Analyses of Reducing Sugars on a Thin-layer Chromatographic Plate with Modified Somogyi and Nelson Reagents, and with Copper Bicinchoninate

1996 ◽  
Vol 60 (4) ◽  
pp. 594-597 ◽  
Author(s):  
Yeon-Kye Kim ◽  
Yoshiyuki Sakano
Keyword(s):  
Thin Layer ◽  
Reducing Sugars ◽  
Thin Layer Chromatographic Plate ◽  
Chromatographic Plate

Quantitation of Sulfamethazine in Pork Tissue by Thin-Layer Chromatography

1993 ◽  
Vol 76 (2) ◽  
pp. 335-341 ◽  
Author(s):  
Joseph Unruh ◽  
Daniel P Schwartz ◽  
Robert A Barford
Keyword(s):  
Thin Layer ◽  
Limit Of Detection ◽  
Solid Phase ◽  
Signal To Noise Ratio ◽  
Internal Standard ◽  
Signal To Noise ◽  
Thin Layer Chromatographic Plate ◽  
Average Accuracy ◽  
Chromatographic Plate ◽  
Layer Chromatography

Abstract Our earlier method to detect and quantitate sulfamethazine (SMZ) in milk at the 10 ppb level was modified to quantitate SMZ in pork tissue. Sulfabromomethazine (SBZ) is added to the tissue as an internal standard. SMZ and SBZ are extracted from the tissue into water as the supernatant of a centrifuged, aqueous homogenate and are cleaned up and concentrated by a series of solid-phase extractions. The sulfonamide-containing eluate is then separated on a silica gel thin-layer chromatographic plate. SBZ and SMZ are derivatized with fluorescamine, and their fluorescence is quantitated with a scanning densitometer. The limit of detection was estimated at 0.25 ppb (signal-to-noise ratio, 3:1). The average accuracy over the analysis range (0.54-21.8 ppb [μg/kg]) was 95.6% (standard deviation = 29.4%, n = 54).

scholarly journals Behavior of migration of some organic compounds on plasma-coated silica gel thin-layer chromatographic plate.

1986 ◽  
Vol 35 (5) ◽  
pp. 496-499 ◽  
Author(s):  
Kikuko YOSHIMURA ◽  
Keiichiro HOZUMI ◽  
Keisuke KITAMURA ◽  
Tatsuya KITADE ◽  
Yukiko OKAMOTO
Keyword(s):  
Thin Layer ◽  
Organic Compounds ◽  
Silica Gel ◽  
Thin Layer Chromatographic Plate ◽  
Chromatographic Plate

scholarly journals A Rapid Thin Layer Chromatographic Method for Simultaneous Screening of Albendazole and Ivermectin in Formulations Prescribed for Human or Veterinary Use

2019 ◽  
Vol 31 (4) ◽  
pp. 896-900
Author(s):  
R.P. Pawar ◽  
P. Mishra ◽  
A. Durgbanshi ◽  
D. Bose
Keyword(s):  
Acetic Acid ◽  
Thin Layer ◽  
Mobile Phase ◽  
Chromatographic Method ◽  
Pharmaceutical Preparations ◽  
Cost Effective ◽  
Dosage Forms ◽  
Thin Layer Chromatographic Plate ◽  
Rf Values ◽  
Chromatographic Plate

An easy and selective thin layer chromatographic method has been developed and experimentally validated for the simultaneous screening of most commonly used anthelmintic drugs i.e. albendazole and ivermectin. Separation of these compounds was attained on silica gel 60 F254 pre-coated thin layer chromatographic plate using an optimized mobile phase of diisopropyl ether:ethyl acetate:glacial acetic acid in the ratio of 7:3:0.1 (v/v), respectively at pH 3.5. The calculated Rf values for albendazole and ivermectin were 0.65 and 0.38, respectively and the LOD was found to be 25 μg/ml and 30 μg/ml for albendazole and ivermectin, respectively. The developed method is selective, sensitive, robust, cost effective, eco-friendly, rapid as well as easy to perform. The developed method was successfully applied for the analysis of albendazole and ivermectin in pharmaceutical preparations marketed as oral suspensions, powder, tablets and injectable of the single or combined dosage forms for human as well as veterinary use. It could also be applied for the simultaneous analysis of both the compounds in other samples.

A Simple Method for the Detection of Benzo[a]pyrene in Smoked Foods

1964 ◽  
Vol 47 (5) ◽  
pp. 894-897
Author(s):  
C Genest ◽  
D M Smith
Keyword(s):  
Thin Layer ◽  
Dimethyl Sulfoxide ◽  
Ultraviolet Light ◽  
Rapid Method ◽  
Small Volume ◽  
Simple Method ◽  
Thin Layer Chromatographic Plate ◽  
Chromatographic Plate ◽  
Benzene Extract

Abstract Benzo[a]pyrene can be used as an index of carcinogens in smoke. A simple and rapid method has been developed for determining this substance. The dried food was extracted with ra-hexane, the hexane was then extracted with dimethyl sulfoxide, and the polynuclear hydrocarbon was displaced from this solvent into benzene by water. The benzene extract was reduced to a small volume and an aliquot was spotted on a thin-layer chromatographic plate beside spots of a standard benzo[a]pyrene solution. The plate was chroma tographed with 2,2,4-trimethyl pentane:benzene (97:3). When observed under ultraviolet light at 3660 Å, 0.002 μg of pure benzo[a]pyrene could be found and the addition of 0.01—0.05 ppm to unsmoked foods could be detected. No smoked food examined contained this level of benzo-[a]pyrene.

Thin-layer chromatographic plate scanner interfaced with a mass spectrometer

1983 ◽  
Vol 55 (14) ◽  
pp. 2285-2289 ◽  
Author(s):  
Louis. Ramaley ◽  
Margaret E. Nearing ◽  
Margaret Anne. Vaughan ◽  
Robert G. Ackman ◽  
W. David. Jamieson
Keyword(s):  
Thin Layer ◽  
Mass Spectrometer ◽  
Thin Layer Chromatographic Plate ◽  
Chromatographic Plate

Laser-Based Photoacoustic Densitometer for Two-Dimensional Scanning of Thin-Layer Chromatographic Plates

1989 ◽  
Vol 43 (2) ◽  
pp. 249-253 ◽  
Author(s):  
Hirofumi Kawazumi ◽  
Edward S. Yeung
Keyword(s):  
Thin Layer ◽  
Spatial Resolution ◽  
Two Dimensional ◽  
Thin Layer Chromatographic Plate ◽  
Rapid Scan ◽  
Scan Time ◽  
Acousto Optic Device ◽  
Chromatographic Plate ◽  
Layer Chromatography ◽  
Scan Modes

Laser-based photoacoustic densitometry was applied to two-dimensional analysis in thin-layer chromatography. An acousto-optic device was used to provide both intensity modulation and a rastering scan. The spatial resolution is 25 × 60 spots for an area of 25 × 50 mm on the thin-layer chromatographic plate. Three detection modes, normal modulation, resonant modulation, and unmodulated rapid scan modes were compared. Detection limits in the most sensitive mode and in the fastest mode are 350 pg with scan time of 153 s and 6.9 ng with scan time of 1.5 s, respectively.

Thin Layer Chromatographic Determination of Ehtyl 0,0-Dimethyldithiophosphoryl-1-phenyl Acetate in Both Technical Cidial and Its 50% Liquid Formulation

1965 ◽  
Vol 48 (6) ◽  
pp. 1118-1120
Author(s):  
B Bazzi ◽  
R Santi ◽  
M Radice ◽  
R Fabbrini
Keyword(s):  
Thin Layer ◽  
Chromatographic Determination ◽  
Phenyl Acetate ◽  
Original Sample ◽  
Liquid Formulation ◽  
Thin Layer Chromatographic Plate ◽  
Chromatographic Plate ◽  
Technical Products ◽  
Phosphorus Determination

Abstract A method based on the phosphorus determination, including thin layer chromatographic separation, has been developed for determining ethyl 0,0,-dimethyldithiophosphoryl- 1 -phenyl acetate in both technical products and its 50% liquid formulation. The insecticide or a convenient amount of an insecticidal preparation is dissolved in benzene, and the solution is spotted on a thin layer chromatographic plate. After development and spraying with the chromogenic reagent, the surface containing Cidial is detached and eluted. The quantity of the active ingredient in the eluate is obtained by estimation of phosphorus as ammonium phosphomolybdate. The concentration of Cidial in the original sample can be derived by calculation.

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