Load-unloading response of intact and artificially degraded articular cartilage correlated with near infrared (NIR) absorption spectra

Author(s):  
I.O. Afara ◽  
S. Singh ◽  
A. Oloyede
2009 ◽  
Vol 17 (4) ◽  
pp. 213-221 ◽  
Author(s):  
Kamaranga H.S. Peiris ◽  
Michael O. Pumphrey ◽  
Floyd E. Dowell

The near infrared (NIR) absorption spectra of deoxynivalenol (DON) and single wheat kernels with or without DON were examined. The NIR absorption spectra of 0.5–2000 ppm of DON in acetonitrile were recorded in the 350–2500 nm range. Second derivative processing of the NIR spectra and spectral subtractions showed DON absorption bands at 1408 nm, 1904 nm and 1919 nm. NIR spectra of sound and Fusarium-damaged kernels were also acquired using two instruments. Subtraction of average absorption spectra and second derivative spectra were evaluated to identify different NIR signatures of the two types of kernel. Differences in peak height and positions of the NIR absorption bands of the kernels were noted. At 1204 nm, 1365 nm and 1700 nm, the differences were in the heights of the absorption peaks. Such differences may be attributed to changes in the levels of grain food reserves such as starches, proteins and lipids and other structural compounds. Shifts in absorption peak positions between the two types of kernels were observed at 1425–1440 nm and 1915–1930 nm. These differences may arise from other NIR active compounds, such as DON, which are not common for the two types of kernel. Since the NIR absorption of DON may have contributed to the shifts between sound and Fusarium-damaged kernels, this study indicates the potential for NIR spectrometry to evaluate Fusarium damage in single kernels based on the DON levels.


Bone ◽  
2013 ◽  
Vol 53 (2) ◽  
pp. 350-357 ◽  
Author(s):  
Isaac Oluwaseun Afara ◽  
Indira Prasadam ◽  
Ross Crawford ◽  
Yin Xiao ◽  
Adekunle Oloyede

2020 ◽  
Vol 6 (2) ◽  
pp. 30
Author(s):  
Yuji Matsukawa ◽  
Kazuo Umemura

It has been reported that even if single-walled carbon nanotubes (SWNTs) are coated with the same polymer, the redox characteristics change of each chirality may differ. Particularly, the addition of hydrogen peroxide (H2O2) minimally affects the near-infrared (NIR) absorption spectra of the dsDNA-(6,5)-enriched SWNT complex (DNA-SWNT complex). Detecting the redox properties of (6,5) chirality using NIR absorption spectra has been one of the issues to be solved. We hypothesized that an oxidizing agent with high oxidizing power is required to detect the absorption spectra of (6,5) chirality. In this study, we used KMnO4, which contains atoms with a high oxidation number. A dispersion was prepared by mixing 0.5 mg of (6,5)-enriched SWNT powder with 1 mg/mL of DNA solution. After adding H2O2 or KMnO4 to this dispersion and oxidizing it, catechin solutions were added to reduce the dispersion. The absorption peak of the DNA-SWNT complex decreased by 23.9% following the addition of KMnO4 (final concentration: 0.5 µM) and recovered 30.7% following the addition of the catechin solution. We revealed that the changes in the absorption spectra change of (6,5) chirality, which could not be detected by H2O2, can be detected by using KMnO4. We also varied the concentration of KMnO4 and verified whether the adsorption of KMnO4 can be modeled as a Langmuir adsorption isotherm.


2007 ◽  
Vol 22 (9) ◽  
pp. 2531-2538 ◽  
Author(s):  
Mei Chee Tan ◽  
Jackie Y. Ying ◽  
Gan Moog Chow

Near infrared (NIR) absorbing nanoparticles synthesized by the reduction of HAuCl4 with Na2S exhibited absorption bands at ∼530 nm, and in the NIR region of 650–1100 nm. The NIR optical properties were not found to be related to the earlier proposed Au2S–Au core-shell microstructure in previous studies. From a detailed study of the structure and microstructure of as-synthesized particles in this work, S-containing, Au-rich, multiply-twinned nanoparticles were found to exhibit NIR absorption. They consisted of amorphous AuxS (where x = 2), mostly well mixed within crystalline Au, with a small degree of surface segregation of S. Therefore, NIR absorption was likely due to interfacial effects on particle polarization from the introduction of AuxS into Au particles, and not the dielectric confinement of plasmons associated with a core-shell microstructure.


2013 ◽  
Vol 15 (20) ◽  
pp. 7666 ◽  
Author(s):  
Honghua Hu ◽  
Olga V. Przhonska ◽  
Francesca Terenziani ◽  
Anna Painelli ◽  
Dmitry Fishman ◽  
...  

2008 ◽  
Vol 23 (1) ◽  
pp. 281-293 ◽  
Author(s):  
Mei Chee Tan ◽  
Jackie Y. Ying ◽  
Gan Moog Chow

Near-infrared (NIR)-absorbing nanoparticles synthesized by the reduction of tetrachloroauric acid (HAuCl4) using sodium sulfide (Na2S) exhibited absorption bands at ∼530 nm and at the NIR region of 650−1100 nm. A detailed study on the structure and microstructure of as-synthesized nanoparticles was reported previously. The as-synthesized nanoparticles were found to consist of amorphous AuxS (x = ∼2), mostly well mixed within crystalline Au. In this work, the optical properties were tailored by varying the precursor molar ratios of HAuCl4 and Na2S. In addition, a detailed study of composition and particle-size effects on the optical properties was discussed. The change of polarizability by the introduction of S in the form of AuxS (x = ∼2) had a significant effect on NIR absorption. Also, it was found in this work that exposure of these particles to NIR irradiation using a Nd:YAG laser resulted in loss of the NIR absorption band. Thermal effects generated during NIR irradiation had led to microstructural changes that modified the optical properties of particles.


2014 ◽  
Vol 18 (08n09) ◽  
pp. 752-761 ◽  
Author(s):  
Tetsuo Okujima ◽  
Yoichi Shida ◽  
Keishi Ohara ◽  
Yuya Tomimori ◽  
Motoyoshi Nishioka ◽  
...  

A series of O-chelated BODIPYs fused with aromatic rings such as benzene and acenaphthylene at β,β-positions was synthesized as a near-infrared dye. The photophysical properties were examined by UV-vis-NIR absorption and fluorescence measurement. Acenaphthylene-fused O-BODIPYs showed a intense absorption at 750–840 nm with the ε of 105 M-1.cm-1. and a fluorescence emission at 770–850 nm with the high Φ value of 0.06–0.43.


1994 ◽  
Vol 91 (9) ◽  
pp. 731-733 ◽  
Author(s):  
N. Mironova ◽  
V. Skvortsova ◽  
U. Ulmanis

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