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. Chinese Trad. Patent Med. (Zhongchengyao) 25 (9), 719-720 (2004). TLC on silica gel with 1) chloroform - methanol - water 13:7:2, 2) chloroform - acetone - formic acid 10:5:2, 3) petroleum ether - ethyl formate - formic acid 15:5:1. Detection 1) by spraying with 10 % H2SO4 in ethanol and heating and under UV 365 nm, 2) by ammonia vapor and under UV 365 nm. Identification by fingerprint techniques. Quantitation of danshensu by HPLC. Discussion of use of the procedures for the quality control of the medicine.
Chinese J. Trad. Patent Med. (Zhongchengyao) 26 (3), 192-195 (2004). TLC of Qufeng medicinal wine on silica gel with 1) n-hexane - ethyl acetate 9:1; 2) ethyl acetate - methanol - water 100:17:13; 3) toluene - ethyl acetate - formic acid - water 20:10:1:1; 4) chloroform - methanol - water 40:10:1; 5) n-hexane - ethyl acetate - chloroform - glacial acetic acid 50:15:5:1. Detection 1) under UV 365 nm; 2) by spraying with 1 % AlCl3 in methanol and under UV 365 nm; 3) by spraying with 5 % H2SO4 in ethanol and heating at 105 ºC; 4) by exposing to ammonia vapor. Identification by fingerprint technique. Quantification of emodin by densitometry at 460 nm. Validation of the method by investigation of its linearity range (0.133-1.330 µg/spot, r=0.9999), precision (RSD=1.44 %, n=6), recovery (99.24 %, RSD=0.74 %, n=12).
Chinese J. Trad. Patent Med. (Zhongchengyao) 26 (4), 341-343 (2004). TLC of Changchun Hongyao capsule extracts on silica gel with n-hexane - ethyl acetate 1:1. Detection by spraying with 5 % solution of potassium iodobismuthate. Identification by fingerprint techniques. Quantification of aconitine by HPLC.
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, 269-273 (2005). HPTLC of flavonoids (hyperoside, isoquercitrin, luteolin, luteolin 7-O glucoside, rutin, vitexin, quercetin, quercitrin as standards) and phenolic acids (caffeic and chlorogenic acid) on silica gel after presaturation with ethyl acetate - acetic acid - formic acid - water 100:11:11:26. Detection by spraying with natural products reagent, followed by spraying with PEG. Visualization under UV light at 254 and 366 nm. Quantitative evaluation by video-densitometry.
leaf powder by high-performance thin-layer chromatography. J. Planar Chromatogr. 18, 305-307 (2005). HPTLC of methanolic extracts of Cinnnamomum tamala leaves and eugenol on silica gel with toluene - ethyl acetate - formic acid 90:10:0.1. Detection and quantitation by densitometry at 280 nm.
J. Pharm. Biomed. Anal 39, 132-138 (2005). A simple, selective, precise and stability-indicating HPTLC method of analysis of curcumin both as a bulk drug and in formulations was developed and validated. HPTLC on silica gel with chloroform-methanol 37:3. This system was found to give compact spots of curcumin (Rf 0.48). Densitometric analysis of curcumin in the absorbance mode at 430 nm. The linear regression analysis data for the calibration plots showed good linear relationship with r =0.996 and 0.994 via peak height and peak area, respectively, in the concentration range of 50-300 ng per spot. The method was validated for precision, recovery, robustness. The LOD and LOQ were 8 and 25 ng per spot, respectively. Curcumin was subjected to acid and alkali hydrolysis, oxidation and photodegradation.
Planta Med. 71, 54-58 (2005). Preparative TLC of microphyllaquinone and (1aS*,1bS*,7aS*,8aS*)-4,5-dimethoxy-1a,7a-dimethyl-1,1a,1b,2,7,7a,8,8a-octahydrocyclopropa[3,4]cyclopenta[1,2-b]naphthalene-3,6-dione on silica gel with hexane - ethyl acetate 7:3 and dichloromethane - chloroform 7:3. Detection under UV light at 250 nm and by spraying with a solution of vanillin - perchloric acid - ethanol, followed by heating at 100 °C for 5 min.