With respect to the comparable complication rate, clinical and radiological outcome of allogenic versus autologous reconstruction of TPF, freeze-dried allograft could be recommended as an appropriate substitute of autograft in this treatment. Nevertheless, the longer follow-up period of the patients could further extend our understanding of the clinical outcome of each component.
Asymmetrically conducting interfaces are the building
blocks of
electronic devices. While p–n junction diodes made of seminal
inorganic semiconductors with rectification ratios close to the theoretical
limits are routinely fabricated, the analogous organic–inorganic
and organic–organic interfaces are still too leaky to afford
functional use. We report fabricating highly rectifying organic–inorganic
interfaces by forming water-mediated hydrogen bonds between the hydrophilic
surfaces of a hole-conducting polymer anode and a polycrystalline
n-type metal oxide cathode. These hydrogen bonds simultaneously strengthen
the anode–cathode electronic coupling, facilitate the matching
between their incompatible surface structures, and passivate the detrimental
surface imperfections. Compared to an analogous directly joined interface,
our hydrogen-bonded Au-PEDOT:PSS–H2O–TiO2-Ti diodes demonstrate 105 times higher rectification
ratios. These results illustrate the strong electronic coupling power
of the hydrogen bonds on a macroscopic scale and underscore the hydrogen-bonded
interfaces as the building blocks of fabricating organic electronic
and optoelectronic devices. The presented interface model is anticipated
to advance designing electronic devices based on the organic–organic
and organic–inorganic hetero-interfaces. Described electronic
implications of hydrogen bonding on the conductive polymer interfaces
are anticipated to be impactful in the organic electronics and neuromorphic
engineering.
A biodegradable micro/nano-structured porous hemostatic gelatin-based sponge as a dentistry surgery foam was prepared using a freeze-drying method. In vitro function evaluation tests were performed to ensure its hemostatic effect. Biocompatibility tests were also performed to show the compatibility of the sponge on human fetal foreskin fibroblasts (HFFF2) cells and red blood cells (RBCs). Then, 10 patients who required the extraction of two teeth were selected, and after teeth extraction, for dressing, the produced sponge was placed in one of the extracavities while a commercial sponge was placed in the cavity in the other tooth as a control. The total weight of the absorbed blood in each group was compared. The results showed a porous structure with micrometric and nanometric pores, flexibility, a two-week range for degradation, and an ability to absorb blood 35 times its weight in vitro. The prepared sponge showed lower blood clotting times (BCTs) (243.33 ± 2.35 s) and a lower blood clotting index (BCI) (10.67 ± 0.004%) compared to two commercial sponges that displayed its ability for faster coagulation and good hemostatic function. It also had no toxic effects on the HFFF2 cells and RBCs. The clinical assessment showed a better ability of blood absorption for the produced sponge (p-value = 0.0015). The sponge is recommended for use in dental surgeries because of its outstanding abilities.
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