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.
Chromatographia 67 (3-4), 259-267 (2008). Investigation of saturated aqueous solutions of 28 different salts used as potential mobile phases for salting-out TLC, on silica gel with a series of four mixed bis-aminocarboxylato cobalt(III) complexes. Confirmation of three alkali metal chlorides, and four alkaline earth metal chlorides, four linear dependences previously established on different adsorbents with (NH4)2SO4 solutions by linear regression analysis of chromatographic data obtained for fifteen mixed aminocarboxylato Co(III) complexes (four series) with solutions of ammonium chloride. With Li+, Mg2+, and Ca2+ chlorides the best separation was achieved.
Phytochem. Anal. 19, 353-358 (2008). HPTLC of galanthamine in the bulbs of Narcissus cv. on silica gel with chloroform - methanol 9:1 with chamber saturation for 30 min. Quantitative determination by absorbance measurement at 288 nm. The hRf value was 72 and selectivity regarding matrix was given. Linearity was in the range of 0.25 and 7.5 µg/spot. The limits of detection and quantification were 47 and 142 ng/spot, respectively. Recovery was 97.8 %. No significant intra- and interday variation was observed. The method proved to be precise, accurate, and rapid in comparison with a reference HPLC method.
J. Planar Chromatogr. 21, 191-195 (2008). HPTLC of fluconazole and clotrimazole (as internal standard) on silica gel with toluene - chloroform - methanol 6:15:2. Quantitation by densitometry at 210 nm.
J. Planar Chromatogr. 21, 21-26 (2008). HPTLC of extracts of Hoodia gordonii with fructose and beta-sitosterol as standards on silica gel with chloroform - methanol - water 70:30:3 in an automatic developing chamber fitted with a twin-trough chamber. The chamber was saturated for 20 min with mobile phase and relative humidity was controlled (33 %). Detection by dipping in anisaldehyde reagent, followed by heating at 100 °C for 3 min. Documentation and evaluation before derivatization under UV 366 nm and after derivatization under white light. The method was validated. It is specific and allows discrimination of Hoodia gordonii from Hoodia currorii, Hoodia parviflora, and the common adulterant prickly pear cactus (Opuntia ficus-indica). The sample is stable in solution and on the plate for at least 3 h, as well as during chromatography (2D test). After derivatization the chromatogram is stable for at least 1 hour. Precision (repeatability, intermediate precision, and reproducibility was good and the method is robust . The method is sensitive to changes in relative humidity. If relative humidity exceeds 47% the plate must be conditioned to 33% RH to ensure proper separation.
J. Liq. Chromatogr. Relat. Technol. 31, 1871-1880 (2008). HPTLC for the determination of neutral lipid profils using a standard mixture (containing cholesterol, oleic acid, triolein, methyl oleate, cholesteryl oleate) on silica gel (plates with 19 scored lanes and a preadsorbent application area, prewashed by development with dichloromethane - methanol 1:1) with petroleum ether - diethyl ether - acetic acid 80:20:1 in a saturated twin-trough chamber. Detection by spraying with 5 % ethanolic phosphomolybdic acid and heating for 10 min at 115 °C. Quantitative determination by absorbance measurement at 610 nm.
Journal of Natural Remedies 8(1), 61-67 (2008). During pharmacognostic studies on Sphaeranthus indicus (Asteraceae) the sesquiterpenoid 7-OH-eudesmanolide was isolated. HPTLC of the ethyl acetate soluble fraction of aqueous alcoholic Sphaeranthus indicus extracts, on silica gel with n-hexane - diethyl ether 3:7. The plant extract and the marker (7-OH-eudesmanolide) were chromatographed simultaneously. Quantitative determination by absorbance measurement at 213 nm.
J. AOAC Int. 91, 1149-1153 (2008). HPTLC of berberine on silica gel prewashed with methanol using n-butanol - acetic acid - water 8:1:1 in a twin-trough chamber with chamber saturation for 5 min at 33 °C at 57 % relative humidity. Quantitative determination by absorbance measurement at 350 nm.
Indian Drugs 45(12), 948-951 (2008). HPTLC of nebivolol hydrochloride and hydrochlorothiazide on silica gel with ethyl acetate - methanol - ammonia 17:2:1. Absorbance measurement at 280 nm. The method was linear in the range of 500-1500 µg/mL and 100-500 µg/mL for nebivolol hydrochloride and hydrochlorothiazide respectively. Recovery was 99.3-101.9 % for both compounds. The method is suitable for routine quality control.