Cumulative CAMAG Bibliography Service CCBS
Our CCBS database includes more than 11,000 abstracts of publications. Perform your own detailed search of TLC/HPTLC literature and find relevant information.
The Cumulative CAMAG Bibliography Service CCBS contains all abstracts of CBS issues beginning with CBS 51. The database is updated after the publication of every other CBS edition. Currently the Cumulative CAMAG Bibliography Service includes more than 11'000 abstracts of publications between 1983 and today. With the online version you can perform your own detailed TLC/HPTLC literature search:
- Full text search: Enter a keyword, e.g. an author's name, a substance, a technique, a reagent or a term and see all related publications
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J. Planar Chromatogr. 32, 475-479 (2019). TLC of enantiomers of (RS)-ketorolac on home-made silica gel plates impregnated with L-Tryp (1), L-Val (2), L-Met (3) or L-His (4) with acetonitrile - methanol - water - chloroform 9:5:2:4 for (1), acetonitrile - methanol - water - dichloromethane 6:2:1:1 for (2), acetonitrile - methanol - water - chloroform 5:3:1:1 for (3) and acetonitrile - methanol - water - chloroform 10:4:1:5 for (4), respectively. Detection by exposure to iodine vapors. The hRF values for (S)-(‒)- and (R)-(+)-ketorolac were 36 and 81 for (1), 30 and 79 for (2), 30 and 87 for (3) and 42 and 85 for (4), respectively. LOD was 0.4 μg/mL.
J. Planar Chromatogr. 32, 7-12 (2019). HPTLC of (RS)-mexiletine on RP-18 plates impregnated with 0.03 mM bovine serum albumin as chiral additive with acetonitrile - dichloromethane - methanol 1:1:1. Detection by exposure to iodine vapors. Resolution was 2.3 for the HPTLC method and 1.9 using an HPLC method. The HPTLC analysis took nearly 7 min, whereas HPLC took nearly 265 min to get the results.
59th Indian Pharmaceutical congress F-211, 440, (2007). TLC of isomers of carvedilol on chiral silica gel (prepared with beta-cyclodextrin) with methanol - water 5:1. Evaluation at 366 nm. The R(+) and the S(-) isomer of carvedilol had hRf values of 89 and 81, respectively. The linearity range was 50 - 500 µg/zone. Limit of detection and quantification was 10, 12 and 40, 42 µg/zone respectively for R(+) and S(-) isomers. The preparation of R(+) and S(-) isomers of carvedilol was found to be in the ratio 3:2 in bulk and formulations.
J. Chromatogr. A 1217(8), 1395-1398 (2010). TLC of atenolol, propranolol and salbutamol and their enantiomers by using different modes of loading/impregnating the Cu(II) complexes of L-proline, L-phenylalanine, L-histidine, N,N-dimethyl-L-phenylalanine, and L-tryptophan on silica gel with 1) the Cu(II)-L-amino acid complex as chiral mobile phase additive, 2) ascending development of plain commercial plates in the solutions of Cu complex, and 3) using a solution of Cu(II)acetate as mobile phase additive for the commercial TLC plates impregnated by development with the amino acid solutions. Detection by exposure to iodine vapor. The detection limit was 0.18 µg for each enantiomer. For the best method performance the Cu(II)cation has to be involved.
J. Planar Chromatogr. 29, 176-183 (2016). HPTLC of atracurium besylate (1) and atropine sulfate (2) on silica gel with acetonitrile – methanol – dichloromethane – glacial acetic acid – water containing 70 mg L-(+)-tartaric acid 70:10:5:7:1, pH 5 for (1), and methanol – water containing 40 mg L-histidine and 20 mg copper(II) acetate 22:3, pH 7 for (2). Quantitative determination by absorbance measurement at 280 nm for (1) and 215 nm for (2). The hRF values for (1) and (2) were 51 and 65, respectively. Linearity was in the range of 2-14 μg/zone for (1) and 5-35 μg/zone for (2). Intermediate precisions were below 1 %. The LOD and LOQ were 0.5 and 1.6 µg/zone for (1) and 1.2 and 3.6 µg/zone for (2). Average recovery was found to be 103.4 % for (1) and 96.6 % for (2).
J. Pharm. Biomed. Anal. 5, 665-673 (1987). Description of a TLC method for enantiomeric separation of chiral carboxylic acids using chiral derivatization and non-chiral TLC conditions to separate diastereomeric carboxamides using „levobase“, (1R, 2R)- (-)-1- (4-nitrophenyl)-2-amino-1, 3-propanediol, and „dextrobase“; the enantiomers of levobase, as chiral derivatizing agents for carboxamide formation in the presence of dicyclohexylcarbodiimide as coupling agent. Good resolution was obtained for a wide range of carboxylic acid enantiomeric pairs containing 1 to 2 chiral centers .
Nachweis mittels DC. (Pure enantiomeric drugs. Identification by densitometry.) Deutsche Apotheker Zeitung 132, 947 –952 (1992). TLC of amino acids, a-methyl amino acids on chiral plates and RP-18 silica with methanol – water – acetonitrile 1:1:4 and 5:5:3, also with methanol – water 1:8 and acetone – methanol – water 10:2:2). Detection by spraying with 0,3% ninhydrin in acetone.
J. Planar Chromatogr. 7, 126-128 (1994). TLC resolution of racemic amino acids on silica gel impregnated with a complex of copper and L-proline. The solvent systems found to be successful were butanol - acetonitrile - water 6:2:3, chloroform - methanol - propionic acid 15:6:4, and acetonitrile - methanol - water 2:2:1. Experimental details for preparing the impregnated plates are described.