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- 저자 : Briseno, Alejandro L. (검색결과 4 건)
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Alba Rita Valenzuela-Briseno,Jeanette Guadalupe Arredondo-D,Antonio Rascon-Careaga,Humberto stiazaran-Garcia,Agustin Gomez-Alvarez,Reynaldo Esquivel-Gonzalez,Roberto Carlos Carrillo-Torres,Enrique Alv 환경독성보건학회 2022 환경독성보건학회지 Vol.37 No.4
This study aimed to evaluate whether aluminum chloride (AlCl₃) causes hematological changes in the peripheral blood of Sprague–Dawley (SD) rats. Five groups of female SD rats were intragastrically administered with 4 different concentrations of AlCl₃ for 5 days a week for a total of 90 days. The aluminum concentration was determined via graphite furnace atomic absorption spectroscopy. Analysis of serum iron-kinetic profiles, blood cytometry outcomes, and blood smears of the blood samples. Scanning electron microscopy (SEM) and Raman spectroscopy were used to search for structural and ultrastructural changes, respectively. Blood aluminum concentration ranged 12.38-16.24 μg/L with no significant difference between experimental treatments. At the AlCl₃ concentration of 40 mg Al/kg bw of rats/day, the mean ferritin value in the serum iron kinetic profile was 29.81±6.1 ng/mL, and this value showed a significant difference between experimental treatments. Blood cytometry revealed that there were 6.45-7.11×10<SUP>6</SUP> cells/μL erythrocytes, 8.91-9.32×10³ cells/μL leukocytes, and 477.2-736.3×10³ cells/μL platelets along with a hemoglobin of 37.38-41.93 g/dL and hematocrit level of 37.38-41.93%; the experimental treatments showed no significant differences. Erythrocyte structural analysis using SEM showed no differences between experimental treatments, whereas ultrastructural evaluation using Raman spectroscopy made it possible to identify the following bands: 741, 1123, 1350, 1578, and 1618 cm<SUP>−1</SUP>, which were respectively associated with the following vibrational modes and compounds: vibration of the tryptophan ring, asymmetric C-O-C stretching of glucose, C-H curve of tryptophan, C=C stretching of the heme group, and C-N stretching of the heme group, with no significant differences between experimental treatments. Therefore, AlCl₃ administration does not induce ultrastructural changes in the erythrocyte membrane. This study revealed that serum ferritin concentration was the only parameter affected by AlCl₃ exposure at 40 mg of Al/kg bw of rats/day.
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Water Processable Polythiophene Nanowires by Photo-Cross-Linking and Click-Functionalization
Kim, Hyeong Jun,Skinner, Matthew,Yu, Hojeong,Oh, Joon Hak,Briseno, Alejandro L.,Emrick, Todd,Kim, Bumjoon J.,Hayward, Ryan C. American Chemical Society 2015 NANO LETTERS Vol.15 No.9
<P>Replacing or minimizing the use of halogenated organic solvents in the processing and manufacturing of conjugated polymer-based organic electronics has emerged as an important issue due to concerns regarding toxicity, environmental impact, and high cost. To date, however, the processing of well-ordered conjugated polymer nanostructures has been difficult to achieve using environmentally benign solvents. In this work, we report the development of water and alcohol processable nanowires (NWs) with well-defined crystalline nanostructure based on the solution assembly of azide functionalized poly(3-hexylthiophene) (P3HT-azide) and subsequent photo-cross-linking and functionalization of these NWs. The solution-assembled P3HT-azide NWs were successfully cross-linked by exposure to UV light, yielding good thermal and chemical stability. Residual azide units on the photo-cross-linked NWs were then functionalized with alkyne terminated polyethylene glycol (PEG–alkyne) using copper catalyzed azide–alkyne cycloaddition chemistry. PEG functionalization of the cross-linked P3HT-azide NWs allowed for stable dispersion in alcohols and water, while maintaining well-ordered NW structures with electronic properties suitable for the fabrication of organic field effect transistors (OFETs).</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/nalefd/2015/nalefd.2015.15.issue-9/acs.nanolett.5b01185/production/images/medium/nl-2015-01185b_0006.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/nl5b01185'>ACS Electronic Supporting Info</A></P>
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Choi, Hyun Ho,Najafov, Hikmet,Kharlamov, Nikolai,Kuznetsov, Denis V.,Didenko, Sergei I.,Cho, Kilwon,Briseno, Alejandro L.,Podzorov, Vitaly American Chemical Society 2017 ACS APPLIED MATERIALS & INTERFACES Vol.9 No.39
<P>Photoinduced charge transfer between semiconductors and gate dielectrics can occur in organic field-effect transistors (OFETs) operating under illumination, leading to a pronounced bias-stress effect in devices that are normally stable while operating in the dark. Here, we report an observation of a'polarization-dependent photoinduced bias-stress effect in two' prototypical single-crystal OFETs, based on rubrene and tetraphenylbis(indolo{l,2-alpha})quinolin. We find that the decay rate of the source-drain current in these OFETs under, illumination is a periodic function of the polarization angle of incident photoexcitation with respect to the crystal axes, with a periodicity of n. The angular positions of maxima and minima of the bias-stress rate match those of the optical absorption coefficient of the corresponding crystals. The analysis of the effect shows that it stems from a charge transfer of 'hot' holes, photogenerated in the crystal within a very short thermafization length (MLT mu m) from the semiconductor-dielectric interface. The observed phenomenon is a type of intrinsic structure-property relationship, revealing how molecular packing affects parameter drift in organic transistors under illumination. We also demonstrate that a photoinduced charge transfer in OFETs can be used for recording rewritable accumulation channels with an optically defined geometry and resolution, which can be used in a number of potential applications.</P>
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