A Colorimetric Method for the Quantitative Measurement of Total Lipids in Tissues

Nature ◽  
1963 ◽  
Vol 197 (4872) ◽  
pp. 1120-1121 ◽  
Author(s):  
R. PHILLIPS DALES
1960 ◽  
Vol 38 (3) ◽  
pp. 253-262 ◽  
Author(s):  
A. M. Marko ◽  
F. B. Reynolds

A qualitative test for indican (indoxyl-O-sulphate, usually as the potassium salt) has been adapted for the quantitative measurement of indican. The method involves the condensation of indican and p-dimethylaminobenzaldehyde in the presence of acid to yield an orange-colored compound. When an excess of sodium acetate is added, the orange-colored reaction product is converted to a cherry-red derivative. The effects of time, acids, temperature, and concentration of reagents on the reaction have been studied and optimum conditions have been selected to obtain a standard curve.Unsatisfactory analytical results are obtained when this method is applied directly to urine samples and a method for the quantitative elution of indican from charcoal columns has, therefore, been devised. With this modification quantitative recoveries have been achieved with indican alone and with indican added to urine samples.In addition a review of the literature pertaining to indican measurement and indigoid pigments is presented.


1970 ◽  
Vol 119 (2) ◽  
pp. 303-306 ◽  
Author(s):  
T. E. Couling ◽  
R. Goodey

The inhibition of N-acetyl-β-d-glucosaminase activity by 2-acetamido-2-deoxy-d-gluconolactone was examined. Separation of the (1→4)- and (1→5)-lactones was achieved by using paper chromatography or countercurrent distribution and identification was obtained by examination of the relative stability of the components of separated material. Quantitative measurement of the two lactones was by kinetic titration or by a colorimetric method based on their reaction with hydroxylamine. It was shown that only the (1→5)-lactone acted as an inhibitor of N-acetyl-β-d-glucosaminase.


1972 ◽  
Vol 55 (1) ◽  
pp. 209-213
Author(s):  
A J Sensabaugh ◽  
Kenneth L Rush

Abstract A method is presented for extracting and determining the starch content of tobacco. Dried tobacco is ground to pass a 60 mesh screen, interfering colored materials are removed from the tobacco by a methanol-water extraction, and the starch is extracted from the tobacco by a perchloric acid treatment. Final quantitative measurement of the starch is made on a colored starch–iodine complex. The absorbance of this colored complex at 600 nm is proportional to the concentration of the starch in solution and can be related to the starch content of the original tobacco sample. Also included is a procedure for the isolation of pure tobacco starch. Such material was prepared for use as a calibration standard needed for the calculation of starch content of tobacco samples from the colorimetric data.


1960 ◽  
Vol 38 (1) ◽  
pp. 253-262
Author(s):  
A. M. Marko ◽  
F. B. Reynolds

A qualitative test for indican (indoxyl-O-sulphate, usually as the potassium salt) has been adapted for the quantitative measurement of indican. The method involves the condensation of indican and p-dimethylaminobenzaldehyde in the presence of acid to yield an orange-colored compound. When an excess of sodium acetate is added, the orange-colored reaction product is converted to a cherry-red derivative. The effects of time, acids, temperature, and concentration of reagents on the reaction have been studied and optimum conditions have been selected to obtain a standard curve.Unsatisfactory analytical results are obtained when this method is applied directly to urine samples and a method for the quantitative elution of indican from charcoal columns has, therefore, been devised. With this modification quantitative recoveries have been achieved with indican alone and with indican added to urine samples.In addition a review of the literature pertaining to indican measurement and indigoid pigments is presented.


2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Swathi Naraparaju ◽  
Durai Ananda Kumar Thirumoorthy ◽  
Sunitha Gurrala ◽  
Asra Jabeen ◽  
Pani Kumar D. Anumolu

Abstract Background A simple and sensitive spectrophotometric method was developed for the quantitative measurement of dolutegravir in pure form and pharmaceutical formulation. The present method was based on redox reaction between dolutegravir and ferric chloride, which upon complexation with 1,10-phenanthroline formed an orange-colored complex that showed absorption maximum at 520.0 nm. Results The developed method obeyed linearity in the concentration range of 40.00–140.00 μg/mL. The method was also validated as per International Council for Harmonization guidelines and the results were within acceptance values. The validated method was employed for the determination of dolutegravir in pharmaceutical dosage form and the percentage assay value was found to be 102.5, which is in agreement with its label claimed. Conclusion The developed redox-based colorimetric method could be used in the routine quality control analysis of dolutegravir present in various pharmaceutical dosage forms.


Sociobiology ◽  
2015 ◽  
Vol 62 (3) ◽  
pp. 334 ◽  
Author(s):  
Edypo Jacob Silva ◽  
Roberto Da Silva Camargo ◽  
Luiz Carlos Forti

The nuptial flight and nest digging are high intensity activities which consume body reserves. The flight and digging effort was quantified by measuring the carbohydrate and total lipids content in males and females before and after the nuptial flight, and the queen’s digging effort during the foundation. The digging effort was quantified by experimentally stimulating the queens to dig a nest – one, two or three consecutive times – compared to the queens that did not dig. The colorimetric method was used to determine the soluble carbohydrates and extraction method of immersion was used to determine the total lipids. The results showed significant loss of carbohydrates and total lipids in males and females after the flight. On average the males contained 0.027 mg of soluble carbohydrates before the nuptial flight, and 0.005 mg after the nuptial flight, and the females contained 0.129 mg of soluble carbohydrates before the nuptial flight, and 0.079 mg after the nuptial flight. For the males the percentage of lipids decreased from 5.27±1.07% to 2.60±0.63% and for females from 36.46±4.86% to 32.62% after the nuptial flight. The digging effort of the queen caused a slight reduction in total carbohydrates, it was without digging 0.054 mg, normal digging 0.055 mg, double digging 0.045 mg (decrease of 20,22 %), and triple digging 0.044 mg  (decrease of 20 %) per queen. Based on our results we conclude that the carbohydrate content is the main energetic resource used for the nuptial flight and nest digging, for males and gynes of leaf-cutting ants.


Author(s):  
William A. Heeschen

Two new morphological measurements based on digital image analysis, CoContinuity and CoContinuity Balance, have been developed and implemented for quantitative measurement of morphology in polymer blends. The morphology of polymer blends varies with phase ratio, composition and processing. A typical morphological evolution for increasing phase ratio of polymer A to polymer B starts with discrete domains of A in a matrix of B (A/B < 1), moves through a cocontinuous distribution of A and B (A/B ≈ 1) and finishes with discrete domains of B in a matrix of A (A/B > 1). For low phase ratios, A is often seen as solid convex particles embedded in the continuous B phase. As the ratio increases, A domains begin to evolve into irregular shapes, though still recognizable as separate domains. Further increase in the phase ratio leads to A domains which extend into and surround the B phase while the B phase simultaneously extends into and surrounds the A phase.


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