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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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.

      132 063
      Development of a high‑performance thin‑layer chromatography‑based method for targeted glycerolipidome profiling of microalgae
      K. MAKAY, C. GRIEHL, Claudia GREWE* (*Research Group of Bioprocess Engineering, Center of Life Sciences of Anhalt University of Applied Sciences, Bernburger Str. 55, 06366 Köthen, Germany)

      Anal. Bioanal. Chem. (2024). HPTLC of monogalactosyldiacylglycerol (1), sulfoquinovosyl diacylglycerol (2), and phosphatidylglycerol (3) in microalgae strains Nannochloropsis granulata, Phaeodactylum tricornutum, Porphyridium purpureum, and Tetraselmis tetrathele on silica gel with methyl acetate - isopropanol - chloroform - methanol - 0.25 % aqueous KCl solution (acidified with glacial acetic acid) 500:500:500:200:87, n-hexane - acetone - isopropanol 16:4:1 and finally with n-hexane - diethyl ether - glacial acetic acid 70:30:1. Detection by dipping into a modified copper sulfate reagent (20 g of CuSO4 × 7 H2O in 200 mL of methanol and acidified with 8 mL of 96 % sulfuric acid and 8 mL of 85 % orthophosphoric acid) for 6 s, followed by heating at 140 °C for 30 min. Quantitative determination by absorbance measurement at 720 nm. Linearity was in the range of 100-2100 ng/zone. Intermediate precisions were below 4 % (n=3). The LOD and LOQ were in the range of 18-29 ng/zone and 63-90 ng/zone, respectively. Recovery was in the range of 93.1-108.1 %.

      Classification: 11c
      132 062
      Quality control and multi-targeted therapeutic approach of Nyctanthes arbor-tristris for management of hepatic disease and associated complications
      S. SALAR*, P. SHARMA, GAURAV (*Department of Pharmaceutical Sciences, Apex University, Jaipur, Rajasthan 302018, India,

      Pharmacogn. Mag. DOI: 10.1177/09731296231189619 (2023). HPTLC of naringenin (1), ferulic acid (2) and caffeic acid (3) in Nyctanthes arbor-tristris on silica gel with toluene - ethyl acetate - formic acid 6:4:1. Quantitative determination by absorbance measurement at 371 nm. Linearity was in the range of 100-4000 ng/zone. Intermediate precisions were below 3 % (n=3). The LOD and LOQ were 30 and 45 ng/zone for (1), 15 and 90 ng/zone for (2) and 17 and 52 ng/zone for (3), respectively. Recovery was in the range of 86.7-96.3 % for (1), 101.6-102.7 % for (2) and 100.8-101.8 % for (3).

      Classification: 7
      132 054
      Euphorbia grantii Oliv. standardized extract and its fraction ameliorate doxorubicin-induced cardiomyopathy in Ehrlich carcinoma bearing mice
      M. SABER*, M. RADI, R. EL-SHIEKH, E. SATTAR, A. EL-HALAWANY (*Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Egypt,

      J. Ethnopharmacol. 321, 117566 (2024). HPTLC of friedelin in Euphorbia grantii on silica gel with hexane – ethyl acetate 19:1. Detection by spraying with para anisaldehyde, followed by heating at 105 °C. Quantitative determination by absorbance measurement at 580 nm. LOD and LOQ were 0.5 and 1.8 μg/zone, respectively. 

      Classification: 14
      132 016
      Active substances of fat-soluble vitamins: Advances in extraction and analysis approaches
      Z. FATIMA, M. QUINTO, J. ZHOU, S. LI (Li Donhao)* (*Department of Chemistry, Yanbian University, Park Road 977, Yanji City, 133002, Jilin Province, China,

      Trends Anal. Chem. 167, 117276 (2023). Review of extraction and chromatographic methods to evaluate active forms of fat-soluble vitamins in various matrices, including HPTLC for the analysis of vitamins K, D, carotenoids in pharmaceutical products, dietary supplements and complex matrices.

      Classification: 27
      132 017
      Advances in screening assays for identifying cholinesterase ligands
      P. DE OLIVEIRA, L. TINOCO, C. CARDOSO, Q. CASS, Marcela DE MORAES* (*BioCrom - Laboratory of Chromatography, Department of Organic Chemistry, Fluminense Federal University, Niteroi, RJ, Brazil,

      Trends Anal. Chem. 168, 117362 (2023). Review of functional and non-functional assays in the study of acetylcholinesterase (AChE) ligand discovery, including HPTLC for the assessing of AChE inhibition and for monitoring of ChE activity.

      Classification: 20
      132 018
      Towards the development of analytical monograph specifications for the quality assessment of the medicinal plant Phyllanthus urinaria
      E. ORMAN, S. BEKOE, S. NKANSAH, I. KRALISCH, J. JATO, V. SPIEGLER, C. AGYARE, E. OPPONG, A. HENSEL* (Institute of Pharmaceutical Biology and Phytochemistry, University of Münster, Münster, Germany,

      Phytochem. 215, 113854 (2023). HPTLC of rutin (1), isoquercitrin (2), gallic acid (3) and phyllanthin (4) on silica gel with ethyl acetate - water - formic acid 15:3:2 for (1) to (3) and toluene – ethyl acetate - formic acid 69:30:1 for (4). Detection by spraying with Natural Product Reagent and polyethylene glycol. Quantitative determination by absorbance measurement at 366 nm. The hRF values for (1) to (4) were 35, 64, 96 and 44, respectively. Linearity was in the range of 100-5000 ng/zone for (1) and (2), 500-5000 ng/zone for (3) and 10-500 ng/zone for (4). Intermediate precisions were below 2 % (n=3). Recovery was 98.5 % for (1), 101.7 % for (2), 100.1 % for (3) and 99.8 % for (4). 

      Classification: 7
      132 020
      A simple, easy, and efficient HPTLC method for simultaneous determination of polyamines (putrescine, spermidine, and spermine) in plant tissues
      M. MOHAJERI, S. AYATOLLAHI, M. KHANDAN, S. MOKHTARI, V. HOSSEINZADEH, F. KOBARFARD* (*Phytochemistry Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran,

      J. Food Compos. Anal. 126, 105835 (2024). HPTLC of putrescine (1), spermidine (2), and spermine (3) on silica gel with chloroform - triethyl amine 4:1. Quantitative determination by absorbance measurement at 254 nm. Linearity was in the range of 0.2-0.8 mg/mL for (1), 0.1-1 mg/mL for (2) and 0.1-0.8 mg/mL for (3). Intermediate precisions were below 4 % (n=3). LOD and LOQ were 0.07 and 0.21 mg/mL for (1), 0.03 and 0.11 mg/mL for (2) and (3). Recovery was in the range of 96.9-109.4 % for (1), 90.1-109.1 % for (2) and 95.9-109.9 % for (3).

      Classification: 17a
      132 023
      Quantitative saccharide release of hydrothermally treated flours by validated salivary/pancreatic on-surface amylolysis (nanoGIT) and high-performance thin-layer chromatography
      Isabel MULLER, Gertrud MORLOCK* (*Institute of Nutritional Science, Chair of Food Science, and Interdisciplinary Research Centre for Biosystems, Land Use, and Nutrition, Justus Liebig University Giessen, Heinrich-Buff-Ring 26􀀀 32, 35392 Giessen, Germany,

      Food Chem. 432, 137145 (2024). HPTLC of glucose (1), maltose (2) and maltriose (3) released from 10 flour samples with the enzymatic (human salivary α-amylase and porcine pancreatic α-amylase in a pancreatin enzyme mixture) and calcium chloride solution, pre-conditioned for 30 min in 70 % relative humidity with saturated sodium carbonate decahydrate solution. Before starting the enzyme reaction by wetting the application area, the upper plate part was covered with another smaller plate, which was sprayed with 2.5 mL 0.1 M sodium chloride solution to start the enzyme reaction, followed by incubation at 37 °C for 60 min. The plate was developed with acetonitrile - water - 2-propanol - acetone 12:3:4:1 or acetonitrile - water - 2-propanol 3:1:1. Detection by spraying with p‑aminobenzoic acid reagent (2 g p-aminobenzoic acid in 252 mL glacial acetic acid - water - acetone - o‑phosphoric acid 25:25:75:1), followed by heating at 140 °C for 5 min. Chromatograms were documented at 366 nm and the fluorescence was measured densitometrically at 366/>400 nm. Linearity was in the range of 5-800 ng/zone for (1), 10-950 ng/zone for (2) and 47-565 ng/zone for (3). Intermediate precisions were below 16 %. Mean recoveries were between 111 and 112 % for (1) and 106 and 115 % for (2).

      Classification: 10a