Magnetic resonance imaging and risk factors for progression of lacunar infarct lesions in Chinese patients

Neuroradiology - The proportion of acute symptomatic lacunar infarction lesions that undergo cavitation and the factors influencing cavity formation are yet unclear, particularly in the Chinese...     

江苏省乳腺X射线摄影频度调查及乳腺癌风险评估

目的 调查估算江苏省乳腺X射线摄影的频度,进而估算乳腺摄影对江苏省女性人口的剂量负担,并评估乳腺摄影对江苏省各年龄组女性人口诱发乳腺癌的风险。方法 采用分层随机抽样调查的方法,通过调查30台乳腺摄影设备年检查人数和受检者年龄分布,估算全省乳腺摄影的频度,并计算乳腺摄影对女性人口的剂量负担。使用美国科学院电离辐射生物效应报告BEIR-Ⅶ中的超额归因风险（EAR）模型估算乳腺摄影检查对3个年龄组诱发乳腺癌的风险。结果 江苏省乳腺摄影检查的频度为3.77次/千人口;乳腺摄影对江苏省女性人口剂量负担为0.02 mGy/人。每次乳腺摄影检查对0~15岁组、16~40岁和>40岁3个年龄组的乳腺癌终生归因风险（LAR）分别为138/10万人、14.7/10万人和1.0/10万人。结论 乳腺摄影对人群乳腺癌诱发风险较小,但低年龄组的风险较大,提示针对低年龄乳腺摄影检查仍应慎重。     

Effects of acid and phosphate on arsenic solidification in a phosphogypsum-based cement backfill process

Phosphogypsum (PG) produced during phosphoric acid production contains significant amounts of arsenic and can potentially cause adverse environmental and health effects. Cement backfill technology is an effective management technique that is used to store PG to prevent such problems. The goal of this paper is to study the influencing factors and mechanism of arsenic stabilization in a PG-based cement backfill process. First, a leaching toxicity test was conducted, which showed that the arsenic concentration in PG batches ranged from 129.1 μg L⁻¹ to 407.1 μg L⁻¹, which were all far above the standard limit (10 μg L⁻¹) set by GB/T 14848-93. In addition, the arsenic content was higher in samples with larger PG particles. Secondly, hydrogen and phosphate ions were added to the backfill to investigate how they influenced arsenic solidification, and the results indicated that phosphate ions, rather than hydrogen ions, delayed the arsenic solidification process. This suggests that controlling the soluble phosphate in PG will help reduce arsenic pollution during backfilling. A toxicity leaching test was carried out after backfill samples were cured for 28 d. All arsenic concentrations were below the standard limit, indicating that the cement backfill technology ensured the long-term solidification and stabilization of arsenic.

Phosphogypsum (PG) produced during phosphoric acid production contains significant amounts of arsenic and can potentially cause adverse environmental and health effects.     

Simple,rapid, sensitive,selective and label-free lincomycin detection by using HAuCl4 and NaOH

A simple, rapid, sensitive, selective and label-free method is presented for the colorimetric determination of lincomycin (Lin) by using HAuCl₄ and NaOH. Upon the addition of Lin, the mixture of HAuCl₄ and NaOH shows a color change from colorless to blue (or dark blue). The limit of colorimetric detection is as low as 1 μM, observed both in Milli-Q water and real samples. The selectivity of Lin detection is excellent compared with 9 other common antibiotics. On the basis of the “three-color” principle of Thomas Young, we extracted the red, green and blue (RGB) alterations of the sensor in the absence and presence of different concentrations of Lin. The color changes are quantitatively illustrated by the total Euclidean distances (EDs = [ΔR² + ΔG² + ΔB²]^1/2). The good linear relationship between the EDs and Lin concentration is used for the quantitative assay of Lin. The developed method demonstrates great potential for the detection of Lin in environmental water and milk.

A simple, rapid, sensitive, selective and label-free method is presented for the colorimetric determination of lincomycin (Lin) by using HAuCl₄ and NaOH.     

LncRNA NEXN-AS1 attenuates proliferation and migration of vascular smooth muscle cells through sponging miR-33a/b

Non-protein-coding RNAs (lncRNAs) are emerging as important regulators in disease pathogenesis, including atherosclerosis (AS). Here, we investigated the role and underlying mechanisms of nexilin F-actin binding protein antisense RNA 1 (NEXN-AS1) on the proliferation and migration of vascular smooth muscle cells (VSMCs). Our data revealed that ox-LDL treatment resulted in decreased NEXN-AS1 expression and increased miR-33a/b levels in human aorta VSMCs (HA-VSMCs) in dose- and time-dependent manners. Overexpression of NEXN-AS1 mitigated the proliferation and migration of HA-VSMCs under ox-LDL stimulation using CCK-8 and wound-healing assays. Moreover, dual-luciferase reporter and RNA immunoprecipitation assays verified that NEXN-AS1 acted as molecular sponges of miR-33a and miR-33b in HA-VSMCs. MiR-33a or miR-33b silencing attenuated the proliferation and migration of ox-LDL-treated HA-VSMCs. Furthermore, miR-33a or miR-33b mediated the inhibitory effects of NEXN-AS1 overexpression on the proliferation and migration of ox-LDL-treated HA-VSMCs. Our study suggested that high level of NEXN-AS1 mitigated VSMC proliferation and migration under ox-LDL stimulation at least partly through sponging miR-33a and miR-33b, illuminating NEXN-AS1 as a novel therapeutic approach for AS treatment.

Non-protein-coding RNAs (lncRNAs) are emerging as important regulators in disease pathogenesis, including atherosclerosis (AS).     

Microporous organic hydroxyl-functionalized polybenzotriazole for encouraging CO2 capture and separation

We report a mild, hydroxyl functionalized and thermal stable benzotriazole-based aerogel (HO-PBTA), which is inspired by phenolic resin chemistry. Taking advantage of the synergistic adsorption interactions between hydroxy-benzotriazole and CO₂, and the phobic effect between benzotriazole and nitrogen (N₂), the CO₂ uptake capacity of the HO-PBTA reaches an encouraging level (6.41 mmol g⁻¹ at 1.0 bar and 273 K) with high selectivity (CO₂/N₂ = 76 at 273 K).

We report a mild, hydroxyl functionalized and thermal stable benzotriazole-based aerogel (HO-PBTA), which is inspired by phenolic resin chemistry.

Nowadays, global warming caused by increased concentrations of carbon dioxide (CO₂) in the atmosphere is one of the most serious environmental problems.^1–3 The development of novel functional materials and new technologies for CO₂ capture and storage has gained great attention. Microporous organic polymers (MOPs) with intrinsic properties including large specific surface area, narrow pore size distribution, good chemical stability, and low skeleton density have exhibited potential applications in gas storage and separation.^4–7 In addition, microporous porous materials with excellent intrinsic properties also made significant breakthroughs in liquid separation.^8,9 The structure and CO₂ adsorption of the MOPs have complicated relationships. Therefore, the design of high performance CO₂ capture materials often involves sophisticated molecular design and careful adjustments of the ingredient ratio. It has been shown that the incorporation of N-containing groups into the pore wall of MOPs has a profound impact on both CO₂ uptake and selectivity by enhancing their physisorption interactions,^10–15 however, it still remains a great challenge to make a facile synthesis of functional MOP materials that capture CO₂ efficiently and selectively.In the application of CO₂ capture, the nitrogen-containing MOPs act as capable storage media due to physisorption that involves an electron donor–acceptor mechanism between a heteroatom nitrogen and CO₂ on the inner surface of the networks.^16–18 The first principles study indicated that nitrogen-containing heteroaromatic groups can form strong physical interactions with CO₂via “dispersive π–π stacking” and electrostatic “in-plane” mechanisms.¹⁹ This theoretical calculation guides us how to design the functional materials that capture CO₂ efficiently and selectively. In previous work, we described a new strategy for CO₂ capture based on the synergistic effect of electrostatic in-plane and dispersive π–π stacking interactions of two functional groups with CO₂, and the proposed synergistic effect can be considered as a new rationale for the design and fabrication of CO₂ capture materials.²⁰ In addition, it has been demonstrated that azo-functionalized MOPs exhibit the N₂ phobicity due to the entropic loss of N₂ gas molecules upon binding, which endows the networks with the unprecedented CO₂ selectivity.²¹ Inspired by these reported studies, we hypothesized that both the CO₂ adsorption capacity and CO₂/N₂ selectivity can be improved greatly by involving multiple, more than two, functional groups in MOP networks where multiple mechanisms work for CO₂ capture and separation. In this work, the synergistic adsorption interactions between the HO-PBTA polymer and CO₂ molecules, the N₂-phobic effect between the HO-PBTA polymer and N₂ have been investigated in details. It is expected that the comprehensive effects of the CO₂-philic and N₂-phobic behaviors will provide new design principles for the development of next-generation functional porous polymers with high CO₂ adsorption capacity and selectivity.To achieve this objective, a benzotriazole-based microporous aerogel (HO-PBTA), with azo, hydroxyl and imino groups in the polymer chains, was fabricated via sol–gel technology involving phenolic resin-inspired chemistry^22–24 and followed by CO₂ supercritical drying (Fig. 1A). The material preparation and characterization are detailed in the ESI.^† The as-prepared HO-PBTA is a dark gray, porous ultralight material, as shown in Fig. 1B. HO-PBTA aerogel was characterized by Fourier transform infrared and ¹³C CP/MAS NMR, and the results were in good agreement with the proposed structures (Fig. 2). The FTIR spectrum of the HO-PBTA is shown in Fig. 2a, in which the absorption peaks at about 3190 cm⁻¹ and 3402 cm⁻¹ correspond to the structure of NH and the OH groups. The peak at 1618 cm⁻¹ is attributed to the vibration of the aromatic ring skeleton. And the absorption at 1536 cm⁻¹ corresponds to the structure of C N in the network. As shown in Fig. 2B, the broad peaks at 150–110 ppm are ascribed to the benzotriazole group carbons, and the peaks at 75–25 ppm corresponds to methylene carbons.Open in a separate windowFig. 1Synthesis of HO-PBTA aerogel. (A) Dark gray aerogel of HO-PBTA was obtained by reacting 4-hydroxy-1H-benzotriazole with formaldehyde, in water at 80 °C in the presence of potassium hydroxide under air conditions; (B) the photograph of the HO-PBTA aerogel.Open in a separate windowFig. 2Chemical structure characterization of the HO-PBTA polymer material. (A) FTIR spectrum, recorded as KBr pellet; (B) ¹³C CP/MAS NMR spectrum.The porosity of the HO-PBTA aerogel was quantified by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and sorption analysis. A SEM image shows that the HO-PBTA aerogel consists of aggregated particles with submicrometer sizes (Fig. 3A). The TEM image (Fig. 3B) reveals the micropore structure, which is an essential requirement for CO₂ capture. The porosity of aerogel was further quantified by sorption analysis using nitrogen (N₂) as the sorbate molecule, and the HO-PBTA aerogel is microporous and exhibits a combination of type I and II N₂ sorption isotherms according to the IUPAC classification (Fig. 4A).²⁵ The increase in the nitrogen sorption at a high relative pressure above 0.9 may arise in part from interparticulate porosity associated with the meso- and macrostructures of the samples and interparticular void.²⁶ According to ref. 27, the specific surface areas calculated in the relative pressure (P/P₀) range from 0.01 to 0.1 shows that the Brunauer–Emmett–Teller (BET) specific surface area of HO-PBTA is up to 2160 m² g⁻¹ (Fig. S3^†). The pore size distribution (PSD) of the network calculated from the adsorption branch of the isotherms with the nonlocal density functional theory (NLDFT) approach indicates that HO-PBTA aerogel exhibits a dominant pore diameter centered at about 0.60 nm (inset in Fig. 4A). Thermal property of HO-PBTA aerogel was evaluated via thermogravimetric analysis (TGA) in nitrogen and air conditions, and the typical TGA curves are shown in Fig. S4.^† HO-PBTA exhibits great thermal stability with high decomposition temperature (T_d, 5% = ∼500 °C) at N₂ atmosphere. The TGA curve indicated that the HO-PBTA aerogel still exhibited good thermal stability at air condition.Open in a separate windowFig. 3Microstructural characterization of HO-PBTA aerogel. (A) Scanning electron microscopy (SEM) image of HO-PBTA aerogel; (B) transmission electron microscopy (TEM) image of HO-PBTA aerogel.Open in a separate windowFig. 4(A) Nitrogen adsorption–desorption isotherms and the pore size distribution calculated by the nonlocal density functional theory (inset) of HO-PBTA aerogel. (B) Gas adsorption isotherms of HO-PBTA aerogel at 273 K.The CO₂ adsorption capacity and selectivity (CO₂/N₂) in HO-PBTA aerogel were evaluated by adsorption isotherm measurements. As shown in Fig. 4B, the CO₂ capture exhibits an increase with the increasing of the pressure. The CO₂ adsorption capacity of the HO-PBTA aerogel is as high as 6.41 mmol g⁻¹ at 1.0 bar and 273 K, while the adsorption capacity of N₂ is only 0.09 mmol g⁻¹ at the same conditions (inset in Fig. 4B). The CO₂ adsorption capacity of the HO-PBTA aerogel is up to 2.3 mmol g⁻¹ at 1 bar and 323 K, and 0.02 mmol g⁻¹ for N₂ at the same conditions (Fig. S5^†). Equilibrium CO₂ adsorption capacity is found to decrease with an increase in temperature due to the exothermic nature of the adsorption process, as expected for physical adsorbents. We found that the CO₂ adsorption capacity of the HO-PBTA aerogel is higher than most of the CO₂ capture MOP materials, and close to some of the MOF materials (Table S1^†).^28–30 This high affinity is a consequence of the favourable interactions of the polarizable CO₂ molecules through multiple adsorption interactions with the framework, and also the inherent microporosity of HO-PBTA aerogel. Additionally, HO-PBTA aerogel also has great CO₂ adsorption capacities and selectivities at 298 and 323 K (Fig. S5^†), and these values are still comparable to the high surface area MOP networks.^31–33For the further CO₂ adsorption, CO₂ was also adsorbed preferentially over N₂ at high temperatures. The selectivities were calculated using the Ideal Adsorbed Solution Theory (IAST) for CO₂/N₂ mixture in the ratio of 0.15 : 0.85. At 1 bar, the IAST CO₂/N₂ selectivities of the HO-PBTA were 76 at 273 K, 97 at 298 K and become 110 at 323 K, which close to the highest one reported to date under the same conditions. Additionally, the HO-PBTA aerogel have the high selectivity of CO₂/N₂ at high temperature than other porous materials (Table S2^†). It is worth noting that the CO₂/N₂ selectivities increased with the temperature increasing, which are essential requirements for high temperature post-combustion CO₂ adsorption. N₂ uptake drops ∼70% at a temperature increase from 273 to 298 K, compared with a ∼60% drop for CO₂. This phenomenon is in line with the conventional CO₂ affinity and the concept of N₂ phobic in nitrogen-rich porous polymers where nitrogen-rich groups (–N N–) will reject N₂ gas selectively.²¹ To further akin to capture from post-combustion gas streams, CO₂ adsorption capacity of HO-PBTA aerogel at higher temperature have been characterized (Fig. S6^†). The HO-PBTA shown the good CO₂ adsorption capacity of 1.8 mmol g⁻¹ at 333 K and 1.5 mmol g⁻¹ 343 K. The N₂ uptakes of HO-PBTA aerogel under the same conditions were 0.016 mmol g⁻¹ and 0.015 mmol g⁻¹, resulting in selectivity of 112 and 101, respectively.The isosteric heat of adsorption (Q_st) for HO-PBTA aerogel was calculated using the virial equations.³⁴ As shown in Fig. S7,^† HO-PBTA has a Q_st value of 33.9 kJ mol⁻¹, and this value can be considered as the optimum for gas adsorption and separation because of a balance between the reversibility and selectivity. The Q_st values is highest among reported values for organic porous polymers and comparable to some MOFs compounds.^21,35,36 The impressive Q_st of 33.9 kJ mol⁻¹ further indicates the strong interaction of HO-PBTA polymers with CO₂ guest molecules. It should be noted that the higher and more optimized Q_st value of the HO-PBTA aerogel can be ascribed to the synergistic effect of azo (–N N–), hydroxyl (–OH) and imino (–NH) units arising from different interaction mechanisms.To illustrate the synergistic adsorption mechanism, we used density functional theory (DFT)^{19,20,37–39} to investigate the interaction of HO-PBTA with CO₂ and to track the CO₂ capture process. The calculation is detailed in the ESI. Fig. 5 shows a series of snapshots for CO₂ capture by 4-hydroxybenzotriazole, as the model compound, where benzotriazole and hydroxyl work synergistically to adsorb multiple CO₂ molecules. The minimum energy structure of the CO₂–azo complex is obtained when CO₂ lies on the azo at a bond distance of 3.06 Å to form the π–π stacking conformation (Fig. 5B). The electrostatic “in-plane” equilibrium conformation of CO₂–HO-PBTA involves two sites: one is the electron deficient central carbon atom of CO₂ to the lone pair of electrons on a nitrogen atom of azo group via dipole–quadrupole interaction; the other is lone pairs of oxygen on CO₂ to a hydrogen atom on the imino group (or a hydrogen atom on the hydroxyl) via hydrogen bonding (Fig. 5C and F). Either dipole–quadrupole interaction or hydrogen bonding cannot stabilize the CO₂–HO-PBTA complex because of their low binding energies.¹⁹ However, previous works and our calculation indicated that simultaneous formation of dipole–quadrupole interaction and hydrogen bonding at both sites cause a much more stable in-plane conformation of CO₂–HO-PBTA complex (Fig. S8^†).^19,20 However, the capture of flowing CO₂ by electrostatic “in-plane” interactions is difficult due to a small binding area by only two atomistic sites. On the other hand, CO₂ can be rapidly adsorbed on the azo group because of its relatively large binding area (Fig. 5A). To our knowledge, the desorption occurs frequently driven by thermal fluctuation. Once CO₂ desorption, the starting speed should be much slower than the bulk speed, resulting in a high probability to be captured by an adjacent hydroxyl and imino groups. The in-plane conformation of CO₂–HO-PBTA complex is, therefore, formed much easily and efficiently with help of the functional azo while retaining the high selectivity of CO₂ over other gas molecules (Fig. 5H). Final coordinates of DFT geometry optimization was shown in Table S3.^†Open in a separate windowFig. 5DFT results to track the full CO₂ capture process. (A) A CO₂ molecule is adsorbed on the face of an electron-rich azo group via the dispersive π–π stacking interaction. (B and C) The desorbed CO₂ molecule can be captured by an adjacent hydroxyl, a stable “electrostatic in-plane” conformation including dipole–quadrupole and hydrogen bond interactions is formed. (D) The second CO₂ molecule comes close to the azo group, (E) and the CO₂ molecule is adsorbed on the azo group. (F) The desorbed CO₂ molecule can be captured by an adjacent imino group. (G) The third CO₂ molecule comes close to the azo group, (H) and the CO₂ molecule is adsorbed on the azo group. The gray, white, blue and red spheres represent C, H, N, and O atoms, respectively.     

醋酸钠林格注射液应用于新生儿腹腔镜手术中补液对血糖及电解质酸碱平衡的影响

目的：探讨醋酸钠林格注射液在新生儿腹腔镜手术中的应用价值。方法：选择ASA分级Ⅰ~Ⅱ级择期行腹腔镜手术的新生儿60例,采用随机数表法分为观察组和对照组各30例,均采用静脉吸入复合全身麻醉,术中分别输注醋酸钠林格注射液和钠钾镁钙葡萄糖注射液补液。于术前和手术结束测定动脉血气分析指标,观察患儿血糖、乳酸、电解质及酸碱平衡的变化。结果：观察组患儿补液前后血糖水平无明显变化（P>0.05）,且术后血糖升高幅度小于对照组（P<0.05）。两组患儿的血pH值、BE值、电解质水平比较差异均无统计学意义（P均>0.05）。结论：和钠钾镁钙葡萄糖注射液相比,醋酸钠林格注射液能够更好地维持新生儿腹腔镜手术围术期的血糖水平,可作为新生儿腹腔镜手术中安全、有效的补液选择。