A method for the simultaneous determinations of total carbohydrate and glycerol in biological samples with the anthrone reagent

1981 ◽  
Vol 4 (3-4) ◽  
pp. 227-231 ◽  
Author(s):  
A. Pons ◽  
P. Roca ◽  
C. Aguiló ◽  
F.J. Garcia ◽  
M. Alemany ◽  
...  
1954 ◽  
Vol 32 (1) ◽  
pp. 218-226
Author(s):  
N. R. Stephenson

Total sugar in a protein-free liver hydrolyzate, determined by copper reduction, provides an acceptable criterion for estimating the response to graded doses of 11-oxycorticosteroids. Total carbohydrate in the liver, measured by the anthrone reagent, may also be used for this purpose. The glycogenic response to adrenal corticoids of fasting adrenalectomized male rats of the Wistar strain, weighing 40 to 50 gm., is increased by the administration of glucose, but appears to be depressed by ethanol. Although the precision of the assay is not influenced unfavorably by using the rats on the day following adrenalectomy, the mortality rate of the adrenalectomized animals is reduced by this procedure.


1975 ◽  
Vol 10 (1) ◽  
pp. 126-131 ◽  
Author(s):  
A. Leduy ◽  
N. Kosaric ◽  
J.E. Zajic

Abstract Spectrophotometric determination of total carbohydrate (TCH) in the wastewater samples by anthrone reagent is a simple and rapid method to follow the utilization of substrate, and hence the reduction of BOD5 load during the biological treatment process with chemoheterotrophs. However, for the coloured wastewater samples or treatment plant effluents, a correction factor was found necessary to compensate the colour inferences. Studies were conducted on various waste sulfite liquors (NH3-, Ca-, Mg-, Mixed- and Na-WSL) which provide a wide range of colours from creamy to black. The correction factor was calculated from the deviation of the standard calibration curves of glucose with and without the presence of WSL. These correction factors depended both on the nature and on the amount of WSL present. Within the practical dilution range of various WSL for the determination of TCH (1:1,000 - 4:1,000 v/v), the correction factors varied from 15 to 40%, which is highly significant if the correction was not made. In all WSL samples, the correction factor became more significant at higher concentration of WSL in the solution. Spectrophotometric studies of WSL at various concentrations within the visible range led to the development of the following empirical equation expressing their colour, $$\Lambda = \Lambda _{\rm s}\left( {1 + {[D_{\rm c}/D]}^2} \right)^{{\rm n/2}}$$ where Λ, Λs, Dc, D and n are the maximum transmitted wavelength of WSL solution, the maximum transmitted wavelength of water (solvent), the critical dilution of WSL, the dilution of WSL (reciprocal concentration of colouring materials) and the chromatic index of WSL respectively.


1954 ◽  
Vol 32 (3) ◽  
pp. 218-226 ◽  
Author(s):  
N. R. Stephenson

Total sugar in a protein-free liver hydrolyzate, determined by copper reduction, provides an acceptable criterion for estimating the response to graded doses of 11-oxycorticosteroids. Total carbohydrate in the liver, measured by the anthrone reagent, may also be used for this purpose. The glycogenic response to adrenal corticoids of fasting adrenalectomized male rats of the Wistar strain, weighing 40 to 50 gm., is increased by the administration of glucose, but appears to be depressed by ethanol. Although the precision of the assay is not influenced unfavorably by using the rats on the day following adrenalectomy, the mortality rate of the adrenalectomized animals is reduced by this procedure.


Author(s):  
W. R. Schucany ◽  
G. H. Kelsoe ◽  
V. F. Allison

Accurate estimation of the size of spheroid organelles from thin sectioned material is often necessary, as uniquely homogenous populations of organelles such as vessicles, granules, or nuclei often are critically important in the morphological identification of similar cell types. However, the difficulty in obtaining accurate diameter measurements of thin sectioned organelles is well known. This difficulty is due to the extreme tenuity of the sectioned material as compared to the size of the intact organelle. In populations where low variance is suspected the traditional method of diameter estimation has been to measure literally hundreds of profiles and to describe the “largest” as representative of the “approximate maximal diameter”.


Author(s):  
C. F. Oster

Although ultra-thin sectioning techniques are widely used in the biological sciences, their applications are somewhat less popular but very useful in industrial applications. This presentation will review several specific applications where ultra-thin sectioning techniques have proven invaluable.The preparation of samples for sectioning usually involves embedding in an epoxy resin. Araldite 6005 Resin and Hardener are mixed so that the hardness of the embedding medium matches that of the sample to reduce any distortion of the sample during the sectioning process. No dehydration series are needed to prepare our usual samples for embedding, but some types require hardening and staining steps. The embedded samples are sectioned with either a prototype of a Porter-Blum Microtome or an LKB Ultrotome III. Both instruments are equipped with diamond knives.In the study of photographic film, the distribution of the developed silver particles through the layer is important to the image tone and/or scattering power. Also, the morphology of the developed silver is an important factor, and cross sections will show this structure.


Author(s):  
Patrick Echlin

A number of papers have appeared recently which purport to have carried out x-ray microanalysis on fully frozen hydrated samples. It is important to establish reliable criteria to be certain that a sample is in a fully hydrated state. The morphological appearance of the sample is an obvious parameter because fully hydrated samples lack the detailed structure seen in their freeze dried counterparts. The electron scattering by ice within a frozen-hydrated section and from the surface of a frozen-hydrated fracture face obscures cellular detail. (Fig. 1G and 1H.) However, the morphological appearance alone can be quite deceptive for as Figures 1E and 1F show, parts of frozen-dried samples may also have the poor morphology normally associated with fully hydrated samples. It is only when one examines the x-ray spectra that an assurance can be given that the sample is fully hydrated.


2019 ◽  
Author(s):  
Ashley Williams ◽  
Deborah Muoio ◽  
Guofang Zhang

Quantative measurements of the glucose analogue, 2-deoxyglucose (2DG), and its phosphorylated metabolite (2-deoxyglucose-6-phosphate (2DG-6-P)) are critical for the measurement of glucose uptake. While the field has long identified the need for sensitive and reliable assays that deploy non-radiolabled glucose analogues to assess glucose uptake, no analytical MS-based methods exist to detect trace amounts in complex biological samples. In the present work, we show that 2DG is poorly suited for MS-based methods due to interfering metabolites. We therefore developed and validated an alternative C18-based LC-Q-Exactive-Orbitrap-MS method using 2-fluoro-2-deoxyglucose (2FDG) to quantify both 2FDG and 2FDG-6-P by measuring the sodium adduct of 2FDG in the positive mode and deprotonation of 2FDG-6-P in the negative mode. The low detection limit of this method can reach 81.4 and 48.8 fmol for both 2FDG and 2FDG-6-P, respectively. The newly developed method was fully validated via calibration curves in the presence and absence of biological matrix. The present work is the first successful LC-MS method that can quantify trace amounts of a nonradiolabeled glucose analogue and its phosphorylated metabolite and is a promising analytical method to determine glucose uptake in biological samples.


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