemical localisation of both lactoferrin and elastase was confined to neutrophils infiltrating cyst walls. These results suggest that lactoferrin in fluid from odontogenic cysts is derived from infiltrating neutrophils and that its presence in aspirated fluids is not a useful diagnostic marker for odontogenic keratocyst.

Biomarkers↗

The odontogenic keratocyst and its occurrence in the nevoid basal cell carcinoma syndrome.

There are histologic differences between odontogenic keratocysts occurring in the basal cell carcinoma syndrome (NBCCS) and as single lesions in otherwise healthy persons. This study identifies certain differences in age, gender, and site between the two groups. The age at removal of the first keratocyst is significantly lower in the syndrome group. On more thorough examination, patients with multiple keratocysts (excluding recurrences) are found to have other features of NBCCS. The term multiple cysts refers to the lifetime history of the patient and does not necessarily imply that more than one cyst is present at any one time.

Adolescent↗

Ridge augmentation using solid and porous hydroxylapatite particles with and without autogenous bone or plaster.

Edentulous areas of dog jaws were augmented with solid or porous particles of hydroxylapatite (HA) alone, or combined with either finely crushed autogenous bone or plaster of paris. At the end of the experiment (24 weeks), the augmented ridges were firm and stable and covered with healthy mucosa. The ridges augmented with only porous particles of HA demonstrated a greater amount of bone ingrowth compared with the solid, dense particles. The new bone formation occurred in those parts of the implants adjacent to the underlying alveolar bone. The addition of autogenous bone to the HA particles did not enhance bony deposition, and none of the autogenous bone chips survived for 24 weeks. The amount of new bone in the ridges augmented with plaster of paris and HA was similar to the other groups, and the plaster did not interfere with healing. There was evidence of resorption of the underlying cortical bone in many of the specimens.

Alveolar Process↗

Immunoglobulin-producing cells in human odontogenic cysts.

Immunohistochemical staining of immunoglobulin-containing plasma cells was performed on odontogenic keratocysts, dental (periapical) and dentigerous cysts. IgG-containing plasma cells were the predominant species in all cyst types examined, with a much lower percentage of IgA- and few IgM-containing plasma cells. Statistically significant differences in the percentage contributions of IgG and IgA plasma cells were observed between the keratocyst and both the dental (periapical) and dentigerous cysts and for IgM between the keratocyst and dental (periapical) cyst. Intense extracellular staining was observed for IgG in all cyst types.

Humans↗

A comparative histological study of odontogenic keratocysts in basal cell naevus syndrome and control patients.

164 odontogenic keratocysts from 60 patients with the basal cell naevus syndrome were compared with a similar number of single keratocysts matched for age and site. Significant differences between the two groups were found in the numbers of satellite cysts, solid islands of epithelial proliferation and odontogenic rests within the capsule, and in the numbers of mitotic figures in the epithelium lining the main cavity. An index of activity derived from these parameters suggests a greater growth potential in syndrome cysts; in addition, the patterns of association of the features support the theory that the odontogenic rests give rise to satellite cysts.

Adolescent↗