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
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- 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.
Indian Drugs 45(8), 663-666 (2008). HPTLC of geranial and luteolin from leaves of Cymbopogon citratus on silica gel with toluene - ethyl acetate 9:1 for geranial and toluene - ethyl acetate - formic acid 10:7:1 for luteolin. Densitometric evaluation at 200 nm (geranial) and 254 nm (luteolin). Alcoholic extracts of the plant leaves were found to contain 1.34 % and 1.49 % of geranial and luteolin respectively.
J. Planar Chromatogr. 21, 263-265 (2008). HPTLC of nimbolide on silica gel in a twin trough chamber with ethyl acetate - hexane 1:1. Quantitative determination by absorbance measurement at 254 nm. The limits of detection and quantification were 3.3 and 1.0 µg/spot, respectively.
Phytochem. Anal.19, 104-115 (2008). TLC of geraniol on silica gel with chloroform - methanol - water 97:24:2 and of geranylacetate with toluene - ethyl acetate 93:7. Detection by spraying with vanillin sulfuric acid reagent.
60th Indian Pharmaceutical Congress PA-217 (2008). HPTLC of oleanolic acid in total methanolic extract of fruits of Randia dumetorum lam. on silica gel with toluene - ethyl acetate - acetic acid 70:30:1 in a twin trough chamber saturated for 10 min. Detection by treatment with 10 % sulphuric acid in methanol, followed by heating at 110 °C and immediate densitometric evaluation. Quantitative determination by absorbance measurement at 540 nm. The method was linear in the range of 50-500 ng/spot. Recovery was in the range of 99.4-100.8 %.
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.
pruriens. Abstract No. 9425, IHCB (2009). HPTLC of L-dopa in Mucuna pruriens seed extract and formulations on silica gel with n-butanol - acetic acid - water 4:1:1. Quantitative determination by absorbance measurement at 280 nm. The method was linear in the range of 100-1200 ng/spot with an average recovery of 100.3 %.
J. Planar Chromatogr. 22, 287-291 (2009). HPTLC of the biomarkers gallic acid, lupeol, oleanolic acid, and stigmasterol and plant extracts on silica gel with toluene - ethyl acetate - formic acid 5:5:1 for gallic acid and with toluene - ethyl acetate 4:1 for lupeol, oleanolic acid, and stigmasterol in a saturated twin trough chamber. Quantitative determination by absorbance measurement at 272 nm. Detection of oleanolic acid, lupeol, and stigmasterol by dipping in anisaldehyde reagent followed by heating at 110 °C for 5 min. Densitometric evaluation at 652 nm.