scholarly journals Factors affecting the detection limit of a flow- injection spectrophotometric procedure

1988 ◽  
Vol 214 ◽  
pp. 447-453 ◽  
Author(s):  
Julian F. Tyson ◽  
Andrew B. Marsden
Keyword(s):  
Detection Limit ◽  
Flow Injection ◽  
Factors Affecting ◽  
Spectrophotometric Procedure

scholarly journals Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent

2018 ◽  
Vol 33 (2) ◽  
pp. 47
Author(s):  
Orlando Fatibello-Filho ◽  
Heberth Juliano Vieira
Keyword(s):  
Standard Deviation ◽  
Detection Limit ◽  
Flow Injection ◽  
Pharmaceutical Formulations ◽  
Injection Method ◽  
Indirect Determination ◽  
Analytical Curve ◽  
Relative Standard ◽  
Injection Procedure

A spectrophotometric flow injection method for the determination of paracetamol in pharmaceutical formulations is proposed. The procedure was based on the oxidation of paracetamol by sodium hypochloride and the determination of the excess of this oxidant using o-tolidine dichloride as chromogenic reagent at 430 nm. The analytical curve was linear in the paracetamol concentration range from 8.50 x 10-6 to 2.51 x 10-4 mol L-1 with a detection limit of 5.0 x 10-6 mol L-1. The relative standard deviation was smaller than 1.2% for 1.20 x 10-4 mol L-1 paracetamol solution (n = 10). The results obtained for paracetamol in pharmaceutical formulations using the proposed flow injection method and those obtained using a USP Pharmacopoeia method are in agreement at the 95% confidence level.

scholarly journals DEVELOPMENT OF FLOW INJECTION METHOD FOR ONLINE DETERMINATION OF THIOCYANATE BASED ON OXIDATION BY PERMANGANATE

2010 ◽  
Vol 10 (2) ◽  
pp. 167-171 ◽  
Author(s):  
Hermin Sulistyarti ◽  
Spas D. Kolev ◽  
Stephanie Lim
Keyword(s):  
Detection Limit ◽  
Thyroid Gland ◽  
Flow Injection ◽  
Hydrogen Cyanide ◽  
Figures Of Merit ◽  
Sample Throughput ◽  
Teflon Membrane ◽  
Developing Method ◽  
Analytical Figures Of Merit

The importance of developing method for thiocyanate becomes obvious, because thiocyanate can inhibit iodine uptake of thyroid gland leading to mumps disease. In this work, thiocyanate is oxidized by permanganate in the acid donor stream to cyanide, which is directly converted to hydrogen cyanide. Then, hydrogen cyanide diffuses through a Teflon membrane into acceptor stream containing nickel(II) in ammoniacal buffer to form tetracyanonickelate(II) which is detected spectrophotometrically at 267 nm. Analytical figures of merit were linear up to 50 mg L-1 for thiocyanate, with RSD of 1.34%, and detection limit of 0.07 mg L-1, respectively. Interfering anions were eliminated under stoichiometric amount of permanganate and sample throughput was 20 h-1. The method was validated for determining thiocyanate samples from synthetic and gold process waters with satisfactory results.   Keywords: Thiocyanate, flow injection, permanganate, spectrophotometry

scholarly journals Determination of Sulfate in Natural and Residual Waters by Turbidimetric Flow-Injection Analysis

2001 ◽  
Vol 84 (1) ◽  
pp. 59-64 ◽  
Author(s):  
Inês P A Morais ◽  
António O S S Rangel ◽  
M Renata S Souto
Keyword(s):  
Detection Limit ◽  
Flow Injection ◽  
Reference Method ◽  
Previous Treatment ◽  
Barium Chloride ◽  
Sulfate Solution ◽  
Injection System ◽  
Residual Water ◽  
Relative Standard

Abstract A turbidimetric flow-injection system was developed for the determination of sulfate in natural and residual water samples, with no previous treatment, using spectrophotometric detection. The precipitating agent, 7.0% (w/v) barium chloride solution prepared in 0.10% (w/v) polyvinyl alcohol, was added by using the merging-zones approach. A 100 mg/L sulfate solution in 0.07M nitric acid was mixed with the sample before it entered the injection loop to improve the detection limit, provide in-line pH adjustment, and prevent the interference of some anionic species. The relative standard deviations of the results were between 1.4 and 3.0% and were in agreement with results obtained by the reference method. Samples within a linear concentration range of 10–120 mg SO42−/L can be analyzed at a rate of 40/h. The detection limit is 5 mg SO42−/L.

Competitive heterogeneous enzyme immunoassay for theophylline by flow-injection analysis with electrochemical detection of p-aminophenol

1990 ◽  
Vol 36 (4) ◽  
pp. 662-665 ◽  
Author(s):  
E P Gil ◽  
H T Tang ◽  
H B Halsall ◽  
W R Heineman ◽  
A S Misiego
Keyword(s):  
Alkaline Phosphatase ◽  
Detection Limit ◽  
Electrochemical Detection ◽  
Flow Injection ◽  
Flow Injection Analysis ◽  
General Procedure ◽  
Amperometric Detection ◽  
Enzyme Label ◽  
Commercial Kit

Abstract A competitive enzyme-linked immunoabsorbent assay based on the flow-injection amperometric detection of p-aminophenol has been investigated with use of the materials and general procedure of a commercial kit for the determination of theophylline in human serum. The antibody is immobilized on glass beads, and the enzyme label is alkaline phosphatase (EC 3.1.3.1). The high currents generated during the electrochemical detection allowed a rapid (35 min) and simple determination of theophylline throughout its therapeutic range (10-20 mg/L) and also in the subtherapeutic range (detection limit of about 80 micrograms/L).

scholarly journals A simple flow-injection method for the determination of blood glucose using a Technicon immobilized enzyme coil

1989 ◽  
Vol 11 (2) ◽  
pp. 87-88 ◽  
Author(s):  
Sveinbjörn Gizurarson
Keyword(s):  
Blood Glucose ◽  
Detection Limit ◽  
Flow Injection ◽  
Immobilized Enzyme ◽  
Single Channel ◽  
Glucose Solution ◽  
Injection System ◽  
Flow Injection System ◽  
Simple Flow

The applicability of a single-channel flow-injection system with immobilized enzyme coil (Technicon) and UV detection to the determination of glucose is described. The method was used for a pure glucose solution and for serum. The detection limit was 0.10 mM, the rate of determination was 20-40 per hour and the precision was satisfactory. The system is very simple and practical when many analysis are to be determined periodically.

scholarly journals Rapid flow injection electrochemical detection of 3,3′,4,4′ tetrachlorobiphenyl using stabilized lipid membranes with incorporated sheep antibody

2013 ◽  
Vol 11 (2) ◽  
pp. 320-323 ◽  
Author(s):  
Dimitrios Nikolelis ◽  
Nikolas Psaroudakis ◽  
Antonis Michaloliakos ◽  
Georgia-Paraskevi Nikoleli ◽  
Michael Scoullos
Keyword(s):  
Detection Limit ◽  
Ethylene Glycol ◽  
Electrochemical Detection ◽  
Flow Injection ◽  
Lipid Membranes ◽  
Electrochemical Biosensor ◽  
Glycol Dimethacrylate ◽  
Lipid Film ◽  
Rapid Flow ◽  
Number Of Cycles

AbstractAn electrochemical biosensor based on a supported polymerized lipid film with incorporated sheep anti-3,3′,4,4′ tetrachlorobiphenyl (PCB congener 77) antibody using flow injection analysis was developed. The polymerized lipid film contained 85% (w/w) dipalmitoylphosphatidylcholine (DPPC) and 15% (w/w) dipalmitoylphosphatidic acid (DPPA), methacrylic acid, ethylene glycol dimethacrylate, AIBN and sheep anti-congener 77 antiserum. Congener 77 was injected into flowing carrier electrolyte and the flow stopped to detect the antigen. These membranes gave only a single transient proportional to log [congener 77] from 10−8 to 10−5 M, with a detection limit of ca. 10−8 M. A membrane containing 35% (w/w) DPPA was used to examine regeneration. The maximum number of cycles was about 5.

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