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971.
972.
Tomoki Yoneda Young Mo Sung Jong Min Lim Dongho Kim Atsuhiro Osuka 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(48):13385-13389
Reductive metalation of [44]decaphyrin with [Pd2(dba)3] provided a Hückel aromatic [46]decaphyrin PdII complex, which was readily oxidized upon treatment with DDQ to produce a Hückel antiaromatic [44]decaphyrin PdII complex. In CH2Cl2 solution the latter complex underwent slow tautomerization to a Möbius aromatic [44]decaphyrin PdII complex which exists as a mixture of conformers in dynamic equilibrium. To the best of our knowledge, these three PdII complexes represent the largest Hückel aromatic, Hückel antiaromatic, and Möbius aromatic complexes to date. 相似文献
973.
Precise characterization method of antibody‐conjugated magnetic nanoparticles for pathogen detection using stuffer‐free multiplex ligation‐dependent probe amplification
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Boram Chung Gi Won Shin Woong Choi Jinmyoung Joo Sangmin Jeon Gyoo Yeol Jung 《Electrophoresis》2014,35(23):3283-3289
Antibody‐conjugated magnetic nanoparticles (Ab‐MNPs) have potential in pathogen detection because they allow target cells to be easily separated from complex sample matrices. However, the sensitivity and specificity of pathogen capture by Ab‐MNPs generally vary according to the types of MNPs, antibodies, and sample matrices, as well as preparation methods, including immobilization. Therefore, achieving a reproducible analysis utilizing Ab‐MNPs as a pathogen detection method requires accurate characterization of Ab‐MNP capture ability and standardization of all handling processes. In this study, we used high‐resolution CE‐single strand conformational polymorphism coupled with a stuffer‐free multiplex ligation‐dependent probe amplification system to characterize Ab‐MNPs. The capture ability of Ab‐MNPs targeting Salmonella enteritidis and nine pathogens, including S. enteritidis, was analyzed in phosphate buffer and milk. The effect of storage conditions on the stability of Ab‐MNPs was also assessed. The results showed that the stuffer‐free multiplex ligation‐dependent probe amplification system has the potential to serve as a standard characterization method for Ab‐MNPs. Moreover, the precise characterization of Ab‐MNPs facilitated robust pathogen detection in various applications. 相似文献
974.
A multiplex single nucleotide polymorphism genotyping method using ligase‐based mismatch discrimination and CE‐SSCP
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Woong Choi Gi Won Shin Hee Sung Hwang Seung Pil Pack Gyu Yong Jung Gyoo Yeol Jung 《Electrophoresis》2014,35(8):1196-1203
Accuracy, simplicity, and cost‐effectiveness are the most important criteria for a genotyping method for SNPs compatible with clinical use. One method developed for SNP genotyping, ligase‐based discrimination, is considered the simplest for clinical diagnosis. However, multiplex assays using this method are limited by the detection method. Although CE has been introduced as an alternative to error prone microarray‐based detection, the design process and multiplex assay procedure are complicated because of the DNA size‐dependent separation principle. In this study, we developed a simple and accurate multiplex genotyping method using reaction condition‐optimized ligation and high‐resolution CE‐based SSCP. With this high‐resolution CE‐SSCP system, we are able to use similar‐sized probes, thereby eliminating the complex probe design step and simplifying the optimization process. We found that this method could accurately discriminate single‐base mismatches in SNPs of the tp53 gene, used as targets for multiplex detection. 相似文献
975.
Rapid and sensitive detection of lower respiratory tract infections by stuffer‐free multiplex ligation‐dependent probe amplification
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Boram Chung Gi Won Shin Chan Kwon Park Woong Choi Yeun‐Jun Chung Hyung Kyu Yoon Gyoo Yeol Jung 《Electrophoresis》2014,35(4):511-514
Lower respiratory tract infection is one of the most common infectious diseases. However, conventional methods for detecting infectious pathogens are time‐consuming, and generally have a limited impact on early therapeutic decisions. We previously reported a rapid and sensitive method for detecting such pathogens using stuffer‐free multiplex ligation‐dependent probe amplification coupled with high‐resolution CE‐SSCP. In this study, we report an application of this method to the detection of respiratory pathogens. As originally configured, this method was capable of simultaneously detecting seven bacterial species responsible for lower respiratory tract infections, but its detection limit and assay time were insufficient to provide useful information for early therapeutic decisions. To improve sensitivity and shorten assay time, we added a target‐specific preamplification step, improving the detection limit from 50 pg of genomic DNA to 500 fg. We further decreased time requirements by optimizing the hybridization step, enabling the entire assay to be completed within 7 h while maintaining the same detection limit. Taken together, these improvements enable the rapid detection of infectious doses of pathogens (i.e. a few dozen cells), establishing the strong potential of the refined method, particularly for aiding early treatment decisions. 相似文献
976.
A novel and direct cross-dehydrogenative coupling (CDC) between benzimidazoles with aldehydes promoted by di-tert-butyl peroxide (DTBP) was developed. The reactions generated the corresponding N-acylbenzimidazoles in good yields under metal-free conditions. This method has broad substrate scope and high efficiency. 相似文献
977.
Nickel(I) complexes were generated in situ from Ni (PPh3)2Cl2 using activated iron and the complexes combined with N,N′-bis(4-fluorobenzylidene) ethane-1,2-diamine (BFBED) were then used as a catalyst for the 1,4-addition reaction of arylboronic acids to α,β-unsaturated substrates. The reaction proceeded to completion and did not require the addition of a base but the addition of potassium iodide is crucial to this cross-coupling reaction. Moreover, experimental observations suggested a possible Ni(I)–Ni(III) catalytic cycle mechanism. 相似文献
978.
Jung-Hoon Choi In-Hak Cho Hee-Chul Eun Hwan-Seo Park Yung-Zun Cho Ki-Rak Lee Geun-Il Park Song-Hyun Kim Chang-Ho Shin Jong-Kyung Kim 《Journal of Radioanalytical and Nuclear Chemistry》2014,299(3):1731-1738
The pyrochemical process, which uses a dry method to recycle used nuclear fuel generates waste LiCl–KCl salt containing radioactive lanthanide elements. To reuse LiCl–KCl salt, the lanthanide elements are separated through a precipitation method promoted by oxygen sparging and the separated fission product of lanthanide oxide should be fabricated into durable wasteforms sustainable for several 1,000 years to store in a final geological repository. Herein, we report the fabrication of a borosilicate glass based wasteform with a glass matrix of SiO2–Al2O3–B2O3 having a high waste loading of 50 wt% lanthanide oxide. Th physical properties of four kinds of wasteforms having a different lanthanide oxide waste composition were evaluated. To investigate the long-term physical stability of each sample having 50 wt% lanthanide oxide waste loading, time–temperature–transformation (TTT) test was conducted at 500 and 700 °C for 60 and 180 h, and the physical properties were evaluated after each TTT test. 相似文献
979.
采用共沉淀法制备了NiFe2O4和NiFe2O4/ZrO2催化剂,用TGA考察了其热化学法,CO2高温分解反应性能。通过对反应前后催化剂的表征发现,反应高温使两种催化剂都发生了明显的烧结,导致在热还原反应中形成的还原态氧化物不能完全被CO2氧化从而降低了催化剂的反应性能;ZrO2的加入对于提高催化剂的热稳定性以及循环反应稳定性具有重要的作用。在高温反应炉中考察了NiFe2O4/ZrO2的CO2分解实验,结果表明,提高热还原温度可以提高CO产量,然而,随着循环次数的增加CO的产量降低得更明显。 相似文献
980.
Simultaneous determination of nine lignans from Schisandra chinensis extract using ultra‐performance liquid chromatography with tandem mass spectrometry in rat plasma,urine, and gastrointestinal tract samples: Application to the pharmacokinetic study of Schisandra chinensis
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You‐Jin Kim Hee Ju Lee Chul Young Kim Sun‐Young Han Young‐Won Chin Young Hee Choi 《Journal of separation science》2014,37(20):2851-2863
The fruit of Schisandra chinensis is a well‐known herbal medicine and dietary supplement due to a variety of biological activities including antihepatotoxic and antihyperlipidemic activities. However, the simultaneous validation methodology and pharmacokinetic investigation of nine lignans of S. chinensis extract in biological samples have not been proved yet. Thus, the present study was undertaken to develop the proper sample preparation method and simultaneous analytical method of schisandrol A, gomisin J, schisandrol B, tigloylgomisin H, angeloylgomisin H, schisandrin A, schisandrin B, gomisin N, and schisandrin C in the hexane‐soluble extract of S. chinensis to apply for the pharmacokinetic study in rats. All intra‐ and interprecisions of nine lignans were below 13.7% and accuracies were 85.1–115% and it is enough to evaluate the pharmacokinetic parameters after both intravenous and oral administration of hexane‐soluble extract of S. chinensis to rats. 相似文献