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
  • Keyword register: select an initial character and browse associated keywords
  • 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.

      129 035
      Exploration and practice on systematic identification strategy of traditional Chinese medicine prescriptions by high‑performance thin‑layer chromatography - with Daqinjiao decoction as an example
      R. CHEN (Chen Ruibiao), S. LIANG (Liang Shengwang), S. WANG (Wang Shumei), Y. XIE (Xie Yuanyuan)* (*School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China, yuanyuan8078@163.com)

      J. Planar Chromatogr. 35, 103-116 (2022). HPTLC of Daqinjiao standard decoction containing the following herbs: Gentianae Macrophyllae Radix (1), Paeoniae Radix Alba (2), Glycyrrhizae Radix et Rhizoma (3), Notopterygii Rhizoma et Radix (4), Saposhnikoviae Radix (5), Angelicae Pubescentis Radix (6), Angelicae Sinensis Radix and Chuanxiong Rhizoma (7), Scutellariae Radix (8) on silica gel with ethyl acetate - methanol - water 15:2:1 for (1) to (5), n-hexane - ethyl acetate 7:3 for (6) and (7) and toluene - ethyl acetate - methanol - formic acid 15:5:1.5:3 for (8). Detection by spraying with 5 % solution of vanillin in sulfuric acid, followed by heating at 105 °C for 5 min for (1) to (3), (5) and (6) and spraying with 2 % iron trichloride for (8). Qualitative identification under UV light at 254 and 366 nm. Reference standards were gentiopicroside for (1), paeoniflorin for (2), liquiritin for (3), nodakenin for (4), 5-O-methylvisammioside for (5), osthole for (6), ligustilide for (7) and baicalein and wogonin for (8). The hRF values for reference standards for (1) to (8) were 40, 35, 46, 28, 24, 37, 65 and 56, respectively.  

      Classification: 8a, 8b
      129 035
      Exploration and practice on systematic identification strategy of traditional Chinese medicine prescriptions by high‑performance thin‑layer chromatography - with Daqinjiao decoction as an example
      R. CHEN (Chen Ruibiao), S. LIANG (Liang Shengwang), S. WANG (Wang Shumei), Y. XIE (Xie Yuanyuan)* (*School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China, yuanyuan8078@163.com)

      J. Planar Chromatogr. 35, 103-116 (2022). HPTLC of Daqinjiao standard decoction containing the following herbs: Gentianae Macrophyllae Radix (1), Paeoniae Radix Alba (2), Glycyrrhizae Radix et Rhizoma (3), Notopterygii Rhizoma et Radix (4), Saposhnikoviae Radix (5), Angelicae Pubescentis Radix (6), Angelicae Sinensis Radix and Chuanxiong Rhizoma (7), Scutellariae Radix (8) on silica gel with ethyl acetate - methanol - water 15:2:1 for (1) to (5), n-hexane - ethyl acetate 7:3 for (6) and (7) and toluene - ethyl acetate - methanol - formic acid 15:5:1.5:3 for (8). Detection by spraying with 5 % solution of vanillin in sulfuric acid, followed by heating at 105 °C for 5 min for (1) to (3), (5) and (6) and spraying with 2 % iron trichloride for (8). Qualitative identification under UV light at 254 and 366 nm. Reference standards were gentiopicroside for (1), paeoniflorin for (2), liquiritin for (3), nodakenin for (4), 5-O-methylvisammioside for (5), osthole for (6), ligustilide for (7) and baicalein and wogonin for (8). The hRF values for reference standards for (1) to (8) were 40, 35, 46, 28, 24, 37, 65 and 56, respectively.  

      Classification: 8a, 8b
      129 036
      High‑performance thin‑layer chromatography‑based quantification of therapeutic phytochemicals in the methanolic extract of Ayurvedic formulation Drakshavaleha
      D. SONA, G. BAGHEL, L. CHANDRAVANSHI, U. SAHU, N. CHAUHAN, A. KUMAR*, P. GUPTA (*Shri Narayan Prasad Awasthi (NPA) Government Ayurved College, Raipur, CG, India, drawanishkr@gmail.com)

      J. Planar Chromatogr. 35, 117-125 (2022). HPTLC of gallic acid (1), piperine (2),
      resveratrol (3), and quercetin (4) in Ayurvedic formulation Drakshavaleha on silica gel with ethyl acetate - toluene - glacial acetic acid - formic acid 10:10:2:1. Quantitative determination by absorbance measurement at 254 and 366 nm. The hRF values for (1) to (4) were 45, 72, 68 and 58, respectively. 

      Classification: 8a
      129 041
      Inherent stability testing of empagliflozin in the presence of metformin HCl by HPTLC and characterization of degradation products of empagliflozin by LC–ESI–QTOF–MS/MS
      V. VICHARE*, V. CHOUDHARI, V. TAMBE, S. DHOLE (*PES Modern College of Pharmacy (for Ladies), Moshi, Pune, Maharashtra, India, vicharevijaya11@gmail.com)

      J. Planar Chromatogr. 35, 61-71 (2022). HPTLC of empagliflozin (1) in the presence of metformin HCl (2) on silica gel with toluene - methanol - ammonia - glacial acetic acid 72:26:1:1. Quantitative determination by absorbance measurement at 230 nm. The hRF values for (1) and (2) were 15 and 48, respectively. Linearity was between 11 and 112 ng/zone for (1) and 85 and 850 ng/zone for (2). Interday and intra-day precisions were below 2 % (n=3). The LOD and LOQ were 0.6 and 1,7 ng/zone for (1) and 5 and 15 ng/zone for (2), respectively. Recovery was found to be in the range of 99.4-101.0 % for (1) and 100.3-101.4 % for (2). Degradation products were characterized by liquid chromatography coupled with electrospray ionizationquadrupole-time of flighttandem mass spectrometry (LCESIQTOFMS/MS).

      Classification: 8b, 17c
      129 046
      A validated high‑performance thin‑layer chromatography method for the simultaneous determination of quercetin and gallic acid in Annona reticulata L.
      K. PATHAK*, R. DAS, N. GOGOI, R. SAIKIA, H. SARMA, A. DAS (*Department of Pharmaceutical Sciences, Faculty of Science and Engineering, Dibrugarh University, Dibrugarh, Assam 786004, India, kalyakster@gmail.com)

      J. Planar Chromatogr. 35, 35-41 (2022). HPTLC of quercetin (1) and gallic acid (2) in the leaves of Annona reticulata on silica gel with toluene - ethyl acetate - formic acid 45:50:8. Quantitative determination by absorbance measurement at 367 nm. The hRF values for (1) and (2) were 71 and 63, respectively. Linearity was between 200 and 1000 ng/zone for (1) and 200 and 1200 ng/zone for (2). Interday and intra-day precisions were below 2 % (n=5). The LOD and LOQ were 21 and 65 ng/zone for (1) and 15 and 55 ng/zone for (2), respectively. Recovery was between 98.0 and 99.1 % for (1) and 99.3 and 100.3 % for (2).

      Classification: 8a
      129 039
      An improved high‑performance thin‑layer chromatographic method to unambiguously assess Ginkgo biloba leaf finished products
      W. PERERA*, D. FROMMENWILER, M. SHARAF, E. REICH (*CAMAG Scientific, Inc., 515 Cornelius Harnett Drive, Wilmington, NC 28401, USA, Wilmer.Perera@camag.com)

      J. Planar Chromatogr. 34, 559-560 (2021). HPTLC fingerprint of Ginkgo biloba finished products on silica gel with n-butyl acetate - methanol - water - formic acid 15:4:2:2. Detection by dipping into anisaldehyde reagent (1 mL of p-anisaldehyde in 200 mL of a mixture of methanol, acetic acid and sulphuric acid 17:2:1). Qualitative identification under UV light at 254 nm and 366 nm. 

      Classification: 8a
      129 031
      Simultaneous determination of betulinic acid, β‑sitosterol and lupeol in fruits, leaves, root and stem bark of Dillenia pentagyna Roxb. by a validated high‑performance thin‑layer chromatography method
      H. SAXENA*, S. PARIHAR, G. PAWAR (*NWFP Section, Silviculture, Forest Management and Agroforestry Division, Tropical Forest Research Institute, Jabalpur, Madhya Pradesh 482021, India, hariomsaxena81@gmail.com)

      J. Planar Chromatogr. 34, 531-542 (2021). HPTLC of betulinic acid (1), β‑sitosterol (2) and lupeol (3) in fruits, leaves, root and stem bark of Dillenia pentagyna on silica gel with petroleum ether - ethyl acetate - acetonitrile 82:18:1. Detection by dipping into anisaldehyde sulfuric acid reagent, followed by heating at 105 °C for 5 min. Quantitative determination by absorbance measurement at 580 nm. The hRF values for (1) to (3) were 17, 23 and 36. Linearity was between 120 and 440 ng/zone for (1), 200 and 1000 ng/zone for (2) and 60 and 220 ng/zone for (3). Interday and intra-day precisions were below 2 % (n=5). The LOD and LOQ were 91 and 276 ng/zone for (1), 304 and 921 ng/zone for (2) and 41 and 125 ng/zone for (3), respectively. Average recovery was 100.7 % for (1), 101.7 % for (2) and 102.0 % for (3). 

      Classification: 8a
      129 027
      High‑performance thin‑layer chromatographic standardization and quantification of marker compounds in an Ayurvedic polyherbal formulation: Krishnadi Churna
      S. PATEL, G. BAGHEL, N. CHAUHAN, S. RATHIYA, U. SAHU, A. PARIHAR, A. KUMAR*, P. GUPTA (*Department of Biotechnology, National Institute of Technology, Raipur, Chhattisgarh, India, drawanishkr@gmail.com)

      J. Planar Chromatogr. 34, 493-502 (2021). HPTLC of quercetin (1), beta-sitosterol (2), piperine (3), gallic acid (4) and resveratrol (5) in Krishnadi Churna on silica gel with toluene - chloroform - methanol 4:4:1 for (3), toluene - ethyl acetate - ethanol - methanol - formic acid 20:15:10:5:1 for (4), toluene - ethyl acetate - methanol - formic acid 50:40:10:2 for (1) and toluene - ethyl acetate - methanol - formic acid 60:30:10:3 for (2) and (5). Quantitative determination by absorbance measurement at 366 nm. The hRF values for (1) to (5) were 52 for (1), 64 for (2), 77 for (3), 61 for (4) and 45 for (5). Linearity was between 2 and 14 µg/mL for (1), (2) and (5), 1 and 18 µg/mL for (3) and 3 and 15 µg/mL for (4). The LOD and LOQ were 3 and 8 µg/zone for (1), 2 and 6 µg/zone for (2), 5 and 16 ng/zone for (3), 8 and 3 µg/zone for (4) and 8 and 3 µg/zone for (5). Average recovery was 99.2 % for (1), 98.4 % for (2), 98.6 % for (3), 98.9 % for (4) and 99.1 % for (5). 

      Classification: 8a