Assay of cerebrospinal fluid protein: a rate biuret method evaluated.

1983 ◽  
Vol 29 (1) ◽  
pp. 126-129 ◽  
Author(s):  
P R Finley ◽  
R J Williams
Keyword(s):  
Cerebrospinal Fluid ◽  
Total Protein ◽  
Protein Concentration ◽  
Protein A ◽  
Colorimetric Method ◽  
Total Protein Concentration ◽  
Reaction Cell ◽  
Biuret Method ◽  
Automated Instrument ◽  
Cerebrospinal Fluid Protein

Abstract We evaluated a rate colorimetric method (Beckman) for measuring total protein in cerebrospinal fluid. The automated instrument we used was Beckman's ASTRA TM. A 100-microL sample of spinal fluid is introduced into the biuret reagent in the reaction cell and the increase in absorbance at 545 nm is monitored for 20.5 s. Solid-state circuits determine the rate of alkaline biuret-protein chelate formation, which is directly proportional to the total protein concentration in the sample. The linear range of measurement is 120 to 7500 mg/L. Day-to-day precision (CV) over the range of 150 to 1200 mg/L ranged from 15.2 to 2.3%. The method was unaffected by radical alteration of the albumin/globulin ratio, but there is a positive interference in the presence of hemoglobin, a suppression in the presence of bilirubin, and no effect by xanthochromia. The method is precise, accurate, rapid, and convenient. The method was compared with the trichloroacetic acid method as performed on the Du Pont aca III, giving a correlation coefficient (r2) of 0.9693. The method is precise, accurate, rapid, and convenient.

scholarly journals Ecological Relevance of Hemolymph Total Protein Concentration in Seven Unrelated Crustacean Species from Different Habitats Measured Predictively by a Density-Salinity Refractometer

2011 ◽  
Vol 2011 ◽  
pp. 1-7 ◽  
Author(s):  
Simonetta Lorenzon ◽  
Marzia Martinis ◽  
Enrico A. Ferrero
Keyword(s):  
Stress Responses ◽  
Total Protein ◽  
Protein Concentration ◽  
Low Cost ◽  
Physiological State ◽  
Colorimetric Method ◽  
Field Method ◽  
Blood Protein ◽  
Total Protein Concentration ◽  
Protein Levels

In recent years, blood metabolites have been investigated as a tool for monitoring physiological condition in wild or cultured crustaceans exposed to different environmental conditions. Blood protein levels fluctuate with changes in environmental and physiological conditions and play fundamental roles in the physiology of crustaceans from O2transport to reproduction up to stress responses. Proteins are major contributors to hemolymph density, and the present study correlates the easy and low cost measure of hemolymph density by a density-salinity refractometer with the total protein concentration, measured with a colorimetric method. Moreover, the study evaluates the accuracy of the relationship and provides a conversion factor from hemolymph density to protein in seven species of crustaceans, representative of taxa far apart in the phylogenetic tree and characterized by different life habits. Measuring serum-protein concentration by using a refractometer can provide a non-destructive field method to assess crustacean populations/species protein-related modifications of physiological state without need of costly laboratory facilities and procedures.

Clinical Utility of Biochemical Analysis of Cerebrospinal Fluid

1995 ◽  
Vol 41 (8) ◽  
pp. 1207-1207
Author(s):  
Mark A Watson ◽  
Mitchell G Scott
Keyword(s):  
Cerebrospinal Fluid ◽  
Case Report ◽  
Early Diagnosis ◽  
Total Protein ◽  
Clinical Utility ◽  
Protein Concentration ◽  
Biochemical Analysis ◽  
Total Protein Concentration ◽  
Vasopressin Secretion ◽  
Hypertonic Saline Infusion

Abstract In the Review by Watson and Scott entitled "Clinical utility of biochemical analysis of cerebrospinal fluid," 1995; 41:343-60, the total protein concentration in Table 1 should have been expressed in grams per liter (g/L), not milligrams per liter. In the Case Report by S. Coyle, M.D. Penney, P.W. Masters, and B.E. Walker entitled "Early diagnosis of ectopic arginine vasopressin secretion." 1933;39:152-4, in column 2, paragraph 3, page 152, and the title of The 1, the concentration of hypertonic saline infusion should have been expressed as 50 grams per liter (g/L), not milligrams per liter.

Determination of Total Protein Concentration in Solution Using Gold Electrode Modified with Silver Nanoparticles

2014 ◽  
Vol 27 (1) ◽  
pp. 253-257 ◽  
Author(s):  
Patrick Marcel Seumo Tchekwagep ◽  
Charles Péguy Nanseu-Njiki ◽  
Emmanuel Ngameni ◽  
Ravi Danielsson ◽  
Thomas Arnebrant ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Total Protein ◽  
Gold Electrode ◽  
Protein Concentration ◽  
Total Protein Concentration

Albumin fraction and measurement of total protein concentration

1993 ◽  
Vol 264 (5) ◽  
pp. H1723-H1726 ◽  
Author(s):  
B. T. Peterson ◽  
R. W. Tate
Keyword(s):  
Total Protein ◽  
Protein Concentration ◽  
Gamma Globulin ◽  
Colorimetric Assay ◽  
Full Range ◽  
Computational Method ◽  
Total Protein Concentration ◽  
Albumin Fraction ◽  
Standard Curve ◽  
Protein Assays

The standard curve of a typical colorimetric assay for total protein is often nonlinear and dependent on the albumin fraction of the protein standard. We developed a simple mathematical transformation to make the standard curve linear and a computational method to correct for differences in albumin concentrations among the samples. This method uses data from total protein assays on two sets of standards (albumin and gamma globulin) and provides accurate measures of total protein over the full range of albumin fractions. Comparison of this two-standard method with the a method that uses only albumin as a standard shows that this method prevents physiologically significant overestimations in total protein concentration and calculated protein osmotic pressure differences in the lungs.

scholarly journals EXERCISE-INDUCED CHANGES IN THE LEVEL OF TOTAL PROTEIN AND ITS FRACTIONS IN THE BLOOD OF HORSES INVOLVED IN RECREATIONAL HORSEBACK RIDING

2020 ◽  
pp. 35-46
Author(s):  
Halyna Tkachenko ◽  
Natalia Kurhaluk ◽  
Irina Tkachova
Keyword(s):  
Total Protein ◽  
Colorimetric Method ◽  
Exercise Session ◽  
Rank Test ◽  
Horseback Riding ◽  
Jugular Veins ◽  
Blood Samples ◽  
Biuret Method ◽  
G Ratio ◽  
Resting Period

The aim of the current study was to do the analysis of the total protein and its fraction in the blood samples of horses, which are involved in recreational horseback riding in the Pomeranian region (Pomeranian Voivodship, northern Poland). Thirteen healthy adult horses from the Pomeranian region in Poland (Strzelinko village, N54°30´48.0´´ E16°57´44.9´´), aged 9.5±2.4 years, including 5 Hucul ponies, 2 Thoroughbred horses, 2 Anglo-Arabian horses, and 4 horses of unknown breed, were used in the current study.Training started at 10:00 AM, lasted 1 hour, and consisted of a ride of cross country by the walking (5 min), the trotting (15 min), the walking (10 min), the trotting (10 min), the walking (5 min), the galloping (5 min), and the walking (10 min). Blood samples were taken from the jugular veins of the animals in the morning time, 90 minutes after feeding, while the horses were in the stables (between 8:30 and 10 AM), and immediately after the exercise session (between 11:00 AM and 2:00 PM). To obtain serum, the blood was collected in plain tubes without anticoagulants. Blood was stored in tubes with K3-EDTA and held on ice until centrifugation at 3,000g for 15 minutes. The plasma was removed.The total protein and its fractions were measured at +23°C by the biuret method with the use of commercially available reagents and a compact semi-automated analyzer RX Monza (Randox Laboratories LTD., UK) according to the procedures described by the manufacturer. The biuret method is the most widely used colorimetric method for the determination of the total protein concentration in serum because of its simplicity, precision, and accuracy. The absorbance of each sample was measured in duplicate.Results are expressed as mean ± S.E.M. All variables were tested for normal distribution using the Kholmogorov-Smirnov test (p>0.05). To find significant differences (significance level, p<0.05) between at the rest and after exercise, the Wilconson signed-rank test was applied to the data. All statistical analyses were performed using STATISTICA 8.0 software (StatSoft, Krakow, Poland). The total protein level in the blood of horses exhibited a non-significant increase (by 7.1%, p>0.05) immediately after exercise as compared to the resting period. Also, the albumin and globulin levels in the blood of horses were non-significantly increased by 5.9% (р>0.05) and 8.1% (р>0.05) after the training sessions. There were no significant differences in serum albumin/globulin ratio between the resting period and after exercise (0.997±0.09 vs. 0.977±0.08). The results of our current study showed that exercise has a statistically non-significant effect on the total proteins and their fractions in equine serum. The fractions and the A/G ratio were within the range of values obtained in horses in other studies. Thus, it was found that total protein and its fractions were increased in horses after training, and this increase was insignificant. This increase has a direct correlation with exercise. In this paper, it is shown that training can change the physiology and affect the biochemistry of hematobiochemical blood parameters in horses subjected to physical exertion.

scholarly journals Role of fibronectin under conditions of doxorubicin action

2015 ◽  
Vol 6 (1) ◽  
pp. 17-22
Author(s):  
A. I. Shevtsova ◽  
G. A. Ushakova
Keyword(s):  
Blood Plasma ◽  
Total Protein ◽  
Protein Concentration ◽  
Male Rats ◽  
Antitumor Action ◽  
Total Protein Concentration ◽  
Monospecific Antibodies ◽  
Anthracycline Chemotherapy ◽  
In Blood Plasma

There is no standard as to treatment of anthracycline chemotherapy complications. The reduction of cytotoxic drugs toxicity without weakening of their antitumor action remains relevant. The extracellular matrix which key component is fibronectin is present in all tissues and it continuously undergoes controlled remodeling. So, the purpose of our work was to study the level of fibronectin in the experimental model of doxorubicin-induced cardiomyopathy and effects of this cytostatic and its co-administration with antioxidants of different nature.The level of fibronectin was measured by ELISA using monospecific antibodies against fibronectin (Sigma, USA), secondary anti-IgG labeled with horseradish peroxidase (Sigma, USA) and fibronectin standard (Sigma, USA). The study was conducted on Wistar male rats with weight of 210 ± 50 g which were divided into 4 groups by 8 animals in each group: 1 – control, rats receiving saline i/p; 2 – doxorubicin 1 mg/kg i/p once a week during 4 weeks; 3 – doxorubicin by the same scheme plus 1% 2-oxoglutarate in drinking water during 4 weeks;4 – doxorubicin by the same scheme and korvitin injection 30 min before doxorubicin application once a week during 4 weeks. Obtained data indicate the effect of doxorubicin to decrease in index mass heart in 38% of animals compared to control animals; decrease in total protein concentration by 8% (Р < 0,05) and increase of the level of fibronectin by 67% (P < 0,001) in blood plasma of rats and decrease in the level of fibronectin in the heart extract by 19% (Р < 0,05) under development of doxorubicin-induced cardiotoxicity. Increased fibronectin concentration in blood plasma had strong correlation with decreased total protein concentration in blood (r=0,80) and heart extract (r=0,59) in rats with doxorubicin-induced cardiomiophaty indicating the sensitive reaction of fibronectin to development of metabolic disorders under doxorubicin influence. 

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