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.
Planta med. 66, 96-98 (2000). TLC of secoiridoids on silica gel with chloroform - methanol 3:1. Detection under UV 366 nm and by spraying successively with 0.2% Fast Red Blue in water and 20% potassium carbonate in water. TLC of g-pyrone compounds (e.g. gentiopicrin, mangiferin) on cellulose with 15% acetic acid in water. Detection under UV 366 nm and by spraying with 5% aluminium chloride solution in ethanol.
Planta med. 68, 640-642 (2002). Analytical and preparative TLC of i. a. (+)-10,11-dioxoerysotrine, erysotrine, syringaresinol, erybraedin, neobavaisoflavone, abyssinone IV, neorautenol, isoneorautenol, shinpterocarpin, and erythrinin B on silica gel with chloroform - ethyl acetate 6:1 by 3-fold development. Visualization under UV light at 254 and 366 nm and by spraying with vanillin - sulfuric acid reagent. TLC bioautography for antibacterial and antifungal assays.
J. Planar Chromatogr. 19, 92-97 (2006). Two-dimensional HPTLC of naringenin, acacetin, flavone, morin, hesperetin, quercetin, narcisin, kaempferol 3,7-dirhamnoside, naringin, rutin, astragalin, quercitrin, kaempferol 3-glyco-7-rhamnoside, naringenin 7-glucoside, ferulic acid, chlorogenic acid, elagic acid, caffeic acid, p-coumaric acid, m-coumaric acid, o-coumaric acid, and gallic acid by connecting diol or silica plates to RP18 plates, with e. g. acetone - water 2:3 or 1:1 in first direction of development and propan-2-ol - ethyl acetate 1:1 or methanol - ethyl acetate 1:9 in second direction of development. Derivatization by use of diphenylboric acid 2-aminoethylester (natural products reagent), followed by PEG 400 reagent; detection under 365 nm.
International Journal of ChemTech Research 1(4), 1122-1128 (2009). TLC on silica gel with toluene - ethyl acetate 3:1. The hRf value of the furanocoumarin psoralen was 47. Densitometric evaluation at 299 nm. The method was linear in the range of 10-100 ng/band. The average recovery was 99.7 %.
CBS 109, 2-4 (2012). Extraction of arabica coffee with 2 to 50 % robusta coffee by accelerated solvent extraction with tBME. A part was saponified with10 % ethanolic KOH solution for 2 h. HPTLC of coffee extracts and standards 16-O-methylcafestol (16-OMC) and 16-OMC esters on silica gel with toluene - ethyl acetate - acetic acid 93:7:1 for 16-OMC esters and with tBME - chloroform 1:1 for 16-OMC. Detection by spraying with vanillin sulfuric acid (1 g in 250 mL ethanol and 2 mL of sulfuric acid, prepared freshly) and heating for 1 min at 80 °C. Quantitative absorption measurement at 530 nm. The LOD was 163 ng/band. After saponification the LOD of free 16-OMC was 43 ng/band. Thus 2 % robusta can be detected in a coffee blend.
Planta Medica 82(4), 371-376 (2016). TLC was applied to compare acetone – water 4:1 extracts from the mycelia and medium of fungus Trichoderma koningiopsis YIM PH 30002; an ethyl acetate fraction of each extract was separated on silica gel (mobile phase unknown) and visualized by three methods: detection with iodine reagent, sulfuric vanillin reagent, and phosphomolybdic acid in ethanol (8 %, w/v); no difference was found. Both extracts were then combined for the further isolation on columns of koninginins A, B and F, koningiopisins A–H, and trichodermaketone C._x000D_
Planta Med 83(05), 412-419 (2017). For the purification of verbascoside, the ethanol-water fractionation through size exclusion chromatography (Sephadex LH-20) of an 80 % ethanolic extract of Lippia citriodora leaves was monitored by TLC on silica gel with chloroform – methanol 7:3, followed by detection with vanillin sulfuric acid reagent.
J. Liquid Chromatogr. 8, 2927-2947 (1985). HPTLC on silica and RP-18 silica with different solvents and solvent mixtures. Detection by UV.