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Evaluation of Ames Seralyzer for the therapeutic drug monitoring of phenobarbital and phenytoin.

Comparison of a reflective photometry assay (Ames Seralyzer) and a fluorescence polarization immunoassay (Abbott TDx) for measuring phenobarbital and phenytoin serum concentration was performed. Routine phenobarbital and phenytoin plasma levels drawn from patients in the pediatric neurology clinic and pediatric intensive care unit were determined in duplicate by the Abbott TDx and Ames Seralyzer systems. A total of 40 samples were assayed. The interday and intraday variability of the Ames system was determined using calibrators of known concentrations (5-25 micrograms/ml). There was significant correlation between the serum phenobarbital or phenytoin concentrations when determined by the Seralyzer and TDx systems. The intraday variability for the measurement of phenytoin when determined by the Seralyzer had coefficients of variation ranging from 2.2 to 8.9%. The interday variability for phenytoin when measured by both the TDx and the Seralyzer correlated well with known calibrators. The utility of the Ames Seralyzer for acute-care facilities, physician offices, and pharmacy satellites is apparent. Based on statistical analysis, the Seralyzer provides accurate phenobarbital and phenytoin serum measurements for clinical use in therapeutic drug monitoring.

Adolescent↗

[Equipment for lyoluminescent dosimetry].

The paper deals with experience gained during construction of photometry set suitable for application in lyoluminiscent dosimetry. Results of stability measurement are presented and possibilities of constructing these apparatuses using Czechoslovak parts are discussed.

Luminescent Measurements↗

Immunophotometric quantification of extravascular immunoglobulin deposits in the synovial membrane of patients with osteoarthritis and rheumatoid arthritis.

The amount of extravascular immunoglobulin deposits in the synovial membrane of patients with osteoarthritis and rheumatoid arthritis was studied in comparison with that of patients suffering from non-joint diseases. Immunoglobulin deposits were immunostained using the three-layer immunoperoxidase method. The staining results were quantified with the help of a microscope photometer connected with a scanning stage. Several experiments involving artificial test substrates, diseases with allegedly increased extravascular deposits or diseases not exhibiting extravascular deposits of immunoglobulins are used to validate the described microspectrophotometrical approach for measuring extravascular immunoglobulin deposits. The scanning photometry demonstrates significantly higher amount of extravascular immunoglobulin deposits in rheumatoid arthritis as compared with osteoarthritis and non-joint diseases.

Arthritis, Rheumatoid↗

Reliability of IL Monarch ion-selective electrode module for sodium, potassium, and chloride measurements.

We evaluated the IL Monarch random-access centrifugal analyzer for measurement of Na+, K+, and Cl- by an indirect potentiometric method. For different concentrations of control material, the total precision (CV) ranged between 0.82% and 1.14% for the three electrolytes; linearity was acceptable within a range of 103 to 215 mmol/L for Na+, 1.6-15.25 mmol/L for K+, and 80-173 mmol/L for Cl-. Data correlated well with those by flame photometry for Na+ and K+ and with those by coulometry for Cl-, both for various biological materials--sera, urines, dialysis fluids--and commercial control materials from various producers. Stability of the potentiometric signal was acceptable: daily variations were 0.2 mV for Na+, 0.05 mV for K+, and 0.03 mV for Cl-. Accordingly, we conclude that the system supplies reproducible and accurate results while being easy to use and requiring little maintenance. The use of indirect potentiometry offers results consistent with those obtained with traditional methods, and easily interpretable by clinical staff. However, better information about the actual ion activity in the tested sample for certain pathologies such as hyperlipemia and dysproteinemia could be obtained by methods involving direct potentiometry.

Centrifugation↗

Effect of an interfering substance on determination of potassium by ion-specific potentiometry in animal urine.

Analytical characteristics of photometry and ion-specific potentiometry for urine from sheep, horses, cows, dogs, and cats were determined, using solutions of sodium and potassium chloride. The performance of both methods were acceptable, but the ion-specific potentiometer (in the mode for urine analysis) was superior in terms of linearity of response and correlation between actual vs measured concentrations. Coefficients of variation of either method for repeated analyses of various concentrations of sodium and potassium were always less than 2.5%. The measurement of sodium concentration in urine samples correlated well between both methods for samples from sheep, horses, cows, dogs, and cats. In contrast, measurement of potassium concentrations in urine samples from sheep, horses, cows, and cats was underestimated consistently by ion-specific potentiometry. The magnitude of the apparent error was variable between species and was often increased with greater urine potassium concentrations. These phenomena were not seen in urine samples from dogs. Sequential dilution of urine samples from sheep before analysis reduced the magnitude of the error observed by ion-specific potentiometry. Seemingly, an equilibrium process existed in which potassium was bound by an anionic or zwitterionic chemical and was sequestered from interaction with the ion-specific electrode. Ultrafiltration experiments indicated the putative potassium chelator was a low molecular weight compound.

Animals↗

Clinical validation of an automated thin-film reflectance method for measurement of magnesium in serum and urine.

We evaluated an automated method for measuring total magnesium in serum, plasma, or urine that utilizes dry multilayered thin-film reagents and reflectance photometry for use on the Kodak Ektachem 400 analyzer. Comparison of magnesium results by this method and by atomic absorption revealed the following: the results on samples from a variety of patients agreed closely, the thin-film methodology was not affected by icteric, hemolyzed, or lipemic samples, and over 100 drugs studied did not interfere. Only very high concentrations of citrate and calcium affected magnesium results by this method. Both the accuracy and versatility of the thin-film method are well suited to routine, fast response, and pediatric testing in the clinical laboratory.

Autoanalysis↗

Comparison of the Seralyzer and EMIT systems for determination of theophylline concentrations.

A reflectance photometry assay for measurement of serum theophylline concentration was evaluated by comparison with an enzyme-multiplied immunoassay technique (EMIT). The concentration of theophylline in blood samples obtained from patients receiving intravenous theophylline therapy in the pediatric intensive-care unit was measured by both the Seralyzer and the EMIT systems. The interday and intraday variability of each method were also determined by means of calibrators of known concentration (5 to 40 micrograms/mL). There was significant correlation between the serum theophylline concentrations determined by the Seralyzer system and the EMIT system. The overall standard error of the estimate was 2.3 micrograms/mL, but with operator experience this improved to 1.3 micrograms/mL. Intraday variability was 1.2 micrograms/mL for the Seralyzer and 0.7 micrograms/mL for EMIT; the respective values for interday variability were 1.4 micrograms/mL and 0.8 micrograms/mL. The Seralyzer method measures theophylline concentrations with reliability, convenience, and speed. It could be potentially useful in a satellite, clinic, or acute-care pharmacy area.

Humans↗

[A study by the National Reference Center for Antibiotics on inocula for antibiotic sensitivity testing].

We compared the diameters of inhibition zones obtained during antibiotic sensitivity testing using two different techniques for preparing and seeding the inoculum, i.e. photometric adjustment followed by flooding, and turbidity adjustment followed by swab streaking. There was no significant difference between the results recorded following photometry-flooding of a light inoculum (2 to 3 X 10(6) CFU/ml) and following swab seeding of a bacterial suspension with a turbidity equal to 0.5 Mac Farland unit. These results indicate that both methods tested answer the NCCLS performance standards for disc antibiotic sensitivity testing and the critical values of the S.F.M. Antibiotic Sensitivity Testing Committee.

Escherichia coli↗

Urinary 3-methylthiopropionate excretion and the effect of D- or L-methionine ingestion studied in healthy subjects.

After overnight fasting, the urinary concentrations of 3-methylthiopropionate in 23 healthy male subjects aged from 17 to 72 were studied by gas chromatography and flame photometry. The urinary 3-methylthiopropionate concentrations after fasting showed an approximately normal distribution in the logarithmic scale (M +/- SD = 0.953 +/- 0.394): 10M = 8.97, 10M-SD = 3.62 and 10M + SD = 22.23 ng/mg Creatinine. In 6 volunteers, a 2g D- or L-methionine loading test was also performed. Following D-methionine ingestion, urinary 3-methylthiopropionate concentrations over a 1-hour period increased 22- to 95-fold above those of the pre- loading values and then decreased in an approximately linear manner on semilogarithmic graph paper during a further 2- or 3-hour observation period, after which the examination ended. The mean amount of 3-methylthiopropionate excreted in the urine 3 hrs after loading was 147.7 micrograms (n = 6). Following L-methionine ingestion, by contrast, the increases in 3-methylthiopropionate concentrations over a 1-hr period were 0.3- to 8.3-fold above those of the preloading values. The mean urinary excretion of 3-methylthiopropionate 3 hrs after loading was 3.58 micrograms (n = 4). Because of the simple and specific analytical procedure, quantitative determination of urinary 3-methylthiopropionate is useful in the study of human methionine metabolism.

Adolescent↗

Measurement of potassium concentration on-line with an ion-specific electrode during hemodialysis.

Patients requiring hemodialysis for end-stage renal disease are vulnerable to wide fluctuations in plasma potassium concentration [K+]p. Dialysis of K+ can result in rapid and large changes of [K+]p and result in significant morbidity. Since blood is routinely diverted extracorporeally to the dialyzer, the measurement of [K+]p could be made 'on-line' in this circuit with an ion-selective electrode (ISE) with negligible additional risk. Valinomycin/tetraphenylborate embedded in polyvinylchloride (PVC) electrodes of high K:Na selectivity were manufactured in our laboratory. The electrodes were calibrated in vitro and placed in a T diverter tube upstream from the dialyzer. Intermittently small amounts of blood were diverted to flow past the electrode allowing measurement of the electrical potential developed between the ISE half cell and a Ag:AgCl electrode placed 4 mm from the valinomycin membrane which could be read as [K+]p ISE. Blood flowing through the T diverter was then collected in glass tubes for measurement of [K+]p by flame photometry. Forty-six comparative measurements were made for 6 patients who had given informed consent for study. Least squares regression analysis for all observations gave a correlation coefficient of 0.95 and a regression equation of y = 1.1 X -0.39. Only six samples were discrepant by 0.5 mmol/l, and all of these had [K+]p greater than 5.0 mmol/l where the ISE measurements were less precise. Although the correlation of the two techniques was less than perfect, the ISE shows potential utility for monitoring trends of [K+]p instantaneously during hemodialysis.

Electrodes↗

ChromoTimeSystem--a new generation of coagulation analyses.

A new system of reagents and a dedicated instrument for coagulation and fibrinolysis assays, the ChromoTimeSystem is described. All assays are performed in the Chromotimer, a microprocessor controlled 4 channel photometer which is connected to micro computer. Most of the reagents use chromogenic substrates. PT, APTT, fibrinogen, reptilase time and thrombin time are all performed with 25 microliters of sample and 250 microliters of reagent. Neither predilution nor preincubation steps are necessary improving these photometric assays in respect to practicability and speed compared to coagulometric techniques. The use of photometry in contrast to the varying physical principles of classical coagulation analysis will be a step forward into standardization.

Antithrombin III↗

Ion-selective electrodes for sodium and potassium: a new problem of what is measured and what should be reported.

For clinical purposes the activities of Na+ and K+ obtained with ion-selective electrodes in undiluted whole blood or serum should be multiplied by an appropriate factor to obtain the same values as the substance concentrations obtained by flame photometry. The factor is primarily dependent on the mass concentration of water in normal plasma divided by the molal activity coefficient of Na+ (or K+) of normal plasma. We discuss the value of the molal activity coefficient of Na+ obtained by theoretical calculations and by direct measurement. The discrepancies between theory and measurement (gamma Na+ of 0.747 and 0.73, respectively) may be due to some binding of Na+ (protein binding or ion pair formation), a small and variable residual liquid-junction potential, or certainty about the appropriate value for the ionic strength of normal plasma (0.16 mol/kg or somewhat higher).

Electrodes↗

Colorimetric determination of potassium in whole blood, serum, and plasma.

This spectrophotometric method for the direct determination of potassium in serum or plasma is based on the selective complexing of potassium by a specific macrocyclic polyether, with the subsequent formation of an ion-pair with a colored anion. The colored anion is extracted into an organic solvent, clarified by centrifugation, and then measured at 415 nm. The absorbance of the chromogen varies linearly with [K+] to at least 15 mmol/L. Results of this colorimetric method (y) correlate well with the results obtained by a flame-photometric method (y = 1.04x - 0.22, r = 0.97, n = 81), with CVs ranging from 2 to 4%. We observed no interferences from lipemia, added bilirubin, or various electrolytes. We also evaluated the use of this reagent in a new automated blood analyzer developed by Abbott, a two-dimensional centrifugal system (Clin Chem 31:1457-1463, 1985). Potassium determined with this system (y) correlated well with results by flame photometry: y = 1.02x + 0.02 (r = 0.94, n = 168). With this system one can use whole-blood specimens in measuring potassium.

Autoanalysis↗

Spectral sensitivity function measured by a rapid scan flicker photometric procedure.

A rapid scan flicker photometric procedure is described whereby continuous spectral sensitivity functions are measured from unpracticed observers in 30 min. The 30 min includes instructions, practice, and data collection. Data are presented from four unpracticed observers age 12 to 42 years. Three practiced observers had their spectral sensitivities measured by both the conventional and rapid scan methods. The conventional method took 1.5 hr, measuring at 25 wavelengths and repeating each three times. The agreement between the rapid scan and conventional methods is satisfactory. Comparison with Judd's correction of CIEV (lambda) yields the same deviations as expected with conventional flicker photometry. The rapid scan procedure is shown to yield acceptably consistent data. The advantages of the rapid scan method for basic and applied vision research is discussed.

Adult↗

Comparison of photometric and weight estimation of Mycobacterium content in homogenous BCG cultures containing Tween 80.

A comparison of the weight and photometric methods of primary assay of BCG vaccine has been made, using a vaccine prepared in albumin-free medium but containing Tween 80. In the weight method, the bacteria were trapped on a membrane filter; for photometry a Pulfrich Elpho photometer and an instrument of Czech origin were used. The photometric results were the more precise, provided that the measurements were made within two days of completion of growth; after this time the optical density of the suspension began to decrease slowly. The lack of precision of the weighing method is probably due to the small weight of culture deposit (which was almost on the limit of accuracy of the analytical balance) and to difficulties in the manipulation of the ultrafilter.

BCG Vaccine↗

[Microfluorimeter for chromosome study].

A microfluorimeter is described for estimating amounts of chemical components in individual cells or in chromosomes, and for registering these components' distribution along the chromosomes. To solve the former problem, photoelectrical photometry of the object's fluorescence intensity is employed. To solve the latter problem, the photographic technique is used--making photos of metaphase plates in automatic or semiautomatic regime of exposure, with the following measuring of the intensity of the chromosome image on the negative performed on the same apparatus. The results of estimation of DNA content in individual chromosomes of Muntiacus muntjak are presented.

Animals↗

Electrical stimulation of experimental nonunions.

Hypertrophic and oligotrophic nonunions were prepared by resection of a portion of the proximal ulna in dogs. In the hypertrophic nonunions, 20 muamps of direct current for eight weeks produced an increase in bone formation compared to the opposite control limb by radiography, photometry, point counting of new bone, and growth rate by sequential fluorochrome labeling and the dynamic uptake of 99mTc-labeled methylene disphosphonate. Oligotrophic nonunions were treated by plating and aspiration grafting in addition to direct-current stimulation. Ony the point counting of new bone showed a significant increase in bone formation with stimulation. Sequential fluorochrome labeling demonstrated that the new bone was laid down on existing bone and not primarily adjacent to the cathode within the fibrous nonunion. This finding supports the cell-mediated rather than physicochemical effect of electrostimulation.

Animals↗

[Screening and detection of the analgesic zomepirac].

The article describes some possibilities for the screening and detection of the analgesic sodium [5-(4-chlorobenzoyl)-1,4-dimethylpyrrol-2-yl]-acetate dihydrate (zomepirac). UV-photometry seems to be the best method for the urine screening. Gas chromatography with and without derivatization and mass spectrometry are recommended as confirming methods.

Analgesics↗