scholarly journals Thin-layer chromatography to monitor cholesterol gallstone dissolution by methyl tert-butyl ether.

1991 ◽  
Vol 157 (1) ◽  
pp. 33-36 ◽  
Author(s):  
H B D'Agostino ◽  
E vanSonnenberg ◽  
C D Schteingart ◽  
A F Hofmann ◽  
G Casola ◽  
...  
1990 ◽  
Vol 23 (4) ◽  
pp. 857-860
Author(s):  
Shigeaki Inoue ◽  
Masaaki Endoh ◽  
Shoichi Shida ◽  
Hiromichi Nakachi ◽  
Mustuo Sasaki ◽  
...  

Author(s):  
Barbara Anders ◽  
Sabrina Doll ◽  
Bernd Spangenberg

AbstractWe present a densitometric quantification method for triclosan in toothpaste, separated by high-performance thin-layer chromatography (HPTLC) and using a 48-bit flatbed scanner as the detection system. The sample was band-wise applied to HPTLC plates (10 × 20 cm), with fluorescent dye, Merck, Germany (1.05554). The plates were developed in a vertical developing chamber with 20 min of chamber saturation over 70 mm, using n-heptane–methyl tert-butyl ether–acetic acid (92:8:0.1, V/V) as solvent. The RF value of triclosan is hRF = 22.4, and quantification is based on direct measurements using an inexpensive 48-bit flatbed scanner for color measurements (in red, green, and blue) after plate staining with 2,6-dichloroquinone-4-chloroimide (Gibbs' reagent). Evaluation of the red channel makes the measurements of triclosan very specific. For linearization, an extended Kubelka–Munk expression was used for data transformation. The range of linearity covers more than two orders of magnitude and is between 91 and 1000 ng. The separation method is inexpensive, fast and reliable.


1992 ◽  
Vol 53 (6) ◽  
pp. 572-577 ◽  
Author(s):  
R. Akimoto ◽  
E. Rieger ◽  
A.R. Moossa ◽  
A.F. Hofmann ◽  
H.E. Wahlstrom

1986 ◽  
Vol 146 (4) ◽  
pp. 865-867 ◽  
Author(s):  
E vanSonnenberg ◽  
AF Hofmann ◽  
J Neoptolemus ◽  
GR Wittich ◽  
RA Princenthal ◽  
...  

Hepatology ◽  
1993 ◽  
Vol 18 (2) ◽  
pp. 373-379 ◽  
Author(s):  
Oliver Esch ◽  
Claudio D. Schteingart ◽  
Dirk Pappert ◽  
Diane Kirby ◽  
Rita Streich ◽  
...  

1968 ◽  
Vol 23 (6) ◽  
pp. 834-838 ◽  
Author(s):  
Falko Grimmer ◽  
Wolfgang Dedek ◽  
Eberhard Leibnitz

The metabolism of dimethoate and its N-butyl homologues in tomato plants has been studied by use of 32P and 35S labelled initial products. The preparation of thiol-35S-labelled dimethoate is described. Formation and break down of dimethoxon and N-tert.-butyl-dimethoxon have been measured by radio-thin layer chromatography. The calculated biological half times have been compared with those in aqueous buffer solutions; remarkable differences between dimethoate and dimethoxon derivatives have been observed. The extension of the N-alkyl chain causes a more rapid biological breakdown. The technique described is also useful for the comparison of other organophosphorus compounds (OPC).


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