A simple solid phase spectrofluorimetric method combined with flow analysis for the rapid determination of salicylamide and salicylic acid in pharmaceutical samples

1999 ◽  
Vol 365 (7) ◽  
pp. 619-624 ◽  
Author(s):  
A. Ruiz Medina ◽  
M. L. Fernández de Córdov ◽  
A. Molina Díaz
Keyword(s):  
Salicylic Acid ◽  
Solid Phase ◽  
Rapid Determination ◽  
Flow Analysis ◽  
Pharmaceutical Samples ◽  
Spectrofluorimetric Method

A FLOW ANALYSIS SYSTEM FOR THE RAPID DETERMINATION OF SULFONAMIDES USING A SOLID PHASE PHOTOMETRIC SENSING ZONE

2002 ◽  
Vol 35 (2) ◽  
pp. 269-282 ◽  
Author(s):  
A. Ruiz Medina ◽  
M. C. Cano García ◽  
A. Molina Díaz
Keyword(s):  
Solid Phase ◽  
Rapid Determination ◽  
Flow Analysis ◽  
Analysis System

Rapid determination of trace Cu2+ by in-syringe membrane SPE and membrane solid-phase spectra technique

2021 ◽  
Author(s):  
Long Li ◽  
Kehan Xu ◽  
Zuohua Huang ◽  
Xinxin Xu ◽  
Jibran Iqbal ◽  
...  
Keyword(s):  
Solid Phase ◽  
Rapid Determination ◽  
Rapid Extraction ◽  
Visible Spectra ◽  
Phase Spectra

A new in-syringe membrane SPE and solid-phase visible spectra method was proposed for the rapid extraction and visible spectra determination of trace Cu2+. The chelation and membrane SPE can be...

A green liquid chromatography method for rapid determination of ergosterol in edible fungi based on matrix solid-phase dispersion extraction and a core–shell column

2020 ◽  
Vol 12 (26) ◽  
pp. 3337-3343 ◽  
Author(s):  
Zhengming Qian ◽  
Zi Wu ◽  
Chunhong Li ◽  
Guoying Tan ◽  
Hankun Hu ◽  
...  
Keyword(s):  
Liquid Chromatography ◽  
Solid Phase ◽  
Rapid Determination ◽  
Edible Fungi ◽  
Chromatography Method ◽  
Matrix Solid Phase Dispersion ◽  
Phase Dispersion ◽  
Liquid Chromatography Method ◽  
Extraction Liquid

A green and rapid matrix solid-phase dispersion extraction-liquid chromatography analytical method for the determination of ergosterol in edible fungi was established.

Solid-phase radioimmunoassay for morphine, with use of an affinity-purified morphine antibody.

1978 ◽  
Vol 24 (2) ◽  
pp. 339-342 ◽  
Author(s):  
M Steiner ◽  
J L Spratt
Keyword(s):  
Affinity Chromatography ◽  
Correlation Coefficient ◽  
Solid Phase ◽  
Rapid Determination ◽  
Biological Fluids ◽  
Inhibitory Effect ◽  
Major Metabolite ◽  
Solid Phase Radioimmunoassay ◽  
Related Compounds

Abstract Morphine antibody purified by affinity chromatography was used to develop a solid-phase radioimmunoassay for morphine in polystyrene tubes. The tubes are coated with an appropriate concentration of the purified antibody, rinsed three times with buffered saline, and stored at -15 degrees C. Using tritiated dihydromorphine, we determined competitive morphine binding by difference when the radioactivity in the assay supernates was measured after incubation (1 h, 37 degrees C). Five standard curves, with use of serum equivalents of morphine ranging from 0 to 6 mug/liter, were linear and had a mean correlation coefficient of 0.98. Uncer conditions of the assay, levorphanol was comparable to morphine in its inhibitory effect on binding of labeled dihydromorphine, whereas dextrorphan was essentially inactive. Morphine-3-glucuronide, a major metabolite, is 55-fold less inhibitory in terms of its capacity to displace the radiolabel. We believe that the sensitivity of the technique, coupled with the simplicity of nonseparatory sampling, renders the system suitable for rapid determination of morphine and related compounds in biological fluids.

Solid-phase sample extraction for rapid determination of methylmalonic acid in serum and urine by a stable-isotope-dilution method.

1989 ◽  
Vol 35 (2) ◽  
pp. 260-264 ◽  
Author(s):  
K Rasmussen
Keyword(s):  
Methylmalonic Acid ◽  
Solid Phase ◽  
Rapid Determination ◽  
Current Method ◽  
Reference Interval ◽  
Cobalamin Deficiency ◽  
Isotope Dilution Method ◽  
Dilution Method ◽  
Selected Ion Monitoring

Abstract Methylmalonic acid concentrations are increased in serum in vitamin B12 (cobalamin) deficiency. Here I demonstrate the successful use of anion-exchange extraction for improving newly developed analytical procedures and describe well-documented, reliable performance of this method for rapid determination of methylmalonic acid. The sorbent counter ion is formate, and the elution solvent is formic acid. The dicyclohexyl derivative is measured by selected ion monitoring. For serum, the assay curve is linear from 0.026 to 200 mumol/L. The normal reference interval is 0.08 to 0.56 mumol/L. Added methylmalonic acid is accurately quantified. The sensitivity and the precision exceed those of the current method by three orders of magnitude. The total and within-day CVs are 4.6% to 7.9% and 2.6% to 4.7%, respectively. Similar figures were obtained for urine. This convenient method is useful for evaluation of cobalamin deficiency, especially in patients with normal or moderately depressed cobalamin concentrations in serum.

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