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.
J. Planar Chromatogr. 22, 301-304 (2009). Analytical and preparative TLC of luteolin-7-rutinoside and luteolin-7-neohesperidoside on silica gel with ethyl acetate - formic acid - acetic acid - water 100:11:11:23, on cellulose with 30 % acetic acid, and on polyamide with chloroform - methanol - 2-butanone - acetyl acetone (= pentane-2,4-dione) 9:4:3:1. Detection by spraying with natural products reagent followed by treatment with PEG 4000, or by aniline phthalate.
Chinese J. Pharm. Anal. 28 (4), 608-610 (2008). TLC of hyperoside in the raw extract of Hypericum perforatum on silica gel with petroleum ether (60-90 °C) – ethyl acetate – methanol 1:4:2. Detection under daylight. Quantification by densitometry at 591 nm. Linearity was given between 0.1 and 14.4 µg/spot (r2 = 0.9892), recovery was between 96.4 and 100.1 %.
J. Planar Chromatogr. 23, 225-226 (2010). OPLC of oregano oil components (carvacrol, thymol, and linalool) on silica gel with dichloromethane. Detection under UV 254 nm, by spraying with vanillin-sulfuric acid reagent (0.1 g vanillin, 100 mL ethanol, and 2.2 mL 95-98 % sulfuric acid) and heating at 110 °C for 3 min, and in the BioArena system (the dried developed plates were dipped for 10 s into an aqueous cell suspension of the soil bacteria Bacillus subtilis and incubated for 2 h at 100 % rel. humidity and 30 °C). Visualizion of antimicrobial compounds was performed by immersing the plates for 5 s in an aqueous solution of MTT reagent (80 mg MTT and 100 mg Triton X-100 in 100 mL water). The layers were further incubated and and documented.
J. Tech. & Sci. of Ningxia Agr. & Forest, 5, 38-39 (2010). For liquorice TLC on silica gel with ethyl acetate - glacial acetic acid - formic acid - water 15:1:1:2, detection by spraying with 10 % sulfuric acid in ethanol and heating at 105 ºC. For Rhizoma zingiberis TLC on silica gel with cyclohexane - diethyl ether 1:1, detection by spraying with 10% vanillin in sulfuric acid and heating at 105 ºC, followed by evaluation in daylight.
Acta Chromatographica 22 (3), 491-497 (2010). HPTLC of lupeol (methanolic Soxhlet extract from the bark of Mimosoups elengi) on silica gel with toluene – ethyl acetate – formic acid 12:2:1. The hRf value of lupeol was 64. Evaluation by densitometry at 220 nm. The linearity was in the range of 1–4 µg/band. The precision was 1.06 and 1.03 %RSD, respectively. Recovery was 97.3 %.
Yunan J. of Chinese Trad. Med. & Pharm. 31(10), 58-60 (2010). TLC of extracts of Cishushi suppository: 1) for Panax notoginseng, on silica gel with chloroform – methanol – water 14:6:1, detection by spraying with 10 % sulfuric acid in ethanol and heating at 105 ºC; 2) for Fructus Cnidii, on silica gel with petroleum ether (60-90 °C) – ethyl acetate 7:3, detection under UV 366 nm; 3) for Borneolum Syntheticum, on silica gel with toluene – ethyl acetate 19:1, detection by spraying with 5 % vanillin-sulfuric acid reagent and heating at 105 °C; 4) for Fructus Sophorae, on silica gel with chloroform – methanol – water – formic acid 700:300:50:1, detection by spraying with 1 % AlCl3 in ethanol, heating and evaluation under UV 366 nm.
J. Planar Chromatogr. 24, 248-252 (2011). TLC of MGDG and DGDG on silica gel with chloroform - methanol -10 % acetic acid 40:10:1. Detection by spraying with a 25 % solution of sulfuric acid in methanol, followed by heating at 105 °C for 5 min. Quantitative determination by densitometry at 477 nm. The hRf values were 48 for DGDG and 80 for MGDG. The limit of detection and quantification was 200 and 500 ng/band for DGDG and 500 and 1500 ng/band for MGDG. The linear range was 0.5-5.5 µg/band for DGDG and 1.5-5.5 µg/band for MGDG, respectively. The recovery (n= 9) was 95.7 % for DGDG and 93.5 % for MGDG. The repeatability and intermediate precision of results, as %RSD, was between 1.7-2.7 % for DGDG and 1.7-2.6 % for MGDG.
J. Planar Chromatogr. 24, 57-59 (2011). HPTLC of piperine on silica gel with toluene - ethyl acetate - diethyl ether 6:3:1 in a saturated twin trough chamber. The hRf of piperine was 40. Quantitative determination by densitometry at 337 nm. Linearity was between 15 and 75 ng/zone. LOD and LOQ was 5 and 15 ng/zone, respectively. The recovery was 94.5 %. The instrumental precision, repeatability, intra-day and inter-day precision (%RSD, n = 6) was 0.6 %, 0.8 %, 0.9 and 0.8 %, respectively.