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Increasing studies have highlighted the significance of milk-derived extracellular vesicles (MEVs) in mother-newborn integration, as well as their application as novel drug delivery systems and diagnostic biomarkers. However, conventional ultracentrifugation (UC) often results in the co-precipitation of casein micelles in MEV pellets. In this study, we compared methods with different principles to screen the optimal pretreatment in caseins removal, and found that isoelectric precipitation by hydrochloric acid (HA) could most effectively remove caseins in porcine milk. We further characterized MEV populations isolated by UC and HA/UC from diverse aspects, including particle methodology via nanoparticle tracking analysis (NTA) and transmission electron microscopy (TEM), RNA and protein contents, and purity analysis. Importantly, the proliferative and anti-inflammatory effects of MEVs were evaluated in vitro, showing the superiority of MEVs via HA/UC in functionality compared with UC. Our results suggest that HA pretreatment before ultracentrifugation could effectively remove caseins and other protein complexes, leading to MEVs via HA/UC with higher purity and more significant effects in vitro. This study provides valuable insights for the advancement of MEVs isolation techniques across different species and accurate function analysis of MEVs.
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The intestinal ecological environment plays a crucial role in nutrient absorption and overall well-being. In recent years, research has focused on the effects of extracellular vesicles (EVs) in both physiological and pathological conditions of the intestine. The intestine does not only consume EVs from exogenous foods, but also those from other endogenous tissues and cells, and even from the gut microbiota. The alteration of conditions in the intestine and the intestinal microbiota subsequently gives rise to changes in other organs and systems, including the central nervous system (CNS), namely the microbiome-gut-brain axis, which also exhibits a significant involvement of EVs. This review first gives an overview of the generation and isolation techniques of EVs, and then mainly focuses on elucidating the functions of EVs derived from various origins on the intestine and the intestinal microenvironment, as well as the impacts of an altered intestinal microenvironment on other physiological systems. Lastly, we discuss the role of microbial and cellular EVs in the microbiome-gut-brain axis. This review enhances the understanding of the specific roles of EVs in the gut microenvironment and the central nervous system, thereby promoting more effective treatment strategies for certain associated diseases.
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Vesículas Extracelulares , Eixo Encéfalo-Intestino , Sistema Nervoso Central , Meio Ambiente , AlimentosRESUMO
Inverse designs are widely used for creating ultra-compact photonic devices, but suffer from high computation power due to the optimization complexity. General Stoke's theorem proves that the overall change present at the outer boundary is equal to the integral of the change over the inner intervals, providing the possibility to divide one sophisticated device into several simple building blocks. Thus, we integrate this theorem with the inverse designs as a novel design methodology for optical devices. Compared with conventional inverse designs, the separated regional-optimisations can reduce the computational complexity significantly. The overall computational time is around five times shorter than optimizing the whole device region. To validate the proposed methodology, a monolithically integrated polarization rotator and splitter is designed and fabricated to demonstrate the performance experimentally. The device achieves polarization rotation (TE00 to TE00 and TM00 modes) and power splitting with the designed power ratio. The exhibited average insertion loss is <1 dB and the crosstalk is <-9.5 dB. These findings confirm the advantages of the new design methodology, as well as its feasibility for achieving multiple functions on one monolithic device.
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Mode localization is widely used in coupled micro-electro-mechanical system (MEMS) resonators for ultra-sensitive sensing. Here, for the first time to the best of our knowledge, we experimentally demonstrate the phenomenon of optical mode localization in fiber-coupled ring resonators. For an optical system, resonant mode splitting happens when multiple resonators are coupled. Localized external perturbation applied to the system will cause uneven energy distributions of the split modes to the coupled rings, this phenomenon is called the optical mode localization. In this paper, two fiber-ring resonators are coupled. The perturbation is generated by two thermoelectric heaters. We define the normalized amplitude difference between the two split modes as: (T M1-T M2)/T M1×100%. It is found that this value can be varied from 2.5% to 22.5% when the temperature are changed by the value from 0K to 8.5K. This brings a â¼ 2.4%/K variation rate, which is three orders of magnitude greater than the variation rate of the frequency over temperature changes of the resonator due to thermal perturbation. The measured data reach good agreement with theoretical results, which demonstrates the feasibility of optical mode localization as a new sensing mechanism for ultra-sensitive fiber temperature sensing.
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Stimulated Brillouin scattering (SBS), originating from the coupling between optical and acoustic waves, has been widely applied in many fields. Silicon is the most used and important material in micro-electromechanical systems (MEMS) and integrated photonic circuits. However, strong acoustic-optic interaction in silicon requires mechanical release of the silicon core waveguide to avoid acoustic energy leakage into the substrate. This will not only reduce the mechanical stability and thermal conduction, but also increase the difficulties for fabrication and large-area device integration. In this paper, we propose a silicon-aluminium nitride(AlN)-sapphire platform for realizing large SBS gain without suspending the waveguide. AlN is used as a buffer layer to reduce the phonon leakage. This platform can be fabricated via the wafer bonding between silicon and commercial AlN-sapphire wafer. We adopt a full-vectorial model to simulate the SBS gain. Both the material loss and the anchor loss of the silicon are considered. We also apply the genetic algorithm to optimize the waveguide structure. By limiting the maximum etching step number to two, we obtain a simple structure to achieve the SBS gain of 2462 W-1m-1 for forward SBS, which is 8 times larger than the recently reported result in unsuspended silicon waveguide. Our platform can enable Brillouin-related phenomena in centimetre-scale waveguides. Our findings could pave the way toward large-area unreleased opto-mechanics on silicon.
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The hyperfluorescence has drawn great attention in achieving efficient narrowband emitting devices based on multiple resonance thermally activated delayed fluorescence (MR-TADF) emitters. However, achieving efficient solution-processed pure blue hyperfluorescence devices is still a challenge, due to the unbalanced charge transport and serious exciton quenching caused by that the holes are easily trapped on the high-lying HOMO (the highest occupied molecular orbital) level of traditional diphenylamine-decorated emitters. Here, we developed two narrowband blue organoboron emitters with low-lying HOMO levels by decorating the MR-TADF core with weakly electron-donating carbazoles, which could suppress the hole trapping effect by reducing the hole traps between host and MR-TADF emitter from deep (0.40â eV) to shallow (0.14/0.20â eV) ones for facilitating hole transport and exciton formation, as well as avoiding exciton quenching. And the large dihedral angle between the carbazole and MR-TADF core makes the carbazole act as a steric hindrance to inhibit molecular aggregation. Accordingly, the optimized solution-processed pure blue hyperfluorescence devices simultaneously realize record external quantum efficiency of 29.2 %, narrowband emission with a full-width at half-maximum of 16.6â nm, and pure blue color with CIE coordinates of (0.139, 0.189), which is the best result for the solution-processed organic light-emitting diodes based on MR-TADF emitters.
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Nowadays numerous thermally activated delayed fluorescence (TADF) polymers have been developed for PLEDs to realize high device performance and tunable emission colors. However, they often possess a strong concentration dependence on their luminescence including aggregation-caused quenching (ACQ) and aggregation-induced emission (AIE). Herein, we first report a nearly concentration-independent TADF polymer based on the strategy of polymerized TADF small molecules. It is found that when a donor-acceptor-donor (D-A-D) type TADF small molecule is polymerized through its long-axis direction, the triplet state is distributed along the polymeric backbone to effectively suppress the unwanted concentration quenching. Unlike the short-axis one with an ACQ effect, the photoluminescent quantum yield (PLQY) of the resultant long-axis polymer remains almost unchanged with the increasing doping concentration. Accordingly, a promising external quantum efficiency (EQE) up to 20 % is successfully achieved in a whole doping control window of 5-100â wt. %.
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In contrast to small-molecule multiple resonance emitters processed via vacuum evaporation technology, the design of multiple resonance dendrimers is presented by introducing the first- and second-generation carbazole dendrons in the periphery of boron, oxygen, nitrogen-doped polycyclic aromatic skeleton, for efficient narrowband blue electroluminescence by a solution process. The multiple resonance dendrimers not only keep the narrowband emission of the polycyclic aromatic skeleton, but also can suppress their intermolecular aggregation by steric carbazole dendrons, overcoming the unwanted spectral broadening in the solid state. The resultant first-generation carbazole dendrimer exhibits narrowband blue emission with promising photoluminescent quantum efficiency of 94% and delayed fluorescence with a lifetime of 139.1 µs in the solid-state film. Solution-processed organic light-emitting diodes based on the dendrimers reveal electroluminescence at 488 nm with full-width at half maximum of 39 nm, the maximum luminous efficiency of 29.2 cd A-1 , and maximum external quantum efficiency of 13.4%.
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BACKGROUND: In patients with acute hypoxemic respiratory failure whose diagnosis is not established after initial evaluation, obtaining a histopathological diagnosis may improve the patients' prognosis. This study aims to compare the safety profile and diagnostic yields between transbronchial lung biopsy (TBLB) and transbronchial lung cryobiopsy (TBLC) in these patients. METHODS: A retrospective comparative study was conducted in a 26-bed intensive care unit over a 5-year period. The consecutive patients with acute hypoxemic respiratory failure who underwent TBLB or TBLC were included to determine the potential etiology. Patients characteristics, procedure related complications, pathological and multidisciplinary discussion (MDD) diagnostic yields, treatment modification and 28-day survival were analyzed. Prognostic factors were identified by Cox regression analysis. RESULTS: Forty-five and 25 consecutive patients underwent TBLB and TBLC, respectively. The patients underwent TBLC were more critical. There was no significant difference in overall procedure related complications of patients underwent TBLB and TBLC [15.6% (7/45) vs 28.0% (7/25), p = 0.212]. The rate of pathological diagnostic yield [72.0% (18/25) vs 37.8% (17/45), p = 0.006], MDD diagnostic yield [84.0% (21/25) vs 55.6% (25/45), p = 0.016] and subsequent treatment modification [84.0% (21/25) vs 57.8% (26/45), p = 0.025] in patients underwent TBLC were significantly higher than those in patients underwent TBLB. Multivariate analysis revealed that MDD diagnosis [HR 0.193 (95% CI 0.047-0.792), p = 0.022] and treatment modification [HR 0.204 (95% CI 0.065-0.638), p = 0.006] may be prognostic protective factors. CONCLUSIONS: TBLC can lead to an increased chance of establishing a diagnosis, which could significantly improve the patients' prognosis, with an acceptable safety profile.
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Doenças Pulmonares Intersticiais , Insuficiência Respiratória , Biópsia/métodos , Broncoscopia/efeitos adversos , Broncoscopia/métodos , Estado Terminal , Humanos , Pulmão/patologia , Doenças Pulmonares Intersticiais/diagnóstico , Insuficiência Respiratória/etiologia , Estudos RetrospectivosRESUMO
Based on Mason's signal flow graph analysis, an analytical model of the optical mode localization based on coupled ring resonators is established. The correctness of the theoretical model is proved by simulation. High sensitivity and common-mode rejection can be achieved by evaluating the modal power ratio from resonant peaks as sensing output. Based on the four-port structure, two output spectrum with mode localization (asymmetric mode splitting) and symmetric mode splitting allows the high-sensitivity sensing and dual-channel calibration to be carried out simultaneously, which can reduce the sensing errors. Monte-Carlo analysis showed that fabrication imperfection changes less than 6% of the performance in 90% cases, thus the construction of practical sensors is possible with appropriate tuning. The optical mode localized sensing has advantages in sensitivity, accuracy, anti-aliasing compared with conventional micro-mechanical mode localized sensor. Various types of high-sensitive sensor can be constructed through coupling parametric perturbation with measurands in different physical domains.
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Donor-acceptor (D-A) conjugated polymers often possess a significant frontier molecular orbital overlap because of the conjugation elongation, leading to no thermally activated delayed fluorescence (TADF) caused by a large singlet-triplet energy splitting (âµEST ). Herein a novel steric locking strategy is proposed by incorporating methyl groups into D-A conjugated polymers. Benefitting from the methyl hindrance, the torsion between the donor and acceptor can be well tuned to form a sterically-locked conformation, so that the unwanted relaxation toward planarity and thus conjugation elongation is prevented to boost hole-electron separation. The resultant D-A conjugated polymer achieves an extremely low ΔEST of 0.09â eV to enable efficient TADF. The corresponding doped and non-doped devices are fabricated via a solution process, revealing a record-high external quantum efficiency (EQE) of 24.0 % (79.4â cd A-1 , 75.0â lm W-1 ) and 15.3 % (50.9â cd A-1 , 47.3â lm W-1 ).
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An electroactive room-temperature phosphorescence (RTP) polymer has been demonstrated based on a characteristic donor-oxygen-acceptor geometry. Compared with the donor-acceptor reference, the inserted oxygen atom between donor and acceptor can not only decrease hole-electron orbital overlap to suppress the charge transfer fluorescence, but also strengthen spin-orbital coupling effect to facilitate the intersystem crossing and subsequent phosphorescence channels. As a result, a significant RTP is observed in solid states under photo excitation. Most noticeably, the corresponding polymer light-emitting diodes (PLEDs) reveal a dominant electrophosphorescence with a record-high external quantum efficiency of 9.7 %. The performance goes well beyond the 5 % theoretical limit for typical fluors, opening a new door to the development of pure organic RTP polymers towards efficient PLEDs.
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Based on a "TADF + Linker" strategy (TADF=thermally activated delayed fluorescence), demonstrated here is the successful construction of conjugated polymers that allow highly efficient delayed fluorescence. Small molecular TADF blocks are linked together using a methyl-substituted phenylene linker to form polymers. With the growing number of methyl groups on the phenylene, the energy level of the local excited triplet state (3 LEb ) from the delocalized polymer backbone gradually increases, and finally surpasses the charge-transfer triplet state (3 CT). As a result, the diminished delayed fluorescence can be recovered for the tetramethyl phenylene containing polymer, revealing a record-high external quantum efficiency (EQE) of 23.5 % (68.8â cd A-1 , 60.0â lm W-1 ) and Commission Internationale de l'Eclairage (CIE) coordinates of (0.25, 0.52). Combined with an orange-red TADF emitter, a bright white electroluminescence is also obtained with a peak EQE of 20.9 % (61.1â cd A-1 , 56.4â lm W-1 ) and CIE coordinates of (0.36, 0.51).
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The meta junction is proposed to realize efficient thermally activated delayed fluorescence (TADF) in donor-acceptor (D-A) conjugated polymers. Based on triphenylamine as D and dicyanobenzene as A, as a proof of concept, a series of D-A conjugated polymers has been developed by changing their connection sites. When the junction between D and A is tuned from para to meta, the singlet-triplet energy splitting (ΔEST ) is found to be significantly decreased from 0.44 to 0.10â eV because of the increasing hole-electron separation. Unlike the para-linked analogue with no TADF, consequently, the meta-linked polymer shows a strong delayed fluorescence. Its corresponding solution-processed organic light-emitting diodes (OLEDs) achieve a promising external quantum efficiency (EQE) of 15.4 % (51.9â cd A-1 , 50.9â lm W-1 ) and CIE coordinates of (0.34, 0.57). The results highlight the bright future of D-A conjugated polymers used for TADF OLEDs.
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A blue-emitting iridium dendrimer, namely B-G2, has been successfully designed and synthesized with a secondgeneration oligocarbazole as the dendron, which is covalently attached to the emissive tris[2-(2,4-difluorophenyl)-pyridyl]iridium(III) core through a nonconjugated link to form an efficient self-host system in one dendrimer. Unlike small molecular phosphors and other phosphorescent dendrimers, B-G2 shows a continuous enhancement in the device efficiency with increasing doping concentration. When using neat B-G2 as the emitting layer, the nondoped device is achieved without loss in efficiency, thus giving a state-of-art EQE as high as 15.3% (31.3 cdA1, 28.9 lmW1) along with CIE coordinates of (0.16, 0.29).
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Correction for 'Solution-processed white OLEDs with power efficiency over 90 lm W-1 by triplet exciton management with a high triplet energy level interfacial exciplex host and a high reverse intersystem crossing rate blue TADF emitter' by Liang Chen et al., Mater. Horiz., 2022, 9, 1299-1308, https://doi.org/10.1039/D1MH02060A.
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Vehicles operating in space need to withstand extreme thermal and electromagnetic environments in light of the burgeoning of space science and technology. It is imperatively desired to high insulation materials with lightweight and extensive mechanical properties. Herein, a boron-silica-tantalum ternary hybrid phenolic aerogel (BSiTa-PA) with exceptional thermal stability, extensive mechanical strength, low thermal conductivity (49.6 mW m-1 K-1), and heightened ablative resistance is prepared by an expeditious method. After extremely thermal erosion, the obtained carbon aerogel demonstrates noteworthy electromagnetic interference (EMI) shielding performance with an efficiency of 31.6 dB, accompanied by notable loading property with specific modulus of 272.8 kN·m kg-1. This novel design concept has laid the foundation for the development of insulation materials in more complex extreme environments.
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The small Extracellular vesicles (sEV) has been recognized to be significant for intercellular communication due to their ability to transfer important cellular cargoes like miRNAs through circulation. The pituitary gland has not been clearly known about the role of its secreted sEV under normal physiological conditions. And Liver disease is a global public health burden. The present study is the first to investigate the effect of pituitary sEV on the liver. Sequencing and qRT-PCR revealed miR-143-3p is one of the richest in the pituitary sEV. MiR-143 Knockout (KO) mice resulted in a remarkable decrease in insulin-like growth factor 1 (IGF-1) levels and a significant increase in insulin-like growth factor binding protein 5 (IGFBP5) levels along with a reduction in liver primary cell growth. More importantly, compared with miR-143-KO-sEV, WT-sEV possesses a more robust capacity to improve miR-143 KO mice liver repair through the Wnt/ß-catenin pathway after an acute injury caused by carbon tetrachloride (CCl4). Our results indicate that pituitary-derived sEV promotes hepatocyte proliferation and liver repair by its cargo miR-143-3p and provides new insight into the regulation mechanism of the pituitary-liver axis, and open a new window for endocrine regulation by using sEV.
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Vesículas Extracelulares , Fígado , Camundongos Knockout , MicroRNAs , Hipófise , Animais , MicroRNAs/genética , MicroRNAs/metabolismo , Vesículas Extracelulares/metabolismo , Hipófise/metabolismo , Camundongos , Fígado/metabolismo , Proliferação de Células , Hepatócitos/metabolismo , Via de Sinalização Wnt , Masculino , Fator de Crescimento Insulin-Like I/metabolismo , Fator de Crescimento Insulin-Like I/genética , Regeneração Hepática/genética , Tetracloreto de Carbono/toxicidadeRESUMO
The general strategy for n-type organic thermoelectric is to blend n-type conjugated polymer hosts with small molecule dopants. In this work, all-polymer n-type thermoelectric is reported by dissolving a novel n-type conjugated polymer and a polymer dopant, poly(ethyleneimine) (PEI), in alcohol solution, followed by spin-coating to give polymer host/polymer dopant blend film. To this end, an alcohol-soluble n-type conjugated polymer is developed by attaching polar and branched oligo (ethylene glycol) (OEG) side chains to a cyano-substituted poly(thiophene-alt-co-thiazole) main chain. The main chain results in the n-type property and the OEG side chain leads to the solubility in hexafluorineisopropanol (HFIP). In the polymer host/polymer dopant blend film, the Coulombic interaction between the dopant counterions and the negatively charged polymer chains is reduced and the ordered stacking of the polymer host is preserved. As a result, the polymer host/polymer dopant blend exhibits the power factor of 36.9 µW m-1 K-1, which is one time higher than that of the control polymer host/small molecule dopant blend. Moreover, the polymer host/polymer dopant blend shows much better thermal stability than the control polymer host/small molecule dopant blend. This research demonstrates the high performance and excellent stability of all-polymer n-type thermoelectric.
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Obesity has been suggested as a risk factor for sarcopenia. Sarcopenic obesity (SO), as a new category of obesity, is a high-risk geriatric syndrome in elderly individuals. However, knowledge about the molecular pathomechanisms of SO is still sparse. In the present study, starting at 13 months, male Sprague-Dawley (SD) rats were fed a high-fat diet (HFD) and normal diet (ND) for 28 weeks to establish a rodent animal model of SO with an identical protocol, which was further assessed and verified as a successful SO model. Through RNA-seq analysis of gastrocnemius muscle in SO rats, we found that differentially expressed genes (DEGs) and alternative splicing events (ASEs) focused mainly on inflammatory, immune-response, skeletal muscle cell differentiation, fat cell differentiation and antigen processing and presentation. Furthermore, as the core regulation factor of skeletal muscle, the mef2c (myocyte enhancer Factor 2C) gene also has a significant alternative 3' splice site (A3SS) and down-regulated expression in HFD-induced SO. The alternative genes targeted by mef2c identified by GO analysis were enriched in transcript regulation of RNA polymerase II promoter. In conclusion, these explorative findings in aging high-fat-fed rats might serve as a firm starting point for understanding the pathway and mechanism of sarcopenic obesity.