scholarly journals Non-invasive analysis of stored red blood cells using diffuse resonance Raman spectroscopy

The Analyst ◽  
2018 ◽  
Vol 143 (24) ◽  
pp. 5950-5958 ◽  
Author(s):  
Rekha Gautam ◽  
Joo-Yeun Oh ◽  
Rakesh P. Patel ◽  
Richard A. Dluhy

A method to acquire the Raman spectra of sub-surface components using diffusely focused radiation in a microscope sampling configuration is described.

The Analyst ◽  
2016 ◽  
Vol 141 (21) ◽  
pp. 6104-6115 ◽  
Author(s):  
Di Yan ◽  
Christian Domes ◽  
Robert Domes ◽  
Timea Frosch ◽  
Jürgen Popp ◽  
...  

Fiber enhanced resonance Raman spectroscopy (FERS) is introduced for chemically selective and ultrasensitive analysis of the biomolecules hematin, hemoglobin, biliverdin, and bilirubin, as well as intact red blood cells.


2006 ◽  
Vol 387 (5) ◽  
pp. 1691-1703 ◽  
Author(s):  
Bayden R. Wood ◽  
Peter Caspers ◽  
Gerwin J. Puppels ◽  
Shveta Pandiancherri ◽  
Don McNaughton

2012 ◽  
Vol 04 (10) ◽  
pp. 792-796
Author(s):  
J. Vijayasekhar ◽  
Srinivasa Rao Karumuri ◽  
Uma Maheswara Rao Velagapudi

1999 ◽  
Vol 19 (1-4) ◽  
pp. 71-74 ◽  
Author(s):  
Xuming Zheng ◽  
David Lee Phillips

We have obtained A-band absorption resonance Raman spectra of 1-chloro-2- iodoethane in cyclohexane solution. We have done preliminary time-dependent wavepacket calculations to simulate the resonance Raman intensities and absorption spectrum in order to learn more about the short-time photodissociation dynamics. We compare our preliminary results for 1-chloro-2-iodoethane with previous resonance Raman results for iodoethane and find that there appears to be more motion along non- C—I stretch modes for 1-chloro-2-iodoethane than for iodoethane. This is consistent with results of TOF photofragment spectroscopy experiments which indicate much more internal excitation of the photoproducts from 1-chloro-2-iodoethane photodissociation than the photoproducts from iodoethane photodissociation.


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Anneli Ehlerding ◽  
Ida Johansson ◽  
Sara Wallin ◽  
Henric Östmark

Resonance-enhanced Raman spectroscopy has been used to perform standoff measurements on nitromethane (NM), 2,4-DNT, and 2,4,6-TNT in vapor phase. The Raman cross sections for NM, DNT, and TNT in vapor phase have been measured in the wavelength range 210–300 nm under laboratory conditions, in order to estimate how large resonance enhancement factors can be achieved for these explosives. The results show that the signal is enhanced up to 250,000 times for 2,4-DNT and up to 60,000 times for 2,4,6-TNT compared to the nonresonant signal at 532 nm. Realistic outdoor measurements on NM in vapor phase at 13 m distance were also performed, which indicate a potential for resonance Raman spectroscopy as a standoff technique for detection of vapor phase explosives. In addition, the Raman spectra of acetone, ethanol, and methanol were measured at the same wavelengths, and their influence on the spectrum from NM was investigated.


Clay Minerals ◽  
1988 ◽  
Vol 23 (1) ◽  
pp. 1-12 ◽  
Author(s):  
Y. Soma ◽  
M. Soma

AbstractResonance Raman spectroscopy has been used to observe the formation of cation radicals in the adsorption of N,N,N',N'-tetramethylbenzidine (TMBD), benzidine, N,Ndimethylaniline (DMA) and aniline on Na-, Cu- and Fe-montmorillonites. Cation radicals of benzidine and TMBD, and their dications were formed at acid sites on the montmorillonite surface, or through the reduction of Cu or Fe interlayer ions, and were adsorbed in the interlayer. Their structures are represented by biphenoquinone type structure, where the inter-ring CC bond and the ring C-N bond have double bond characters. It was demonstrated from Raman spectra that DMA and aniline adsorbed on Cu-montmorillonite from the vapour phase dimerize to form TMBD and benzidine dications.


Transfusion ◽  
2021 ◽  
Author(s):  
Martha Z. Vardaki ◽  
Hans Georg Schulze ◽  
Katherine Serrano ◽  
Michael W. Blades ◽  
Dana V. Devine ◽  
...  

2017 ◽  
Vol 31 (16-19) ◽  
pp. 1744067 ◽  
Author(s):  
Yu-Chao Wang ◽  
Long-Xing Su ◽  
Yu Zhao ◽  
Jian-Feng Liu ◽  
Zheng-Chuan Shen ◽  
...  

Resonance Raman spectra of Be[Formula: see text]Zn[Formula: see text]O alloy materials were studied using 325 nm Laser. The research showed that the Raman spectra of Be[Formula: see text]Zn[Formula: see text]O alloys presents a dual-mode vibration. Compare Be[Formula: see text]Zn[Formula: see text]O alloy with ZnO single crystal, the A1 (LO) phonon vibration mode of Be[Formula: see text]Zn[Formula: see text]O alloy moved to the larger wave number direction. The position of A1 (LO) phonon vibration modes of Be[Formula: see text]Zn[Formula: see text]O and Be[Formula: see text]Zn[Formula: see text]O was 580 cm[Formula: see text] and 582 cm[Formula: see text], respectively. In addition, the temperature-dependent Raman spectroscopy was employed for Be[Formula: see text]Zn[Formula: see text]O, and the phonon mode frequency shift with temperature was studied in detail. Finally, the stability of the polar and nonpolar Be[Formula: see text]Zn[Formula: see text]O alloy materials was studied using resonance Raman spectroscopy. The results showed that the A1 (LO) phonon mode frequency of polar Be[Formula: see text]Zn[Formula: see text]O alloy remained in the same position, while the nonpolar Be[Formula: see text]Zn[Formula: see text]O alloys moved nearly 3.5 cm[Formula: see text] to larger direction after being placed in the air for two years. The reason may be that the stability of the nonpolar Be[Formula: see text]Zn[Formula: see text]O alloy is relatively poor upon interaction with molecule such as H2O, O2 in the air.


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