Notes

Dose-dense ABVD since first-line remedy within early-stage unfavorable Hodgkin lymphoma: link between a prospective, multicenter double-step cycle Two study through Fondazione Italiana Linfomi.
As label-free biomarkers, electrical properties of single cells have been widely used for cell-type classification and cell-status evaluation. However, as intrinsic bioelectrical markers, previously reported membrane capacitance and cytoplasmic resistance (e.g., specific membrane capacitance Cspecific membrane and cytoplasmic conductivity σcytoplasm ) of tumor subtypes were derived from tens of single cells, lacking statistical significance due to low cell numbers. In this study, tumor subtypes were constructed based on phenotype (treatment with 4-methylumbelliferone) or genotype (knockdown of ROCK1) modifications and then aspirated through a constriction-channel based impedance flow cytometry to characterize single-cell Cspecific membrane and σcytoplasm . Thousands of single tumor cells with phenotype modifications were measured, resulting in significant differences in 1.64 ± 0.43 μF/cm2 vs. 1.55 ± 0.47 μF/cm2 of Cspecific membrane and 0.96 ± 0.37 S/m vs. 1.24 ± 0.47 S/m of σcytoplasm for 95C cells (792 cells of 95C-control vs. 1529 cells of 95C-pheno-mod); 2.56 ± 0.88 μF/cm2 vs. 2.33 ± 0.56 μF/cm2 of Cspecific membrane and 0.83 ± 0.18 S/m vs. 0.93 ± 0.25 S/m of σcytoplasm for H1299 cells (962 cells of H1299-control vs. 637 cells of H1299-pheno-mod). check details Furthermore, thousands of single tumor cells with genotype modifications were measured, resulting in significant differences in 3.82 ± 0.92 vs. 3.18 ± 0.47 μF/cm2 of Cspecific membrane and 0.47 ± 0.05 vs. 0.52 ± 0.05 S/m of σcytoplasm (1100 cells of A549-control vs. 1100 cells of A549-geno-mod). These results indicate that as intrinsic bioelectrical markers, specific membrane capacitance and cytoplasmic conductivity can be used to classify tumor subtypes.Inorganic Na3 Zr2 Si2 PO12 is prospective with a high ionic conductivity but suffers large interfacial resistance and stability issues against sodium metal, hindering its practical application in all-solid-state sodium batteries. A surface potential regulation strategy is adopted to address these issues. Na3 Zr2 Si2 PO12 (NZSP) ceramic with homogeneously-sintered surface is synthesized by a simple two-step sintering method to promote its uniform surface potential, which is favorable for mitigating the potential fluctuations at the interface against Na metal and enhancing interfacial compatibility. The Na/NZSP interface can be stabilized for over 4 months with a low interfacial resistance of 129 Ω cm2 at 25 °C. The symmetrical Na/NZSP/Na cell exhibits ultra-stable sodium platting/stripping cycling for over 1000 cycles under 0.1 mA cm-2 . Superior interfacial performance is well retained even under 0.2 mA cm-2 at room temperature. The robust interface is further signified by its excellence under higher current densities of up to 0.85 mA cm-2 at 60 °C. A 4 V all-solid-state Na3 V1.5 Cr0.5 (PO4 )3 /NZSP/Na metal battery is demonstrated at ambient conditions, which exhibits superior rate capability and delivers a high reversible capacity of 103 mA h g-1 under 100 mA g-1 for over 400 cycles with a Coulombic efficiency of over 99%.Simultaneous reductive amination of C=O and C-OH in 5-hydroxymethylfurfural (HMF) into C-NH2 in 2,5-bis(aminomethyl)furan (BAMF) is challenging. In this work, reductive amination of C=O in HMF was firstly studied, in which HMF can be converted into 5-hydroxymethyl furfurylamine (HMFA) with a 99.5 % yield over Raney Co catalyst. BAMF was then directly synthesized with 82.3 % yield from HMF over Raney Ni catalyst at 160 °C for 12 h. An even higher yield of 88.3 % could be obtained through a stepwise reductive amination process, in which the reaction started at 120 °C for the first 2 h over Raney Co mainly for amination of C=O and then continued at 160 °C for another 10 h over Raney Ni mainly for amination of C-OH. Under optimized reaction conditions, the catalyst could be reused four times without obvious loss in catalytic performance. XRD and XPS characterization of the reused catalyst indicated that the formation of Ni3 N and the adsorption of alkyl amines could be the main reasons for the deactivation of the catalyst. Moreover, plausible reaction pathways were proposed to originate the detected by-products according to the kinetic profiles.Poly(lactic acid) (PLA) and its copolymer, poly(lactic-co-glycolic acid) (PLGA), based aliphatic polyesters have been extensively used for biomedical applications, such as drug delivery system and tissue engineering, thanks to their biodegradability, benign toxicity, renewability, and adjustable mechanical properties. A rapidly growing field of cancer research, the development of therapeutic cancer vaccines or treatment modalities is aimed to deliver immunomodulatory signals that control the quality of immune responses against tumors. Herein, the progress and applications of PLA and PLGA are reviewed in delivering immunotherapeutics to treat cancers.
The use of paracetamol or nefopam for postoperative pain control is limited by the need of high doses associated with unwanted effects. Previous works suggest positive interactions between both compounds that may be exploited to obtain potentiation of antinociception.

Mechanical and heat antinociception induced by oral doses of paracetamol, nefopam or their combination was studied by isobolographic analysis in a murine model of postsurgical pain. The effective doses that produced 50% antinociception (ED
) were calculated from the log dose-response curves for each compound. Subsequently, the effects of ED
s, ED
s, ED
s and ED
s of nefopam and paracetamol combined were assessed.

Oral paracetamol induced dose-dependent relief of postoperative sensitivity and showed higher efficacy reducing mechanical hypersensitivity (ED
177.3±15.4mg/kg) than heat hyperalgesia (ED
278.6±43mg/kg). Oral nefopam induced dose-dependent antinociception with similar efficacy for mechanical and heat hypersensitivitywe identify in a mouse model of postoperative pain a potent synergistic oral combination consisting of low paracetamol and nefopam doses that provides relief of postsurgical hypersensitivity to mechanical and thermal stimuli. Oral multimodal paracetamol-nefopam mixtures represent a potential clinically available pharmacological strategy for the relief of incisional sensitivity and the promotion of patient recovery.
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