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. AOAC Int. 91, 1227-1236 (2008). HPTLC on silica gel using chloroform - ethanol - water - triethylamine 5:5:1:5 for separation of phospholipids and chloroform - acetone - methanol - acetic acid - water 46:17:15:14:8 and chloroform - methanol - acetic acid 13:5:2 for separation of glycolipids. Visualization by spraying with primuline reagent (Direct Yellow) and observation under UV light at 366 nm. Also MALDI-TOF-MS analysis.
Biochem. Biophys. Res. Commun. 399, 150-154 (2010). HPTLC of the lipids from mouse primary macrophages on silica gel with butanol - acetic acid - water 3:1:1. Detection by imaging using Fujifilm intelligent dark box in SYBR green fluorescent light. Quantitative determination with a TLC plate imaging software.
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.
Food Chem. 239, 848-857 (2018). HPTLC of lipids in raw milk on silica gel with n-hexane – diethyl ether – acetic acid 85:15:2. Detection by spraying with phosphomolybdic acid in ethanol. Quantitative determination by absorbance measurement at 650 nm. The identified peaks corresponded to phospholipids, 1,3-diglycerols, 1,2-diglycerols, sterols, free fatty acids and triacylglycerols.
Chromatographia 18, 512-516 (1984). The retention behavior of 8 substituted benzoic acids was tested on R-18 silica in the presence of ammonium bromide and various tetraalkylammonium compounds with different alkyl chain lengths. Developing solvents made up of water, acetonitrile, acetone, dioxane, methanol and THF. Scanning by absorbance at 254 nm.
Biochemical Systematics and Ecology 13
Part 2: Optimization of the system. J. High Resol. Chromatogr. 8, 838-842 (1985). Examination of influence of sorbent modifier, elution temperature and polarity of elution solvent upon resolution of polar lipids. HPTLC of 23 polar lipids on silica with 9 different eluents. Quantification by densitometry.
J. Chromatogr. 382, 308-313 (1986). TLC of 5 phospholipids, 5 neutral lipids, 4 cholesterol ester subfractions on silica with 2 successive runs with chloroform - methanol - water 65:25:4 and n-hexane - acetone 100:1. Analysis of lipids in human blood.