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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J. Liq. Chromatogr. Relat. Technol. 34, 902-919 (2011). HPTLC of seven sugars (D-glucose, D-galactose, D-mannose, beta-D-fructose, alpha-D-fructose, sucrose, maltose, lactose) in food samples on silica gel with n-butanol - isopropanol - acetic acid - boric acid solution (200 mg boric acid in 10 mL water) 6:14:1:3. Detection by dipping into either aniline diphenylamine o-phosphoric acid reagent or p-aminobenzoic acid reagent. Quantitative determination by absorbance measurement at 370 nm. The HPTLC method was more sensitive by a factor of 8 for detection of sugars when compared to HPLC; only fructose showed a slightly better LOQ (difference by factor of 3). LOQ was better than 63 ng for HPTLC and about 500 ng for HPLC. Method comparison showed a good correlation and only a mean difference between both methods of 1.5 % sugar content for many food samples analyzed. HPTLC is a fully compliant method for determination of sugars in food. Application in the bioanalytical field was shown as well.
J. Planar Chromatogr. 23, 353-358 (2010). TLC of aclarubicin and doxycycline on silica gel, RP-18, cellulose, polyamide 11, and HPTLC on silica gel and RP-18 with a wide range (from 0 to 100 %) of mixtures of n-alcohols with DMSO, hexamethyldisiloxane, acetonitrile, and water in chambers saturated with mobile phase at room temperature. Detection by spraying with sulfuric acid - methanol 1:4, anisaldehyde - methanol - acetic acid - orthophosphoric acid - sulfuric acid 1:100:10:10:5 (for cellulose) and 5 % aluminium chloride in methanol (for polyamide). The effect of mobile and stationary phases on the chromatographic behavior of the compounds was studied.
J. AOAC Int. 93, 1836-1843 (2010). HPTLC of 1) lamivudine-zidovudine on silica gel with ethyl acetate - toluene - methanol 12:5:3, quantitative determination by absorbance measurement at 289 nm; of 2) metronidazole with ethyl acetate - ammonia 50:1, quantitative determination by absorbance measurement at 313 nm; of 3) neviparine with ethyl acetate - toluene 3:1, quantitative determination by absorbance measurement at 289 nm; and of 4) quinine with ethyl acetate - toluene - acetone 22:3:5, quantitative determination by absorbance measurement at 327 nm in a twin-trough chamber lined with wetted filter paper and saturated for 20 min. The average repeatability (within-laboratory) was 1.9 %, with 73 % less than 2 % and 97 % at 2.6 % or less. The average reproducibility (among-laboratory) was 2.7 %. Mean hRf values for lamivudine, metronidazole, neviparine, quinine, and zidovudine were 19, 28, 34, 33, 57.
Planta Med. 74, 352-353 (2008). HPTLC of tetraphyllin, turneradiffusin, beta-arbutin, terniflorin, echinaticin, turneradin and methanolic extracts of Turnera diffusa on silica gel with ethyl acetate - acetic acid - water 190:10:1. Quantitative determination by densitometric absorbance measurement at 254 nm.
J. Liq. Chromatogr. Relat. Technol. 34, 817-828 (2011). HPTLC of diclofenac (1) and ibuprofen (2) in aqueous environmental samples, on cyano phase with dichloromethane - methanol - cyclohexane 19:1:8. Detection by dipping into a Vibrio fisheri bacteria suspension for 3 sec. Then a glass plate was placed on top of the layer and a light-sensitive camera was used to measure the luminescence for 1 to 10 min. Linearity was between 10 and 2000 ng/zone. Limits of detection and quantification were 89 and 129 ng/band for (1), and 20 and 26 ng for (2). The coupling of HPTLC with a luminescent bacteria assay is suitable to determine drugs in aqueous environmental samples.
J. Planar Chromatogr. 24, 166-171 (2011). HPTLC of brimonidine tartrate as the bulk drug and in formulations on silica gel with methanol - toluene - triethylamine 10:35:2. The hRf value was 48. Quantitative determination by densitometry in absorbance mode at 247 nm. Linearity was between 100 and 600 ng/band (r² = 0.9965). LOD and LOQ were 9 and 28 ng/band, respectively. The intra-day and inter-day precision (%RSD, n = 3) was 1.1-1.2 % and 0.5-1.0 %, respectively. Recovery was between 98.7-100.4 %. The repeatability of application (%RSD, n = 6), was 1.6 %.
Asian Journal of Chemistry 23 (5), 2098-2100 (2011). HPTLC of glycyrrhizic acid in herbal formulation on silica gel with chloroform - glacial acetic acid - methanol - water 15:8:3:2. The hRf value of glycyrrhizic acid was 28. Quantitative evaluation by absorbance measurement at 254 nm. The method was found to be linear in the range of 100-500 ng/band with average recovery between 99-102 %.
J. Trad. Chinese Veterinary Med. 5, 53-55 (2010). TLC of stachydrine on silica gel with acetone - ethanol - hydrochloric acid 10:6:1. Detection by spraying with bismuth potassium iodide - 1 % iron(III)chloride in ethanol 5:1 and heating at 100 ºC. Identification by comparison of the hRf value and zone color with the standard. Quantification of stachydrine by densitometry at 510 nm. Precision (%RSD within plate, n = 8) was 3.7 %. Stability of measurement (%RSD within 120 min, n = 5) was 4.5 %. Linearity was in the range of 3.2-38.3 µg/zone (r=0.997, n = 6). The recovery (by standard addition) was 96.6 % with a %RSD of 2.0 % (n = 6).