Poly[(N,N-dimethyl­formamide-κO)tris­(μ-naphthalene-1-acetato)terbium(III)]

In title compound, [Tb(C12H9O2)3(C3H7NO)]n, the Tb atom is nine-coordinated by nine O atoms from three naphthalene-1-acetate and one N,N-dimethyl­formamide ligands. The Tb atoms are linked by three bridging naphthalene-1-acetate ligands into a chain parallel to the b axis. Further stabilization of the structure is accomplished by non-classical C—H⋯O hydrogen bonds and C—H⋯π interactions

PREPARATION OF MACROPOROUS TIO2 BY STARCH MICROSPHERES TEMPLATE WITH ASSISTANCE OF SUPERCRITICAL CO2

In this work a green route is reported to prepare a TiO2 macroporous network using corn starch microspheres flake as a bio-template. The starch microspheres prepared by emulsion technology were used as a template into which precursor tetrabutyl titanate (TBOT) was permeated using supercritical carbon dioxide (scCO2) as a forceful carrier or infiltration media, resulting in the formation of an organic/inorganic hybrid material; then the coated template was gelled and dried during the scCO2-coating and the depressurization processes, followed by removal of the template by calcination at 700°C; finally, TiO2 inverse-opals-like material reversely replicating the starch microspheres template was obtained. Scanning electron microscopy (SEM), nitrogen sorption measurements, and X-ray diffraction (XRD) indicated that the products were the inverse replicas from their templates. The obtained TiO2 inverse opals-like material showed a wide dispersion of pore sizes from mesopores to macropores – a few nanometers to several micrometers –with the BET surface area up to 103 m2/g, and a predominantly anatase crystalline phase. In addition, the wall thickness of the macropores varied with tunable pressure for closed cells or open-cell foams. So this facile and environmentally friendly process for the preparation of high-surface area, thermally-stable, metal-oxide catalysts and supports by a starch microsphere templating approach may have widespread potential applications in catalysis, absorbents, photoelectric materials, and so on

The Diagnostic and Prognostic Potential of MicroRNAs for Hepatocellular Carcinoma

Hepatocellular carcinoma (also termed hepatocarcinoma) is the third cancer-related cause of death worldwide. To our knowledge, markers such as α-fetoprotein display poor performance in the early diagnosis and prognosis prediction of hepatocarcinoma. MicroRNAs are an evolutionarily conserved class of small noncoding single-stranded RNA typically consisting of 18–24 nucleotides. They have been reported to act as tumor suppressors or oncogenes via reversely regulating gene expression. Recent evidence has revealed that microRNAs, especially in body fluids such as the blood and urine, display important diagnostic and prognostic potential for hepatocarcinoma. Here, we reviewed currently available data on microRNAs and hepatocarcinoma, with emphasis on the biogenesis and function of microRNAs and their potential diagnostic and prognostic value for hepatocarcinoma. We also discussed the clinical utility perspectives of microRNAs in hepatocarcinoma and possible challenges

Comparison of preprocessing methods and storage times for touch DNA samples

Aim To select appropriate preprocessing methods for different substrates by comparing the effects of four different preprocessing methods on touch DNA samples and to determine the effect of various storage times on the results of touch DNA sample analysis. Method Hand touch DNA samples were used to investigate the detection and inspection results of DNA on different substrates. Four preprocessing methods, including the direct cutting method, stubbing procedure, double swab technique, and vacuum cleaner method, were used in this study. DNA was extracted from mock samples with four different preprocessing methods. The best preprocess protocol determined from the study was further used to compare performance after various storage times. DNA extracted from all samples was quantified and amplified using standard procedures. Results The amounts of DNA and the number of alleles detected on the porous substrates were greater than those on the non-porous substrates. The performances of the four preprocessing methods varied with different substrates. The direct cutting method displayed advantages for porous substrates, and the vacuum cleaner method was advantageous for non-porous substrates. No significant degradation trend was observed as the storage times increased. Conclusion Different substrates require the use of different preprocessing method in order to obtain the highest DNA amount and allele number from touch DNA samples. This study provides a theoretical basis for explorations of touch DNA samples and may be used as a reference when dealing with touch DNA samples in case work

High temperature superconducting FeSe films on SrTiO3 substrates

Interface enhanced superconductivity at two dimensional limit has become one of most intriguing research directions in condensed matter physics. Here, we report the superconducting properties of ultra-thin FeSe films with the thickness of one unit cell (1-UC) grown on conductive and insulating SrTiO3 (STO) substrates. For the 1-UC FeSe on conductive STO substrate (Nb-STO), the magnetization versus temperature (M-T) measurement shows a diamagnetic signal at 85 K, suggesting the possibility of superconductivity appears at this high temperature. For the FeSe films on insulating STO substrate, systematic transport measurements were carried out and the sheet resistance of FeSe films exhibits Arrhenius TAFF behavior with a crossover from a single-vortex pinning region to a collective creep region. More intriguing, sign reversal of Hall resistance with temperature is observed, demonstrating a crossover from hole conduction to electron conduction above Tc in 1-UC FeSe films

The Serum MicroRNA Expression Modified the Genic Toxicity Caused by Aflatoxin B1

The serum microRNAs have been reported as potential biomarkers for hepatocellular carcinoma (HCC); however, their role in genic toxicity related to aflatoxin B1 (AFB1), such as TP53 mutation and DNA damage, has not yet been evaluated. Here, we conducted a hospital-based case-control study, including 558 patients with pathologically diagnosed HCC and positive AFB1 and healthy controls (n = 630) without any evidence of liver diseases. Genic toxicity related to AFB1 was evaluated using the hot-spot mutation at the codon 269 of TP53 gene (TP53M) and AFB1-DNA adducts. Through serum microRNA PCR microarray screening analysis, we observed 10 differentially expressed microRNAs (including miR-7-2-3p, miR-4651, miR-127-3p, miR-192-5p, miR-382-5p, miR-10b-5p, miR-532-3p, miR-16-5p, miR-106b-5p, and miR-4688) among HCC cases with positive AFB1 and controls with positive AFB1. The miR-4651 and miR-382-5p were further identified to be significantly higher in AFB1-positive HCC cases compared to controls. This kind of increasing serum levels was significantly and positively associated with frequency of TP53M and the levels of AFB1-DNA adduct. Furthermore, these microRNAs also modified the prognosis of HCC related to AFB1. These results suggest that the serum levels of microRNAs might be able to modify AFB1-induced genic toxicity, and microRNA-4651 and miR-382-5p, are such potential candidates

Clincal Observation of Grouping Responsibility Model of Immersion foot nursing In Maternity Ward

目的：责任制护理是一种以病人为中心，在护理过程中运用医学、护理、心理、生理、社会等学科的知识，观察分析病人的全面健康情况，进行有计划和系统的护理，从而提高护理质量和护理人员的素质。引入浸足1号进行整体护理，观察其临床效果。方法：在产科实施分组责任制护理，可以使护士为病人提供连续、全程、无缝隙的护理服务。引入浸足1号护理分为试验组和对照组，使试验组患者增加了家的感觉，并促进了产妇体质的尽快恢复。结果：在实施过程中，我们改变了原来的排班模式，使病人在住院期间有固定的责任护士，增强了护士的责任心，调动了护士的积极性，加强了护患沟通，减少了护理差错和纠纷，提高了护理质量，同时把护士的被动服务变为了主动服务，大大提高了护理质量，促进了产妇康复进程，试验组与对照组比较，护理质量明显提高，统计学比较有显著差异，P<0.05。结论：引入浸足1号护理提高了病人、医生的满意度，提高了护士的自身价值。Objective: Nursing responsibility system is patient centered system, using medicine, nursing, psychology, social and other disciplines of knowledge in the process of nursing, observing and comprehensively analyzing the health condition of patient, proceeding with a systematic nursing plan, so as to improve the quality of nursing and nursing staff quality. Introduction of immersion foot 1 of holistic nursing care, to observe its clinical effect. Methods:The implementation of the system of grouping responsibility nursing in obstetrics, can enable nurses to provide continuous, full, and non-breaking nursing service for patients . Introduction of immersion foot 1 nurses were divided into experimental group and control group, the experimental group increases the feeling of home, which promote maternal physical recovery. Results:In the process of implementation, we changed the original scheduling model, so as to make the patient had the fixed nurses during hospitalization, to strengthen the responsibility of nurses, to arouse the enthusiasm of nurses, to strengthen communication between nurses and patients, to reduce nursing errors and disputes, to improve the quality of care. Meanwhile the nurses change passive service in order to active service, which greatly improved the quality of nursing and promoted maternal rehabilitation process. Compare the experimental group with control group, and significantly improved the quality of nursing, there was statistical significant difference between the groups P<0.05. Conclusion: Introduction of immersion foot 1 care improves patient, physician satisfaction, and the nurses' value

Establishment of a sensitive UPLC-MS/MS method to quantify safinamide in rat plasma

A fast, simple, and sensitive ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was established for the quantification of safinamide in rat plasma. Plasma samples were treated with acetonitrile for protein precipitation, and diazepam was used as an internal standard (IS). The analytes were separated on an Acquity UPLC C18 (2.1 mm × 50 mm, 1.7 μm) chromatographic column with gradient elution using a mobile phase (0.1% formic acid-acetonitrile). Then, the eluates were detected by electrospray ionization (ESI) in positive ion mode. The analytes were quantified by multiple reaction monitoring (MRM) using the transition m/z 303.3→215.0 of safinamide and m/z 285.0→154.0 of IS. Safinamide had good linearity in the concentration range of 1.0–2000 ng/mL, and the lower limit of quantitation (LLOQ) was 1.0 ng/mL. The intra- and inter-day precision and accuracy of safinamide were less than 7.63%, while the average recovery rate was 92.98%–100.29%. The method was validated to be stable and had low noise, short chromatographic run time, wide linear range, small sample volumes, low sample injection volumes, and high sensitivity. Therefore, it can be used in pharmacokinetics and preclinical and clinical studies