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
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- 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.
Food Chem. 362, 130167 (2021). HPTLC of monosaccharides rhamnose, xylose, arabinose, mannose, glucose, galactose and sucrose in cladodes from Opuntia ficus-indica and Opuntia joconostle on silica gel with acetonitrile - 0.3 % ammonium hydroxide 17:3. Detection by dipping into thymol (0.2 %) and sulfuric acid (5 %) in methanol reagent, followed by heating at 95 °C for 2 min.
Planta Med. 85(2), 154-159 (2019). Two new cycloartane triterpene heterosides (cimiheraclein F and a shengmanol derivative) isolated from Actaea heracleifolia aerial parts (Ranunculaceae) were submitted to acid hydrolysis (HCl 0.4 M in methanol 60 %, 90°C, 2 h). The glycone moieties were purified and developed on TLC silica gel with ethyl acetate – chloroform – methanol – water 3:2:2:1. Detection after spraying with sulfuric acid 10 % in water and heating. The glycones were identified in both cases as L-arabinopyranose by comparison of the RF values (and of specific optical rotation) to a standard.
J. Planar Chromatogr. 33, 489-499 (2020). HPTLC of fructose (1), glucose (2) and sucrose (3) in honey on silica gel with 1-butanol-2-propanol - boric acid - water 3:5:1. Detection by spraying with 2 mL of aniline diphenylamine phosphoric acid reagent, followed by heating at 110 ºC for 10 min. The hRF values for (1) to (3) were 14, 32 and 27, respectively. Linearity was between 250 and 1250 ng/zone for (1) to (3). Intermediate precision was below 7 % (n=3). The LOD and LOQ were 22 and 67 ng for (1), 33 and 100 ng for (2) and 21 and 64 ng for (3), respectively. Average recovery was 100.7 % for (1), 101.4 % for (2) and 104.0 % for (3).
J. Planar Chromatogr. 32, 109-114 (2019). HPTLC of fructose (1), glucose (2), maltose (3), raffinose (4) and sucrose (5) in the roots of the seven Asparagus species A. adscendens, A. racemosus, A. retrofractus, A. officinalis, A. densiflorus, A. falcatus, and A. sprengeri on silica gel with propanol - ethyl acetate - water 6:3:1. Detection by spraying with a methanolic solution of diphenylamine, aniline, and ortho-phosphoric acid, followed by heating at 140 °C for 2-3 min. Quantitative determination by absorbance measurement at 600 nm. The hRF values for (1) to (5) were 55, 50, 31, 11 and 46, respectively. Linearity was between 100 and 500 ng for (1) to (5). The intermediate precision was below 2 % (n=3). The LOD and LOQ were 22 and 66 ng for (1), 13 and 40 ng for (2), 51 and 155 ng for (3), 13 and 39 ng for (4) and 76 and 229 ng for (5), respectively. Average recovery was 97.9 % for (1), 99.9 % for (2), 99.3 % for (3), 98.3 % for (4) and 97.8 % for (5).
J. Planar Chromatogr. 20, 411-417 (2007). HPTLC of sucralose in dietetic products on silica gel impregnated with 0.1 M dipotassium hydrogen phosphate solution, and on amino phase with acetonitrile - water 17:3. Also a mixture of sucralose, sucrose, glucose, fructose was separated on amino phases with acetonitrile - water 3:1. Detection by dipping in 2-naphthol sulfuric acid reagent and aniline diphenylamine ortho-phosphoric acid reagent, followed by heating at 120 °C. Post-chromatographic derivatization on aluminium-backed amino plates was performed by heating the plate 190 °C for 20 min. Evaluation under UV light at 366 nm. For fluorescence enhancement the amino plate was dipped into a 1:2 solution of paraffin in n-hexane. Densitometric quantification by fluorescence measurement at 366 nm and by absorbance measurement at 500 and 405 nm.
J. Liq. Chromatogr. Relat. Technol. 32, 1711-1732 (2009). The authors described the TLC methods available for the analysis of acidic monosaccharides, disaccharides, and oligosaccharides derived from natural sources. TLC methods for the separation and visualization of monosaccharides are examined, as well as the successful application of TLC for ganglioside analysis and the application of these separations to neoglycolipids prepared from less tractable oligosaccharides and strong acidic animal polysaccharides, such as glycosaminoglycans.
Food Res. Int. 89, 565-573 (2016). HPTLC of galacturonic acid (1), galactose (2), glucose (3), mannose (4), arabinose (5), xylose (6) and rhamnose (7) in neutral hydrolysates from 5 plant secondary raw materials (sugar beet pulp, walnut shell, cocoa bean husk, onion peel and pea pods) on silica gel, impregnated by immersion in 0.5 M solution of monosodium phosphate, three times with acetonitrile – water – ethyl acetate – 1-propanol 17:3:4:4. Detection by dipping into diphenylamine-aniline-phosphoric acid reagent (2 % solution of diphenylamine and aniline, each in phosphoric acid – methanol 1:4), followed by heating at 150 ºC for 3 min. Qualitative identification using white light illumination. The hRF values for (1) to (7) were 1, 15, 22, 28, 37, 54 and 83, respectively.
Anal. Chem. 59, 1320-1326 (1987). TLC of monosaccharide dabsylhydrazones on silica with e.g. water saturated n-butanol - triethylamine 30:1, acetonitrile - benzene - ethyl acetate 15:15:1 or benzene - CHCl3 - EtOH 15:15:10. Dabsylhydrazones of D-glucose, palactose, mannose, fructose, arabinose, xylose, ribose, deoxyribose, glycerose.