strontium chloride
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2021 ◽  
Vol 1 (38) ◽  
pp. 30-34
Author(s):  
G. Lyubomirskiy ◽  
R. Matveev

Taking into account the high demand for professional teeth whitening in patients, as well as a significant high percentage of hyperesthesia after this medical manipulation, the urgency of solving this problem becomes obvious. Our study was carried out in 17 patients aged 20 to 35 years with complaints of hyperesthesia after professional teeth whitening with a diode laser with a wavelength of 810 nm using President Sensitive toothpaste with potassium nitrate and strontium chloride at home. All patients underwent professional oral hygiene before teeth whitening, recommended toothpaste and a brush, and received training in home care and teeth cleaning. According to our research, the toothpaste with potassium nitrate and strontium chloride has a pronounced desensitive effect and corresponds to the declared parameters. Thus, after professional whitening with a diode laser with a wavelength of 810 nm and subsequent application of toothpaste with potassium nitrate and strontium chloride, a decrease in tooth sensitivity, remineralization of hard tissues and suppression of bacterial growth were revealed. However, the selection should be individualized, taking into account all medical indications and properties of hygiene products.


Author(s):  
Aman Mallick ◽  
Gaurav Malhotra ◽  
Pradeep Shukla ◽  
Prerna Kataria ◽  
C. S Joshi

Introduction: Dentine hypersensitivity (DH) occurs on exposed dentine and is dependent on the patency of dentinal tubules. This study compared the effectiveness of toothpaste containing Strontium Chloride, Novamine, Pro-Arginine in occluding dentine tubules along with comparision of those. Materials and Method: 45 freshly extracted teeth were randomly divided (15 each) into 3 groups: Group 1 15 Teeth treated with toothpaste containing Strontium Chloride. Group 2 15 Teeth treated with toothpaste containing Novamine Group 3 15 Teeth treated with toothpaste containing Pro-Arginine. Each specimen was brushed with the dentifrice slurries and examined under SCM. Result: The mean of occluded dentinal tubules on the dentin surface after brushing with three dentifrices were significant among them Pro-arginine group showed maximum occlusion. Conclusion: The present in vitro SEM study results revealed that:  All the experimental agents– Strontium chloride, novamin, Pro- Argenine were effective in occluding dentinal tubules & the percentage (%) of occluded tubules was found to be highest for Pro- Argenine as compared to the other groups. Keywords: SCM, DH


Pharmaceutics ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1799
Author(s):  
Rui Sun ◽  
Jiaxin Zhang ◽  
Robert A. Whiley ◽  
Gleb B. Sukhorukov ◽  
Michael J. Cattell

This work demonstrated for the first time the synthesis of novel chlorhexidine particles containing strontium and zinc, to provide an effective, affordable, and safe intervention in the treatment of recurrent infections found in Medicine and Dentistry. The CHX-SrCl2 and CHX-ZnCl2 particles were synthesized by co-precipitation of chlorhexidine diacetate (CHXD) and zinc chloride or strontium chloride, where particle size was manipulated by controlling processing time and temperature. The CHX-ZnCl2 and CHX-SrCl2 particles were characterized using SEM, FTIR, and XRD. UV-Vis using artificial saliva (pH 4 and pH 7) was used to measure the drug release and ICP-OES ion release. The antibacterial properties were examined against P. gingivalis, A. actinomycetemcomitans, and F. nucleatum subsp. Polymorphum, and cytotoxicity was evaluated using mouse fibroblast L929 cells. The novel particles were as safe as commercial CHXD, with antibacterial activity against a range of oral pathogens. UV-Vis results run in artificial saliva (pH 4 and pH 7) indicated a higher release rate in acidic rather than neutral conditions. The CHX-ZnCl2 particles provided the functionality of a smart Zinc and CHX release, with respect to environmental pH, allowing responsive antibacterial applications in the field of medicine and dentistry.


Energy ◽  
2021 ◽  
pp. 122308
Author(s):  
Hong Zhang ◽  
Ting Yan ◽  
Nan Yu ◽  
Z.H. Li ◽  
Q.W. Pan

PLoS ONE ◽  
2021 ◽  
Vol 16 (4) ◽  
pp. e0250501
Author(s):  
Danielle da Silva Pompeu ◽  
Brennda Lucy Freitas de Paula ◽  
Antônia Patricia Oliveira Barros ◽  
Samir Costa Nunes ◽  
Alexandra Melo Pingarilho Carneiro ◽  
...  

Objective This split-mouth randomized controlled clinical trial assessed the effect of 10% strontium chloride in combination with photobiomodulation (PBM) for the control of tooth sensitivity (TS) post-bleaching. Methods The upper/lower, right and left quadrants of fifty volunteers were randomized and allocated to four groups (n = 25): PLACEBO—placebo gel + simulation of PBM; Placebo + PBM; STRONTIUM—10% strontium chloride + simulation of PBM; and PBM + STRONTIUM—10% strontium chloride + PBM. All groups received tooth bleaching treatment with 35% hydrogen peroxide. For the PBM treatment, the laser tip was positioned in the apical and cervical regions of the teeth bleached in the respective hemi-arch. The laser system was operated in continuous mode, using 1.7 J of energy. A dose of 60 J/cm2 was applied to each point for 16 seconds under 808 nm near-infrared light (100mW of power), with a point area of 0.028 cm2. TS was assessed during a 21-day follow-up, using the modified visual analogue scale. Results In the intragroup assessment, the Friedman test indicated that PBM + STRONTIUM promoted the greatest reduction in TS after the second week of treatment (p ≤ 0.05). The Wilcoxon-Mann-Whitney test indicated that the groups Placebo + PBM, STRONTIUM, and STRONTIUM + PBM did not differ statistically (p ≥ 0.05) in the first and third weeks of treatment The group PLACEBO exhibited the greatest TS in the first three days after each bleaching session. Conclusion The combination of 10% strontium chloride with PBM was effective in reducing post-bleaching TS; however, the combination of 10% strontium chloride with PBM was effective in reducing post-bleaching TS; however, it did not differ from the individual use of Placebo + PBM or STRONTIUM groups assessed after 21 days of follow-up.


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