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.
(TLC in pharmacy: buckthorn bark.) Deutsche Apotheker Zeitung 132, 70-72 (1992). TLC of 1,8-dihydroxayanthracen and derivatives on silica with ethyl acetate – methanol – water 77:13:10. Visualization by spraying with 10 % KOH in methanol, heating at 105 °C for 15 min. and under UV 254 and 365 nm or under visible light.
J. Chin. Trad. Med. (Zhongguo Zhongyao Zazhi) 20, (1) 33-34 (1995). TLC of baicalin on silica with toluene - ethyl acetate - formic acid 10:15:11. Quantification by densitometry at 280 nm.
J. Planar Chromatogr. 20, 61-64 (2007). HPTLC of flavonoids (catechin, epicatechin, gallocatechin, catechin gallate as standards) on RP-18 with acetonitrile - water - formic acid 10:40:3. The best separation of catechin and epicatechin was achieved by multiple gradient development with increasing concentrations of acetonitrile (from 20 to 22%) in the water - formic acid mixture. UV detection at 282 and 500 nm (after derivatization with vanillin-phosphoric acid) for estimation of catechin content.
J. Planar Chromatogr. 26, 336-342 (2013). HPTLC of diosmin (1), hesperidin (2), and ascorbic acid (3) on silica gel with ethyl acetate - methanol - water 15:3:2 for (1) and (2) and ethyl acetate - methanol - water - acetic acid 15:10:2:1 for (3). Quantification by absorbance measurement at 340 nm for (1), 286 nm for (2) and 265 nm for (3). The hRf values for (1), (2) and (3) were 34, 40 and 56, respectively. Linearity was in the range of 100-800 ng/zone for (1) and (2) and 50-400 ng/zone for (3). LOD and LOQ were 6 and 17 ng/zone for (1), 4 and 13 ng/zone for (2) and 4 and 13 ng/zone for (3), respectively. Recoveries were in the range of 98.1-99.3 % for (1), 98.4-99.5 % for (2) and 98.0-99.1 % for (3). Intermediate/interday/intra-day precision was below 2 % (n=6).
J. Sep. Sci. 37, 2797-2804 (2014). HPTLC of six flavonoids ((1) rutin, (2) luteolin-7-o-glucoside, (3) chamaemeloside, (4) apigenin-7-o-glucoside, (5) luteolin, (6) apigenin) and one coumarin, (7) umbelliferone, from chamomile plant samples and dietary supplements on amino silica gel with dichloromethane - acetonitrile - ethylformate - glacial acetic acid formic acid 44:10:12:5:5. Detection by spraying with 1 % methanolic solution of diphenylboric acid-beta-ethylamino ester, followed by air drying at 50 °C for 5 min. Quantitation by absorbance measurement at 450 nm for (1), (2) and (5), 360 nm for (3), (4) and (6) and 320 nm for (7). The hRF values for (1) to (7) were 7, 22, 27, 33, 58, 69 and 77. Linearities were in the range of 30-240 ng/zone for (1), 40-160 ng/zone for (2), 55-220 ng/zone for (3), 50-200 ng/zone for (4), 16-65 ng/zone for (5), 30-120 ng/zone for (6) and 21-85 ng/zone for (7). The intermediate intra-day and inter-day precisions were below 5 %. The LOD and LOQ were 10 and 30 ng/zone for (1), 13 and 40 ng/zone for (2), 18 and 55 ng/zone for (3), 17 and 50 ng/zone for (4), 6 and 16 ng/zone for (5), 10 and 30 ng/zone for (6) and 7 and 21 ng/zone for (7), respectively. Recoveries for the compounds were >90 %.
Phytochem. Anal. 27, 222-228 (2016). HPTLC fingerprinting of luteolin, quercetin and their corresponding glycosidic derivatives luteolin-7-O-glucoside and rutin (quercetin-3-O-rutinoside) in Soldanella alpina on silica gel with formic acid – water – ethyl methyl ketone – ethyl acetate 1:1:3:5. A solution of 2,5-dihydroxybenzoic acid in 70 % methanol (100 mg/mL) was used as a matrix for HPTLC-MALDI-TOF MS analysis.
J. Ethnopharmacol. 193, 627-636 (2016). HPTLC of hyperoside (1), rutoside (2), apigenin (3), spiraeoside (4), quercetin (5), and isoquercitrin (6) on silica gel with ethyl acetate – formic acid – glacial acetic acid – water 100:11:11:26. Detection by spraying with natural product/PEG reagent, followed by drying for 10 min. Quantitative determination by absorbance measurement at 366 nm. The hRF values for (1) to (6) were 55, 37, 95, 6, 92 and 57, respectively._x000D_
J. Planar Chromatogr. 30, 521-526 (2017). HPTLC of eupalitin-3-O-β-D-galactopyranoside in Boerhavia diffusa on silica gel with n-butanol – acetic acid ‒ water 8:1:1. Quantitative determination by absorbance measurement at 274 nm. The hRF value was 55. Linearity was between 0.05 and 2.5 μg/zone. LOD and LOQ were 1 and 4 ng/zone. The intermediate precision was <2 % (n=5). Average recovery was 98.3 %.