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The performance of a stirred bioreactor was evaluated in this study in terms of the bubble hydrodynamics and the mass transfer efficiency, using a non‐viscous Newtonian fluid of water, a viscous non‐Newtonian fluid of xanthan, and a viscous non‐Newtonian fluids of xanthan with dispersed soybean powder, respectively. The computational fluid dynamics–population balance model (CFD‐PBM) method coupled with the viscosity model and the mass transfer model is established to simulate the gas–liquid mass transfer process and bubble size distribution in the stirred bioreactor. The results demonstrate that the rheological properties of the fluid play an important role in determining the gas holdup, the mass transfer efficiency, and the bubble size distribution. Viscosity of the fluid exhibits a negative impact on gas–liquid mass transfer rate and gas holdup. Moreover, by properly adjusting the operating conditions such as the stirrer speed, it is possible to modulate the gas dispersion and mass transfer rate in the reactor. [ABSTRACT FROM AUTHOR]

Precise control over sequence structure in copolymers is essential for chemical product engineering. The complexity of sequence structures results in the challenging characterization of monomer sequences. Herein, a chemical composition model (CD model) is developed to record the distribution density of monomers in the chain segment, where the deviation of the chemical composition function between a copolymer and its ideal sequence structure can directly map the sequence structure quality. The application of the CD model in randomly generated virtual copolymers demonstrates that the model has great sensitivity and discrimination to evaluate sequence structures accurately. Furthermore, the CD model is combined with the kinetic Monte Carlo algorithm to explicitly track the evolution of sequence structure quality in the copolymerization process. The CD model provides an insight into the evolution of sequence structure, which is conducive to building the bridge between molecular structure and properties for the development of chemical product engineering. [ABSTRACT FROM AUTHOR]

Empirical research using the Empathic Accuracy Task (EAT) has suggested that schizophrenia patients and people with schizotypal personality disorder exhibit lower empathic accuracy than healthy people. However, empathic accuracy in a subclinical sample with high levels of schizotypy has seldom been studied. Our study aimed to investigate empathy in a subclinical sample using the Chinese version of the EAT and a self‐report empathy measure. Forty participants with high levels of schizotypy (HS participants) and 40 with low levels of schizotypy (LS participants), as measured by the Schizotypal Personality Questionnaire (SPQ), were recruited. All participants completed the Chinese version of the EAT and the self‐report Questionnaire of Cognitive and Affective Empathy. Empathic accuracy (EA) scores and the intra‐individual variability of EA scores were calculated. Independent samples t tests and Pearson correlation analyses were performed to examine group differences in empathy and the relationship between empathy and schizotypy respectively. HS participants exhibited reduced EA for both positive and negative videos, and larger intra‐individual variability of EA for negative videos than LS participants. However, HS and LS participants did not differ in self‐report cognitive empathy. Moreover, the interpersonal dimension of the SPQ was negatively correlated with EAT performance and self‐report cognitive empathy in LS participants. Individuals with HS show poorer performance‐based EA but relatively intact self‐report cognitive empathy. This study provides empirical evidence for the ontogeny of empathy deficits in subclinical populations at risk of developing schizophrenia, supporting early interventions for social cognitive deficits. [ABSTRACT FROM AUTHOR]

Type 2 diabetic osteoporosis (T2DOP) is a skeletal metabolic syndrome characterized by impaired bone remodeling due to type 2 diabetes mellitus, and there are drawbacks in the present treatment. Osteoking (OK) is widely used for treating fractures and femoral head necrosis. However, OK is seldom reported in the field of T2DOP, and its role and mechanism of action need to be elucidated. Consequently, this study investigated whether OK improves bone remodeling and the mechanisms of diabetes‐induced injury. We used db/db mice as a T2DOP model and stimulated MC3T3‐E1 cells (osteoblast cell line) with high glucose (HG, 50 mM) and advanced glycation end products (AGEs, 100 µg/mL), respectively. The effect of OK on T2DOP was assessed using a combined 3‐point mechanical bending test, hematoxylin and eosin staining, and enzyme‐linked immunosorbent assay. The effect of OK on enhancing MC3T3‐E1 cell differentiation and mineralization under HG and AGEs conditions was assessed by an alkaline phosphatase activity assay and alizarin red S staining. The AGEs/insulin‐like growth factor‐1(IGF‐1)/β‐catenin/osteoprotegerin (OPG) pathway‐associated protein levels were assayed by western blot analysis and immunohistochemical staining. We found that OK reduced hyperglycemia, attenuated bone damage, repaired bone remodeling, increased tibial and femoral IGF‐1, β‐catenin, and OPG expression, and decreased receptor activator of nuclear kappa B ligand and receptor activator of nuclear kappa B expression in db/db mice. Moreover, OK promoted the differentiation and mineralization of MC3T3‐E1 cells under HG and AGEs conditions, respectively, and regulated the levels of AGEs/IGF‐1/β‐catenin/OPG pathway‐associated proteins. In conclusion, our results suggest that OK may lower blood glucose, alleviate bone damage, and attenuate T2DOP, in part through activation of the AGEs/IGF‐1/β‐catenin/OPG pathway. [ABSTRACT FROM AUTHOR]

Diabetic neuropathic pain (DNP), one of the most common complications of diabetes, is characterized by bilateral symmetrical distal limb pain and substantial morbidity. To compare the differences is aimed at serum metabolite levels between 81 DNP and 73 T2DM patients without neuropathy and found that the levels of branched‐chain amino acids (BCAA) are significantly lower in DNP patients than in T2DM patients. In high‐fat diet/low‐dose streptozotocin (HFD/STZ)‐induced T2DM and leptin receptor‐deficient diabetic (db/db) mouse models, it is verified that BCAA deficiency aggravated, whereas BCAA supplementation alleviated DNP symptoms. Mechanistically, using a combination of RNA sequencing of mouse dorsal root ganglion (DRG) tissues and label‐free quantitative proteomic analysis of cultured cells, it is found that BCAA deficiency activated the expression of L‐type amino acid transporter 1 (LAT1) through ATF4, which is reversed by BCAA supplementation. Abnormally upregulated LAT1 reduced Kv1.2 localization to the cell membrane, and inhibited Kv1.2 channels, thereby increasing neuronal excitability and causing neuropathy. Furthermore, intraperitoneal injection of the LAT1 inhibitor, BCH, alleviated DNP symptoms in mice, confirming that BCAA‐deficiency‐induced LAT1 activation contributes to the onset of DNP. These findings provide fresh insights into the metabolic differences between DNP and T2DM, and the development of approaches for the management of DNP. [ABSTRACT FROM AUTHOR]

Sepsis arises from an uncontrolled inflammatory response triggered by infection or stress, accompanied by alteration in cellular energy metabolism, and a strong correlation exists between these factors. Alpha‐ketoglutarate (α‐KG), an intermediate product of the TCA cycle, has the potential to modulate the inflammatory response and is considered a crucial link between energy metabolism and inflammation. The scavenger receptor (SR‐A5), a significant pattern recognition receptor, assumes a vital function in anti‐inflammatory reactions. In the current investigation, we have successfully illustrated the ability of α‐KG to mitigate inflammatory factors in the serum of septic mice and ameliorate tissue damage. Additionally, α‐KG has been shown to modulate metabolic reprogramming and macrophage polarization. Moreover, our findings indicate that the regulatory influence of α‐KG on sepsis is mediated through SR‐A5. We also elucidated the mechanism by which α‐KG regulates SR‐A5 expression and found that α‐KG reduced the N6‐methyladenosine level of macrophages by up‐regulating the m6A demethylase ALKBH5. α‐KG plays a crucial role in inhibiting inflammation by regulating SR‐A5 expression through m6A demethylation during sepsis. The outcomes of this research provide valuable insights into the relationship between energy metabolism and inflammation regulation, as well as the underlying molecular regulatory mechanism. [ABSTRACT FROM AUTHOR]

Cell surface engineering with exogeneous receptors holds great promise for various applications. However, current biological methods face problems with safety, antigen escape, and receptor stoichiometry. The purpose of this study is to develop a biochemical method for displaying polyvalent antibodies (PAbs) on the cell surface. The PAbs are synthesized through the self‐assembly of DNA‐Ab conjugates under physiological conditions without the involvement of any factors harsh to cells. The data show that PAb‐functionalized cells can recognize target cells much more effectively than monovalent controls. Moreover, dual Ab incorporation into the same PAb with a defined stoichiometric ratio leads to the formation of a polyvalent hybrid Ab (DPAb). DPAb‐functionalized cells can effectively recognize target cell models with antigen escape, which cannot be achieved by PAbs with one type of Ab. Therefore, this work presents a novel biochemical method for Ab display on the cell surface for enhanced cell recognition. [ABSTRACT FROM AUTHOR]

Objectives: This study aims to elucidate the role of Fe2+ overload in kainic acid (KA)‐induced excitotoxicity, investigate the involvement of ferritinophagy selective cargo receptor NCOA4 in the pathogenesis of excitotoxicity. Methods: Western blotting was used to detect the expression of FTH1, NCOA4, Lamp2, TfR, FPN, and DMT1 after KA stereotaxic injection into the unilateral striatum of mice. Colocalization of Fe2+ with lysosomes in KA‐treated primary cortical neurons was observed by using confocal microscopy. Desferrioxamine (DFO) was added to chelate free iron, a CCK8 kit was used to measure cell viability, and the Fe2+ levels were detected by FerroOrange. BODIPY C11 was used to determine intracellular lipid reactive oxygen species (ROS) levels, and the mRNA levels of PTGS2, a biomarker of ferroptosis, were measured by fluorescent quantitative PCR. 3‐Methyladenine (3‐MA) was employed to inhibit KA‐induced activation of autophagy, and changes in ferritinophagy‐related protein expression and the indicated biomarkers of ferroptosis were detected. Endogenous NCOA4 was knocked down by lentivirus transfection, and cell viability and intracellular Fe2+ levels were observed after KA treatment. Results: Western blot results showed that the expression of NCOA4, DMT1, and Lamp2 was significantly upregulated, while FTH1 was downregulated, but there were no significant changes in TfR and FPN. The fluorescence results indicated that KA enhanced the colocalization of free Fe2+ with lysosomes in neurons. DFO intervention could effectively rescue cell damage, reduce intracellular lipid peroxidation, and decrease the increased transcript levels of PTGS2 caused by KA. Pretreatment with 3‐MA effectively reversed KA‐induced ferritinophagy and ferroptosis. Endogenous interference with NCOA4 significantly improved cell viability and reduced intracellular free Fe2+ levels in KA‐treated cells. Conclusion: KA‐induced excitotoxicity activates ferritinophagy, and targeting ferritinophagy effectively inhibits downstream ferroptosis. Interference with NCOA4 effectively attenuates KA‐induced neuronal damage. This study provides a potential therapeutic target for excitotoxicity related disease conditions. [ABSTRACT FROM AUTHOR]

Multifunctional metallo‐/ionic‐covalent organic polymers (TCTB@Zn‐iCOPs) were constructed through one‐pot multicomponent reaction in a deep eutectic solvent at room temperature. The structures of various TCTB@Zn‐iCOPs were characterized, demonstrating their successful integration of multiple sites and excellent structural stability. Then TCTB@Zn‐iCOPs were employed to transform atmospheric CO2 into cyclic carbonates. The results showed that satisfactory product yields were obtained under mild and additive‐free conditions, with a high TOF value of 101 h−1; furthermore, the optimized TCTB@Zn‐iCOP2 exhibited excellent versatility in catalyzing the cycloaddition reactions between various substituted epoxides and CO2, and its activity did not significantly decrease after being reused for five times. Compared with previously reported nonmetallic iCOPs, the TCTB@Zn‐iCOP2 shows significantly improved activity and stability. Finally, DFT calculations were conducted along with a comparison of energy barriers for possible reaction paths, gaining an in‐depth understanding of the synergistic catalytic mechanism involving multiple sites. [ABSTRACT FROM AUTHOR]

Pathogenic bacterial membrane proteins (MPs) are a class of vaccine and antibiotic development targets with widespread clinical application. However, the inherent hydrophobicity of MPs poses a challenge to fold correctly in living cells. Herein, we present a comprehensive method to improve the soluble form of MP antigen by rationally designing multi‐epitope chimeric antigen (ChA) and screening two classes of protein‐assisting folding element. The study uses a homologous protein antigen as a functional scaffold to generate a ChA possessing four epitopes from transferrin‐binding protein A of Glaesserella parasuis. Our engineered strain, which co‐expresses P17 tagged‐ChA and endogenous chaperones groEL‐ES, yields a 0.346 g/L highly soluble ChA with the property of HPS‐positive serum reaction. Moreover, the protein titer of ChA reaches 4.27 g/L with >90% soluble proportion in 5‐L bioreactor, which is the highest titer reported so far. The results highlight a timely approach to design and improve the soluble expression of MP antigen in industrially viable applications. [ABSTRACT FROM AUTHOR]

Mitochondrial dynamics has emerged as an important target for neuronal protection after cerebral ischaemia/reperfusion. Therefore, the aim of this study was to investigate the mechanism by which ARMC10 regulation of mitochondrial dynamics affects mitochondrial function involved in ischaemic stroke (IS). Mitochondrial morphology was detected by laser scanning confocal microscopy (LSCM), and mitochondrial ultrastructural alterations were detected by electron microscopy. The expression of mitochondrial dynamics‐related genes Drp1, Mfn1, Mfn2, Fis1, OPA1 and ARMC10 and downstream target genes c‐Myc, CyclinD1 and AXIN2 was detected by RT‐qPCR. Western blot was used to detect the protein expression of β‐catenin, GSK‐3β, p‐GSK‐3β, Bcl‐2 and Bax. DCFH‐DA fluorescent probe was to detect the effect of ARMC10 on mitochondrial ROS level, Annexin V‐FITC fluorescent probe was to detect the effect of ARMC10 on apoptosis, and ATP assay kit was to detect the effect of ARMC10 on ATP production. Mitochondrial dynamics was dysregulated in clinical IS samples and in the OGD/R cell model, and the relative expression of ARMC10 gene was significantly decreased in IS group (p < 0.05). Knockdown and overexpression of ARMC10 could affect mitochondrial dynamics, mitochondrial function and neuronal apoptosis. Agonist and inhibitor affected mitochondrial function and neuronal apoptosis by targeting Wnt/β‐Catenin signal pathway. In the OGD/R model, ARMC10 affected mitochondrial function and neuronal apoptosis through the mechanism that regulates Wnt/β‐catenin signalling pathway. ARMC10 regulates mitochondrial dynamics and protects mitochondrial function by activating Wnt/β‐catenin signalling pathway, to exert neuroprotective effects. [ABSTRACT FROM AUTHOR]

In this paper, a coupled concrete‐filled multicellular steel tube composite shear walls structure (CCSSW) is proposed. A finite element model (FEM) is developed to investigate the seismic behavior of CCSSW, and the model was validated by the tests. The effects of four parameters including axial compression ratio (ACR) on the hysteretic behavior of the CCSSW were studied. Then, a theoretical model for predicting the ultimate shear capacity (USC) of CCSSW was established. The results show that the failure mode of coupled walls exchanged from flexural failure to flexural‐shear failure with increasing the ACR, and it is recommended that the ACR should less than 0.6 to ensure the ductility requirement. To better realize the function of the first line of defense of steel coupling beam (SCB), following recommendations are concluded: the span‐to‐depth ratio range of SCB is 4.0–6.0, the wall stiffness ratio is 2.4–4.7, and low yield strength material should be used for SCB. The maximum error on USC between FEM results and theoretical results is 12.8%, and most of them are less than 10%, indicating the effectiveness of the proposed theoretical model. [ABSTRACT FROM AUTHOR]

Objective: The genomic and molecular ecology involved in the stepwise continuum progression of lung adenocarcinoma (LUAD) from adenocarcinoma in situ (AIS) to minimally invasive adenocarcinoma (MIA) and subsequent invasive adenocarcinoma (IAC) remains unclear and requires further elucidation. We aimed to characterize gene mutations and expression landscapes, and explore the association between differentially expressed genes (DEGs) and significantly mutated genes (SMGs) during the dynamic evolution from AIS to IAC. Methods: Thirty‐five patients with ground‐glass nodules (GGNs) lung adenocarcinomas were enrolled. Whole‐exome sequencing (WES) and transcriptome sequencing (RNA‐Seq) were conducted on all patients, encompassing both tumor samples and corresponding noncancerous tissues. Data obtained from WES and RNA‐Seq were subsequently analyzed. Results: The findings from WES delineated that the predominant mutations were observed in EGFR (49%) and ANKRD36C (17%). SMGs, including EGFR and RBM10, were associated with the dynamic evolution from AIS to IAC. Meanwhile, DEGs, including GPR143, CCR9, ADAMTS16, and others were associated with the entire process of invasive LUAD. We found that the signaling pathways related to cell migration and invasion were upregulated, and the signaling pathways of angiogenesis were downregulated across the pathological stages. Furthermore, we found that the messenger RNA (mRNA) levels of FAM83A, MAL2, DEPTOR, and others were significantly correlated with CNVs. Gene set enrichment analysis (GSEA) showed that heme metabolism and cholesterol homeostasis pathways were significantly upregulated in patients with EGFR/RBM10 co‐mutations, and these patients may have poorer overall survival than those with EGFR mutations. Based on the six calculation methods for the immune infiltration score, NK/CD8+ T cells decreased, and Treg/B cells increased with the progression of early LUAD. Conclusions: Our findings offer valuable insights into the unique genomic and molecular features of LUAD, facilitating the identification and advancement of precision medicine strategies targeting the invasive progression of LUAD from AIS to IAC. [ABSTRACT FROM AUTHOR]

To overcome the limitations of empirical synthesis and expedite the discovery of new polymers, this work aims to develop a data‐driven strategy for profoundly aiding in the design and screening of novel polyester materials. Initially, we collected 695 polyesters with their associated glass transition temperatures (Tgs) to develop a quantitative structure–property relationship (QSPR) model. The model underwent rigorous validation (i.e., external validation, internal validation, Y‐random, and application domain analysis) to demonstrate its robust predictive capabilities and high stability. Subsequently, by employing an in‐silico retrosynthesis strategy, over 95,000 virtual polyesters were designed, largely expanding the available space for polyester material family. External assessments were performed, highlighting good extrapolation ability of the QSPR model. Furthermore, we experimentally synthesized 10 designed polyesters with predicted Tgs covering a large temperature range from −42.52 to 103.61°C, and characterization results gave an average absolute error of 17.40°C relative to the predicted ones. It is believed that such data‐driven approach can drive future product development of polymer industry. [ABSTRACT FROM AUTHOR]

Deep eutectic solvent (DES) is used as both photocatalyst and solvent for photoinduced reversible complexation‐mediated polymerization (photo‐RCMP), which enables a rapid polymerization to produce polymers with predictable molar mass and low molar mass dispersity (Đ). This work illustrates a comprehensive understanding of DES‐accelerated RCMP's mechanism and kinetic features through quantum chemical calculations and kinetic modeling. According to the results, electrons transferring from hydrogen bond in DES to iodine atom in alkyl iodide (RI) initiator under light irradiation lowers the decomposition free energy of complex RI‐DES. This procedure facilitates the generation of primary radicals, thus contributing to the DES‐accelerated phenomenon. In the meantime, the reaction paths are identified by computation as (i) decomposition of RI‐DES under light irradiation generates active radicals and ·I‐DES complex and (ii) combination of two ·I‐DES releases iodine (I2) and regenerates DES. In addition, kinetic modeling based on the method of moments successfully identifies kinetic features of polymerization in the presence and absence of DES, respectively. Kinetic modeling shows a fast increase in primary radicals concentration and rapid build‐up of the photo‐RCMP activation‐deactivation equilibrium, demonstrating that DES is a beneficial photocatalyst and solvent to enable the rapid generation of primary radicals and accelerate the completion of catalytic cycle. This research provides an in‐depth understanding of DES‐involved photo‐RCMP and lays a theoretical foundation for expanding the application of DES to other polymerization systems. [ABSTRACT FROM AUTHOR]

Background: Bacterial prophylaxis with a fluoroquinolone (FQ) during autologous stem cell transplant (ASCT) is common, although not standardized among transplant centers. The addition of doxycycline (doxy) to FQ prophylaxis was previously linked to reduced neutropenic fever and bacteremia in multiple myeloma (MM) patients undergoing ASCT although several confounders were present. We compared the incidence of neutropenic fever and bacteremia between MM patients variably receiving prophylaxis with FQ alone and FQ‐doxy during ASCT. Methods: Systematic retrospective chart review of MM patients who underwent ASCT between January 2016 and December 2021. The primary objective was to determine the effect of bacterial prophylaxis on neutropenic fever and bacteremia within 30 days of ASCT. Multivariable logistic regression for neutropenic fever and univariate logistic regression for bacteremia accounted for differences in subject characteristics between groups. Results: Among 341 subjects, 121 received FQ and 220 received FQ‐doxy for prophylaxis. Neutropenic fever developed in 67 (55.4%) and 87 (39.5%) subjects in the FQ and FQ‐doxy groups, respectively (p =.005). Bacteremia was infrequent, with 5 (4.1%) and 5 (2.3%) cases developing in the FQ and FQ‐doxy groups, respectively (p =.337). Among Gram‐negative bacteremia events, 7/7 Escherichia coli strains were FQ‐resistant, and 5/7 were ceftriaxone‐resistant. Conclusion: The FQ‐doxy prophylaxis group had fewer cases of neutropenic fever than the FQ group, however, there was no significant difference in bacteremia. High rates of antibiotic resistance were observed. An updated randomized controlled trial investigating appropriate prophylaxis for ASCT in the context of current oncology standards and changing antimicrobial resistance rates is warranted. [ABSTRACT FROM AUTHOR]

Objective: Bioengineered tracheal grafts are a potential solution for the repair of long‐segment tracheal defects. A recent advancement is partially decellularized tracheal grafts (PDTGs) which enable regeneration of host epithelium and retain viable donor chondrocytes for hypothesized benefits to mechanical properties. We propose a novel and tunable 3D‐printed bioreactor for creating large animal PDTG that brings this technology closer to the bedside. Methods: Conventional agitated immersion with surfactant and enzymatic activity was used to partially decellularize New Zealand white rabbit (Oryctolagus cuniculus) tracheal segments (n = 3). In parallel, tracheal segments (n = 3) were decellularized in the bioreactor with continuous extraluminal flow of medium and alternating intraluminal flow of surfactant and medium. Unprocessed tracheal segments (n = 3) were also collected as a control. The grafts were assessed using the H&E stain, tissue DNA content, live/dead assay, Masson's trichrome stain, and mechanical testing. Results: Conventional processing required 10 h to achieve decellularization of the epithelium and submucosa with poor chondrocyte viability and mechanical strength. Using the bioreactor reduced processing time by 6 h and resulted in chondrocyte viability and mechanical strength similar to that of native trachea. Conclusion: Large animal PDTG created using our novel 3D printed bioreactor is a promising approach to efficiently produce tracheal grafts. The bioreactor offers flexibility and adjustability favorable to creating PDTG for clinical research and use. Future research includes optimizing flow conditions and transplantation to assess post‐implant regeneration and mechanical properties. Level of Evidence: NA. [ABSTRACT FROM AUTHOR]

Introduction: Severe spinal cord injury results in the loss of neurons in the relatively intact spinal cord below the injury area and skeletal muscle atrophy in the paralyzed limbs. These pathological processes are significant obstacles for motor function reconstruction. Objective: We performed tail nerve electrical stimulation (TNES) to activate the motor neural circuits below the injury site of the spinal cord to elucidate the regulatory mechanisms of the excitatory afferent neurons in promoting the reconstruction of locomotor function. Methods: Eight days after T10 spinal cord transection in rats, TNES was performed for 7 weeks. Behavioral scores were assessed weekly. Electrophysiological tests and double retrograde tracings were performed at week 8. Results: After 7 weeks of TNES treatment, there was restoration in innervation, the number of stem cells, and mitochondrial metabolism in the rats' hindlimb muscles. Double retrograde tracings of the tail nerve and sciatic nerve further confirmed the presence of synaptic connections between the tail nerve and central pattern generator (CPG) neurons in the lumbar spinal cord, as well as motor neurons innervating the hindlimb muscles. Conclusion: The mechanisms of TNES induced by the stimulation of primary afferent nerve fibers involves efficient activation of the motor neural circuits in the lumbosacral segment, alterations of synaptic plasticity, and the improvement of muscle and nerve regeneration, which provides the structural and functional foundation for the future use of cutting‐edge biological treatment strategies to restore voluntary movement of paralyzed hindlimbs. [ABSTRACT FROM AUTHOR]

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Objective: Composite tracheal grafts (CTG) combining decellularized scaffolds with external biomaterial support have been shown to support host‐derived neotissue formation. In this study, we examine the biocompatibility, graft epithelialization, vascularization, and patency of three prototype CTG using a mouse microsurgical model. Study Design: Tracheal replacement, regenerative medicine, biocompatible airway splints, animal model. Method: CTG electrospun splints made by combining partially decellularized tracheal grafts (PDTG) with polyglycolic acid (PGA), poly(lactide‐co‐ε‐caprolactone) (PLCL), or PLCL/PGA were orthotopically implanted in mice (N = 10/group). Tracheas were explanted two weeks post‐implantation. Micro‐Computed Tomography was conducted to assess for graft patency, and histological analysis was used to assess for epithelialization and neovascularization. Result: Most animals (greater than 80%) survived until the planned endpoint and did not exhibit respiratory symptoms. MicroCT confirmed the preservation of graft patency. Grossly, the PDTG component of CTG remained intact. Examining the electrospun component of CTG, PGA degraded significantly, while PLCL+PDTG and PLCL/PGA + PDTG maintained their structure. Microvasculature was observed across the surface of CTG and infiltrating the pores. There were no signs of excessive cellular infiltration or encapsulation. Graft microvasculature and epithelium appear similar in all groups, suggesting that CTG did not hinder endothelialization and epithelialization. Conclusion: We found that all electrospun nanofiber CTGs are biocompatible and did not affect graft patency, endothelialization and epithelialization. Future directions will explore methods to accelerate graft regeneration of CTG. Level of Evidence: N/A Laryngoscope, 134:1155–1162, 2024 [ABSTRACT FROM AUTHOR]

In most non‐fullerene organic solar cells comprising bulk‐heterojunction active layers, the inter‐domain connectivity of small‐molecule acceptors is generally inferior to those of polymeric donors due to their intrinsic short‐range ordering. This issue is even exacerbated by the physiochemical mismatch between acceptor‐phases and metal‐oxide electron transport layers in most inverted n‐i‐p devices, leading to inefficient electron collection. By pre‐depositing an ultra‐thin acceptor primer layer, it develops a novel acceptor‐enriched‐bottom active layer to reinforce the acceptor‐phase continuity. It is however challenging to preserve the primer layer during non‐orthogonal solvent processing. Thus, sequential n‐type doping is implemented on the surface of the primer layer, which allows to slightly reduce the acceptor solubility by polarity regulation, as well as stabilize the film structure via strong π–π interaction between dopant/host acceptor. Upon acceptor enrichment, higher interfacial electron density enhances the built‐in potential while the enlarged domains suppress both charge‐transfer state and bimolecular recombination. Consequently, the champion device efficiency is greatly improved from ca. 16.1% to 18.0%, mainly resulting from the simultaneously elevated fill factor and short‐circuit current density. [ABSTRACT FROM AUTHOR]

Background: Current methods utilizing preoperative magnetic resonance imaging (MRI)‐based radiomics for assessing lymphovascular invasion (LVI) in patients with early‐stage breast cancer lack precision, limiting the options for surgical planning. Purpose: This study aimed to develop a sophisticated deep learning framework called "Prior Clinico‐Radiological Features Informed Multi‐Modal MR Images Convolutional Neural Network (PCMM‐Net)" to improve the accuracy of LVI prediction in breast cancer. By incorporating multiparameter MRI and prior clinical knowledge, PCMM‐Net should enhance the precision of LVI assessment. Methods: A total of 341 patients with breast cancer were randomly divided into training and validation groups at a ratio of 7:3. Imaging features were extracted from T1‐weighted, T2‐weighted, and contrast‐enhanced T1‐weighted MRI sequences. Stepwise univariate and multivariate logistic regression were employed to establish a clinico‐radiological model for LVI prediction. The radiomics model was built using redundancy and the least absolute shrinkage and selection operator. Then, two deep learning frameworks were developed: the Multi‐Modal MR Images Convolutional Neural Network (MM‐Net), which does not consider prior radiological features, and PCMM‐Net, which incorporates multiparameter MRI and prior clinical knowledge. Receiver operating characteristic curves were used, and the corresponding areas under the curves (AUCs) were calculated for evaluation. Results: PCMM‐Net achieved the highest AUC of 0.843. The clinico‐radiological features displayed the lowest AUC value of 0.743, followed by MM‐Net with an AUC of 0.774, and radiomics with an AUC of 0.795. Conclusions: This study introduces PCMM‐Net, an innovative deep learning framework that integrates prior clinico‐radiological features for accurate LVI prediction in breast cancer. PCMM‐Net demonstrates excellent diagnostic performance and facilitates the application of precision medicine. [ABSTRACT FROM AUTHOR]

Many traditional fermented foods and beverages industries around the world request the addition of multi‐species starter cultures. However, the microbial community in starter cultures is subject to fluctuations due to their exposure to an open environment during fermentation. A rapid detection approach to identify the microbial composition of starter culture is essential to ensure the quality of the final products. Here, we applied single‐cell Raman spectroscopy (SCRS) combined with machine learning to monitor Oceanobacillus species in Daqu starter, which plays crucial roles in the process of Chinese baijiu. First, a total of six Oceanobacillus species (O. caeni, O. kimchii, O. iheyensis, O. sojae, O. oncorhynchi subsp. Oncorhynchi and O. profundus) were detected in 44 Daqu samples by amplicon sequencing and isolated by pure culture. Then, we created a reference database of these Oceanobacillus strains which correlated their taxonomic data and single‐cell Raman spectra (SCRS). Based on the SCRS dataset, five machine‐learning algorithms were used to classify Oceanobacillus strains, among which support vector machine (SVM) showed the highest rate of accuracy. For validation of SVM‐based model, we employed a synthetic microbial community composed of varying proportions of Oceanobacillus species and demonstrated a remarkable accuracy, with a mean error was less than 1% between the predicted result and the expected value. The relative abundance of six different Oceanobacillus species during Daqu fermentation was predicted within 60 min using this method, and the reliability of the method was proved by correlating the Raman spectrum with the amplicon sequencing profiles by partial least squares regression. Our study provides a rapid, non‐destructive and label‐free approach for rapid identification of Oceanobacillus species in Daqu starter culture, contributing to real‐time monitoring of fermentation process and ensuring high‐quality products. [ABSTRACT FROM AUTHOR]

A challenge for high‐impact polystyrene (HIPS) production and design is the more accurate and low computational cost prediction of the phase separation and phase inversion conversion, the first conversion determining the onset of the two‐phase system and the second conversion defining the pathway toward a complex, for example, salami‐like morphology. In this work, a two‐phase deterministic method of moments (MoM) model running in several minutes is therefore developed in the intermediate styrene conversion range (up to around 30%), considering for simplicity only diffusional limitations on termination on an average basis. It is showcased that the phase separation conversion can be taken as 2 m%, and the phase inversion conversion should be calculated by algebraic means. Interestingly, the latter conversion varies with the initial reaction conditions either on a time basis (e.g., variation of initial radical concentration) or both a time and conversion basis (e.g., relative contribution of rubber and St partitioning coefficient). A comparison with the commonly used pseudo‐homogeneous MoM model reveals that by accounting for mass transfer in a more representative two‐phase model, the amount of monomer consumed is slightly reduced, the grafting efficiency decreases with increasing conversion instead of increasing, and the styrene composition in the graft copolymer decreases. The current work additionally puts forward two‐phase MoM data to facilitate future benchmarking with other (stochastic) modeling approaches and enables kinetic insights into heterogeneous grafting polymerization, further promoting the production of multiphase industrial polymer products. [ABSTRACT FROM AUTHOR]

The oxidation of cyclohexanone with nitric acid in microreactors, as a representative chemical reaction with in situ gas production, was selected as the model reaction for computational fluid dynamics (CFD) modeling. The reaction kinetics was coupled with the CFD model by user‐defined functions (UDFs) to obtain the velocity field of liquid phase, the concentration field of products, and the temperature field of gas–liquid phases during the reaction process. The simulation results were then validated by the experimental data. Based on the established model, the fluid flow behavior and mass transfer characteristics during the in situ gas production process in a microreactor were further analyzed. Finally, the effects of channel diameter and bubble velocity on gas–liquid interfacial mass transfer were investigated. This work provides an effective method for studying in situ gas production processes through modeling and simulation, which is valuable in the design and optimization of tubular reactors. [ABSTRACT FROM AUTHOR]

The numerical manifold method (NMM) has been widely utilized to solve problems involving complicated boundaries, cracks, and interfaces. Recently, strain or gradient smoothing techniques have been incorporated into NMM to improve its performance. The resulting smoothed NMMs (SNMMs) normally possess enhanced numerical properties, for example, higher accuracy, convergence, and efficiency. A challenging issue rooted in NMM and other enhanced finite element methods using unfitted meshes is the ill‐conditioning induced by extremely small cut element. In this study, we investigate the behaviors of SNMMs in the case of small cut element. It is demonstrated that the cut‐induced ill‐conditionings also exist for two types of SNMMs, namely, edge‐based SNMM and physical‐patch‐based SNMM. Furthermore, a preconditioner based on the normalization of basis functions is proposed to resolve the ill‐conditioning. Several benchmark problems demonstrate the performances of SNMMs regarding accuracy, convergence, and stability. [ABSTRACT FROM AUTHOR]

The smoothed particle finite element method (SPFEM) is an effective framework for large deformation analysis. The original SPFEM possesses the rank deficiency issue due to the direct nodal integration technique, which can be overcome by incorporating the strain gradient stabilization method. However, an extra volumetric locking due to the strain gradient stabilization term has been found. In this study, we propose a simple and efficient approach, the B‐dev approach, which only considers the deviatoric part of the smoothed strain gradient for stabilization to overcome the volumetric locking issue. First, the correctness of the stabilized SPFEM method is verified by an elastic cantilever beam vibration problem without considering incompressibility. Then, through the example of the strip footing penetration problem, the volumetric locking in the stabilized SPFEM is demonstrated and the capability of the proposed B‐dev approach in terms of overcoming the volumetric locking is verified. Furthermore, the stabilized SPFEM with B‐dev approach is applied to two types of elastoplastic problems in geotechnical engineering. All numerical results illustrate that the proposed approach can improve the performance of the stabilized SPFEM in dealing with incompressible and large deformation problems in geomechanics. [ABSTRACT FROM AUTHOR]

Objective: Long‐segment tracheal defects require tissue replacement for successful reconstruction. Rapid revascularization is imperative to maintain graft function. We previously showed that partially decellularized tracheal grafts (PDTG) and composite tracheal grafts (CTG; PDTG supported by a 3‐dimensionally printed external splint) regenerate respiratory epithelium and may support the regeneration of endothelial cells (CD31+). However, the capability of graft endothelial cells to organize or contribute to tracheal revascularization remains unclear. In this study, we quantified endothelial cells (CD31+) and neovessel formation in PDTG and CTG. We hypothesize that PDTG and CTG support tracheal neovascularization to a similar extent as surgical (syngeneic tracheal graft [STG]) and native trachea (NT) controls. Study Design: The animal study, a randomized control trial. Setting: Center for Regenerative Medicine, Nationwide Children's Hospital. Methods: PDTG was created via an established decellularization protocol. Segmental tracheal reconstruction was performed with STG, PDTG, or CTG using a mouse microsurgical model. NT was used as a nonsurgical control. At 1 month, mice were euthanized, grafts harvested, sectioned, and stained with CD31 and hematoxylin and eosin. Neovessel formation was quantified by the number of formed blood vessels in the lamina propria and vessel size (vessel/graft area, mm2). Results: Decellularization eliminated all endothelial cells and there were no perfused vessels at implantation. At 1 month, PDTG and CTG supported neovessel formation with tubular vessels lined with endothelial cells. There was no difference in the number or size of vessels compared to controls. Conclusion: PDTG and CTG support tracheal endothelial cell regeneration and neovessel formation. Future directions to assess the function, kinetics, and distribution of graft neovessels are needed. [ABSTRACT FROM AUTHOR]

More and more attention has been paid to the important roles of external fields in controlled radical polymerization (CRP). However, their essential roles have not been studied thoroughly yet, which hinders the in‐depth understanding of the mechanism and kinetics. Herein, a strategy combining quantum chemical calculations (QCC) and kinetic modeling was adopted to identify the essential roles of light and ultrasonication in the dual‐stimuli regulated bulk atom transfer radical polymerization (ATRP). At the molecular level, the impact of light on Cu‐catalyzed ATRP was investigated. The CuIIBr/Me6TREN has high absorbance at an experimental wavelength of 365 nm (main excitation S0 → D7 accounts for 84.93%). Electron transfer reactions involving Me6TREN are more favorable paths for photochemical reactions, and the mechanism of the copper activation/deactivation pathway is inner sphere electron transfer. At the micro‐scale, a kinetic model based on the method of moment was established with a "series" encounter pair model to consider the influence of ultrasound on diffusional limitation. Simulation results show that the changes of the reaction rate coefficients ka, kda, and kt at high conversion reflect the degree of diffusional limitation by ultrasound. The multiscale modeling strategy applied in this study identifies the essential roles of photo and ultrasonication in dual‐stimuli regulated model systems, which can be extended to other external‐field regulated CRP to improve the mechanistic understanding. [ABSTRACT FROM AUTHOR]

There is currently no suitable autologous tissue to bridge large tracheal defects. As a result, no standard of care exists for long‐segment tracheal reconstruction. Tissue engineering has the potential to create a scaffold from allografts or xenografts that can support neotissue regeneration identical to the native trachea. Recent advances in tissue engineering have led to the idea of partial decellularization that allows for the creation of tracheal scaffolds that supports tracheal epithelial formation while preserving mechanical properties. However, the ability of partial decellularization to eliminate graft immunogenicity remains unknown, and understanding the immunogenic properties of partially decellularized tracheal grafts (PDTG) is a critical step toward clinical translation. Here, we determined that tracheal allograft immunogenicity results in epithelial cell sloughing and replacement with dysplastic columnar epithelium and that partial decellularization creates grafts that are able to support an epithelium without histologic signs of rejection. Moreover, allograft implantation elicits CD8+ T‐cell infiltration, a mediator of rejection, while PDTG did not. Hence, we establish that partial decellularization eliminates allograft immunogenicity while creating a scaffold for implantation that can support spatially appropriate airway regeneration. [ABSTRACT FROM AUTHOR]

d‐Galactose (d‐gal) and l‐glutamate (l‐glu) impair learning and memory. The mechanism of interaction between the gut microbiome and brain remains unclear. In this study, a model of cognitive impairment was induced in tree shrews by intraperitoneal (ip) injection of d‐gal (600 mg/kg/day), intragastric (ig) administration with l‐glu (2000 mg/kg/day), and the combination of d‐gal (ip, 600 mg/kg/day) and l‐glu (ig, 2000 mg/kg/day). The cognitive function of tree shrews was tested by the Morris water maze method. The expression of Aβ1‐42 proteins, the intestinal barrier function proteins occludin and P‐glycoprotein (P‐gp), and the inflammatory factors NF‐κB, TLR2, and IL‐18 was determined by immunohistochemistry. The gut microbiome was analyzed by 16SrRNA high‐throughput sequencing. After administering d‐gal and l‐glu, the escape latency increased (p <.01), and the times of crossing the platform decreased (p <.01). These changes were greater in the combined administration of d‐gal and l‐glu (p <.01). The expression of Aβ1‐42 was higher in the perinuclear region of the cerebral cortex (p <.01) and intestinal cell (p <.05). There was a positive correlation between the cerebral cortex and intestinal tissue. Moreover, the expression of NF‐κB, TLR2, IL‐18, and P‐gp was higher in the intestine (p <.05), while the expression of occludin and the diversity of gut microbes were lower, which altered the biological barrier of intestinal mucosal cells. This study indicated that d‐gal and l‐glu could induce cognitive impairment, increase the expression of Aβ1‐42 in the cerebral cortex and intestinal tissue, decrease the gut microbial diversity, and alter the expression of inflammatory factors in the mucosal intestines. The dysbacteriosis may produce inflammatory cytokines to modulate neurotransmission, causing the pathogenesis of cognitive impairment. This study provides a theoretical basis to explore the mechanism of learning and memory impairment through the interaction of microbes in the gut and the brain. [ABSTRACT FROM AUTHOR]

In the present study, a combined kinetic and heat transfer model was developed to study the kinetics and predict thermal runaway of vinyl chloride (VC) suspension polymerization. Reactor temperature, monomer conversion, mole of initiator, radical concentrations in the two phases (i.e., VC‐rich phase and PVC‐rich phase), and average molecular properties were mapped during non‐isothermal processes. Meanwhile, the risk of thermal runaway was evaluated using S–Z (divergence) and H–J criteria. Simulation results show that a lower jacket temperature Tj and a larger heat transfer coefficient U are able to postpone or even avoid the risk of thermal runaway. Both of the criteria serve well for the prediction of thermal runaway during non‐isothermal processes. To prevent the occurrence of thermal runaway to the greatest extent, model‐based design of strategies for an isothermal polymerization process was done. Specifically, either jacket temperature Tj or heat transfer coefficient U can be fine‐tuned to maintain a 50°C isothermal process. [ABSTRACT FROM AUTHOR]

The drag force model is vital for capturing gas–solid flow dynamics in many simulation approaches. Most of the homogeneous drag models in the literature are expressed as a function of phase fraction (ε) and particle Reynolds number (Res). In this work, we use a "big data" approach to analyze ~108 data points for drag coefficient (Fd) for Geldart Group A particles at atmospheric pressure and find that the contribution of Res on Fd is much less than ε based on the Maximal information coefficient analysis. Thus, these drag models are separately reduced to machine learning and conventional expressions only related to ε. The reduced models achieve almost the same predictive performance as the originals in bubbling, turbulent, and jet fluidizations. Moreover, the reduced models provide better numerical stability for coarse grid simulations. These findings provide new insights into the drag coefficient for Geldart Group A particles under full fluidization conditions. [ABSTRACT FROM AUTHOR]

Photocatalytic hydrogen (H2) production is significant to overcome challenges like fossil fuel depletion and carbon dioxide emission, but its efficiency is still far below that which is needed for commercialization. Herein, we achieve long‐term stable H2 bubbling production from water (H2O) and lactic acid via visible‐light‐driven photocatalysis in a porous microreactor (PP12); the catalytic system benefits from photocatalyst dispersion, charge separation, mass transfer, and dissociation of O−H bonds associated with H2O. With the widely used platinum/cadmium‐sulfide (Pt/CdS) photocatalyst, PP12 leads to a H2 bubbling production rate of 602.5 mmol h−1 m−2, which is 1000 times higher than that in a traditional reactor. Even when amplifying PP12 into a flat‐plate reactor with an area as large as 1 m2 and extending the reaction time to 100 h, the H2 bubbling production rate still remains at around 600.0 mmol h−1 m−2, offering great potential for commercialization. [ABSTRACT FROM AUTHOR]

The molecular mechanisms underlying uric acid (UA)‐induced mitochondrial dysfunction and apoptosis have not yet been elucidated. Herein, we investigated underlying mechanisms of UA in the development of mitochondrial dysfunction and apoptosis. We analyzed blood samples of individuals with normal UA levels and patients with hyperuricemia. Results showed that patients with hyperuricemia had significantly elevated levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, which may indicate liver or mitochondrial damage in patients with hyperuricemia. Subsequently, lipidomic analysis of mouse liver tissue mitochondria and human liver L02 cell mitochondria was performed. Compared with control group levels, high UA increased mitochondrial phosphatidylserine (PS) and decreased mitochondrial phosphatidylethanolamine (PE) levels, whereas the expression of mitochondrial phosphatidylserine decarboxylase (PISD) that mediates PS and PE conversion was downregulated. High UA levels also inhibited signal transducer and activator of transcription 3 （STAT3） phosphorylation as well as mitochondrial respiration, while inducing apoptosis both in vivo and in vitro. Treatment with allopurinol, overexpression of PISD, and lyso‐PE (LPE) administration significantly attenuated the three above‐described effects in vitro. In conclusion, UA may induce mitochondrial dysfunction and apoptosis through mitochondrial PISD downregulation. This study provides a new perspective on liver damage caused by hyperuricemia. [ABSTRACT FROM AUTHOR]

In summary, ABO1009-DP demonstrated a good safety profile and well tolerability administered as a booster vaccination. Safety and immunogenicity of boosting with a severe acute respiratory syndrome coronavirus 2 omicron variant mRNA vaccine in healthy adults: An open-label, and single-arm Phase 1 study As an Omicron-specific mRNA vaccine, a single dose of ABO1009-DP booster induced excepted humoral and cellular immunity against Omicron variant BA.1. [Extracted from the article]

Background: Although ileal faecal diversion is commonly used in clinical settings, complications accompany it. Elucidating the intestinal changes caused by ileal faecal diversion will help resolve postoperative complications and elucidate the pathogenic mechanisms of associated intestinal disorders, such as Crohn's disease (CD). Therefore, our study aimed to provide new insights into the effects of ileal faecal diversion on the intestine and the potential mechanisms. Methods: Single‐cell RNA sequencing was performed on proximal functional and paired distal defunctioned intestinal mucosae from three patients with ileal faecal diversion. We also performed in vitro cellular and animal experiments, tissue staining and analysed public datasets to validate our findings. Results: We found that the epithelium in the defunctioned intestine tended to be immature, with defective mechanical and mucous barriers. However, the innate immune barrier in the defunctioned intestine was enhanced. Focusing on the changes in goblet cells, we demonstrated that mechanical stimulation promotes the differentiation and maturation of goblet cells through the TRPA1‐ERK pathway, indicating that the absence of mechanical stimulation may be the main cause of defects in the goblet cells of the defunctioned intestine. Furthermore, we found obvious fibrosis with a pro‐fibrotic microenvironment in the defunctioned intestine and identified that monocytes may be important targets for faecal diversion to alleviate CD. Conclusions: This study revealed the different transcription landscapes of various cell subsets and the potential underlying mechanisms within the defunctioned intestine, when compared to the functional intestine, based on the background of ileal faecal diversion. These findings provide novel insights for understanding the physiological and pathological roles of the faecal stream in the intestine. [ABSTRACT FROM AUTHOR]

Using network analysis, this study investigated how family communication patterns (Conversation and Conformity) were related to and predictive of adolescent overall depression severity and specific symptoms. A community sample of adolescents (10–17 years, n = 1327) completed the Children's Depression Inventory and the Revised Family Communication Pattern Instrument. Depressive symptoms were also re‐assessed 6 months later. Results showed that Conversation orientation protected against, whereas Conformity orientation increased the risk of adolescent depression. Family communication particularly influenced the child's feeling of being unloved, and feeling unloved was the only symptom prospectively predicted by two communication orientations at baseline. These findings revealed the path linking family factors to adolescent depression and may have implications for future family‐based interventions. [ABSTRACT FROM AUTHOR]

A detailed heterogeneous model considering the thermodynamic incompatibility was developed to simulate polyurethane/poly(methyl methacrylate) (PU/PMMA) interpenetrating polymer network (IPN) formation. The Gibbs free energy was calculated to predict the phase separation point and a two‐film theory was used to quantify the mass transfer between the PU‐rich phase and the PMMA‐rich phase. Compared with the homogeneous model, the cross‐linking density of PMMA increases rapidly during the network formation, because the monomer dispersion in two phases improves the possibility of free radical cross‐linking reaction, whereas the cross‐linking density of PU is unaffected. Simulations show that the partitioning of monomer significantly affects the PMMA network structure. The phase separation is strongly dependent on the onset of MMA polymerization. The proposed model allows visualizing of the IPN formation process and provides direction for reducing the extent of phase separation. Moreover, the structural information derived from the simulations can be further related to the properties. [ABSTRACT FROM AUTHOR]

Aim: To gain a better understanding of the use of sentinel lymph node mapping by Chinese oncologists for endometrial cancer staging and analyze factors influencing its application. Methods: Questionnaires were collected online before and by phone after the symposium to evaluate the general characteristics of oncologists who participated in the endometrial cancer seminar and factors associated with the application of sentinel lymph node mapping in endometrial cancer patients. Results: Gynecologic oncologists from 142 medical centers participated in the survey. 35.4% of doctors employed sentinel lymph node mapping for endometrial cancer staging, 57.3% chose indocyanine green as the tracer. Multivariate analysis revealed that cancer research center (odds ratio = 4.229, 95% CI 1.747–10.237), physician familiarity with sentinel lymph node mapping (odds ratio = 126.188, 95% confidence interval 43.220–368.425) and the use of ultrastaging (odds ratio = 2.657, 95% confidence interval 1.085–6.506) were related to the doctors' selection of sentinel lymph node mapping. There was a significant difference in the surgical procedure for early endometrial cancer, the number of removed sentinel lymph node, and the reason for not adopting sentinel lymph node mapping before and after the symposium. Conclusions: The theoretical knowledge of sentinel lymph node mapping, the use of ultrastaging, and cancer research center are related to a higher acceptance of sentinel lymph node mapping. Distance learning is conducive to the promotion of this technology. [ABSTRACT FROM AUTHOR]

Single atomic metal (SAM) doping is reported as an effective strategy to promote the electrochemical property of carbon‐based anode materials for high‐power sodium‐ion batteries (SIBs). However, the effects of SAM with different configurations on solid electrolyte interphase (SEI) and energy storage mechanism of Na+ are not revealed. Herein, Cr single atoms (CrSAs) are reported with controllable configurations (Cr–N4 or Cr–N2) implanted on the N, P co‐doped carbon (NPC) anode materials (denoted as CrN4SAs/NPC or CrN2SAs/NPC). The CrN4SAs/NPC anode displays a high specific capacity (318.2 mAh g−1 at 0.05 A g−1) and outstanding rate performance (145.1 mAh g−1 at 5 A g−1), better than those of CrN2SAs/NPC and NPC. The superiority is originated from the difference of SEI and the energy storage mechanism of sodium ions during electrochemical process, which are unveiled through ex situ characterization and theoretical calculation. The full cell assembled with CrN4SAs/NPC anode and Na3V2(PO4)2F3@C cathode displays a high energy density at a high power density. [ABSTRACT FROM AUTHOR]

The mesoporous carbon‐supported metal catalysts are important materials in heterogeneous catalysis. From the standpoint of process intensification, the current synthesis methods still suffer from several issues, such as the excessive use of toxic solvents, the time‐consuming self‐assembly process, and the difficulty of continuous production. Herein, we report a solvent‐free and continuous route to synthesize mesoporous carbon‐supported metal catalysts. Interestingly, the use of cyclic extrusion could promote mixing, coordination, and assembly of catalyst precursors (tannin‐metal salts‐additives) by shearing and squeeze force. The as‐made mesoporous carbon‐supported nickel materials showed high surface areas (up to 512 m2 g−1), narrow pore size distribution (~10 nm), and good performance in the selective hydrogenation of nitrobenzene to aniline (Conv. >99%; Sel. >99%). In addition, the fluid property of catalyst precursors and the geometry of the twin‐screw extrusion channel were studied, and the essence of this cyclic extrusion process is also discussed. [ABSTRACT FROM AUTHOR]

Background: ABO blood groups has been associated with risk of several cancers; however, the results for an association with ovarian cancer are inconsistent and little is known about the expression of histo‐blood group (ABH) antigens and ABO gene in ovarian tumor tissues. Methods: To assess the impact of genotype‐derived ABO blood types on the risk of EOC, we conducted a case–control study in 1,870 EOC and 4,829 controls. Expression of A and B antigen in 70 pairs of ovarian tumor tissues and adjacent normal tissues were detected by immunohistochemistry. Gene expression and DNA methylation profiling was conducted in ovarian tumor tissues. Results: We identified that blood group A was associated with increased risk for EOC compared to blood group O (OR = 1.18, 95% CI = 1.03–1.36, p = 0.019). Increased frequency of aberrant expression of histo‐blood group antigens was observed in patients with blood group A (76.5%) compared to patients with blood group O (21.1%) and B (5.0%) by immunohistochemistry (p < 0.001). ABO gene expression was down‐regulated in ovarian tumor tissues compared with paired adjacent normal tissues (p = 0.027). In addition, ABO gene expression was positively correlated with NFYB (r = 0.38, p < 0.001) and inversely correlated with DNA methylation level of four CpG sites on ABO gene (cg11879188, r = − 0.3, p = 0.002; cg22535403, r = − 0.30, p = 0.002; cg13506600, r = − 0.22, p = 0.025; cg07241568, r = − 0.21, p = 0.049) in ovarian tumor tissues. Conclusion: We identified blood group A was associated with increased EOC risk in Chinese women and provided the clues of the possible molecular mechanisms of blood group A related to ovarian cancer risk. We identified blood group A was associated with increased EOC risk in Chinese women. We provided the clues of the possible molecular mechanisms of blood group A related to ovarian cancer risk. [ABSTRACT FROM AUTHOR]

Background: To explore the value of human data from the Zhuang population via predicting the diameter of the hamstring tendon autograft in anterior cruciate ligament (ACL) reconstruction and determining the feasibility of preoperative ultrasound for prediction. Methods: In total, 24 Zhuang patients who underwent ACL reconstruction with a 4‐strand semitendinosus and gracilis tendon autograft (4 S‐STG) were enrolled in this study. Before the operation, the affected semitendinosus tendon (ST) was examined by ultrasonography, and its length, diameter, cross‐sectional area, and circumference were measured. The patients' basic information and body data, ie, height, weight, body mass index, lower limb length injured, and thigh circumference injured, were recorded. Their ST and gracilis tendon lengths and diameters and 4 S‐STG diameter were measured during the operation. A correlation analysis was conducted between the ultrasound measurement results and human data and intraoperative tendon measurements. Results: The ST diameter measured by ultrasound was correlated with the ST length and ST diameter measured during operation, and the ST circumference measured by ultrasound was correlated with the ST diameter measured during operation. The patients' body weight can be used to distinguish a 4 S‐STG diameter of ≥8 mm (P <.01, mean difference = 11.59). The area under the receiver operating characteristic curve of body weight was 0.829. The final graft diameter ≥8 mm could be predicted with a body weight of 61.5 kg as the cutoff point; the sensitivity and specificity were 72.2% and 83.3%, respectively. Conclusion: In Zhuang patients undergoing ACL reconstruction with 4 S‐STG, body weight more accurately predicted graft diameter than preoperative semitendinosus diameter. [ABSTRACT FROM AUTHOR]

Objectives/Hypothesis: Partially decellularized tracheal scaffolds have emerged as a potential solution for long‐segment tracheal defects. These grafts have exhibited regenerative capacity and the preservation of native mechanical properties resulting from the elimination of all highly immunogenic cell types while sparing weakly immunogenic cartilage. With partial decellularization, new considerations must be made about the viability of preserved chondrocytes. In this study, we propose a multimodal approach for quantifying chondrocyte viability for airway tissue engineering. Methods: Tracheal segments (5 mm) were harvested from C57BL/6 mice, and immediately stored in phosphate‐buffered saline at −20°C (PBS‐20) or biobanked via cryopreservation. Stored and control (fresh) tracheal grafts were implanted as syngeneic tracheal grafts (STG) for 3 months. STG was scanned with micro‐computed tomography (μCT) in vivo. STG subjected to different conditions (fresh, PBS‐20, or biobanked) were characterized with live/dead assay, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), and von Kossa staining. Results: Live/dead assay detected higher chondrocyte viability in biobanked conditions compared to PBS‐20. TUNEL staining indicated that storage conditions did not alter the proportion of apoptotic cells. Biobanking exhibited a lower calcification area than PBS‐20 in 3‐month post‐implanted grafts. Higher radiographic density (Hounsfield units) measured by μCT correlated with more calcification within the tracheal cartilage. Conclusions: We propose a strategy to assess chondrocyte viability that integrates with vivo imaging and histologic techniques, leveraging their respective strengths and weaknesses. These techniques will support the rational design of partially decellularized tracheal scaffolds. Level of Evidence: N/A Laryngoscope, 133:512–520, 2023 [ABSTRACT FROM AUTHOR]

Statins have been proven to be effective in minimizing the risk of cardiovascular adverse events, however, their effect on BP variability is debatable with respect to their significance and their use as a potential anti‐hypertensive. Using a meta‐analysis approach, the aim of this study was to explore whether certain statins have the potential to lower blood pressure (BP). For the period 2002–2022, Scopus, PubMed, Web of Science, and the Cochrane Central Register of Controlled Trials databases were searched for the studies that examined the effect of statins on blood pressure in normotensive or hypertensive individuals. Randomized controlled clinical trials that investigated this effect were included based on our inclusion criteria. Our primary outcomes were changes in systolic and diastolic blood pressure (DBP). The final analysis of the study included 49 RCTs involving 45 173 participants randomized to receive either statins or placebo. Among the two groups, the total weighted mean difference (WMD) for systolic blood pressure (ΔSBP) was –1.42 (95% CI: –2.38, –0.46; p =.004) and diastolic blood pressure (ΔDBP) was 0.82 (95% CI: –1.28, –0.36; p =.0005). Despite various studies suggesting the efficacy of statins in blood pressure lowering to be significant and non‐significant both, we observed a decrease in SBP and DBP both, although the change was not as large and could be considered significant. A large multicenter, multi‐ethnic, large sample pool size, and a long period follow‐up study is still required to assert these claims. [ABSTRACT FROM AUTHOR]