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
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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.
J. Agric. Food Chem. 50, 3208-3213 (2002). TLC of plant extracts (e.g. thymol, carvacrol, naphthalinol) on silica gel with chloroform - methanol 9:1 (best resolution) 3:2, n-propanol - water-ethyl acetate 7:1:2, chloroform- methanol - triethylamine 90:9:1, NH3 - butanol 2:5, chloroform - methanol - acetic acid 90:10:1. After drying for 1 h at 37°C, the plates were sprayed with 2 mL of potato-dextrose broth containing a spore suspension of the test organism Cladosporium.
J. Chinese Trad. Patent Med., (Zongchengyao) 25 (2), 125-127 (2003). TLC of isoimperatorin on silica gel with petroleum ether (60-90°C) - ethyl acetate 5:1. Detection under UV. Identification by fingerprint technique. Quantitation by densitometry at 305 nm.
Proc. Intern. Symp. on Planar Separations Plan. Chrom. 203-208 (2003). Description of the novel on-plate solid-liquid continuous extraction (SLCE) with preparative layers. The fine powdered sample to be extracted has to be introduced into a preparative layer on a 200 mm x 30 mm plate which is placed into a special device. The prepared preparative plate is covered with a glass plate, and with the help of a thick filter paper the extraction can be started with the appropriate extraction solvent. HPTLC of furocoumarins on silica gel under unsaturated conditions with ether - dichloromethane - tetrahydrofuran - hexane 10.71:9.68:7.5:72.11. Quantitation by densitometry at 313 nm.
CBS 92, 13-15 (2004). HPTLC on silica gel with toluene - ethyl acetate - methanol - ammonia 25 % 10:10:50:3 over 70 mm with chamber saturation for 30 min. Detection by dipping in iodine solution (0.05 g in 10 mL ethanol 96 %). Visual evaluation under white light. Quantitative determination by absorbance measurement at 210 nm. Repeatability measuring 6 replicates of the same sample on one plate is between 1.6 % and 3.7 %, repeatability of the means from 3 different plates is 1.2 %.
CBS 85, 14-15 (2000). HPTLC on silica gel with ethyl acetate - formic acid - water 45:5:3. Detection by spraying with dichloroquinonechlorimide followed by spraying with 10 % aqueous sodium carbonate solution. Visual evaluation.
J. Planar Chromatogr. 17, 300-304 (2004). TLC of essential oils and thymol, carvacrol, geraniol as standards and streptomycin and gentamycin as positive controls on silica gel with toluene - ethyl acetate 93:7. Detection with ethanolic vanillin sulfuric acid. Quantitative determination at 500 nm. For bioautography the developed plates were dipped for 10 s in approximately 50 mL culture medium containing the test organism followed by drying for 2 min. After storage of the plates at 26 - 28 °C for 17 h they were dipped for 10 s in an aqueous solution (0.1 g / 60 mL) of 3-{4,5-dimethylthiazol-2-yl}-2,5-diphenyltetrazolium bromide (MTT) the layers were incubated at 28 °C for 2 h and then dipped in 70 % ethanol and dried at room temperature.
J. AOAC Int. 88, 1568-1570 (2005). HPTLC of alliin on silica gel with n-butanol - acetic acid - water 3:1:1 at 25 +/- 2 °C and 40 % relative humidity. Detection by dipping in ninhydrin reagent (0.3 g ninhydrin in 100 mL n-butanol and 3 mL acetic acid) for 2 s, followed by heating at 110 °C for 5 min. Quantitative determination by densitometric evaluation of peak areas at 540 nm. Linearity within the range of 250-1500 ng/spot, correlation coefficient of 0.998 and RSD of 2.87 %; mean recovery 98.4 %.
Planta Med. 72, 351-357 (2006). Analytical and preparative TLC of ergosta-4,6,8(14),22-tetraen-3-one, beta-sitosterone, 2,6,11-trimethyldodeca-2,6-10triene, and stigma-4-ene-3,6-dione on silica gel with n-hexane - ethyl acetate 6:1. Preparative TLC of tsangin A with dichloromethane - acetone 25:1; of tsangin B and beilschmien C with dichloromethane - acetone 20:1; of beilschmien A and B with n-hexane - ethylacetate 2:1. Detection under UV light at 254 nm.