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
- Browse and search by CBS classification: Select one of the 38 CBS classification categories where you want to search by a keyword
- Keyword register: select an initial character and browse associated keywords
- Search by CBS edition: Select a CBS edition and find all related publications
Registered users can create a tailor made PDF of selected articles throughout CCBS search – simply use the cart icon on the right hand of each abstract to create your individual selection of abstracts. You can export your saved items to PDF by clicking the download icon.
Simultaneous analysis of seven tetracyclines in honey. J. Chromatogr. 400, 253-261 (1987). TLC of residual oxytetracycline, tetracycline, chlortetracycline, doxycycline, methacycline, dimethylchlortetracycline and minocycline in honey on silica and RP-8 silica with chloroform - methanol - 5% aqueous Na2EDTA 65:20:5 (lower phase) and methanol - acetonitrile - 0.5M aqueous oxalic acid 1:1:4 (pH 3.0), resp. Detection by spraying with 0.2M aqueous magnesium chloride and 10% TEA in methanol, resp., and then observing under UV at 360 nm. Detection limits 0.1 ppm in honey.
J. Chromatogr. 463, 469-473 (1989). Description of a number of TLC systems and spray reagents for separating and identifying the cation and anion parts of benzathine and embonic acid salts of ampicillin, amoxycillin, cephalexin and talampicillin embonate. Use of the methods for assessing the purity of the synthesized embonate and benzathine salts of ß-lactam antibiotics.
J. Agric. Food. Chem. 38, 538-541 (1990). TLC on silica RP-18 with methanol - acetonitrile - water 1:1:1, visualization by short-wave UV and by spraying with diazotised sulfanilic acid.
J. Planar Chromatogr. 5, 62-63 (1992). TLC of DNS-streptomycin and DNS-neomycin on silica with 20% disodium monohydrogen phosphate solution for 4 cm and (after drying) with the organic phase from butanol – ether – 20% aqueous Na2HPO4 35:10:20. Quantification by fluoro densitometry at 313/>400 nm resp. 366/>400 nm. Simple TLC method for routine analysis.
Shokuhin Eiseigaku Zasshi (J. Food Hyg. Soc. of Jap.) 34, 517-523 (1993). Establishment of a confirmation method using reverse-phase TLC/FABMS for identifying residual tetracycline antibiotics. oxytetracycline, tetracycline, chlortetracycline and doxycycline in thiaglycerol as matrix.
Proc. 9th Internat. Symp. Instr. Chromatogr., Interlaken, April 9.-11., 15-46 (1997). HPTLC of chloramphenicol and impurities (e.g. 1-(4'-nitrophenyl)-2-amino-1,3-propanediol, 4-nitrobenzaldehyde) on silica with chloroform - methanol - water 90:10:1. Detection under UV 254 nm; quantification by densitometry at 280 nm.
J. AOAC Int. 82, 1 - 8 (1999). TLC of antibiotics (avilamycin, avoparcin, Zn-bacitracin, erythromycin, flavomycin, furazolidone, lasalocid, monensin, narasin, penicillin, salinomycin, spiramycin, tetracyclines, tylosin, virginiamycin) after sample extraction on silica gel using butanol - methanol - 0.8% oxalic acid 8:2:5 or ethyl acetate - toluene - isopropanol 36:4:1. Detection by bioautography using a variety of test media and bacteria. Carbadox can be detected under UV prior to bioautography. Semiquantitative determination by measuring the size of the inhibition zones.
J. Liq. Chrom. & Rel. Technol. 24, 1501-1510 (2001). TLC of ampicillin on silica gel with butanol - water - acetic acid 4:1:1. Quantitation by densitometry at 485 nm after dipping in 0.2% ethanolic ninhydrin solution. The method was validated for linearity, detection limit, and accuracy by the method of Funk as well as for selectivity, and precision. Selective, precise, and accurate procedure.