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:
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J. Planar Chromatogr. 35, 383-393 (2022). HPTLC of baicalin in the stem barks of Oroxylum indicum on silica gel with acetone - ethyl acetate - water - formic acid 4:20:1:1. Quantitative determination by absorbance measurement at 318 nm. The hRF value for baicalin was 49. Linearity was between 0.2 and 1.0 µg/zone. Interday and intra-day precisions were below 1 % (n=3). The LOD and LOQ were 56 and 188 ng/zone. Average recovery was 99.2 %.
J. Planar Chromatogr. 35, 281-285 (2022). HPTLC of vanillin (1) and ethyl vanillin (2) in flavoring agents on silica gel with toluene - chloroform - acetone 7:8:2. Detection under UV light at 254 and 366 nm. The hRF values for (1) and (2) were 46 and 55, respectively.
J. Planar Chromatogr. 35, 299-311 (2022). HPTLC of powdered herbal drugs and finished products (leaves of Mentha piperita, Olea oleuropea, Ginkgo biloba and Camellia sinensis, fruits of Styphnolobium japonicum and Piper nigrum, roots of Angelica species (A. gigas, A. sinensis, A. dahurica, A. acutiloba, and A. pubescens, Curcuma longa and poly-herbal products containing powdered extracts of Curcuma longa root and Piper nigrum fruits) on silica gel with three complementary developing solvents (CDS): low polar developing solvent (toluene - ethyl acetate 9:1); medium polar developing solvent (cyclopentyl methyl ether - tetrahydrofuran - water - formic acid 40:24:1:1); and high polar developing solvent (ethanol - dichloromethane - water - tetrahydrofuran 16:16:4:1). Detection by heating at 100 °C for 3 min, followed by spraying with NP reagent (1.0 g of 2-aminoethyl diphenylborinate in 100 mL of methanol). For Olea oleuropea and Ginkgo biloba, the derivatization with NP was followed by spraying with anisaldehyde sulfuric acid reagent and heating at 100 °C for 3 min. Analysis was performed under UV light at 254 and 366 nm. Performance of the Universal HPTLC mix (UHM) was assessed in terms of precision. The hRF values for all substances were between 20 and 80.
J Chromatogr A, 1598, 209-215 (2019). Samples were methanolic extracts of honeys from Robinia pseudoacacia (Fabaceae) or from Tilia spp. (Tiliaceae / Malvaceae), as well as standards: abscisic acid (sesquiterpenoid), caffeic acid, chlorogenic acid, cinnamic acid, ferulic acid (phenolic acids), chrysin (flavone), myricetin, quercetin (flavonols), naringenin (flavanone). HPTLC on silica gel with chloroform – ethyl acetate – formic acid 5:4:1. Visualization under UV 254 nm and 366 nm, before and after derivatization by spraying with aluminium chloride (1 % in methanol), which rendered flavone bands bright yellow. Quantitative absorbance measuremet by densitometry at 366 nm. Linearity was in the range of 12,5–200 µg/mL for most standards (25–400 µg/mL for chrysin). Main differences observed in samples: 1) abscisic acid (hRF 56) and chrysin (hRF 82) were present only in Tilia honey samples, quercetin (hRF 55) only in Robinia honey; 2) ferulic acid (hRF 60) was the most prominent blue band in Tilia honey samples (1.35–18.73 g/kg of honey), and less intense in Robinia honey (0–1.24 g/kg of honey). Multivariate analysis was performed in two different ways with principal component analysis.
J Chromatogr Sci, 60 (9), 832-839 (2022). Establishment of two TLC methods for the synchronous estimation of cinnarizine (Cinn) and acefyline heptaminol (Acef) in the presence of reported Cinn/Acef degradation products, as well as theophylline (Theo) as potential impurity of Acef. TLC on silica gel (1) for Cinn with dichloromethane - methanol - formic acid 30:2:1 and (2) for Acef with the same solvents in ratio 150:7.5:4. Quantitative determination by densitometry at 254 nm showed that Cinn and Acef are well separated from their degradation products. The concentration range was 0.2 - 1.8 and 2 - 18 μg/zone for Cinn and Acef, respectively, with mean percentage recoveries of 99.2 / 99.8 and 99.2 / 99.7 for method 1 and method 2, respectively. The method is selective, robust and retained its accuracy in up to 50 % of Cinn/Acef reported degradation products and Theo. Application of the two methods to a coformulated drug product comprising Cinn and Acef with satisfactory results showing statistically no significant differences compared with those obtained by reference ones.
Drug Standards of China 22 (3), 259-264 (2021). Gentianella acuta (Michx.) Hulten is a herbal traditional Chinese medicine, containing mainly efficacy components like diphenylpyrione, cycloether terpenoids, flavonoids, and triterpenoids. It has liver protection, hypoglycemic, anti-inflammatory and other pharmacological activities, and is used clinically to treat jaundice, headache, fever, dry mouth and bile fever etc. To establish a quality standard of the herb, TLC was used for the investigation of the chemical composition and fingerprints. TLC of methanolic extracts of 10 batches of Gentianella acuta collected from different regions (A) for cycloether terpene components (gentiopicroside and swertimarin), on silica gel with ethyl acetate - methanol - water 4:1:1, detection under UV 254 nm, identification by comparison of the fingerprints with those of the standards gentiopicroside and swertimarin; (B) for terpenoids (oleanolic acid), on silica gel with chloroform - methanol - ammonium hydroxide 20:6:1, detection under UV 254 nm, identification by comparison of the fingerprints with those of the oleanolic acid standard; (C) for aqueous extracts (water-soluble components such as flavonoids and phenolic acids), on silica gel with 1-butanol - acetic acid - water 9:3:2, detection by spraying with 5 % aluminium trichloride solution and evaluation under UV 366 nm, identification by comparison of the fingerprints with those of the oleanolic acid standard. The results showed that the TLC profiles of 10 batches were very similar, and well consistent with the HPLC fingerprint results. In addition, gentiopicroside, swertimarin and oleanolic acid were identified by TLC in the medicine, thus can be used as the target components of the identification. Therefore, the results of this study can be used as the basis for the authenticity identification and quality evaluation of the medicine.
J Chromatogr Sci, 60 (6), 606-612 (2022). Simultaneous determination of sofosbuvir and daclatasvir, co-formulated as directly acting antiviral agents used for treatment of hepatitis C virus, by TLC on silica gel with ethyl acetate - hexane - methanol 18:1:1. Both substances were quantitatively separated in one analytical run. Quantitative determination by densitometry at 280 nm with linearity range of 0.4 - 25.4 μg/band for sofosbuvir and 0.4 - 12.8 μg/band for daclatasvir. The method is time- and cost-saving, which is even more important for some combinations on the market, such as Darvoni® tablets.
J Strait Pharm 33 (8), 46-48 (2021). Yinling Heji is a TCM drug, containing Artemisia capillaris Thunb., Scutellaria L., Radix Rehmanniae Preparata etc. It clears heat and dampness, is mainly used for the prevention and treatment of neonatal jaundice, and has a good effect on children with mild diseases. For quality control, microemulsion thin-layer chromatography on polyamide layer, (A) for Herba Artemisiae Scopariae, of methanol extracts of the test sample (TCM prescription drug), methanol extracts of the test sample without Herba Artemisiae Scopariae, methanolic extracts of Herba Artemisiae Scopariae and standard chlorogenic acid in methanol, (B) for Scutellaria L., methanol extracts of the test sample, methanol extracts of the test sample without Scutellaria L., methanolic extracts of Scutellaria L. and standard baicalin in methanol, (C) for Rhei Radix et Rhizoma, methanol extracts of the test sample, methanol extracts of the test sample without Rhei Radix et Rhizoma, methanolic extracts of Rhei Radix et Rhizoma, and standard emodin in methanol. Development with (sodium dodecyl sulfate - n-butanol - cyclohexane - water 27:63:10:300) - formic acid 9:1.