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
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Abstract GP-41, IPC (2005). HPTLC of tizanidine in tablets on silica gel with ethyl acetate - methanol - acetic acid 60:4:1. Linearity range was 0.5-0.6 µg, LOQ 0.5 µg, and average recovery was 99.4-101.6 %. The method was validated according to ICH guidelines.
Indian Drugs 42 (7), 465-468 (2005). HPTLC of tizanidine and diclofenac in tablet formulations on silica gel with chloroform - methanol 4:1. Quantitative determination by absorbance measurement at 230 nm. Cetrizine was used as an internal standard. The solvent system was found to give compact spots for diclofenac sodium (Rf value 0.86), tizanidine (0.26) and cetrizine (0.52). The method was validated for linearity, accuracy and precision. Linearity for tizanidine was 0.6-1.4 µg/mL, and for diclofenac sodium 7.5-17.5 µg/mL . The mean recoveries obtained for tizanidine and diclofenac sodium were 98.73 % and 99.70 %, respectively. The proposed method was accurate, precise, selective and rapid for simultaneous estimation of tizanidine and diclofenac sodium in tablets.
J. Planar Chromatogr. 19, 348-354 (2006). HPTLC of puerarin, daidzein, daidzin, and 3’-methoxypuerarin on silica gel, pre-washed with methanol, in an unsaturated twin-trough chamber with chloroform - methanol - ethyl acetate - water 16.2:18.8:52:3. Quantitative determination by absorbance measurement at 254 nm. The relative standard deviation of Rf values, retention times and peak area percentages all meet the national standards.
using high-performance thin-layer chromatography. J. AOAC Int. 89, 1467-1474 (2006). HPTLC of eugenol, luteolin, ursolic acid, and oleanolic acid on silica gel in a twin trough chamber with toluene - ethyl acetate - formic acid 35:15:1 at 25 °C and 40 % relative humidity. Quantitation in absorbance mode at 280 nm for eugenol, at 350 nm for luteolin, and at 530 nm for ursolic acid and oleanolic acid after derivatization with anisaldehyde-sulfuric acid reagent and heating at 105°C. The methods were validated for precision, repeatability, and accuracy.
J. Planar Chromatogr. 19, 383-385 (2006). HPTLC of apigenin on silica gel, pre-washed with methanol, in a saturated twin-trough chamber with toluene - methanol 5:1. Densitometric evaluation at 343 nm.
Innovative Food Science and Emerging Technologies 1, 239-243 (2001). HPTLC of commercial herbal spirits (alcoholic or hydroalcoholic solutions of volatile substances with flavoring or medicinal properties) and one red wine on silica gel with toluene – ethyl formate – formic acid 79:20:1. Antioxidative components were detected by dipping for 30 s in a soybean oil solution (3 % in n-hexane, previously treated with active carbon). Quantitative determination in UV light at 254 nm after different times of UV-exposure (30 min – 20 h). The antioxidant activity could be evaluated from the fluorescence-persisting time of the respective spots and was correlated with linoleic acid oxidation and DPPH-titration methods. Although the nature of the active herbal antioxidants remains to be established, phenolic compounds seem to be key candidates.
J. Liq. Chromatogr. Relat. Technol. 28, 267-275 (2005) . TLC of allylestrenol on silica gel in a twin-trough chamber with n-hexane - ethyl acetate - dichloromethane 45:10:1. Detection by spraying with anisaldehyde-sulfuric acid reagent followed by heating at 100 °C for 5 min. Quantitative determination by absorbance measurement at 609 nm.
Indian Drugs 44 (3), 205-208 (2007). HPTLC of frusemide (= furosemide) and spironolactone on silica gel with toluene - acetonitrile - glacial acetic acid 70:30:2, with chamber saturation for 15 min at room temperature. Development over 8 cm, followed by air drying. Quantitative determination by densitometry at 254 nm. Linearity was between 8 - 32 ng/µL and 20 - 80 ng/µL for frusemide and spironolactone respectively. The method was validated for accuracy and precision. The limit of detection and quantification for frusemide was 3 ng/µL and 8 ng/µL respectively, and for spironolactone 2 ng/µL and 6 ng/µL, respectively. Recovery by standard addition was 99.4-101% for both compounds.