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[Display omitted] Despite the flourishing studies of droplet interfacial boiling, the boiling upon vibratory surfaces, which may cause vigorous liquid–vapor-solid interactions, has rarely been investigated. Enhanced boiling normally can be gained from rapid removal of vapor and disturbance of liquid–vapor interface. We hypothesize that the vibratory surfaces enhance both effects with new intriguing phenomena and thus, attain an enhanced boiling heat transfer. We experimentally investigated the impacting fluid dynamics and coupled heat transfer patterns of multiple droplets and a single droplet impinging on still and vibratory surfaces of various materials and different wettability. The boiling under vibratory surfaces with increased vibration velocity amplitude and enhanced wettability can be enhanced by 80% in heat transfer coefficient and Nusselt number, which is attributed to several reasons: shortened bubble lifespan, thinner and smaller bubbles, and enhanced disturbances in liquid–vapor interfaces. The vibration also delays the Leidenfrost point when the droplet impacts a descending surface, which shows that the droplet impact moment (vibration phase angle) is particularly crucial. The descending surface releases the generated vapor actively and facilitates liquid–solid contact, thereby delaying the Leidenfrost. From fundamentals to application, this article strengthens our understanding of vibrated interfacial boiling in scenarios closer to multiple natural processes and practical industries. [ABSTRACT FROM AUTHOR]

Diquat (DQ) is a commonly used bipyridine herbicide known for its toxic properties and adverse effects on individuals. However, the mechanism underlying DQ-induced damage remain elusive. Our research aimed to uncover the regulatory network involved in DQ-induced damage. We analyzed publicly accessible gene expression patterns and performed research using a DQ-induced damage animal model. The GSE153959 dataset from the Gene Expression Omnibus collection and the animal model of DQ-induced kidney injury were used to identify differentially expressed genes (DEGs). Pathways including the regulation of DNA-templated transcription in response to stress, RNA polymerase II transcription regulator complex and transcription coregulatory activity were shown to be enriched in 21 DEGs. We used least absolute shrinkage and selection operator (LASSO) regression analysis to find possible diagnostic biomarkers for DQ-induced damage. Then, we used an HK-2 cell model to confirm these results. Additionally, we confirmed that 3-hydroxy-3-methylglutaryl-CoA synthase 2 (HMGCS2) was the major gene associated with DQ-induced damage using multi-omics screening. The sample validation strongly suggested that HMGCS2 has promise as a diagnostic marker and may provide new targets for therapy in the context of DQ-induced damage. • DQ caused kidney and liver toxicity. • The database and mouse model results revealed that DQ increased Hmgcs2 expression. • The metabolome and proteome data revealed DQ increased HMGCS2 expression. [ABSTRACT FROM AUTHOR]

Perfluorinated compounds (PFCs) are man-made chemicals used in the manufacture of many products with water and dirt repellent properties. Many diseases have been proved to be related to the exposure of PFCs, including breast fibroadenoma, hepatocellular carcinoma, breast cancer and leydig cell adenoma. However, whether the PFCs promote the progression of prostate cancer remains unclear. In this work, through comprehensive bioinformatics analysis, we discovered the correlation between the prostate cancer and five PFCs using Comparative Toxicogenomics Database (CTD), Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) databases. In addition, further analysis showed that several PFCs-related genes demonstrated strong prognostic value for prostate cancer patients. The survival analysis and receiver operating characteristic (ROC) curves revealed that PFCs-related genes based prognostic model held great predictive value for the prognosis of prostate cancer, which could potentially serve as an independent risk factor in the future. In vitro experiments verified the promotive role of perfluorooctanoic acid (PFOA) and perfluorononanoic acid (PFNA) in the growth of prostate cancer cells. This study provided novel insights into understanding the role of PFCs in prostate cancer and brought attention to the environmental association with cancer risks and progression. • Many diseases including cancers are proved to be related to the increased exposure of Perfluorinated compounds (PFCs). • The water solubility of PFCs theoretically increases the exposure risks of genitourinary systems. • Online analysis exhibited the association between PFCs-related genes and the progression of prostate cancer. • Prognostic model based on PFCs-related genes distinguished prostate cancer patients with diverse long-term survival. • Proliferation of prostate cancer cells were induced by high concentration of PFOA and PFNA validated by in vitro assays. [ABSTRACT FROM AUTHOR]

Sepsis-associated acute renal injury (SA-AKI) is a common critical clinical disease. It is associated with increased mortality and increased risk of progression to chronic kidney disease. However, its pathogenesis is not fully known. We hypothesized that metabolic interactions mediate cell apoptosis and AKI. We found that phosphatidylcholine content in human renal tubular epithelial cells following lipopolysaccharide-induced injury was increased. The activity of lysophosphatidylcholine acyltransferase 3 (LPCAT3), a key enzyme in phospholipid metabolism, was increased, while the expression of miR-124-3p.1, which targets LPCAT3, was decreased. We also found that in the serum of SA-AKI patients, LPCAT3 activity was increased, and miR-124-3p.1 expression was decreased. Further experiments confirmed the specific binding of exocrine miR-124-3p.1 to LPCAT3. Our data reveal the molecular mechanisms of phospholipid metabolic disorder in early SA-AKI as well as the role of the miR-124-3p.1/LPCAT3 pathway in SA-AKI, which leads to ferroptosis. These results could provide the scientific basis for early diagnosis and renal replacement therapy in SA-AKI. • In early SA-AKI, the phospholipid metabolic disordered. • MiR-124-3p.1 can regulate LPCAT3 expression and affect lipid metabolism, which leads to ferroptosis. • These results could provide the scientific basis for early diagnosis and renal replacement therapy in SA-AKI. [ABSTRACT FROM AUTHOR]

To elucidate the impact of CYP3A4 activity inhibition and genetic polymorphism on the metabolism of crizotinib. Enzymatic incubation systems for crizotinib were established, and Sprague-Dawley rats were utilized for in vivo experiments. Analytes were quantified using LC-MS/MS. Upon screening 122 drugs and natural compounds, proanthocyanidins emerged as inhibitor of crizotinib metabolism, exhibiting a relative inhibition rate of 93.7%. The IC 50 values were 24.53 ± 0.32 μM in rat liver microsomes and 18.24 ± 0.12 μM in human liver microsomes. In vivo studies revealed that proanthocyanidins markedly affected the pharmacokinetic parameters of crizotinib. Co-administration led to a significant reduction in the AUC (0–t) , C max of PF-06260182 (the primary metabolite of crizotinib), and the urinary metabolic ratio. This interaction is attributed to the mixed-type inhibition of liver microsome activity by proanthocyanidins. CYP3A4, being the principal metabolic enzyme for crizotinib, has its genetic polymorphisms significantly influencing crizotinib's pharmacokinetics. Kinetic data showed that the relative metabolic rates of crizotinib across 26 CYP3A4 variants ranged from 13.14% (CYP3A4.12, 13) to 188.57% (CYP3A4.33) when compared to the wild-type CYP3A4.1. Additionally, the inhibitory effects of proanthocyanidins varied between CYP3A4.12 and CYP3A4.33, when compared to the wild type. Our findings indicate that proanthocyanidins coadministration and CYP3A4 genetic polymorphism can significantly influence crizotinib metabolism. • Procyanidins significantly inhibited crizotinib metabolism both in vitro and in vivo. • CYP3A4 genetic polymorphism affected the metabolic kinetics of crizotinib. • CYP3A4 variation also determined the intensity of procyanidins inhibition of crizotinib metabolism. [ABSTRACT FROM AUTHOR]

[Display omitted] • Mono-metal Relay catalysis for one-pot bis-alkoxycarbonylation of alkynes. • Relay catalysis over Pd-catalyst induced by two divergent di-phosphines. • Synthesis of N,P-hybrid di-phosphines with bulky steric hindrance. • Two independent and compatible Pd-catalysts modified by two divergent di-phosphines. The mono-metal relay catalysis is a good strategy for one-pot multi-step cascade process in which the specific catalysis can be switched upon the ligand exchange to match the requirements for each independent reaction but without mutual interference and quenching problem. Herein, the one-pot cascade bis-alkoxycarbonylation of terminal alkynes was achieved by taking advantages of the mono-metallic (Pd) relay catalysis, wherein the two kinds of divergent di-phosphines of L1 and DTBPMB were involved. In this Pd(OAc) 2 - L1 -DTBPMB system, due to the steric bulkiness of L1 and DTBPMB, the two type of catalysts including Pd(OAc) 2 - L1 and Pd(OAc) 2 -DTBPMB co-existed independently and compatibly. Pd(OAc) 2 - L1 system was only in charge of the first-step carbonylation of alkynes towards the branched α,β-unsaturated esters with gem -positioned double bond. Subsequent, Pd(OAc) 2 -DTBPMB system took over the carbonylation of the branched α,β-unsaturated esters to afford the target diesters. It was indicated Pd(OAc) 2 -L1 system was an efficient and stable catalyst which could be recycled upon 15 runs for the first-step carbonylation. Anyway, Pd(OAc) 2 -DTBPMB system easily underwent deactivation, which degraded the recyclability of the Pd(OAc) 2 - L1 -DTBPMB coupling system for this cascade bis-alkoxycarbonylation. [ABSTRACT FROM AUTHOR]

Ligand-controlled divergent regioselectivity in Pd-catalyzed alkoxycarbonylation of alkenes. [Display omitted] • Synthesis of pinwheel-like tridentate phosphines. • Ligand-controlled divergent regioselectivity in Pd-catalyzed alkoxycarbonylation of alkenes. • Flexible tridentate phosphine in charge of anti -Markovnikov's alkoxycarbonylation of alkenes. • Rigid tridentate phosphine in charge of Markovnikov's alkoxycarbonylation of alkenes. The elaborate control of regioselectivity regulated by the involved ligands with specific structural skeleton and compositions is always demanded in alkoxycarbonylation of alkenes. Herein, a series of pinwheel-like tridentate phosphine ligands with rotatable flexibility (L3) or hard rigidity (L5–L7) were synthesized and characterized for the first time, in which the incorporated three PPh 2 -fragments are located at meta-positions of phenyl groups. It was proved that the tridentate phosphine of L3 with the flexible configuration favorably corresponded to the linear regioselectivity with l/b ratio of 98/2, whereas L7 with the rigid configuration absolutely did favor to the branched regioselectivity with l/b ratio of 1/99. The presence of the three PPh 2 -frgaments in L3 did contribute to the remarkable performance of L3 -Pd(TFA) 2 system in terms of activity, linear regioselectivity and stability, subjected to 10-run recycling uses in anti -Markovnikov's methoxycarbonylation of styrene without activity loss and Pd-black precipitation. In comparison, although the optimal L7 -Pd(MeCN) 2 Cl 2 system could catalyze Markovnikov's alkoxycarbonylation of alkenes to afford the branched esters with excellent regioselectivity in the fresh use, its stability was too poor to support the recycling experiments. L3 -Pd(TFA) 2 and L7 -Pd(MeCN) 2 Cl 2 catalytic systems were both applicable to a wide range of substrates in alkoxycarbonylation of alkenes to afford the target esters in the isolated yields of 41–91 %, with the well maintained divergent regioselectivity. [ABSTRACT FROM AUTHOR]

Ibuprofen is the most commonly used analgesic. CYP polymorphisms are mainly responsible for the differences in drug metabolism among individuals. Variations in the ability of populations to metabolize ibuprofen can lead to drug exposure events. The aim of this study was to evaluate the effects of CYP2C19 and CYP3A4 polymorphisms on ibuprofen metabolism in a Chinese population. First, 31 CYP2C19 and 12 CYP3A4 microsomal enzymes were identified using an insect expression system. Then, variants were evaluated using a mature incubation system. Moreover, ibuprofen metabolite content was determined via ultra-performance liquid chromatography-tandem mass spectrometry analysis. Finally, kinetic parameters of CYP2C19 and CYP3A4 genotypes were determined via Michaelis-Menten curve fitting. Most variants exhibited significantly altered intrinsic clearance compared to the wild type. In the CYP2C19 metabolic pathway, seven variants exhibited no significant alterations in intrinsic clearance (CL int), six variants exhibited significantly high CL int (121–291%), and the remaining 15 variants exhibited substantially reduced CL int (1–71%). In the CYP3A4 metabolic pathway, CYP3A4*30 was not detected in the metabolite content due to the absence of activity, and 10 variants exhibited significantly reduced CL int. To the best of our knowledge, this is the first study to assess the kinetic characteristics of 31 CYP2C19 and 12 CYP3A4 genotypes on ibuprofen metabolism. However, further studies are needed on poor metabolizers as they are more susceptible to drug exposure. Our findings suggest that the kinetic characteristics in combination with artificial intelligence to predict the toxicity of ibuprofen and reduce any adverse drug reactions. • We firstly evaluate the catalytic activities of 31 CYP2C9 and 12 CYP3A4 variants toward ibuprofen in vitro. • Most variants exhibit decreased catalytic activity toward ibuprofen. • We need to focus on PMs with severely abnormal metabolic function. [ABSTRACT FROM AUTHOR]

The development, protection, and restoration of bays require works in scientific research and applications, and the success of which depends on a well deployment of monitoring stations for marine water quality. However, for bays without historical data, it is difficult to carry out related research on deployment of the monitoring stations, resulting in very few research works. This paper has introduced the affinity propagation (AP) clustering algorithm and achieved good results by correcting the preferences. The results show that under the given preference, that is, when the value of M is −6800, the number of monitoring stations in the Xincun lagoon area is 24. Simultaneous the sensitivity analysis of preferences shows that the number of exemplars decreases with lower preferences, that is, when M decreased from −4000 to −12000, the number also decreased from 70 to 36. However, some exemplars remain unchanged or being changed to adjacent positioning. This shows the stability of computation results and the rationality of AP. The research results can be well applied to other bays, even open waters. • AP clustering can be used to layout seawater monitoring stations. • Multi-dimensional feature parameters is used to modify the bias parameters of the algorithm. • Sensitivity analysis shows that AP clustering can be applied in bays lacking historical data. [ABSTRACT FROM AUTHOR]

Critical melting pretreatment for granular swelling and soluble starch release was performed before freeze-thawing (FT) to enhance the effect of FT treatment on structure modification of potato starch. The critical melting temperature applied was based on the onset melting temperature (T o) of the native potato starch. After pretreatment, the effect of multiple FT cycles on the morphology, structure, and functionality was investigated. The pretreatment effectively induced granular swelling and partial disruption of the crystalline structure by increasing the volume of water molecules inside the granules. The pasting pattern changed obviously after treatments with the significantly increased final viscosity (up to 5000 from 2900 mPa s) and decreased breakdown (1/5th of native starch). Soluble starch released due to the both critical melting and FT treatments had a strong tendency to reassociate outside the granules, which effectively raised the thermal stability of starch granules. Moreover, increased water (∼109–∼164%) and oil (∼56–∼64%) absorption of starch at room temperature were observed. The synergistic effect of the combination of critical melting pretreatment and mechanical force of ice crystals effectively modified the properties of potato starch, suggesting a useful clean-label method for starch modification. [Display omitted] • Pretreatment enhanced modification effect of freeze-thawing on potato starch (PS). • Critical melting pretreatment applied is based on onset melting temperature of PS. • The combined treatment changed the morphology, structure, and functionality of PS. • Thermal stability of PS granules raised significantly after the combined treatment. • Partial disruption of chain arrangement and soluble starch release plays a key role. [ABSTRACT FROM AUTHOR]