Corrosion Sealing of Amalgam Restorations In Vitro

10.2341/08-94 ◽  
2009 ◽  
Vol 34 (3) ◽  
pp. 312-320 ◽  
Author(s):  
D. B. Mahler ◽  
B. V. Pham ◽  
J. D. Adey

Clinical Relevance After placement, amalgam restorations exhibit a gap between the restoration and tooth structure, which fills with corrosion products during time in clinical service. To reduce the time necessary to fill this gap, an amalgam that exhibits a small initial gap shortly after setting and an amalgam that contains zinc is recommended.

2010 ◽  
Vol 35 (3) ◽  
pp. 314-323 ◽  
Author(s):  
C. L. Roggenkamp ◽  
F. A. Berry ◽  
H. Lu

Clinical Relevance Freshly mixed amalgam added to existing amalgam restorations as a means of repair and allowed to set completely may be expected to join with nearly original strength, if sufficient condensation time and pressure are used.


2011 ◽  
Vol 12 (3) ◽  
pp. 164-170 ◽  
Author(s):  
Indra Gupta ◽  
Satyendra Gupta ◽  
Anjali Kothari

ABSTRACT Aim To compare the retention of amalgam restorations in bonded amalgam restoration and restorations with undercuts. Background With improvement in adhesive technology problem associated with conventional preparation for amalgam restorations mainly compromised resistance form of tooth structure have been largely overcome. Materials and methods Forty caries free extracted molars were used. A basic box preparation was done proximally with buccoproximal and linguoproximal walls diverging at 45° angle and the axial wall is 1.3 mm in dentin. Group 1 – Teeth with basic box preparation. Group 2 – Teeth with box preparation for bonded amalgam. Group 3 – Teeth with box preparation and proximal retention grooves. Group 4 – Teeth with box preparation and occlusal dovetail. Group 1, 3 and 4 were restored with silver amalgam and group 2 restored with resin-bonded amalgam. All samples were subjected to simulated occlusal load against marginal ridge using a blunt stainless steel point in an Instron testing machine. The force in kilogram required to dislodge the restorations as well as the type and location of failure were recorded. Result The main force required to dislodge the restoration was least in group 1 and 3 and maximum in group 2. Conclusion The in vitro study showed that the amalgam bonding technique, using an adhesive resin liner in proximal box form preparation, was more effective than either box form with proximal grooves or dovetails or proximal box only in providing resistance to displacement. Clinical significance Amalgam bonding eliminates the unnecessary removal of sound tooth structure during cavity preparations. How to cite this article Gupta I, Gupta S, Kothari A. Revisiting Amalgam: A Comparative Study between Bonded Amalgam Restoration and Amalgam Retained with Undercuts. J Contemp Dent Pract 2011;12(3):164-170.


2010 ◽  
Vol 35 (6) ◽  
pp. 641-648 ◽  
Author(s):  
T. Alptekin ◽  
F. Ozer ◽  
N. Unlu ◽  
N. Cobanoglu ◽  
M. B. Blatz

Clinical Relevance The lining of amalgam restorations showed no significant effect on microleakage around restoration margins. In vivo and in vitro evaluations confirmed that microleakage was higher in resin composite restorations than in amalgam.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yasaman Barekatain ◽  
Jeffrey J. Ackroyd ◽  
Victoria C. Yan ◽  
Sunada Khadka ◽  
Lin Wang ◽  
...  

AbstractHomozygous deletion of methylthioadenosine phosphorylase (MTAP) in cancers such as glioblastoma represents a potentially targetable vulnerability. Homozygous MTAP-deleted cell lines in culture show elevation of MTAP’s substrate metabolite, methylthioadenosine (MTA). High levels of MTA inhibit protein arginine methyltransferase 5 (PRMT5), which sensitizes MTAP-deleted cells to PRMT5 and methionine adenosyltransferase 2A (MAT2A) inhibition. While this concept has been extensively corroborated in vitro, the clinical relevance relies on exhibiting significant MTA accumulation in human glioblastoma. In this work, using comprehensive metabolomic profiling, we show that MTA secreted by MTAP-deleted cells in vitro results in high levels of extracellular MTA. We further demonstrate that homozygous MTAP-deleted primary glioblastoma tumors do not significantly accumulate MTA in vivo due to metabolism of MTA by MTAP-expressing stroma. These findings highlight metabolic discrepancies between in vitro models and primary human tumors that must be considered when developing strategies for precision therapies targeting glioblastoma with homozygous MTAP deletion.


2006 ◽  
Vol 31 (6) ◽  
pp. 688-693 ◽  
Author(s):  
B. A. C. Loomans ◽  
N. J. M. Opdam ◽  
F. J. M. Roeters ◽  
E. M. Bronkhorst ◽  
R. C. W. Burgersdijk

Clinical Relevance When placing a Class II resin composite restoration, the use of sectional matrix systems and separation rings to obtain tight proximal contacts is recommended.


2010 ◽  
Vol 35 (6) ◽  
pp. 655-662 ◽  
Author(s):  
M. Özcan ◽  
G. Schoonbeek ◽  
B. Gökçe ◽  
E. Çömlekoglu ◽  
M. Dündar

Clinical Relevance For reliable repair of amalgam restorations, including dentin fractures, the amalgam surface should first be silica coated; dentin/enamel should be etched, washed and rinsed thoroughly. Then, amalgam should be silanized and primer/bonding should be applied onto dentin.


10.2341/05-26 ◽  
2006 ◽  
Vol 31 (2) ◽  
pp. 261-265 ◽  
Author(s):  
A. R. Yazici ◽  
A. Müftü ◽  
G. Kugel ◽  
R. D. Perry

Clinical Relevance The thickness of the residual dentin is a critical factor in the reducing thermal transfer to pulp, and this transfer varies with the curing unit used.


2011 ◽  
Vol 36 (1) ◽  
pp. 72-79 ◽  
Author(s):  
L. Korkut ◽  
H. S. Cotert ◽  
H. Kurtulmus

Clinical Relevance Fitting accuracy and microleakage dominate prognostic covariates for the long-term durability of crown restorations. The fitting accuracy and microleakage potential of zirconia infrastructures might be influenced by manufacturing technology.


2018 ◽  
Author(s):  
Soo-Hyun Kim ◽  
Richard P. Redvers ◽  
Lap Hing Chi ◽  
Xiawei Ling ◽  
Andrew J. Lucke ◽  
...  

ABSTRACTBreast cancer brain metastasis remains largely incurable. While several mouse models have been developed to investigate the genes and mechanisms regulating breast cancer brain metastasis, these models often lack clinical relevance since they require the use of immune-compromised mice and/or are poorly metastatic to brain from the mammary gland. We describe the development and characterisation of an aggressive brain metastatic variant of the 4T1 syngeneic model (4T1Br4) that spontaneously metastasises to multiple organs, but is selectively more metastatic to the brain from the mammary gland than parental 4T1 tumours. By immunohistochemistry, 4T1Br4 tumours and brain metastases display a triple negative phenotype, consistent with the high propensity of this breast cancer subtype to spread to brain. In vitro assays indicate that 4T1Br4 cells have an enhanced ability to adhere to or migrate across a brain-derived endothelial monolayer and greater invasive response to brain-derived soluble factors compared to 4T1 cells. These properties are likely to contribute to the brain-selectivity of 4T1Br4 tumours. Expression profiling and gene set enrichment analyses demonstrate the clinical relevance of the 4T1Br4 model at the transcriptomic level. Pathway analyses implicate tumour-intrinsic immune regulation and vascular interactions in successful brain colonisation, revealing potential therapeutic targets. Evaluation of two histone deacetylase inhibitors, SB939 and 1179.4b, shows partial efficacy against 4T1Br4 metastasis to brain and other sites in vivo and potent radio-sensitising properties in vitro. The 4T1Br4 model provides a clinically relevant tool for mechanistic studies and to evaluate novel therapies against brain metastasis.SUMMARY STATEMENTWe introduce a new syngeneic mouse model of spontaneous breast cancer brain metastasis, demonstrate its phenotypic, functional and transcriptomic relevance to human TNBC brain metastasis and test novel therapies.


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