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. 16, 377-380 (2003). TLC of diosmin on silica gel with chloroform - methanol - water 23:12:2 with chamber saturation with 25% NH3. Quantitation by densitometry at 344 nm. Repeatable and accurate results were obtained, limit of detection was 20 ng; satisfactory recovery (99.8 to 100.3%); linearity is given from 5 to 50 mg/mL. New and simple procedure.
CBS 90, 10-11 (2003). HPTLC of periwinkle cell samples on prewashed silica gel with ethylacetate - diethylamine 9:1 in horizontal developing chamber over 25 mm. Detection by radiation with short-wave UV 254 nm. Quantitative determination by fluorescence measurement at 254 nm or 365 nm.
CBS 88, 14-15 (2002). HPTLC of mushroom extracts on silica gel with dichloromethane - ethyl acetate - methanol 3:1:1 and HPTLC of hydroquinone, rutin, resorcinol, and ascorbic acid on silica gel with toluene - methanol - acetic acid 45:8:4 over 80 mm with chamber saturation. Determination of bioactivity with DPPH-biotest by spraying with 5 mg (2,2-di-(4-tert-octylphenol)-1-picrylhydrazyl in 10 mL acetone.
Chinese J. Trad. Pat. Med. (Zhongchengyao) 26 (8), Append. 9-11 (2004). TLC on silica gel previously immersed in 0.5 % NaOH solution, developed with 1) ethyl acetate - methanol - water 100:17:13; and 2) with the upper phase of toluene - ethyl acetate - formic acid - water 20:10:1:1. Detection by spraying with AlCl3 solution and under UV 365 nm. Identification by fingerprint technique and comparison with the standard. Quantification of scutellarin by HPLC.
J. Planar Chromatogr. 18, 34 -38 (2005). Considering the latest technical and methodological developments, modern high-performance thin-layer chromatography, also known as planar chromatography, is a reliable and powerful analytical technique, in full compliance with current good-manufacturing practice (cGMP). With the proper equipment TLC is the method of choice when many samples must be analysed at low cost per sample. Advantages of HPTLC are shown in the analysis of botanicals: 1) Identification (separation of Stephania tetrandra root extracts with tetrandrine as standard on silica gel with toluene - ethyl acetate - methanol -ammonia 100:100:50:3; detection under UV at 254 and 366 nm, under white light after derivatization with iodine, and under UV at 366 nm after derivatization with anisaldehyde. 2) Semi-quantitative assessments in process control and stability tests (separation of fatty acids of Saw Palmetto products on RP-18 by two fold development with dichloromethane - acetic acid - acetone 2:4:5. 3) Quantitfication of marker compounds, like curcumin measured at 366 nm/>400 nm on silica gel with toluene - acetic acid 4:1. 4) Choice of stationary phase (separation of flavonoids on conventional TLC plates and on HPTLC plates with formic acid - water - ethyl methyl ketone - ethyl acetate 10:10:30:50 and detection with natural products reagent; switching to HPTLC reduced analysis time to a quarter and gave sharper bands). 5) Choice of mobile phase; 6) Derivatization and 7) Chromatogram evaluation.
Chinese J. Chromatogr. 26 (1), 50-55 (2008). TLC of some endophytic fungi isolated by column chromatography from selected medicinal plants on silica gel plates with 1) chloroform - methanol 7:1, 2) chloroform - acetonitrile 7:3, 3) ethyl acetate - 2-propanol 19:1, 4) methylene chloride - tetrahydrofuran 3:1, 5) methylene chloride - methanol - dimethylformamide 90:9:1. Detection by spraying with 1 % vanillin sulfuric acid reagent after gentle heating. Also HPTLC on silica gel with chloroform - methanol 9:1. Detection by densitometry at 254 nm and 366 nm. If taxol was present, derivatization by spraying with 1 % vanillin sulfuric acid reagent and heating for 2 min, then detection under UV 366 nm and white light. Only 13 fungal species produced taxol in the artificial culture medium of the 20 screened fungi.
Planta Med. 71, 194-196 (2005). Analytical TLC of glaucopines A and B on silica gel with dichloromethane - methanol 19:1. Detection by spraying with 50 % sulfuric acid.
(Chromatographic determination of acetyldigoxin in quality control.) Dtsch. Apoth. Ztg. 123, 1022-1026 (1983). TLC of alpha-acetyldigoxin on silica with chloroform - acetone 1 3:9. Detection with HCl vapors and drying at 120 °C for 10 minutes. In situ evaluation.