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. The saved items can be printed to PDF using the print function of your web browser.
J. Planar Chromatogr. 20, 407-410 (2007). TLC of the color pigments from different sorts of red wine (Cabernet Sauvignon, Merlot, and Burgundy) on RP-18 with acetonitrile - water - formic acid 20:29:1 in a saturated chamber. Evaluation in visible light and under UV light at 366 nm, and by spraying with a methanolic solution of 0.5 mg/mL DPPH radical (2,2.diphenyl-1-picrylhydrazyl). Densitometric evaluation. RP-TLC is a tool for monitoring wine, for identification of the origin, and for detection of adulteration.
J. Planar Chromatogr. 25, 361-362 (2012). HPTLC of pigments in wheatgrass on sucrose-impregnated silica gel prepared by dipping the plates into a sucrose solution (400 g granulated sucrose/1 L distilled water), followed by heating at 110 °C for 20 min. Development with n-hexane - acetone 37:13. Detection by absorbance measurement between 400 and 800 nm. Sucrose impregnation prevents the degradation of the pigments during the analysis.
(Chinese). J. Lanzhou Univ., Nat. Sci. 23, 109-113 (1987) (Lanzhou Daxue Xuebao, Ziran Kexueban). TLC of 9 pigments (neoxanthin, violaxanthin, antheraxanthin, lutein, chlorophyll b, chlorophyll a, cryptoxanthin, pheophytins, ß-carotene) on silica with benzene - tert.butanol 9:10. Quantification by densitometry.
Biochemical Systematics and Ecology 18, 303-306 (1990). TLC of 19'-hexanoyloxyfucoxanthin, fucoxanthin, diadinoxanthin, 19-hexanoyloxyparacentrone-3-acetate, diatoxanthin and ß,ß-carotene on silica with 40% acetone in hexane, hexane – acetone – isopropanol 68,5:40:1,5 or hexane – acetone – isopropanol – benzene 17:33:1,3:17.
Biochemical Systematics and Ecology 22, 31-41, (1994). Separation of carotenoids on silica with acetone - hexane in different proportions. Preparative TLC on silica with the same hexane - acetone mixtures.
J. Agric. Food Chem. 48, 22-26 (2000). TLC of e.g. pelargonidin 3-O-, 3-O-malyl, and 3,5-di-O-glucoside on cellulose with hydrochloric acid - acetic acid - water 3:15:82 and 1-butanol - acetic acid - water 4:1:5, upper phase. Visualization under UV 365 nm.
Acta Chrom. 12, 151-158 (2002). HPTLC of lutein in nutrition supplements on RP-18 (with concentration zone, pre-washed with dichloromethane – methanol 1:1) with petroleum ether – acetonitrile – methanol 1:2:2. All sample solutions and developing chambers were wrapped in aluminum foil to protect the labile pigment from photo-decomposition. Densitometry at 448 nm. Three products containing lutein as the free alcohol or dipalmitate ester plus other ingredients were analyzed.
J. Sep. Sci. 30, 3311-3315 (2007). HPTLC of lawsone in the leaves of Lawsonia alba on silica gel with chloroform – methanol 17:3. Quantitative determination by absorbance measurement at 334 nm. The hRf value of lawsone was 40 and selectivity regarding matrix was given. Linearity was between 100 and 1000 ng/zone. The precision was 1.72 % and recovery (by standard addition) was 98.8 %.