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. 37, 2797-2804 (2014). HPTLC of six flavonoids ((1) rutin, (2) luteolin-7-o-glucoside, (3) chamaemeloside, (4) apigenin-7-o-glucoside, (5) luteolin, (6) apigenin) and one coumarin, (7) umbelliferone, from chamomile plant samples and dietary supplements on amino silica gel with dichloromethane - acetonitrile - ethylformate - glacial acetic acid formic acid 44:10:12:5:5. Detection by spraying with 1 % methanolic solution of diphenylboric acid-beta-ethylamino ester, followed by air drying at 50 °C for 5 min. Quantitation by absorbance measurement at 450 nm for (1), (2) and (5), 360 nm for (3), (4) and (6) and 320 nm for (7). The hRF values for (1) to (7) were 7, 22, 27, 33, 58, 69 and 77. Linearities were in the range of 30-240 ng/zone for (1), 40-160 ng/zone for (2), 55-220 ng/zone for (3), 50-200 ng/zone for (4), 16-65 ng/zone for (5), 30-120 ng/zone for (6) and 21-85 ng/zone for (7). The intermediate intra-day and inter-day precisions were below 5 %. The LOD and LOQ were 10 and 30 ng/zone for (1), 13 and 40 ng/zone for (2), 18 and 55 ng/zone for (3), 17 and 50 ng/zone for (4), 6 and 16 ng/zone for (5), 10 and 30 ng/zone for (6) and 7 and 21 ng/zone for (7), respectively. Recoveries for the compounds were >90 %.
J. Planar Chromatogr. 28, 30-35 (2015). HPTLC of lupeol in the leaves of F. carica, F. nitida, F. ingens, F. palmata, and F. vest, on silica gel with toluene – methanol 9:1. Detection by spraying with p-anisaldehyde reagent, followed by heating. Quantitative determination by absorbance measurement at 540 nm. The hRF value of lupeol was 32. Linearity was between 100 and 800 ng/zone. The intermediate intra-day and inter-day precisions were below 2 % (n=6). The LOD and LOQ were 31 and 94 ng/zone, respectively. Recoveries were in the range of 99.2-99.7 %.
J. Planar Chromatogr. 27, 377-384 (2014). HPTLC of metformin in urine on silica gel with chloroform – methanol – ammonia 27 % 25:25:1. Quantitative determination by absorbance measurement at 237 nm. The hRF value of metformin was 25. Linearity was between 200 and 2000 ng/zone. The intermediate inter-day and intra-day precisions were below 9 % (n=5). The LOD and LOQ were 40 and 120 ng/zone, respectively. Recoveries were in the range of 92-94 %.
J. Planar Chromatogr. 28, 12-16 (2015). HPTLC of acrylic acid (as trans-cinnamic acid after labeling through a coupling reaction with iodobenzene at 60 ºC for 30 min) in water samples on silica gel with chloroform - methanol - acetic acid mixture 90:10:1. Quantitative determination by absorbance measurement at 254 nm. The hRF value for labeled acrylic acid was 47. Linearity was between 0.1 and 1 mM. The intermediate precisions were below 1.2 % (n=3). The LOD for the labeled acrylic acid was 0.1 nmol. Recoveries were in the range of 97-103 %.
leaves by a validated HPTLC–photodensitometry method. Phytochem. Anal. 26, 253-260 (2015). HPTLC of oleacein (1), oleuropein (2) and echinacoside (3) in the leaves of Ligustrum vulgare on silica gel with dichloromethane - methanol - formic acid - water 160:50:8:3. Detection by dipping into anisaldehyde (0.5 %, methanolic) and sulfuric acid (5 %, methanolic), followed by heating at 105 °C for 10 min. Quantitative determination by absorbance measurement at 240 nm and 350 nm. The hRF values of (1) to (3) were 82, 58 and 12, respectively. Linearity was in the range of 625-1875 μg/mL for (1), 100-300 μg/mL for (2) and 180-540 μg/mL for (3). LOD and LOQ were 0.58 and 1.77 μg/mL for (1), 0.20 and 0.61 μg/mL for (2) and 0.32 and 0.97 μg/mL for (3), respectively. Intra-day and inter-day precisions were below 3 % (n=3). Average recoveries varied from 102 to 113 % for (1), 106 and 112 % for (2) and 99 and 101 % for (3), respectively.
J. Agric. Food. Chem. 63, 2893-2901 (2015). HPTLC of lecithins such as phosphatidylcholine (1) and phosphatidylethanolamine (2) in soybean and sunflower used for chocolate production on silica gel with chloroform - methanol - water - ammonia 30:17:2:1. Detection by dipping into a primuline solution (100 mg of primuline in 200 mL of acetone - water, 4:1). Quantitation by fluorescence measurement at UV 366 nm. The hRF values of (1) and (2) were 30 and 41-43, respectively. Quantitation was also performed by HPTLC-positive ionization electrospray ionization mass spectrometry (ESI-MS) and by scanning HPTLC-matrix-assisted laser desorption ionization-time-of-flight mass spectrometry (MALDI-TOFMS). Mean LODs ranged from 8 to 40 mg/kg for HPTLC-FLD, 10 to 280 mg/kg for HPTLC-ESI and 15 to 310 mg/kg for HPTLC-FLD-ESI-MS.
Int. J. Pharm. 492, 109-119 (2015). HPTLC of sildenafil on silica gel with chloroform - ethanol 9:1. Quantitative determination by absorbance measurement at 254 nm.
Chromatographia 78, 1409-1413 (2015). HPTLC of oligosaccharides (derived from native chondroitin sulfate and hyaluronan) on silica gel aluminum foils of either "standard" or MS grade with 1-butanol - formic acid - water 3:4:1. Detection by staining with orcinol/sulfuric acid reagent or by MALDI-TOF MS. The hRf values of the unsaturated disaccharides of chondroitin sulfate (C4S, one sulfate residue per disaccharide unit) and chondroitin (C0S, no sulfate) were 43 and 55, respectively. The thickness of the silica gel layer (200 or 100 µm) influenced the quality of the mass spectra: a thinner layer improved the achievable signal-to-noise ratio and minimized unwanted formylation of the GAG oligosaccharides.