Humans ; Lead ; Spectrometry, Fluorescence ; Spectrophotometry, Atomic ; Uncertainty

OBJECTIVETo study the conjugation reaction characteristics of caffeic acid micromolecule cistanoside F and bovine serum albumin.

METHODThe interaction between bovine serum albumin (BSA) and cistanoside F that was separated from Callicarpa plant for the first time and abbreviated CF was detected by fluorescence (FS), UV-vis absorbance and circular dichroism (CD) under simulative physiological conditions.

RESULTCF-BSA's static apparent binding constant (K(a)), number of binding sites (n), efficiency of energy transfer (E), spatial distance (r), thermodynamic parameters deltaG, deltaH and deltaS and changes in alpha-helical structure content in BSA before and after CF's effect were calculated to define the binding site of CF in BSA and analyze the impact of several common metal ions on the interaction of CF and BSA.

CONCLUSIONGround state compounds formed by CF and BSA could cause intrinsic fluorescence quenching. Their binding constant K(a) of cistanoside F with BSA was 4.36 x 10(4) L x mol at 25 degrees C, the number of binding site n was 1, and the spatial distance r was 3.09 nm. The results indicated that the hydrogen bond played a major role in cistanoside F-BSA association. The displacement experiments confirmed that cistanoside F can bind to site I of BSA. In addition, the binding constant of cistanoside F with BSA was enhanced after the addition of some common metal ions Mg2+, Fe3+, Cu2+ and Zn2+. The intrinsic fluorescence of BSA was quenched by cistanoside F via forming cistanoside F-BSA complex and non-radiation energy transfer. CD spectra showed that the binding of cistanoside F with BSA induced conformational changes in BSA.

Animals ; Caffeic Acids ; chemistry ; Catechols ; chemistry ; Cattle ; Circular Dichroism ; Glycosides ; chemistry ; Serum Albumin, Bovine ; chemistry ; Spectrometry, Fluorescence ; Spectrophotometry, Ultraviolet ; Thermodynamics

The chrome content of 8 Korean cements and 11 Korean bleaching detrgents was analyzed by the qualitative DPC method and the quantitative atomic absorption spectrophotometry and UV-visible spectrophotometry. In cements, there was no detectable chrome in 1 sample and the range of chrome content in other 7 samples was 1.32 5.29ppm. The qualitative result was welJ. correlated with the quantitative result. In bleaching detergents, there was no detectable chrome in 4 samples and the range of chrome content in other 7 samples was 0.0329 0.362ppm. However, the qualitative result was not correlated with the quantitative result.
Detergents* ; Spectrophotometry ; Spectrophotometry, Atomic

No abstract available.
Spectrophotometry, Atomic*

Animals ; Humans ; Reproducibility of Results ; Selenium ; analysis ; Spectrometry, Fluorescence ; Spectrophotometry, Atomic

Humans ; Mercury ; blood ; urine ; Spectrometry, Fluorescence ; methods ; Spectrophotometry, Atomic ; methods

OBJECTIVETo determine the composition, structure, trace elements and thermal stability of Tibetan medicine Nanhanshuishi.

METHODThe trace elements, the structure, and the thermal stability of Nanhanshuishi were assayed and calculated by X-ray fluorescence spectrometry (XRF), inductively coupled plasma optical emission spectrometer (ICP-OES), atomic fluorescence spectrometry (AFS), inductively coupled plasma mass spectrometry (ICP-MS), X-ray power diffraction (XRD), TG-DTA.

RESULTThe results indicated that the phase is mainly made up of CaCO3 (Rhombohedral, R-3c) in Nanhanshuishi. The analysis of elements show that Nanhanshuishi is rich in Ca and O, and contains other more than 20 minor elements, such as Si, Mg, Fe, Al, Na, K, Zn, Mn, Pb, As, Hg etc. The result of TG-DTA show that the weight of Nanhanshuishi starts to decline from near 700 degrees C and get steady above 850 degrees C.

CONCLUSIONThe study provided scientific data for the establishment of quality standards of Tibetan medicine Nanhanshuishi.

Drug Stability ; Mass Spectrometry ; Medicine, Tibetan Traditional ; Minerals ; Spectrometry, X-Ray Emission ; Spectrophotometry, Atomic ; Trace Elements ; analysis

The objective of the present study was to describe two non-invasive methods for fat quantification in normal canine liver by using magnetic resonance imaging (MRI) and spectroscopy. Eleven adult beagle dogs were anesthetized and underwent magnetic resonance examination of the cranial abdomen by performing morphologic, modified Dixon (mDixon) dual gradient echo sequence, and proton magnetic resonance spectroscopy (¹H MRS) imaging. In addition, ultrasonographic liver examination was performed, fine-needle liver aspirates and liver biopsies were obtained, and hepatic triglyceride content was assayed. Ultrasonographic, cytologic, and histologic examination results were unremarkable in all cases. The median hepatic fat fraction calculated was 2.1% (range, 1.3%–5.5%) using mDixon, 0.3% (range, 0.1%–1.0%) using ¹H MRS, and 1.6% (range 1.0%–2.5%) based on triglyceride content. The hepatic fat fractions calculated using mDixon and ¹H MRS imaging were highly correlated to that based on triglyceride content. A weak correlation between mDixon and ¹H MRS imaging was detected. The results show that hepatic fat content can be estimated using non-invasive techniques (mDixon or ¹H MRS) in healthy dogs. Further studies are warranted to evaluate the use of these techniques in dogs with varying hepatic fat content and different hepatic disorders.
Abdomen ; Adult ; Animals ; Biopsy ; Dogs ; Humans ; Liver ; Magnetic Resonance Imaging ; Proton Magnetic Resonance Spectroscopy ; Protons ; Spectrum Analysis ; Triglycerides

Antimony ; urine ; Flow Injection Analysis ; Spectrometry, Fluorescence ; methods ; Spectrophotometry, Atomic ; methods

Humans ; Lead ; urine ; Sensitivity and Specificity ; Spectrometry, Fluorescence ; methods ; Spectrophotometry, Atomic ; methods