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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Part VII. J. Planar Chromatogr. 7, 389-393 (1994). TLC of stereoisomeric menthols and thujols (menthol, neomenthol, isomenthol, neoisomenthol, thujol, neothujol, isothujol, neoisothujol) on silica with hexane - ethanol 85:15 for menthols and benzene for thujols, each plate was developed three times. A new stereoisomeric topological index has been proposed (ISTI) which enables distinction between stereoisomers with hydroxyl groups in axial and equatorial positions.
J. Chromatogr. A 787, 227-233 (1997). Examination of the influence of temperature and mobile phase composition on retention of a-, b-, and g-cyclodextrins and two macrocyclic antibiotics. Measurement of RF values of the solutes at temperature from 5 to 60°C. Estimation of the change of enthalpy (DH°) and entropy (DS°) from linear Van't Hoff plots. Discussion of temperature as useful parameter for designing an enantioselective chromatographic system in which Rf values of the chiral phases modifier should be equal to 0 or 1.
J. Chromatogr. B 737 (1/2), 39-45 (2000). Development of a new strategy for isolating biologically active SIOOAI protein in order to further investigate the multiple functions of SIOOAI in various assay systems. Purification by octyl-sepharose hydrophobic interaction chromatography and HiTrapQ anion-exchange chromatography after EDTA extraction of myocardium of recombinant bacteria. Analysis of the products by silver-stained SCS-PAGE, silver stained two-dimensional PAGE and SDS-PAGE techniques.
Chromatographia 62 (11-12), 653-657 (2005). TLC of S(+) and R(-) ibuprofen on RP phase with beta-cyclodextrin - methanol 15:1. The UV densitometric detection was carried out at 222 nm. Limit of detection for S(+) and R(-) ibuprofen is 1 µg/mg. Precision and repeatability are good, the obtained results are within the range x mean ± 2. Recovery for both isomers is approximately 99 % and linearity was found to be in the range of 0.01-0.3 %. The presence of both isomers S(+) and R(-) ibuprofen was observed in all preparations at comparable concentrations from 56-66% for S(+) isomer and from 34-44 % for R(-) isomer.
J. Planar Chromatogr. 23, 7-13 (2010). TLC of the enantiomers of racemic atenolol, metoprolol, propanolol, and labetalol on silica gel using vancomycin as chiral impregnating agent or as chiral phase additive. With vancomycin as impregnating agent, resolution of the enantiomers of atenolol, metoprolol, propanolol, and labetalol was achieved with acetonitrile - methanol - water - dichloromethane 7:1:1:1, acetonitrile - methanol - water 6:1:1, acetonitrile - methanol - water - dichloromethane - glacial acetic acid 14:2:2:2:1, and acetonitrile - methanol - water 15:1:1. With vancomycin as mobile phase additive, resolution of the enantiomers of metoprolol, propanolol, and labetalol was achieved using acetonitrile - methanol - 0.56 mM aqueous vancomycin (pH 5.5) 15:1:2, and acetonitrile - methanol - 0.56 mM aqueous vancomycin (pH 5.5) - dichloromethane 18:2:3:2, respectively. Chromatograms were developed in glass chambers previously equilibrated with the mobile phase at 16 +/- 2 °C for 10-15 min. Detection by exposure to iodine vapor. The detection limits were 1.3, 1.2, 1.5. and 1.4 µg for each enantiomer of atenolol, metoprolol, propanolol, and labetalol, respectively.
J. Planar Chromatogr. 29, 108-112 (2016). HPTLC of water-soluble vitamins (B1, B2, B6, C, and B12), amino acids and β-blocker enantiomers (carvedilol, (S)-(−)-propranolol hydrochloride, (±)-propranolol hydrochloride, and (±)-sotalol hydrochloride) on novel core–shell polymers consisting of hyperbranched (poly(ethyleneimine)) core surrounded by oligosaccharide shell (PEI-OS) as a component of the silica gel phase. The influence of the weight of the hyperbranched PEI core (5 and 25 kDa) was investigated. β-blocker enantiomers were separated using acetonitrile - methanol 7:3. PEI-maltose and PEI-lactose were the most effective polymers for the chiral separation of β-blockers.
J. Chromatogr. 450, 241-252 (1988). Description of the separation of enantiomers using forced-flow planar chromatographic techniques such as OPLC and rotation planar chromatography. Discussion of the operating conditions for circular and linear developments with the separation of D, L-a-methylserine as an example.