Automatic Titration with Direct Read-out of Chloride Concentration

1961 ◽  
Vol 7 (3) ◽  
pp. 285-291 ◽  
Author(s):  
Ernest Cotlove ◽  
Hiroshi H Nishi

Abstract Direct read-out of chloride concentration is provided by an auxiliary designed for use with the automatic coulometric-amperometric titrator of Cotlove et al. (1). The circuitry, construction, and operation of the auxiliary are described. Automatic titration of samples of biologic fluids such as serum, cerebrospinal fluid, urine, sweat, and gastrointestinal fluids requires no prior preparation and the usual titration is completed within 1 min. The chloride concentration of the sample appears on a digital register directly in milliequivalents per liter. In routine use by various technologists in a clinical chemistry laboratory, the auxiliary-titrator combination has proved to be simple to operate and consistently accurate. The procedure requires only 0.1 ml. of solutions containing 10-400 mEq./L. of chloride (or 1 ml. of solutions with lower concentrations down to 1 mEq./L.). Optimal accuracy with a 0.1-ml. sample was in the concentration range above 40 mEq./L., in which the coefficient of variation was about ± 0.5 per cent.

1995 ◽  
Vol 41 (3) ◽  
pp. 343-360 ◽  
Author(s):  
M A Watson ◽  
M G Scott

Abstract In addition to microbial culture, cytology, and immunological studies, physicians rely on the clinical chemistry laboratory for biochemical analysis of patients' cerebrospinal fluid (CSF). However, apart from routine glucose and protein determinations, the clinical value of other CSF analytes is often unclear. Here, we review the literature pertaining to the use of CSF biochemical measurements in managing patients with infectious disease, neoplasia, stroke and trauma, and dementia. Although a small number of studies demonstrate potential usefulness of some markers, we conclude that, without further study, the data are insufficient to support the routine clinical use of most of the analytes examined.


Author(s):  
Nataša Stojanović ◽  
Dunja Rogić ◽  
Ana Stavljenić-Rukavina

AbstractThe Konelab 20XT (Thermo Electron Oy, Finland) is a clinical chemistry analyzer for colorimetric, immunoturbidimetric and ion-selective electrode measurements. The aim of our work was to evaluate the analytical performances of the Konelab 20XT according to the European Clinical Chemistry Laboratory Standards Guidelines. A total of 30 analytes including substrates, enzymes, electrolytes and specific proteins were tested. Investigation results showed low imprecision (within-run coefficient of variation was below 3.5% and between-day coefficient of variation was less than 2.5% for most analytes at all three levels studied) and acceptable accuracy of the analyzer. No significant sample- or reagent-related carry-over was found. It was demonstrated that the analytical system operates within the claimed linearity ranges. The results compared well with those obtained by instruments routinely used in our laboratory (Olympus AU2700, Behring Nephelometer II). In general, the data on interference by hemoglobin, hyperbilirubinemia and turbidity are in accordance with known facts. However, slight hemolysis was found to interfere with the alkaline phosphatase (ALP) assay and mild lipemia affected the glucose assay. The Konelab 20XT is an easy-to-use analyzer that is suitable for routine and emergency analyses in small laboratories.


1970 ◽  
Vol 16 (10) ◽  
pp. 856-860 ◽  
Author(s):  
Aron O Lurie ◽  
Richard J Patterson

Abstract A simple method for the assay of progesterone in nonpregnancy plasma was designed specifically for the clinical chemistry laboratory. One technician can readily perform 22 assays in less than one work day. Although no chromatographic step was used, the method was highly specific. Repro-ducibility studies indicated that the assay had a coefficient of variation of 7.5% for pregnancy plasma, 11.5% for nonpregnancy plasma. Clinical application of the method to specimens obtained from subjects during the normal menstrual cycle yielded values very similar to those obtained by more laborious and costly assay techniques.


1962 ◽  
Vol 8 (5) ◽  
pp. 538-545 ◽  
Author(s):  
Nathan Radin

Abstract A punched-card system was developed to simplify the administrative aspects of the clinical chemistry laboratory. In it a three-part requisition and samples are matched and given a laboratory number. The third copy of the original laboratory requsition is a charge card also used as a name file for the day. Prepunched cards, coded for laboratory tests, are used for each test requested. The laboratory number is stamped and punched on each test card. All test cards are then sorted into laboratory test groups, after which the laboratory data and results are recorded on them. Cards are then sorted for laboratory number and rematched with the original laboratory requisitions, which remained in numerical order. Results are then copied directly onto the requisitions. The system is more efficient, less susceptible to error, and simpler than other laboratory record systems.


1983 ◽  
Vol 14 (3) ◽  
pp. 301-316
Author(s):  
ARVIND K. N. NANDEDKAR ◽  
A. BLANK ◽  
JACOB ROOTENBERG

PEDIATRICS ◽  
1982 ◽  
Vol 69 (6) ◽  
pp. 833-833
Author(s):  
Joe Rutledge ◽  
Larry Miller

The Committee on Nutrition, American Academy of Pediatrics has recently reported on the "Use of Intravenous Fat Emulsions in Pediatric Patients" (Pediatrics 68:738, 1981). The committee recommends restriction of the amount of fat emulsion given infants because of a lack of accurate and appropriate means of monitoring serum fatty acid and triglyceride concentrations. Such is not the case for triglycerides. The pediatric clinical chemistry laboratory has the ability to measure serum triglyceride concentrations to support hyperalimentation therapeutic monitoring.


2019 ◽  
Vol 4 (2) ◽  
pp. 31-36
Author(s):  
Pier Angeli Medina ◽  
◽  
Jenny Matibag ◽  
Sarah Jane Datay-Lim ◽  
Elizabeth Arcellana-Nuqui

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