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.
J. Sep. Sci. 43, 2981-2988 (2020). HPTLC of citicoline (1) and piracetam (2) in presence of their degradation products on silica gel with methanol - chloroform - ammonium chloride buffer 9:1:2. Quantitative determination by absorbance measurement at 230 nm. The hRF values for (1) and (2) were 15 and 85, respectively. Linearity was between 0.2 and 4 µg/zone for both (1) and (2). Intermediate precision was below 2 % (n=3). The LOD and LOQ were 56 and 180 ng/zone for (1) and 53 and 170 ng/zone for (2), respectively. Average recovery was 100.9 % for (1) and 99.8 % for (2).
J. Planar Chromatogr. 33, 219-229 (2020). HPTLC of carbamazepine (1) and its degradation product iminostilbene (2) on silica gel with petroleum ether - acetone 7:3. Quantitative determination by absorbance measurement at 230 nm. The hRF values for (1) and (2) were 12 and 63, respectively. Linearity was between 0.1 and 1.4 µg/zone for (1) and 0.1 and 1.2 µg/zone for (2). Intermediate precision was below 2 % (n=3). The LOD and LOQ were 0.03 and 0.09 µg/zone for (1) and 0.03 and 0.09 µg/zone for (2), respectively. Average recovery was 99.7 % for (1) and 99.7 % for (2).
Food Control. 22, 1154-1157 (2011). TLC of histamine in fish and fishery products on cellulose with ammonia - ethanol 1:3. Detection by spraying with Pauly's reagent (equal mixture of 20 mM sulfanilic acid in a 1 M HCl solution and 200 mM sodium nitrite solution, followed by adding 10 % anhydrous sodium carbonate in a 5 % ethanol solution). Color intensity was recorded using a digital camera, followed by imaging processing. Linearity was between 30 and 1000 ng/zone for histamine. Intermediate precision was below 5 % (n=3). The LOD was 20 ppm (2 mg/100 g). Recovery rate was between 93 and 98 %.
Food Control. 103, 111-118 (2019). Thin layer chromatography in tandem with surface-enhanced Raman scattering (TLC-SERS) of histamine in tuna samples on diatomaceous earth plates with ethanol - ammonia 3:1. Detection by spraying with Pauly's reagent (equal mixture of 20 mM sulfanilic acid in a 1 M HCl solution and 200 mM sodium nitrite solution, followed by adding 10 % anhydrous sodium carbonate in a 5 % ethanol solution). Gold nanoparticles were deposited on the plate zone and measurements were performed using a Raman spectrometer with an excitation laser wavelength of 785 nm.
J. Ethnopharmacol. 235, 361-374 (2019). HPTLC of colchicine (1) and withaferin A (2) in the polyherbal ayurvedic formulation Peedantak Vati (PV) on silica gel with chloroform -
methanol - water - formic acid 140:13:2:4. Quantitative determination by absorbance measurement at 218 nm. The hRF values for (1) and (2) were 22 and 28, respectively. LOD and LOQ were 40 and 120 ng/zone for (1) and 120 and 240 ng/zone for (2), respectively.
J. Chromatogr. A 1432, 140-144 (2016). 2-Aminoacetophenone (AAP) is closely correlated with the appearance of the sensory phenomenon of untypical aging off-flavor (UTA) in wine and is generally analyzed by GC/MS after being extracted from wines by liquid-liquid, solid-liquid or solid phase microextraction. Presentation of a rapid, selective and sensitive method for the determination of AAP in wine by HPTLC of the extracts, obtained by liquid-liquid extraction with t-butyl methyl ether followed by a basic cleanup, on amino layer with methylene chloride – toluene 7:3. Detection by dipping into n-hexane-paraffin solution and quantification by densitometry at 366/>400 nm using 2-amino-4-methoxyacetophenone as internal standard. The LOD and LOQ were 0.1 and 0.3 μg/L, respectively. The recovery was near 100 % for model, white and red wines, while AAP concentrations were >0.5 μg/L in UTA. The results indicated that the method enables the analysis of AAP in wines clearly below the odor thresholds and represents a rapid and convenient screening alternative to existing GC/MS methods.
(Hungarian). (Dehydrogenation accompanied decomposition of pyrido-pyrimidine carboxamide). TLC of 1,6-dimethyl-4-ox-1,6,7,8,9,9a-hexahydropyrido- (1,2a)-pyrimidine-3-carboxamide on silica with chloroform - methanol 92:8. Detection by UV. Photometry after elution.
J. Agric. Food Chem. 38, 1877-1880 (1990). One- and two-dimensional TLC on silica with dichloromethane - methanol 9:1, hexane - benzene - acetone 7:3:1; GC/MS after elution with methanol. Visualization under UV and by autoradiography.