Label-free determination of lipid composition and secondary protein structure of human salivary noncancerous and cancerous tissues by Raman microspectroscopy

The Analyst ◽  
2015 ◽  
Vol 140 (7) ◽  
pp. 2107-2113 ◽  
Author(s):  
Beata Brozek-Pluska ◽  
Monika Kopec ◽  
Izabela Niedzwiecka ◽  
Alina Morawiec-Sztandera

The applications of optical spectroscopic methods in cancer detection open new possibilities in oncological diagnostics.

2013 ◽  
Vol 85 (19) ◽  
pp. 8996-9002 ◽  
Author(s):  
Stanislav O. Konorov ◽  
H. Georg Schulze ◽  
James M. Piret ◽  
Michael W. Blades ◽  
Robin F. B. Turner

1988 ◽  
Vol 42 (8) ◽  
pp. 1441-1450 ◽  
Author(s):  
A. Wang ◽  
P. Dhamelincourt ◽  
G. Turrell

The first attempt to determine the cation distributions in amphiboles by Raman microspectroscopy is described. The Raman spectra of five amphibole samples were obtained. It was observed that the Raman bands of the OH stretching modes were narrower than the corresponding infrared bands previously reported. However, even with the use of the most sophisticated Raman instruments, it was not possible to distinguish the bands due to the different cation arrangements of one particular configuration. Nevertheless, the experimental results and the theoretical analysis developed here allowed approximate calculations of the site occupancies to be made for four samples. These results yield a better understanding of the problems involved in the determination of the cation distributions in amphiboles with the use of vibrational spectroscopic methods.


The Analyst ◽  
2017 ◽  
Vol 142 (20) ◽  
pp. 3848-3856 ◽  
Author(s):  
Esen Efeoglu ◽  
Alan Casey ◽  
Hugh J. Byrne

Raman microspectroscopy as anin vitrolabel-free, high content screening technique to determine spectral markers of cytogenotoxicity.


1981 ◽  
Vol 46 (12) ◽  
pp. 3063-3073 ◽  
Author(s):  
Jana Podlahová ◽  
Bohumil Kratochvíl ◽  
Vratislav Langer ◽  
Josef Šilha ◽  
Jaroslav Podlaha

The equilibria and mechanism of addition of protons to the ethylenediphosphinetetraacetate anion (L4-) were studied in solution by the UV, IR, 1H and 31P NMR spectroscopic methods. A total of six protons can be bonded to the anion. They are added stepwise, first with partial formation of zwitterions containing P-H bonds, which then dissociate with formation of the free acid, H4L, where all four protons are bonded in carboxyl groups. The formation of zwitterions is strongly dependent on the concentration. In the final stage, the acid bonds two additional protons to form the bis-phosphonium cation, H6L2+. A number of isostructural salts containing this cation, H4L.2 HX (X = Cl, Br, I), have been prepared. The X-ray crystal structure determination of the bromide confirmed the expected arrangement. The bromide crystals are monoclinic, a = 578.2, b = 1 425.0, c = 1 046.7 pm, β = 103.07° with a space group of P21/c, Z = 2. The final R factor was 0.059 based on 1 109 observed reflections. The structure consists of H6L2+ cations containing protons bonded to phosphorus atoms (P-H distance 134 pm) and of bromide anions, located in gaps which are also sufficiently large for I- anions in the isostructural iodide. The interbonding of phosphonium cations proceeds through hydrogen bonds, C-OH...O=C, in which the O...O distance is 275.3 pm.


1991 ◽  
Vol 32 (2) ◽  
pp. 371-374
Author(s):  
M Muraca ◽  
MT Vilei ◽  
L Miconi ◽  
P Petrin ◽  
M Antoniutti ◽  
...  

2013 ◽  
Vol 67 (9) ◽  
pp. 1101-1105 ◽  
Author(s):  
Christian Vogel ◽  
Christian Adam ◽  
Don McNaughton

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