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. Liq. Chromatogr. Relat. Technol. 42, 1-8 (2019). HPTLC of phospholipids (phosphatidylcholines, phosphatidylethanolamines, cardiolipins and phosphatidylglycerols) associated to membrane proteins in Rhodobacter (Rb.) blasticus, Rhodospirillum (R.) rubrum and Rhodobaca (Rbc.) bogoriensis on silica gel with a 7-step gradient based on methanol - water - ethyl acetate. HPTLC was coupled to electrospray mass spectrometry (ESI-MS) using an elution head-based interface for the identification of several phospholipid species.
Anal. Chem. 79, 5793-5808 (2007). HPTLC of phospholipids (phosphatidylcholine, phosphatidylethanolamine, phosphatidylglycerol, phosphatidic acid, cardiolipin, sphingomyelin) on silica gel in a saturated chamber with chloroform-methanol - 2-propanol - triethylamine - 0.25 % potassium chloride solution 30:9:23:18:6. Detection by dipping in molybdenum blue reagent for 1 s and quantitative evaluation by densitometry. The sensitivity was in the range of 10 to 150 pmol/spot (depending on phospholipid acidity, hRf value, and ion polarity).
Food Chem. 168, 520-528 (2015). HPTLC of lipids and fatty acids in mussels (Mytilus sp.) on silica gel with methyl acetate - isopropanol - chloroform - methanol - 0.25 % potassium chloride 25:25:25:10:9 as the polar solvent and further developed with hexane - diethyl ether - glacial acetic acid 40:10:1. Detection by spraying with a copper acetate reagent (10 % cupric sulfate in 8 % aqueous phosphoric acid). Quantitative determination by absorbance measurement at 535 nm.
Phytochemistry. 124, 68-78 (2016). HPTLC of polar lipids in ten species of microalgae included in two main linages (Plantae and Chromista) on silica gel with methyl acetate – isopropanol – chloroform – methanol – 0.25 % potassium chloride 25:25:25:10:4. Detection of phosphorous containing lipids by spraying with molybdenum reagent (molybdenum trioxide and metallic molybdenum in concentrated sulfuric acid followed by dilution with water). Those bands that gave negative response to the molybdenum reagent and migrate according to betaine lipid references from Chlamydomonas reinhardtii and Pavlova lutheri were subsequently visualized with iodine solution and scratched off. These isolated betaine lipids were eluted with 5 mL of chloroform – methanol 2:1.
J. AOAC Int. 101, 1993-2000 (2018). HPTLC of neutral lipids in fatty acid methyl ester (FAME)-derived biodiesel (1) and sphingolipids in human plasma (2) on LiChrospher or silica gel with a 4-step gradient based on t-butyl methyl ether, dichloromethane, and n-heptane for (1) and a 7-step gradient based on methanol and dichloromethane for (2). Detection of neutral lipids by dipping into a methanolic primuline solution (0.02 g/100 mL), followed by fluorescence recording at 366/>400 nm. Detection of sphingolipids by absorbance measurement at 190 nm. Zones of interest were eluted into an electrospray ionization-ion trap MS (ESI-MS) using a TLC-MS interface. _x000D_
J. Chromatogr. 299, 460-464 (1984). Two-dimensional TLC of triglycerides on silica having a strip of octadecyl-bonded silica along one side. Development with dry acetone - acetonitrile 4:1, three times along the reversed-phase band, then with dried toluene - ethanol - free chloroform 1:1 at right angles, after impregnating the plate with silver nitrate solution. Visualization with molybdatophosphoric acid reagent.
A comparison to serum lipid pattern. V. Danube Symposium on Chromatography, Yalta, November 11-16, 1985. Two dimensional TLC of lipids on silica with 1.) chloroform - methanol - water - acetic acid - heptane 65:25:4:1:1, 2.) heptane - ether - acetic acid 95:4:1. Detection by charring at 140 °C after copper acetate spray; densitometry. Identification of lysophosphatidylcholine, sphingomyelin, phosphatidylcholina, sulfatide, phosphatidylethanolamine, cerebroside.
J. Agric. Food Chem. 34, 904-907 (1986). Chromatography of oils and lipids on silica with petrol ether - ether - acetic acid 90:10:1 or chloroform - methanol - water 65:25:4. Detection with 5 0 % aq. sulfuric acid or Dragendorff reagent.