Relationship between the chromatographic behaviour of dermorphin-related oligopeptides and the composition of the mobile phase in reersed-phase thin-layer chromatography: comparison of extrapolated RF values

1984 ◽  
Vol 287 ◽  
pp. 259-270 ◽  
Author(s):  
A.M. Barbaro ◽  
M.C. Pietrogrande ◽  
M.C. Guerra ◽  
G.Cantelli Forti ◽  
P.A. Borea ◽  
...  
1973 ◽  
Vol 56 (2) ◽  
pp. 367-372
Author(s):  
David L Stalling ◽  
James N Huckins

Abstract The components of Aroclors® 1232, 1248, 1254, and 1260; Halowaxes® 1099, 1013, and 1014; and several chlorinated pesticides are resolved by reverse phase thin layer chromatography (RPTLC), which permits component separation by partition between a nonpolar stationary phase and a polar mobile phase. Rf values of resulting spots were calculated for 2 of 4 new solvent systems (mobile phases). RPTLC patterns were reproducible and characteristic of each material examined. The spots were recovered from the plates and characterized by gas-liquid chromatography (GLC) and/or GLC-mass spectrometry. In some cases, single GLC peaks of Aroclor standards were resolved into more than one component by RPTLC, whereas some RPTLC spots of Halowaxes were resolved into as many as 4 GLC peaks. The analysis of environmental residues of chlorinated compounds was facilitated by this technique.


2014 ◽  
Vol 21 (1) ◽  
pp. 11-15
Author(s):  
Daiva Kazlauskienė ◽  
Guoda Kiliuvienė ◽  
Palma Nenortienė ◽  
Giedrė Kasparavičienė ◽  
Ieva Matukaitytė

By conducting the toxicological analysis it is meaningful to determine the analytical system that could identify simultaneously several medicinal preparations quickly and precisely. The purpose of this work was to create and validate the method of thin-layer chromatography that would be suitable to separate the components of antidepressant mixture (amitriptyline hydrochloride, paroxetine hydrochloride, sertraline hydrochloride, fluvoxamine maleate and buspirone hydrochloride) and to identify them. The system was validated with regard to the sensitivity, repetition of data, resistance and particularity. The solvent systems with potential of high separation of components in their mixture were created: acetonitrile, methanol, ammonia solution 25 percent (85:10:5); acetonitrile, methanol, ammonia solution 25 percent (75:20:5); dichlormethane, 1,4-dioxane, ammonia solution 25 percent (50:45:5); dichlormethane, 1,4-dioxane, ammonia solution 25 percent (42:55:3); trichlormethane, 1,4-dioxane, ammonia solution 25 percent (25:70:5); trichlormethane, 1,4-dioxane, ammonia solution 25 percent (60:36:4). One of the most suitable solvent systems for separation of the analyzed mixture (sertraline, amitriptyline, paroxetine, buspirone, fluvoxamine) was determined – acetonitrile, methanol, ammonia solution 25 percent (85:10:5). When this solvent system was used, the average Rf values of the analyzed compounds differed the most. Validation was conducted – the relative standard deviation (RSD, percent) of the average Rf value of the analyzed compounds varied from 0,6 to 1,8 percent and did not exceed the permissible error of 5 percent. The sensitivity of methodology was determined by assessing the intensity of the mixture’s spots on the chromatographic plate. The detection limit of buspirone was 0,0012 µg; sertraline – 0,0008 µg; amitriptyline – 0,0004 µg; fluvoxamine – 0,0004 µg; paroxetine – 0,0008 µg. The resistance of results to the changed conditions – it was determined that when the amounts of the solvents acetonitrile and methanol were increased or decreased to two milliliters, the average Rf values of the analyzed compounds did not change statistically significantly


Talanta ◽  
1992 ◽  
Vol 39 (8) ◽  
pp. 953-958 ◽  
Author(s):  
I POLITZER ◽  
K CRAGO ◽  
K AMOS ◽  
K MITCHELL ◽  
T HOLLIN

INDIAN DRUGS ◽  
2015 ◽  
Vol 52 (12) ◽  
pp. 42-48
Author(s):  
P. J. Patel ◽  
◽  
D. A Shah ◽  
F. A. Mehta ◽  
U. K. Chhalotiya

A simple, sensitive and precise high performance thin layer chromatographic (HPTLC)method has been developed for the estimation of ondansetron (OND) and ranitidine (RAN) in combination. The method was employed on thin layer chromatography (TLC) and aluminium plates were precoated with silica gel 60 F254 as the stationary phase, while the solvent system was methanol. The Rf values were observed to be 0.5 ± 0.02, and 0.3 ± 0.02 for OND and RAN, respectively. The separated spots were densitometrically analyzed in absorbance mode at 299 nm. This method was linear in the range of 25-300 ng/band for OND and 50-600 ng/band for RAN. The limits of detection for OND and RAN were found to be 3.47 and 1.83 ng/band, respectively. The limits of quantification for OND and RAN were found to be 10.53 and 5.55 ng/band, respectively. The proposed method was validated with respect to linearity, accuracy, precision and robustness. The method was successfully applied to the estimation of OND and RAN in combined dosage form.


Sign in / Sign up

Export Citation Format

Share Document