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Introduction. LAMA1, also known as laminin subunit α1, is a member of the laminin family, which is widely reported to be a key basement membrane molecule that affects various biological activities and is associated with many kinds of diseases. We aimed to investigate the association between LAMA1single-nucleotide polymorphisms and the occurrence and progression of esophageal squamous cell carcinoma in the Chinese population. Method. 2,186 participants were collected retrospectively between October 2008 and January 2017, including 1,043 ESCC patients and 1,143 noncancer patients. A 2 mL blood sample was obtained intravenously for the LDR for SNP analysis. The 6 SNP loci of LAMA1 were selected and examined. We analyzed the association of several genetic models of 6 LAMA1 SNP loci, sex, age, smoking and drinking status, and the occurrence of esophageal squamous cell carcinoma. Results. In the rs62081531 G > A locus, genotype GA was a protective factor for ESCC compared with GG (OR: 0.830, P = 0.046 ), especially among the younger and nondrinkers. At rs607230 T > C, genotype TC was linked with a lower risk of ESCC compared with TT. (OR: 0.613, P = 0.034 ). Haplotype Frequencies revealed that Ars62081531Grs621993Ars539713Trs566655Ars73938538Crs607230 (OR: 0.803, P = 0.028 ) and Grs62081531Grs621993Ars539713Trs566655Crs73938538Crs607230 (OR: 0.679, P = 0.010 ) were strongly associated with lower susceptibility of ESCC. Conclusion. The LAMA1 rs62081531, rs539713, rs566655, and rs607230 polymorphisms were demonstrated to be related to susceptibility to ESCC in the Chinese population. LAMA1 SNPs may have a significant impact on the occurrence of esophageal cancer and may serve as potential diagnostic biomarkers.

Feng Su,1,&ast; Yong Fang,1,&ast; Jinjie Yu,1 Tian Jiang,1 Siyun Lin,1 Shaoyuan Zhang,1 Lu Lv,2 Tao Long,2 Huiwen Pan,2 Junqing Qi,2 Qiang Zhou,3 Weifeng Tang,4 Guowen Ding,2 Liming Wang,5 Lijie Tan,1 Jun Yin1 1Department of Thoracic Surgery, Zhongshan Hospital of Fudan University, Shanghai, People’s Republic of China; 2Department of Cardiothoracic Surgery, Affiliated People’s Hospital of Jiangsu University, Jiangsu, People’s Republic of China; 3Department of Thoracic Surgery, Sichuan Cancer Hospital & Institute, Sichuan, People’s Republic of China; 4Department of Cardiothoracic Surgery, Nanjing Drum Tower Hospital, Jiangsu, People’s Republic of China; 5Department of Respiratory, Shanghai Xuhui Central Hospital, Shanghai, People’s Republic of China&ast;These authors contributed equally to this workCorrespondence: Jun Yin; Lijie Tan, Zhongshan Hospital of Fudan University, 180 Fenglin road, Xuhui District, Shanghai, 200032, People’s Republic of China, Email jun_yin@fudan.edu.cn; tan.lijie@zs-hospital.sh.cnBackground: The σ 1A subunit of the adaptor protein 1 (AP1S1) participates in various intracellular transport pathways, especially the maintenance of copper homeostasis, which is pivotal in carcinogenesis. It is therefore rational to presume that AP1S1 might also be involved in carcinogenesis. In this hospital-based case-control study, we investigated the genetic susceptibility to ESCC in relation to SNPs of AP1S1 among Chinese population.Methods: A database containing a total of 1303 controls and 1043 ESCC patients were retrospectively studied. The AP1S1 SNPs were analyzed based on ligation detection reaction (LDR) method. Then, the relationship between ESCC and SNPs of AP1S1 was determined with a significant crude P< 0.05. Then the logistic regression analysis was used for the calculation for adjusted P in the demographic stratification comparison if a significant difference was observed in the previous step.Results: AP1S1 rs77387752 C>T genotype TT was an independent risk factor for ESCC, while rs4729666 C>T genotype TC and rs35208462 C>T genotype TC were associated with a lower risk for ESCC, especially in co-dominant model and allelic test for younger, male subjects who are not alcohol-drinkers nor cigarette smokers.Conclusion: AP1S1 rs77387752, rs4729666 and rs35208462 polymorphisms are associated with susceptibility to ESCC in Chinese individuals. AP1S1 SNPs may exert an important role in esophageal carcinogenesis and could serve as potential diagnostic biomarkers.Keywords: AP1S1, single nucleotide polymorphism, SNP, esophageal squamous cell carcinoma, ESCC

The effect of a self-assembly nucleating agent, N , N ′, N ″-tricyclohexyl-1,3,5-benzenetricarboxylamide (BTCA), on the crystallization behavior of poly(lactic acid) (PLA) was probed by time-resolved Fourier transform infrared spectroscopy (FTIR) and wide angle X-ray diffraction (WAXD). The vibrational changes associated with inter- and intra-chain interactions during crystallization were monitored. In the initial period of crystallization, the order of intensity changes is as follows: 1458 cm −1 > 1210 cm −1 » 921 cm −1 , 1458 cm −1 ∼ 1210 cm −1 > 921 cm −1 , and 1458 cm −1 ∼ 1210 cm −1 ∼ 921 cm −1 for neat PLA, PLAs containing 0.1 wt% and 0.3 wt% BTCA, respectively. This indicates that BTCA can accelerate both the formation of skeletal conformational-ordered structure and, especially, the 10 3 helix one. The incorporation of BTCA changes the crystallization mechanism but has no impact on the crystal form of PLA.

This research focused on development of a new type of re-centering damper consisting of the Ni-Ti Shape Memory Alloy (SMA) rods and friction wedges. Compared with the other existing types of SMA-based dampers, the proposed damper offers an improved energy absorption capacity. In addition, strength and deformation capacity of the proposed damper can be conveniently adjusted if needed. To verify the perceived benefits of the damper, a series of tests were performed on an experimental specimen. It was found that the proposed damper can exhibit stable hysteretic energy dissipation response and reliable re-centering performance without developing any visible damage in the damper components. The test results also show that the damper is not sensitive to the different loading protocols imposed. Beyond the experimental work, a theoretical model for the proposed damper was established and validated by the test results. The theoretical model can be used to design the damper in the future. Furthermore, a three-dimensional computer model was developed for the tested damper. The computer model was found to be able to accurately replicate the nonlinear responses of the experimental specimen. The modelling approaches and assumptions adopted in the computer model can be used for future analysis and design.

This research focused on a new type of re-centering beam-to-column connection for use in low-rise steel moment-resisting frames (MRFs). A new material model was first developed and validated to accurately, conveniently, and efficiently simulate the nonlinear behavior of the critical components of the connection. To demonstrate its potential, a representative low-rise MRF previously investigated was revisited and re-designed with the considered re-centering connection. Specifically, the re-centering beam-to-column connections in the re-designed system are controlled to have the same flexural resistances as the corresponding ones in the original system under the connection rotation angle of 0.025 rad. Computer simulations were conducted to compare different aspects the original and re-designed systems under the design basis earthquake level excitations. It was found that the re-designed system is overall superior to the original one based on a comprehensive performance measure established in this research that considers the peak transient and residual inter-story drift angles as well as the peak base shear demand. Moreover, compared with the original system, the re-designed system was found to have similar seismic demands on the acceleration-sensitive or velocity-sensitive nonstructural components but larger seismic demands on the displacement-sensitive nonstructural components. Accordingly, the displacement-sensitive nonstructural components should be designed with caution in the low-rise MRF with the re-centering beam-to-column connections.

This paper focuses on a new type of base connection for wide-flange columns. The base connection consists of a pair of steel angles and a shear plate that connect the flanges and the web of a wide-flange column to the foundation through a set of high-strength bolts, respectively. To investigate the response of the bolted base connection under the combined column axial compression and weak-axis lateral load, three specimens were prepared and tested. The test parameter varied in the specimens was the technology used to develop the angles in the bolted base connection. The three specimens adopted the hot rolled angles, the angles cold folded from steel plates, and the angles welded from steel plates, respectively. All the specimens were tested with the same axial compression and the same cyclic lateral loading protocol. It was found that all the specimens behaved in the same ductile manner while dissipating significant amounts of hysteretic energy. Moreover, all the specimens sustained the weak-axis rotation of 0.06 rad without developing any in-cycle strength degradations. The tests provided clear evidence that the cold folded and welded angles can be used as the surrogates to the hot rolled angles in the bolted base connection under the considered combined loading. This research further established a simplified model to approximate the backbone response of the lateral resistance of the bolted base connection under the considered combined loading. Result comparisons show that the simplified model can provide reasonable estimates.

Composite electrodes that possess both appropriate integration and reasonable structures are needed to provide eminent electrochemical performance in energy storage devices. At this work, an innovative electrode material with a composite structure of Ni3S2/NiV-LDH nanosheets fixed on the reduced graphene oxide/Ni Foam (rGO/NF) was fabricated by a convenient two-step hydrothermal process. The intriguing compositional/componental advantages significantly facilitate the efficient penetration of the electrolytes and increase active sites of redox reactions in energy storage application. The Ni3S2/NiV-LDH/rGO/NF electrode reaches a standout specific capacitance of 3004.3 F g−1 at a current density of 1 A g−1 and a superb cycle stability with 92.2% capacitance retention after 5000 cycles. Furthermore, an asymmetric supercapacitor (Ni3S2/NiV-LDH/rGO/NF//AC) was also assembled, achieving a high energy density of 59.4 Wh kg−1 at 852.3 W kg−1 and favourable cycle life, where 98.3% of the capacitance was retained after 8000 cycles. These consequences show that Ni3S2/NiV-LDH/rGO/NF composite is a potential electrode material in the future.

Poly(lactic acid)/poly(e-caprolactone) (PLA/PCL) blends are among the most widely investigated biomaterials for tissue engineering scaffolds. Incorporating carboxylic multi-walled carbon nanotubes (MWCNTs) into the blend can further tune the microphase distribution and interface adhesion which conversely dominates the micromechanical properties. In this work, atomic force microscope (AFM) based quantitative nanomechanical measurements were applied on PLA/PCL/MWCNTs bionanocomposites for gaining knowledge at the nanoscale. Results show that MWCNTs are mainly dispersed in the PCL phase which is adjacent to the PLA phase. The microphase structures and the onsite microscopic Young's moduli distributions have significant changes with the introduction of MWCNTs. No obvious intermediate layer in the PLA/MWCNTs and PCL/MWCNTs interfaces is observed in the Young's moduli map, indicating weak interactions in the polymer/MWCNTs interface. Moreover, microscopic structure-property relationships of PLA/PCL/MWCNTs nanocomposites were discussed and correlated to the macroscopic mechanical properties. A better understanding of these properties would be helpful in tailoring the PLA/PCL based bionanomaterials for applications in tissue engineering scaffolds, where the nanomechanical information is critical.

To improve bioavailability of pueraria flavones (PF), a self-microemulsifying drug delivery system (SMEDDS) dropping pills composed of PF, Crodamol GTCC, Maisine 35-1, Cremophor RH 40, 1,2-propylene glycol and polyethylene glycol 6000 (PEG6000) was developed. Particle size, zeta potential, morphology and in vitro drug release were investigated, respectively. Pharmacokinetics, bioavailability of PF-SMEDDS dropping pills and commercial Yufengningxin dropping pills were also evaluated and compared in rats. Puerarin treated as the representative component of PF was analyzed. Dynamic light scattering showed the ability of PF-SMEDDS dropping pills to form a nanoemulsion droplet size in aqueous media. The type of media showed no significant effects on the release rate of PF. PF-SMEDDS dropping pills were able to improve the in vitro release rate of PF, and the in vitro release of these dropping pills was significantly faster than that of Yufengningxin dropping pills. There was a dramatic difference between the mean value of t1/2, peak concentration (Cmax), the area of concentration-time curve from 0 to 6 h (AUC0-6 h) of PF-SMEDDS dropping pills and that of commercial Yufengningxin dropping pills. A pharmacokinetic study showed that the bioavailability of PF was greatly enhanced by PF-SMEDDS dropping pills. The value of Cmax and relative bioavailability of PF-SMEDDS dropping pills were dramatically improved by an average of 1.69- and 2.36-fold compared with that of Yufengningxin dropping pills after gavage administration, respectively. It was concluded that bioavailability of PF was greatly improved and that PF-SMEDDS dropping pills might be an encouraging strategy to enhance the oral bioavailability of PF.

Naproxen is an anti-inflammatory pharmaceutical that has been detected in natural and engineered aquatic environments. The primary aim of this research was to study chemical transformations of naproxen following chlorine oxidation, which is common in water and wastewater treatment systems. Synthetic waters containing elevated concentrations of naproxen were oxidized by free chlorine at naproxen:chlorine molar ratios of 0.02-3:1 and pH values of 5-9. The formation of naproxen products was dependent on pH, chlorine dosage and contact time. This study demonstrates that naproxen readily reacts with free chlorine and forms disinfection products. The formation of specific reaction products can vary depending on the characteristics of the water or wastewater and treatment operating conditions. More research is needed to identify intermediate and chemical reaction end products and to understand the reaction kinetics of naproxen chlorination for a range of water and wastewater treatment conditions. A secondary aim of this research was to study effects of naproxen and its chlorination products on biofilm processes, which are common in water and wastewater treatment systems and natural aquatic environments. A bioreactor was fed a naproxen solution and then fed a solution at the same naproxen concentration following contact with free chlorine. Results indicate that naproxen was not degraded biologically for the conditions of this study. In contrast, the naproxen solution containing products of chlorination caused an adverse response by discharging biomass from the bioreactor. Results therefore demonstrate that naproxen products of chlorination can adversely affect a biofilm process, which potentially can impact the performance of biofilm processes in natural and engineered aquatic environments. More research is needed to study naproxen chlorination reactions at low concentrations and in complex matrices, and to understand the toxicological relevance of naproxen and its products of chlorination in natural and engineered aquatic environments.

Endocrine disrupting compounds (EDCs), represented by steroid hormones, organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and bisphenol A have been determined in four sediment cores from the Gulf of Mexico, from New Orleans surface water (Lake Pontchartrain and Mississippi River), and from the influent and effluent of a New Orleans municipal sewage treatment plant. During the five-month monitoring of selected EDCs in the Mississippi River (MR) and Lake Pontchartrain (LP) in 2008, 21 of 29 OCPs in MR and 17 of 29 OCPs in LP were detected; bisphenol A was detected in all of the samples. Steroid hormones (estrone, 17β-estradiol and 17α-ethinylestradiol) were detected occasionally. Total EDC (OCPs + PCBs + steroid hormones + bisphenol A) concentrations in the two surface water samples were found to vary from 148 to 1112 ng L(-1). Strong correlation of the distribution of total OCPs, total PCBs and total EDCs between solid and water phases was found in LP, while moderate or no correlation existed in MR. OCPs, PCBs, steroid hormones, and bisphenol A were all detected in the ocean sediments, and total EDCs were measured in the range of 77 to 1796 ng g(-1) dry sediment weight. The EDCs were also found in untreated and treated municipal sewage samples with a removal efficiency of 83% for OCPs but no removal efficiency for 17α-ethinylestradiol.

Samples were collected from two stormwater canals and a recreational urban waterway known as Bayou St. John in New Orleans, Louisiana, USA and analyzed for a range of pharmaceuticals and personal care products (PPCPs) and endocrine disrupting chemicals (EDCs). Concentrations of 7 PPCPs and EDCs were measured by a method that provides for simultaneous extraction and quantification of the following compounds: clofibric acid, naproxen, ibuprofen, fluoxetine, clorophene, triclosan, bisphenol A. The method also was used as an indicator of the occurrence of estrogenic compounds by targeting estrone and 17beta-estradiol. The two canals (Orleans and London) are used to drain a portion of the city's stormwater directly into the Mississippi River or Lake Pontchartrain. Bayou St. John is located between the two canals and supplied with water from Lake Pontchartrain. Results from the 6-month sampling period indicated the following concentration ranges for the two stormwater canals: naproxen (ND - 145 ng/l), ibuprofen (ND - 674 ng/l), triclosan (ND - 29 ng/l) and bisphenol A (1.9-158 ng/l). Concentrations of these target analytes increased with cumulative rainfall. For bayou waters, only naproxen (2.1-4.8 ng/l) and bisphenol A (0.9-44 ng/l) were detected. Estrone was detected but determined non-quantifiable for multiple sampling events at the 3 sites. None of the other target analytes (clofibric acid, fluoxetine, clorophene, and 17beta-estradiol) were detected above their method detection levels. Results of this study demonstrate the occurrence of PPCPs and EDCs in New Orleans stormwater canals and Bayou St. John. Results also demonstrate the use of this analytical technique as an indicator of non-point source sewage contamination in New Orleans stormwater canals.