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.
Food Chem. 113, 640-644 (2009). HPTLC of curcumin (1), demethoxycurcumin (2), and bisdemethoxycurcumin (3) from the rhizomes of Curcuma longa on silica gel with chloroform - methanol 24:1. Quantitative determination by absorbance measurement at 425 nm. The hRf values of (1), (2), and (3) were 66, 48, and 30, respectively. Selectivity regarding matrix was given. Linearity was between 1 and 20 µg/spot for all curcuminoids. The intermediate precision of the method was satisfactory. Recovery was 98.7 % for (1), 96.3 % for (2), and 97.2 % for (3). The limit of detection for the substances was 100 ng/spot.
Chromatographia 65 (3-4), 239-243 (2007). TLC of solasodine in various Solanum species on silica gel with a developing solvent containing an organic acid to form ion pair complexes of solasodine with the acid dye. The resulting colored complex was quantified by absorbance measurement at 461 nm. Linearity was between 79 and 495 ng/spot with a correlation coefficient of 0.995. The method eliminates post derivatization steps and the problem of background interference. Application of the method to determine solasodine content in various herb samples, herb extract and their formulations showed an accuracy of 98.5 ± 2.8 % without matrix interference.
60th Indian Pharmaceutical Congress PA-202 (2008). HPTLC of allyl disulphide (an active ingredient of Allium sativum, garlic) on silica gel with n-hexane. The hRf value was 52. Quantitative determination by absorbance measurement at 298 nm. The linearity range was 200-1200 ng/spot. Several polyherbal formulations containing garlic were analyzed with the proposed method using allyl disulphide as marker.
J. Pharm. Biomed. Anal. 47, 790-794 (2008). HPTLC of the steviolbioside, stevioside and rebaudioside A in Stevia rebaudiana leaves on silica gel with ethyl acetate - ethanol - water 20:5:3. Detection by spraying with acetic anyhdride - sulphuric acid - ethanol 1:1:10 reagent. Quantitative determination by absorbance measurement at 510 nm. Linearity was in the range of 160-960 ng/spot for steviolbioside, 1-6 µg/spot for stevioside and 0.5-3 µg/spot for rebaudioside A with good correlation coefficients (0.998-0.999). The method was used for the assay of steviol glycosides in S. rebaudiana leaves collected from ten different locations.
60th Indian Pharmaceutical Congress PG-263 (2008). HPTLC of rutin in methanolic extracts of fresh leaves of Moringa pterygosperma on silica gel with ethyl acetate - formic acid - glacial acetic acid - water 100:11:11:26. Quantitative determination by absorbance measurement at 254 nm. The method provided good resolution of rutin from other constituents of the plant.
J. Sep. Sci. 32, 3239-3245 (2009). HPTLC of shikonin (1), acetylshikonin (2), and beta-acetoxyisovalerylshikonin (3) in four species of Arnebia on RP-18 with acetonitrile - methanol - 5 % formic acid 20:1:4. Quantitative determination by absorbance measurement at 520 nm. Linearity was in the range of 100-600 ng/zone for (1) and (2) and 100-1800 ng/zone for (3). The limits of detection for (1), (2) and (3) were 18, 15 and 12 ng/zone, respectively, while the limits of quantification were 60, 45 and 40 ng/zone, respectively.
Learned J. Dali Acad. (General Issue) 8 (10), 3-6 (2009). TLC of puerarin (in extracts obtained from different parts of Radix Puerariae) on silica gel with trichloromethane – methanol – water 14:5:1. Detection under UV 254 nm. The maximum amount of puerarin was found in the bine of the drug, followed by that in the root, whereas no puerarin was found in the flower and fruit.
International Seminar on Herbal Drug Research, PN-013 (2009). HPTLC of ethyl acetate extracts of seeds of Eugenia jambolana on silica gel with chloroform - acetone - formic acid 150:33:17. The antioxidant activity of different extract was assessed by DPPH method. The proposed method was applied to plant extract as well as to polyherbal formulation. The ethyl acetate extract was found to have good antioxidant activity. For HPLC fingerprint profiling a RP18 column was used with 80 % methanol as mobile phase.