CHO Group Research Articles

Mn(I)‐Catalyzed C−H Allylation of Indoles with 2‐Vinylaziridines

AbstractMn(CO)5Br‐catalyzed reaction of 1‐(2‐pyrimidyl)indoles with 1‐sulfonyl‐2‐vinylaziridines in THF in the presence of 0.25 equiv. of NaOAc affords 2‐allylated indoles in 31 % to 100 % yields. The protocol suits for 3‐, 4‐, 5‐, 6‐, and 7‐substituted indoles and N‐(2‐pyrimidyl)pyrroles as well as various 1‐(arylsulfonyl)‐2‐vinylaziridines such as 1‐(phenylsulfonyl)‐2‐vinylaziridine, 1‐(naphthalen‐2‐ylsulfon‐yl)‐2‐vinylaziridine, and 1‐(substituted phenylsulfonyl)‐2‐vinylazirid‐ines. Functional groups including alkyl, alkoxy, halogen, CHO, COOMe, CF3, CN, and NO2 groups are tolerated.

A low-carbohydrate, high-fat diet leads to unfavorable changes in blood lipid profiles compared to carbohydrate-rich diets with different glycemic indices in recreationally active men.

In addition to recent discussions of low-carbohydrate, high-fat diets (LCHF) from a performance perspective, there is a paucity of knowledge regarding influence of the combined effect of an exercise and nutritional intervention, which varies in carbohydrate (CHO) intake and glycemic indices, on blood lipid levels in recreationally active men. A total of 65 male runners (VO2 peak = 55 ± 8 mL·min-1·kg-1) completed a 10-week ad libitum nutritional regimen (LOW-GI: ≥ 65% low GI CHO per day, n = 24; HIGH-GI: ≥ 65% high GI CHO per day, n = 20; LCHF: ≤ 50 g CHO daily, n = 21) with a concurrent prescribed endurance training intervention. Fasting total cholesterol (TC), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C) were determined before and after the intervention. Additionally, 24-h dietary recalls were completed twice weekly. Following the intervention, TC was significantly higher in LCHF (196 ± 37 mg·dL-1) compared to both LOW-GI (171 ± 41 mg·dL-1) and HIGH-GI (152 ± 28 mg·dL-1, p < 0.001). Additionally, LDL-C levels increased in LCHF (+17 ± 21 mg·dL-1, p = 0.001), while they decreased in both CHO groups (p < 0.05, respectively). Only the HIGH-GI group demonstrated a significant reduction in HDL-C (-3 ± 9 mg·dL-1, p = 0.006), while a decrease in TG was only significant in LOW-GI (-18 ± 36 mg·dL-1, p = 0.008). Although mean blood lipid levels remained within the normal range, the data indicate that a low-carbohydrate, high-fat (LCHF) diet leads to unfavorable changes in individual blood lipid profiles compared to carbohydrate-rich diets. Therefore, it is recommended that the impact of a low-carbohydrate diet on blood lipids be considered when counseling active and healthy individuals.

Is severe carbohydrate restriction necessary for appetite suppression? The ASKED randomized controlled trial.

This trial aimed to compare three low-energy diets (LEDs) with different amounts of carbohydrates (CHO) on ketosis and changes in hunger feelings in adults with obesity. A total of 101 adults (51 female) with obesity (BMI, mean [SEM], 34.7 [0.4] kg/m2) were randomized to follow three isocaloric LEDs (1000 kcal/day) for 8 weeks, containing either low, medium, or high CHO (70, 100, and 130 g/day, respectively), and 4 weeks of refeeding and weight stabilization. Body weight (BW) and composition, hunger and other appetite ratings, concentrations of β-hydroxybutyrate (βHB), and appetite-related hormones were measured at baseline and at the end of weeks 8 and 12. At week 8, weight loss and βHB concentrations were significantly different among groups: Low CHO group versus Medium CHO group (BW: 2.32 [0.95] kg, 95% CI: 0.44 to 4.21, p = 0.016; βHB: -0.40 [0.09] mM, 95% CI: -0.67 to -0.09, p < 0.001); Low CHO group versus High CHO group (BW: 2.29 [0.96] kg, 95% CI: 0.39 to 4.19, p = 0.016; βHB: -0.644 [0.10] mM, 95% CI: -0.84 to -0.44, p < 0.001); and Medium CHO group versus High CHO group (BW: -0.03 [0.94] kg, 95% CI: -1.89 to 1.84, p = 0.977; βHB: -0.15 [0.08] mM, 95% CI: -0.30 to 0.002, p = 0.054). No significant differences in hunger were found among groups: Low CHO group versus Medium CHO group (-10.87 [5.92] mm, 95% CI: -0.82 to 22.57, p = 0.068); Low CHO group versus Medium CHO group (7.74 [7.36] mm, 95% CI: -6.77 to 22.26, p = 0.294); and Medium CHO group versus High CHO group (-3.13 [7.48] mm, 95% CI: -17.89 to 11.63, p = 0.676). Although the findings of this trial are not definitive, changes in hunger ratings with weight loss did not differ among groups. Additional studies with CHO intake of up to 130 g in 1000-kcal/day LEDs are warranted to replicate these findings.

The Characteristics Analysis of Hyaluronic Acid Modified By Cold Atmospheric Plasma and Its Performance in Hydrogel Preparation

ABSTRACTHyaluronic acid (HA) is extensively utilized in biomedical applications, and its functionality can be enhanced by introducing aldehyde groups (─CHO) through oxidation. In this study, cold atmospheric plasma (CAP) was used to treat aqueous HA solutions, resulting in the formation of plasma‐modified HA (PMHA) containing ─CHO groups. The free radicals generated from interactions between water molecules and CAP particles reacted with HA, leading to the oxidation of hydroxyl groups into ─CHO and the cleavage of glycosidic bonds, causing molecular depolymerization. The PMHA was then used to synthesize hydrogels in combination with carboxymethyl chitosan and ɛ‐polylysine. This study presents an effective approach for generating HA with aldehyde functionalities and offers insights into the interaction between CAP and polysaccharides.

Boosting lithium/magnesium separation performance of selective electrodialysis membranes regulated by enamine reaction

Monovalent cation exchange membranes (MCEMs) have progressively played an important role in the field of ion separation. However, according to transition state theory (TST), synchronously tuning the enthalpy barrier (△H) and entropy barrier (△S) for cation transport to improve ion separation performance is challenging. Here, the enamine reaction between the -NH- and -CHO groups is applied to regulate the subsequent Schiff-base reaction between the -CHO and -NH2 groups, which reduces the positive charges of the selective layer but increases the steric hindrance. The increased -T△S (△S term) for cation transport plays an important role in improving Li+/Mg2+ separation performance. The optimal positively-charged glutaraldehyde@piperazine/polyethyleneimine assembled membrane (M-Glu@PIP/PEI) has a perm-selectivity (Li+/Mg2+) of 31.83 with a Li+ flux of 1.87 mol·m-2·h-1, surpassing the Li+/Mg2+ separation performance of state-of-the-art monovalent ion selective membranes (MISMs). Most importantly, the selective electrodialysis (S-ED) process with M-Glu@PIP/PEI can be directly applied to treat simulated salt-lake brines (SLBs), and its superior Li+/Mg2+ separation performance and operational stability enables 74.44% of the lithium resources with a Li+ purity of 34.02% to be recovered. This study presents new insights into the design of high-performance MCEMs for energy-efficient resource recovery.

Mimicking biological method with inorganic and organic compounds modified clays for continuous controlling of Microcystis aeruginosa

Although clay dispersion is one of the few techniques currently used in the field to control cyanobacterial harmful algal blooms (CyanoHABs), low flocculation efficiency and resuspension of flocculated algal cells are its main drawbacks. This study simulated the "flocculatio-lysis-degradation-nutrient regulation" model of biocontrol technique to develop a modified clay (ECRE-CS-PFS-CPL) using polyferric sulfate (PFS), chitosan (CS) and Eichhornia crassipes root extracts (ECRE) to modify the clinoptilolite (CPL). The results revealed that ECRE-CS-PFS-CPL introduced functional groups, specifically aldehyde group —CHO and amide group —CO-NH—, leading to an enhanced void structure. At 0.2 g/L concentration, ECRE-CS-PFS-CPL demonstrated a removal efficiency of 98.02 % within 30 min. ECRE-CS-PFS-CPL exhibited a positive charge in nature water, leveraging charge neutralisation to expedite the flocculation of M. aeruginosa cells. The combination of coated CS and algal cells resulted in the formation of large, dense flocs through net sweeping and bridging, which was 58.28 times larger than control. Subsequently, the loaded ECRE inhibited the algal cells via allelopathy. The inhibition activated the antioxidant system of M. aeruginosa, with significant increases in catalase (CAT) and superoxide dismutase (SOD) activities. Photosynthetic pigments (Chl-a), photosynthetic efficiency (Fv/Fm) and maximum relative photosynthetic electron transfer rate (ETRmax) were markedly reduced, indicating the damage to photosynthetic system. Furthermore, Chl-a remained consistently low during extended monitoring, registering at 4.98 % of control after 40 days. ECRE-CS-PFS-CPL effectively reduced microcystins by 81.48 % and phosphate levels in algal cultures by 91.92 % compared to control. Consequently, ECRE-CS-PFS-CPL offers an efficient, environmentally safe and sustainable solution for CyanoHABs control.

Enhancing CO2 reduction with formamide-Ni@TiO2 catalyst

Formamide condensation with Ni can generate the NC structure, widely recognized as an efficient catalyst for electrocatalytic CO2 reduction reaction (CO2RR). To improve the utilization efficiency of Ni atoms, we introduced metal oxides as substrates to modulate the growth of a formamide-Ni (FA-Ni) condensate. FA-Ni@TiO2 demonstrated 2.8 times higher partial CO current density and Ni turnover frequency than FA-Ni, which were also higher than those of other FA-Ni@metal oxides, including ZrO2, Al2O3, Fe2O3, and ZnO. The improved performance of CO2RR can be attributed to the Ni content exposed on FA-Ni@TiO2 being twice that of the raw FA-Ni condensate. The Fourier transform infrared results suggested that formamide was adsorbed on TiO2 via the -CHO group, exposing -NH2 for potential interaction with Ni. As a result, Ni atoms were predispersed on the TiO2 surface. By contrast, the dispersion of Ni atoms was not enhanced by other metal oxides, such as Al2O3, Fe2O3, and ZnO, owing to the robust acidity of their surface sites. These metal oxides adsorbed formamide via -NH2, leading to the absence of extra -NH2 available for binding to Ni atoms. This study provides new insights into the development of appropriate substrates for single-atom catalysts.

Spatial and Size Distributions of Ti(C5H7O2)2[(CH3)2CHO]2 Mist Particles in a Tubular Furnace for Conformal and Uniform Deposition of Amorphous TiO2 Thin Films

The spatial and size distributions of titanium diisopropoxide bisacetylacetonate [(C5H7O2)2[(CH3)2CHO]2, also known as Ti(acac)2(OiPr)2] mist, diluted in CH3OH, are investigated in a tubular furnace using atmospheric‐pressure mist chemical vapor deposition (mist CVD). The focus is on the deposition of amorphous (a)‐TiO2 films with tubular furnace temperature and mesh bias as variables. When the furnace temperature reaches 350 °C, the number density of mist particles increases without significant changes in their size distribution, leading to a higher film deposition rate. Further, the deposition rate and average size of the mist particles with lower adhesion coefficient decrease with increasing spatial distance from the furnace inlet. Furthermore, applying a mesh bias results in an increase in the maximum number density of mist particles with a narrower size distribution; however, the overall film deposition rate decreases. These variations are attributed to the chemical reactivity of the mist precursors produced by pyrolysis and mesh bias. The fine mist precursors, which are strongly charged, coordinate with CH3OH and CHO groups through solvation, enhancing their chemical stability and lifetime. This process yields a dense and rigid a‐TiO2 network, improving the junction properties at the a‐TiO2/c‐Si interface.

Hierarchically porous carbon confined cobalt nanoparticles for highly efficient oxidative esterification of 5‐hydroxymethylfurfural

AbstractHerein, we report a controllable and versatile strategy for the synthesis of highly dispersed Co nanoparticles embedded in open‐channel hierarchically porous N/O‐doped carbon skeleton. Moreover, the pore sizes of the hierarchical structures can be easily tuned by adjusting the size of precursors. The as‐obtained Co@NC‐2ST exhibits unprecedented activity and selectivity in the oxidative esterification of 5‐hydroxymethylfurfural (HMF) to dimethyl furan‐2,5‐dicarboxylate under base‐free and atmospheric conditions. In particular, the achieved turnover frequency value is an order of magnitude higher than that of the state‐of‐art heterogeneous catalysts reported to date. A combination of experimental and density function theory studies reveals that the unique features of Co@NC‐2ST enable a novel reaction route, that is, the CHO group of HMF is preferentially esterified instead of the OH group. This can be attributed to the nucleophilic addition reaction caused by the attack of methoxy anion on the CHO group of HMF.

Starch exploration in Nelumbo nucifera and Trapa natans: Understanding physicochemical and functional variations for future perspectives

The current research emphasis on identifying unconventional starch sources with varied properties to broaden industrial applications. The focus of this research is on the search for alternative sources of starch with different properties in order to expand their potential use in the industrial sector. Starch was extracted from Trapa natans and Nelumbo nucifera and analyzed for their physicochemical and functional properties. They had similar protein (0.35 %) and ash contents, but the nitrogen-free extract was slightly higher in Nelumbo starch (87.58 %) than in Trapa starch (85.09 %). The amylose and amylopectin contents were 23.89 % and 76.11 % in Trapa starch and 15.70 % and 84.30 % in Nelumbo starch, respectively. Fourier-transform infrared spectroscopy identified both as polysaccharides. The characteristic absorption bands assigned to the stretching of OH groups (3324 cm−1; 3280 cm−1), the asymmetric and symmetric stretching of aliphatic chain groups (2925 cm−1; 2854 cm−1), the bending vibration of CHO groups (1149 cm−1; 1144 cm−1) were present in both the starch samples, with the exception of CH3 which could not be detected in Trapa natans starch. X-ray diffraction confirmed hexagonal and orthorhombic crystal structures in Nelumbo nucifera and Trapa natans starch. Scanning electron microscopy revealed a smooth oval and a rough cuboidal shape for lotus and chestnut starch, respectively. Rheological analysis showed that both starch solutions exhibited gel behavior, with Trapa showing stronger gel behavior after the crossover point. These results suggest potential applications in various industries, including the food industry and beyond.

Preoperative Oral Carbohydrates for Children: A Meta-Analysis and Systematic Review.

Background: Many studies have reported the use of preoperative oral carbohydrates (CHO) in children, but the results are inconsistent. The aim of this meta-analysis is to assess the effectiveness and safety of oral CHO administration in children prior to surgery, with the goal of offering a dependable reference for clinical nursing practices and surgical interventions. Methods: Two authors searched PubMed, Clinical trials, Web of Science, Embase, Cochrane Library, China national knowledge infrastructure (CNKI), Wanfang and Weipu databases for randomized controlled trial (RCT) on the effects of preoperative oral CHO in children up to April 12, 2024. We used RevMan 5.4 software for data analysis. Results: Nine RCTs involving a total of 1279 children were included. The meta-analysis showed that there was statistical difference in the pH of gastric juice (MD = 1.54, 95%CI: 1.40-1.67, p < .001), intraoperative sedation score (MD = 0.62, 95%CI: 0.27-0.97, p < .001), and the incidence of postoperative nausea and vomiting (OR = 0.40, 95%CI: 0.20-0.80, p = .009) between the CHO and control groups. There was no statistical difference in the RGV (MD = -0.23, 95%CI: -0.47-0.01, p = .06) and the postoperative blood glucose level (MD = -0.91, 95%CI: -5.03-3.21, p = .67) between the CHO and control groups. Egger regression analysis showed that there were no publication biases amongst the synthesized outcomes (all p > .05). Conclusion: The administration of oral CHO to children before surgery is safe and practicable. There is a need for additional, well-conducted studies with more participants to further elucidate the role of preoperative CHO administration.

Comparison of water-soluble and water-insoluble organic compositions attributing to different light absorption efficiency between residential coal and biomass burning emissions

Abstract. There are growing concerns about the climate impacts of absorbing organic carbon (also known as brown carbon, BrC) in the environment, yet its chemical composition and association with the light absorption capabilities remain poorly understood. This study characterized water-soluble and water-insoluble organic carbon (WSOC and WIOC) from residential solid fuel combustion at the molecular level and evaluated their quantitative relationship with mass absorption efficiency (MAE). The MAE values at λ = 365 nm from biomass burning were significantly higher than those from coal combustion (p &lt; 0.05). Thousands of peaks were identified in the m/z range of 150–800, with the most intense ion peaks occurring between m/z 200–500 for WSOC and m/z 600–800 for WIOC, respectively. The CHO group predominated in the WSOC extract from biomass burning emissions, while sulfur-containing compounds (SOCs) including CHOS and CHONS were more intense in the WIOC extract, particularly from coal emissions. Emissions of the CHON group were positively correlated with the fuel nitrogen content (r = 0.936; p &lt; 0.05), explaining their higher abundance in coal emissions compared to biomass. The SOC emissions were more predominant during flaming phases, as indicated by a positive correlation with modified combustion efficiency (MCE) (r = 0.750; p &lt; 0.05). The unique formulas of coal combustion aerosols were in the lower H/C and O/C regions, with higher unsaturated compounds in the van Krevelen (VK) diagram. In the WIOC extract, coal combustion emissions contained significantly higher fractions of condensed aromatics (32 %–59 %) compared to only 4.3 %–9.7 % in biomass burning emissions. In contrast, the CHOS group in biomass burning emissions was characterized by larger condensed aromatic compound fractions than those in coal combustion. Moreover, the CHOS aromatic compound fractions were positively correlated with MAE values in both WSOC (r = 0.714; p &lt; 0.05) and WIOC extracts (r = 0.929; p &lt; 0.001), suggesting that these compounds significantly contributed to MAE variabilities across different fuels.

Pre-operative carbohydrate drink in pediatric spine fusion: randomized control trial.

As rapid discharge protocols for pediatric spine fusion shorten stays, gastrointestinal (GI) complications are uncovered and cause delays in discharge. A pre-operative carbohydrate (CHO) drink has been shown to improve perioperative GI symptoms and functional return but has not been examined in pediatric spine patients. We aimed to determine if a preoperative CHO drink is safe in pediatric spine fusion patients, and if it improves their comfort scores and return of bowel function. We prospectively randomized ASA-1 and -2 pediatric spine fusion patients to either a pre-anesthesia carbohydrate drink 2h prior to surgery or to a control group (standard 8h NPO), blinded to surgical team. We documented time to return to flatus, bowel movement, GI symptoms, and comfort scores for 72h post-operatively or until discharge. 62 patients were randomized. There was no significant differences between the groups' pre-operative characteristics, surgical details, nor post-operative morphine dose equivalents, except for EBL (405cc control, 340cc CHO drink, p = 0.044). There were no perioperative complications related to ingestion of the CHO drink. CHO group had a positive trend for earlier return of flatus (21% vs. 3% return at 12h), and comfort scores for anxiety and abdominal pain, but no statistically significant differences. There was no difference in length of stay or time to first bowel movement. There were no complications related to ingestion of a CHO drink 2h prior to pediatric spinal fusion surgery. Further studies are needed to develop a study blinded to the participants with larger sample size. Level of evidenceI.

Synergy of metallic Co and oxygen vacancy sites in Co/Ce-MOF catalysts for efficiently promoting lignin derived phenols and macromolecular lignin hydrodeoxygenation

The enhanced utilization of biomass-derived chemicals for the generation of high value aromatics through an advanced catalytic strategy has captured considerable attention within the realm of eco-friendly manufacturing. This work presented four innovative three-dimensional rod-shaped mesoporous Ce-based MOF materials, which were coupled with a H-donor solvent to facilitate vanillin hydrodeoxygenation and macromolecular lignin. Under the optimized conditions (30 mg CoCe@C catalyst, 2 MPa N2 pressure, 15 mL isopropanol, 190 °C, and 5 h), the CoCe@C catalyst achieved nearly complete conversion of vanillin and demonstrated 87.8 % selectivity in the hydrogen-donor solvent. The characterization findings suggested that the synergy between metallic Co and oxygen vacancy sites enabled the effective activation of CHO group in vanillin, leading to formation of reactive product MMP. In addition, the optimal CoCe@C catalyst could also achieve macromolecular lignin hydrodeoxygenation to obtain high yield of lignin oil products with narrower molecular weight distribution. This study presented a viable approach for the concurrent utilization of lignin derivatives in the generation of high value fuels and chemicals.

Acid-Catalyzed Activation and Condensation of the =C5H Bond of Furfural on Aldehydes, an Entry Point to Biobased Monomers.

Furfural is an industrially relevant biobased chemical platform. Unlike classical furan, or C-alkylated furans, which have been previously described in the current literature, the =C5H bond of furfural is unreactive. As a result, on a large scale, C=C and C=O bond hydrogenation/hydrogenolysis is mainly performed, with furfuryl alcohol and methyl tetrahydrofuran being the two main downstream chemicals. Here, we show that the derivatization of the -CHO group of furfural restores the reactivity of its =C5H bond, thus permitting its double condensation on various alkyl aldehydes. Overcoming the recalcitrance of the =C5H bond of furfural has opened an access to a biobased monomer, whose potential have been investigated in the fabrication of renewably-sourced poly(silylether). By means of a combined theoretical-experimental study, a reactivity scale for furfural and its protected derivatives against carbonylated compounds has been established using an electrophilicity descriptor, a means to predict the molecular diversity and complexity this pathway may support, and also to de-risk any project related to this topic. Finally, by using performance criteria for industrial operations in the field of fuels and commodities, we discussed the industrial potential of this work in terms of cost, E-factor, reactor productivity and catalyst consumption.

Synthesis and performance of a nanosensing platform for homocysteine detection: A series of iridium(III) complexes containing aldehyde group as probe and MOF as supporting substrate

The low cost and simple detection method for Hcy (homocysteine) is highly desired in analytical and biological fields since Hcy has been regarded as a bio-marker for multiple diseases. In this work, five Ir(C^N)2(N^N)+ compounds having –CHO group in their C^N or N^N ligand were synthesized and tried for Hcy sensing. Electron-donating groups such as –NH2 and –CH3 were incorporated into the C^N or N^N ligand. Their geometric structure, electronic structure, and optical parameters (with or without Hcy) were analyzed and compared carefully to explore their Hcy sensing potential. The sensing mechanism was revealed by NMR titration and theoretical simulation as a cyclization reaction between the –CHO group and Hcy. The optimal compounds, which showed increased emission quantum yield (2.5-fold) and emission blue-shift (by ∼ 100 nm) upon Hcy, were then covalently grafted into a porous host bio-MOF-1. Linear working plots were fitted, with good selectivity, LOD of 0.15 μM, and response time of 33 s. The novelty of this work was the eye-sensitive emission color change of this nanosensing platform from red (without Hcy) to green (with Hcy).

Facile synthesis of mechanically robust and injectable tetra-polyethylene glycol/methacrylate chitosan double-network hydrogel cartilage repair

The development of advanced hydrogel scaffolds with good biocompatibility, mechanical strength and bioactive property is highly desirable in cell growth, proliferation, and differentiation for the cartilage tissue regeneration. Herein, we reported a simple, inexpensive, feasible, and environmentally benign strategy to synthesize a biocompatible polyethylene glycol-based methacrylate-modified chitosan (PCSMA) double network (DN) hydrogel via the reversible Schiff base reaction and successive photopolymerization between the tetra-poly (ethylene glycol) aldehyde (Tetra-PEG-CHO) and methacrylate-modified chitosan (CSMA) in mild conditions. The four-terminated CHO groups were hypothesized to not only construct the whole architectural network through the dynamic pH-responsive Schiff base but also contribute to the injectable behavior and good tissue adhesion, which may furnish the surgeon with the availability of injectable and shapeless ability to fill in the gaps. Compared to the single PCS hydrogel with the main similar components of the tetra-PEG-CHO and pure CS moieties, the post-fabrication of PCSMA DN hydrogel possessed slower degradation time, denser network, and stronger mechanical stability, which could facilitate the bone marrow mesenchymal stem cell (BMSCs) activity and promote the chondrogenic differentiation for facilitating cartilage regeneration. Our study highlights the positive effects on chondrogenic performance and supports the PCSMA hydrogel as a promising tissue-engineered scaffold for the cartilage defect repair.

Effects of Preoperative Oral Carbohydrate on Perioperative Maternal Outcomes Undergoing Cesarean Section: A Systematic Review and Meta-Analysis.

Preoperative oral carbohydrate (CHO) is a rapid postoperative rehabilitation protocol that improves perioperative outcomes and is widely used in adult surgical patients. However, pregnant women are excluded because of the possibility of aspiration due to delayed gastric emptying. This meta-analysis was conducted to evaluate the efficacy of preoperative oral CHO in elective cesarean section. PubMed, Embase, Web of Science, and the Cochrane Library were searched from inception to July 2023. Randomized controlled trials were included. The risk of bias was assessed using the Cochrane tool. Risk ratios and 95% confidence intervals were calculated. Meta-analysis was performed using random-effects models to estimate risk ratios and mean differences (MDs) with 95% confidence intervals (CIs). The outcomes included thirst and hunger scores, incidence of vomiting and nausea, time to flatus, and homeostatic model assessment of insulin resistance (HOMA-IR). A total of nine studies with 1211 patients were included in the analysis. The levels of thirst and hunger were evaluated using a 10-point visual analog scale, with 0 representing the best and 10 representing the worst. The severity of hunger (weighted mean difference (WMD: -2.34, 95% CI: -3.13 to -1.54), time to flatus (WMD: -3.51 hours, 95% CI: -6.85 to -0.17), and HOMA-IR (WMD: -1.04, 95% CI: -1.31 to -0.77) were significantly lower in the CHO group compared to the control group. However, there were no significant differences in the severity of thirst or the incidence of vomiting and nausea between the CHO and control groups. Preoperative oral CHO during cesarean section alleviates thirst and hunger, shortens the time of postoperative flatus, and reduces HOMA-IR. However, the available evidence is insufficient to reach a clear consensus on the benefits or harms of preoperative oral CHO during cesarean section. Therefore, it is premature to make a definitive recommendation for or against its routine use.

A Randomized Trial of Healthy Weight Gain in Athletic Individuals.

The purpose of this study is to evaluate the outcomes of a 10-wk diet and exercise regimen designed to promote healthy weight gain with excess energy from peanut-containing or high-carbohydrate foods. Nineteen male and 13 female athletes were randomly assigned to receive an additional 500 kcal·d -1 above typical intake through provision of either peanut-based whole foods/snacks (PNT group) or a similar, high-carbohydrate, peanut-free snack (CHO group) along with supervised, whole-body RT (3 d·wk -1 for 60-120 min). Body composition was assessed by dual-energyx-ray absorptiometry at baseline and postintervention. Total body mass (TBM) increased 2.2 ± 1.3 kg with 1.5 ± 1.1 kg as LBM after week 10. The PNT group ( n = 16; 27 ± 7 yr; 10 men, 6 women) gained less TBM than the CHO group ( n = 16; 23 ± 3 yr; 9 men, 7 women) (1.6 ± 1.1 kg vs 2.7 ± 1.2 kg, respectively, P = 0.007) with no differences in LBM (1.2 ± 1.1 kg vs 1.9 ± 1.0 kg, P = 0.136). These results suggest that the addition of 500 kcal·d -1 from whole foods/snacks in combination with a rigorous RT program promotes a similar weight gain of ~0.22 kg·wk -1 , primarily as LBM, over 10 wk in both male and female athletes. However, snack macronutrient content may impact the effectiveness of this regimen.

The Me(almIM)&lt;sub&gt;2&lt;/sub&gt; structural ZIFs: Synthesis, characterization and application

The Me(almIM)2 structural ZIFs are formed from the metal ions Me2+ and the linker 4-methyl-5-imidazolecarboxaldehyde (HalmIM), with the Me–almIM–Me bond angle similar to the Si–O–Si angle in zeolites (145o). Depending on the type of bond formed, Me(almIM)2 material has RHO or SOD structure with good thermal and chemical stability. With pore diameter of about 3.0-3.7 Å connected to large cavities with sizes from 9.1-17.9 Å and a structural frameworks containing two groups –CH3 and –CHO with hydrophilic properties, when the –CHO groups is modified by amine groups through imine condensation reaction, we can create hydrophobic materials for diverse applications in adsorption, separation, sensing, biomedical and catalysis. This review report collects results from more than 100 research papers related to Me(almIM)2 from 2010 to present and provides some recommendations on their synthesis, characterization and application in the future.