Hebertfitch6830

Supplementation of CaP-based bone graft substitutes with bioinorganics such as strontium, zinc or silicon is an interesting approach to increase the biological performance in terms of bone regenerative potential of calcium phosphate (CaP)-based bone substitutes. However, the in vivo efficacy of this approach has not been systematically analyzed, yet. Consequently, we performed a systematic review using the available literature regarding the effect of bioinorganic supplementation in CaP-based biomaterials on new bone formation and material degradation in preclinical animal bone defect models and studied this effect quantitatively by performing a meta-analysis. Additional subgroup analyses were used to study the effect of different bioinorganics, animal model, or phase category of CaP-based biomaterial on bone formation or material degradation. Results show that bioinorganic supplementation increases new bone formation (standardized mean difference [SMD] 1.43 SD, confidence interval [CI] 1.13-1.73). Additional subgroup analysis showed that strontium, magnesium and silica significantly enhanced bone formation, while zinc did not have any effect. This effect of bioinorganic supplementation on new bone formation was stronger for DCPD or β-TCP and biphasic CaPs than for HA or α-TCP (p less then 0.001). In general, material degradation was slightly hindered by bioinorganic supplementation (mean difference [MD] 0.84%, CI 0.01-1.66), with the exception of strontium that significantly enhanced degradation. Overall, bioinorganic supplementation represents an effective approach to enhance the biological performance of CaP-based bone substitutes.A high-performance gas separation membrane for hydrogen (H2) purification is still highly desirable for the sustainable development of our society. GS0976 Based on the structure of γ-graphyne, we theoretically designed the two-dimensional nanomaterials γ-C4X (X = O, S or Se) with intrinsic pores that may be suitable for gas separation. By first-principles calculations, we obtained the geometric structures of γ-C4X, and confirmed that γ-C4O and γ-C4S are stable at room temperature. Due to the moderate size of the intrinsic pores, γ-C4O exhibits a lower diffusion barrier and higher permeance for H2 than those of γ-C4S. It is worth noting that at room temperature, the high selectivity (1019) for separating H2 from a H2/CH4 mixture by γ-C4O shows great potential for H2 purification. Moreover, the classic molecular dynamics simulations at 300 K demonstrate that H2 can easily permeate through the intrinsic pores of γ-C4O membranes with high permeability and selectivity, which supports our first-principles calculations.The vibrationally resolved spectra of the pyrene cation and doubly-dehydrogenated pyrene cation (C16H10˙+; Py+ and C16H8˙+; ddPy+) are presented. Infrared predissociation spectroscopy is employed to measure the vibrational spectrum of both species using a cryogenically cooled 22-pole ion trap. The spectrum of Py+ allows a detailed comparison with harmonic and anharmonic density functional theory (DFT) calculated normal mode frequencies. The spectrum of ddPy+ is dominated by absorption features from two isomers (4,5-ddPy+ and 1,2-ddPy+) with, at most, minor contributions from other isomers. These findings can be extended to explore the release of hydrogen from interstellar PAH species. Our results suggest that this process favours the loss of adjacent hydrogen atoms.Herein, we report a FnCas12a/crRNA assisted Dumbbell-PCR method for the detection of isomiRs with double specificity and magnification. The single nucleotide variant of isomiRs in terminals and/or inner sequence could be discriminated by this strategy. Using this method, let-7a isomiRs in MCF-7 and MCF-7R cell lines were analyzed.Correction for 'Substrate and product binding inside a stimuli-responsive coordination cage acting as a singlet oxygen photosensitizer' by Sonja Pullen et al., Dalton Trans., 2020, 49, 9404-9410, DOI 10.1039/D0DT01674H.Circulating tryptophan/large neutral amino acids (tryptophan/LNAA) ratio, an indicator of brain serotonin levels, may be important in appetite regulation, together with gastrointestinal (gastric emptying, plasma cholecystokinin) mechanisms. We have compared effects of intragastric tryptophan ('Trp') on the plasma tryptophan/LNAA ratio in lean and obese men, and the associations of the tryptophan/LNAA ratio, gastric emptying and CCK concentrations with energy intake. Lean and obese male participants (n = 16 each) received 3 g Trp or volume-matched control intragastrically, 15 min before a mixed-nutrient drink (300 mL, 400 kcal) (t = 0 min) in randomised, double-blind fashion. Plasma amino acid (for calculation of the plasma tryptophan/LNAA ratio) and CCK concentrations were measured from t = -20-60 min. Gastric emptying was assessed from t = 0-60 min, and ad-libitum energy intake from a standardised buffet-style meal from t = 60-90 min. The increase in the plasma tryptophan/LNAA ratio was less in obese, than lean, participants (P 0 kcal) after Trp compared with those who did not (by ≤0 kcal) (P less then 0.05). Moreover, in participants who reduced their energy intake, the ratio was lower in obese, than in lean (P less then 0.05). There was a trend for an inverse correlation between energy intake with the plasma tryptophan/LNAA ratio in lean (r = -0.4, P = 0.08), but not in obese, participants. There was no significant difference in gastric emptying or CCK between participants who reduced their energy intake and those who did not. In conclusion, the plasma tryptophan/LNAA ratio appears to be a determinant of the suppression of energy intake in response to tryptophan in normal-weight people, but not in those with obesity. The role of the plasma tryptophan/LNAA ratio to regulate energy intake, and potential changes in obesity, warrant evaluation in prospective studies.Correction for 'Pyridine N-oxide promoted hydrosilylation of carbonyl compounds catalyzed by [PSiP]-pincer iron hydrides' by Guoliang Chang et al., Dalton Trans., 2020, 49, 9349-9354, DOI 10.1039/D0DT00392A.Highly transparent and active Pt-Mo2C counter electrodes were successfully fabricated by the strong metal-support interaction, with high dispersity of Pt nanoclusters on Mo2C support, which endowed bifacial dye-sensitized solar cells with a rear-to-front efficiency ratio as high as 0.75.