Comparison of the shear bond strength of 3D printed temporary bridges materials, on different types of resin cements and surface treatment

Thus, purpose of this study was to compare the shear bond strength of the resin cement and the resin modified glass ionomer cement on 3D printed temporary material for crowns and bridges in combination with different surface treatment modalities. Test specimens VarseoSmile Temp material (Bego, Bremen, Germany) (n=64) in the form of rectangular blocks (n=32) and cylindrical test specimens (n=32) were printed using the Varseo S 3D printer (Bego, Bremen, Germany). The specimens were divided into 4 groups, with 8 specimens of each kind. Two groups (n=16 pairs) were blasted with Perlablast® Micro [PM] 50µm (Bego, Bremen, Germany) and two groups (n=16 pairs) were blasted with alumina [AL] 50µm. The cylindric specimen were cemented on the rectangular block with a load of 20N using a Zwick/Roell machine (Ulm, Germany), to ensure a comparable cementing process. One group (n=8) of each pre-treatment was cemented with Fuji Cem 2 [Fuji+AL & Fuji+PM] and one of each with Variolink® Esthetic [Vario+AL & Vario+PM]. The Fuji Cem 2 was chemically cured while dual curing Variolink® Esthetic was additionally light cured using LED (Bluephase II, Ivoclar Vivadent, Ellwagen, Germany; light intensity, >1,000 mW/cm2, high power modus). The shear strength was performed with Zwick/Roell universal test machine (speed, 0.8 mm/min), fracture and statistical analysis was performed (T-test, p<0.05). T-test showed a significant difference Fuji Cem 2 (Fuji+AL & Fuji&PM) and Variolink® Esthetic (Vario+AL &Vario+PM) (p=0.000). Fuji+AL & Fuji+PM showed a significant difference for surface pre-treatment (p=0.002). Vario+AL & Vario+PM no significance (p=0.872) for pre-treatment method was detectable. Variolink® Esthetic showed a higher bond strength compared to Fuji Cem 2 and an increasing bond strength for Fuji Cem 2 with alumina pre-treatment. There was no significant difference for Vario+AL and Vario+PM

Improving Patient Experience by Providing Consistent Education Regarding Medication Side Effects

https://digitalcommons.psjhealth.org/stvincent-bootcamp/1033/thumbnail.jp

Modeling the dynamics of hypoxia inducible factor-1α (HIF-1α) within single cells and 3D cell culture systems

HIF (hypoxia inducible factor) is an oxygen-regulated transcription factor that mediates the intracellular response to hypoxia in human cells. There is increasing evidence that cell signaling pathways encode temporal information, and thus cell fate may be determined by the dynamics of protein levels. We have developed a mathematical model to describe the transient dynamics of the HIF-1α protein measured in single cells subjected to hypoxic shock. The essential characteristics of these data are modeled with a system of differential equations describing the feedback inhibition between HIF-1α and prolyl hydroxylases (PHD) oxygen sensors. Heterogeneity in the single-cell data is accounted through parameter variation in the model. We previously identified the PHD2 isoform as the main PHD sensor responsible for controlling the HIF-1α transient response, and make here testable predictions regarding HIF-1α dynamics subject to repetitive hypoxic pulses. The model is further developed to describe the dynamics of HIF-1α in cells cultured as 3D spheroids, with oxygen dynamics parameterized using experimental measurements of oxygen within spheroids. We show that the dynamics of HIF-1α and transcriptional targets of HIF-1α display a non-monotone response to the oxygen dynamics. Specifically we demonstrate that the dynamic transient behaviour of HIF-1α results in differential dynamics in transcriptional targets

Assessing the Efficacy of Nano- and Micro-Sized Magnetic Particles as Contrast Agents for MRI Cell Tracking

Iron-oxide based contrast agents play an important role in magnetic resonance imaging (MRI) of labelled cells in vivo. Currently, a wide range of such contrast agents is available with sizes varying from several nanometers up to a few micrometers and consisting of single or multiple magnetic cores. Here, we evaluate the effectiveness of these different particles for labelling and imaging stem cells, using a mouse mesenchymal stem cell line to investigate intracellular uptake, retention and processing of nano- and microsized contrast agents. The effect of intracellular confinement on transverse relaxivity was measured by MRI at 7 T and in compliance with the principles of the ‘3Rs’, the suitability of the contrast agents for MR-based cell tracking in vivo was tested using a chick embryo model. We show that for all particles tested, relaxivity was markedly reduced following cellular internalisation, indicating that contrast agent relaxivity in colloidal suspension does not accurately predict performance in MR-based cell tracking studies. Using a bimodal imaging approach comprising fluorescence and MRI, we demonstrate that labelled MSC remain viable following in vivo transplantation and can be tracked effectively using MRI. Importantly, our data suggest that larger particles might confer advantages for longer-term imaging