光敏抗菌剂及其在纺织材料上的应用研究进展

光敏抗菌剂是一种光敏分子,在日光和UVA的照射下吸收能量而激发,生成对生物物种产生氧化损伤的活性氧。将光敏抗菌剂负载在纺织材料上使其在日光或紫外光的照射下具有抗菌特性,是近年来抗菌材料的研究热点。光敏抗菌剂主要包括卟啉类、杂蒽类、噻吩类、天然光敏剂、无机纳米光敏抗菌剂等,其在纺织品上的应用方法也有多种,包括涂层法、化学改性法、静电吸附法、静电纺丝法等。因此,本文对几种光敏抗菌剂的化学结构、光反应效率、抗菌机理、在纺织材料上的应用研究及负载到纺织材料上后所出现的问题进行综述,并对未来智能光敏抗菌纺织材料的研发重点进行展望。

QUANTIFICATION OF P4HA2 mRNA OF FIBROBLASTS WITH SYBR GREEN BASED RT-PCR FOR CORRECTING CMV INACTIVATION EFFICIENCY IN DONOR BLOOD

Objective To quantify proline 4-hydroxylase, alpha polypeptide ii （ P4HA2 ） mRNA of human embryo lung fibroblast （HELF） with SYBR green based reversed transcript PCR （RT-PCR） for correcting cytomegalovirus （CMV） inactivation or clearance efficiency in donor blood. Methods A pair of specific primers of exon 12a of P4HA2 was designed, and the related PCR-reaction system and condition were optimized. Then the recombinant plasmid containing the target fragment was constructed for making standard curve with SYBR green based real-time RT-PCR. Finally, the sensitivity, reproducibility, and specificity of this method were fully estimated. Results The sensitivity of the method was 1.5E ＋ 04 copies/mL of P4HA2 mRNA, corresponding to 10^3 fibroblasts. In addition, existence of 8. 67E ＋ 06 leukocytes could not interfere with the accurate quantification of HELF in the large dynamic range. The intra-assay variability and inter-assay variability both varied in different concentrations, being higher in low concentrations and lower in high concentrations. But all of them were below 13. 76% in variation, which showed acceptable stability of this method. Conclusion SYBR green and specific primer based real-time RT-PCR show up a good quality for quantifying HELF P4HA2 mRNA with good specificity, stability, and high sensitivity. Approximate 10 copies of P4HA2 mRNA per cell in average can be detected by the method. Therefore, this method can be used to deduct fibroblast-associated CMV for correcting CMV inactivation efficiency in leukocytes.

Rutile TiO2 Microspheres with Exposed Nano-Acicular Single Crystals for Dye-Sensitized Solar Cells

Uniquely structured rutile TiO2 microspheres with exposed nano-acicular single crystals have been successfully synthesized via a facile hydrothermal method. After calcination at 450 ℃ for 2 h, the futile TiO2 microspheres with a high surface area of 132 m2/g have been utilized as a light harvesting enhancement material for dye-sensitized solar cells （DSSCs）. The resultant DSSCs exhibit an overall light conversion efficiency of 8.41% for TiO2 photoanodes made of futile TiO2 microspheres and anatase TiO, nanoparticles （mass ratio of 1：1）, significantly higher than that of pure anatase TiO2 nanoparticle photoanodes of similar thickness （6.74%）. Such a significant improvement in performance can be attributed to the enhanced light harvesting capability and synergetic electron transfer effect. This is because the photoanodes made of futile TiO2 microsphere possess high refractive index which improves the light utilisation efficiency, suitable microsphere core sizes （450-800 nm） to effectively scatter visible light, high surface area for dye loading, and synergetic electron transfer effects between nanoparticulate anatase and nano-acicular futile single crystals phases giving high electron collection efficiency.

In situ FT-IR investigation on the reaction mechanism of visible light photocatalytic NO oxidation with defective g-C_3N_4

The g-C_3N_4 with different structures was prepared by heat treatment using urea(CN-U) and thiourea(CN-T) as precursors under the same conditions. The microstructure and optical properties of the photocatalyst were analyzed with advanced tools. The results showed that the CN-U has a porous structure, a high specific surface area and a wide band gap in comparison with CN-T. The in situ FT-IR technique was used to monitor the adsorption and reaction process of visible photocatalytic NO oxidation on g-C_3N_4. The corresponding reaction mechanism was proposed based on the results of reaction intermediate observation and electron paramagnetic resonance(EPR) radical scavenging. It was revealed that(1) the presence of defective sites favored the adsorption of gas molecules and electronically compensated it leading to promoted formation of the final products;(2) the high separation efficiency of photogenerated electron-hole pairs enhanced the production of radicals during the photocatalytic reaction;(3) the hydroxyl radicals(-OH) are not selective for the decomposition of pollutants, which are favorable to the complete oxidation of the reaction intermediates. The above three aspects are the main reasons for the CN-U possessing the efficient visible light photocatalytic activity. The present work could provide new insights and methods for understanding the mechanism of photocatalysis.