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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      132 025
      TLC–MS-bioautographic identification of antityrosinase compounds and preparation of a topical gel formulation from a bioactive fraction of an RSM-optimized alcoholic extract of Rubia cordifolia L. stem
      A. INSAF, R. PARVEEN, V. SRIVASTAVA, M. SAMAL, M. KHAN, S. AHMAD* (*Jamia Hamdard, Department of Pharmaceutics, School of Pharmaceutical Education & Research, New Delhi 110062, India, sahmad_jh@jamiahamdard.ac.in)

      J. AOAC Int. 106, 1598-1607 (2023). HPTLC bioautography of Rubia cordifolia on silica gel impregnated with kojic acid with toluene - ethyl acetate - formic acid 5:4:1. Antityrosinase activity by spraying with 2 mM L-tyrosine and incubated at room temperature for 10 min. The plate was the sprayed with tyrosinase solution (1 mL of mushroom tyrosinase enzyme (3333 units) in 10 mL PBS - sodium phosphate buffer solution, pH 6.8), followed by incubation at room temperature for 45 min. Clear white zones of tyrosinase enzyme inhibition allowed the detection of presence of active compounds. Further analysis by MS allowed the identification of purpurin with antityrosinase potential.

      Classification: 4e
      132 033
      Antioxidant profiles of 19 lemon balm extracts by high-performance thin-layer chromatography–radical scavenging assay versus respective microtiter plate assay
      Agnes MORICZ*, V. LAPAT, G. MORLOCK (*Plant Protection Institute, Centre for Agricultural Research, Herman O. Str. 15, 1022 Budapest, Hungar, moricz.agnes@atk.hun-ren.hu)

      J. Liq. Chromatogr. Relat. Technol. doi:10.1080/10826076.2023.2284706 (2023). HPTLC of 19 lemon balm leaf samples on cyano phase with acetonitrile - water - acetic acid 20:30:1. Free radical scavenging activity was detected by dipping into a 0.02 % methanolic 1,1-diphenyl-2-picrylhydrazyl (DPPH) solution. Rosmarinic acid was identified by HPTLC–high-resolution mass spectrometry (HRMS). 

      Classification: 7
      132 034
      Emerging approaches for the detection of trimethylamine N-oxide: A gut derived metabolite
      A. KOTTARATHIL, D. S. RAJKUMAR, R. PADMANABAN* (*Immunodynamics and Interface Laboratory, Centre of Advanced Study in Crystallography and Biophysics, University of Madras, Chennai, India, drprajashree@gmail.com)

      J. Liq. Chromatogr. Relat. Technol. doi:10.1080/10826076.2023.2284737 (2023). HPTLC of quercetin (1), myricetin (2), tannic acid (3), gallic acid (4), ellagic acid (5), ascorbic acid (6) and humic acid (7) on silica gel with toluene - ethyl acetate - formic acid - methanol 15:15:4:2 in the first dimension and toluene - ethyl acetate - formic acid 6:3:1 in the second dimension for (1) to (4) and ethyl acetate - acetone - water - formic acid 5:3:1:1 for (5) and (6). Quantitative determination by absorbance measurement at 254 nm. The hRF values for (1) to (5) were 15, 73, 80, 21 and 62, respectively. Linearity was in the range of 100-600 ng/zone for (1) to (5) and (7) and 200-1200 ng/zone for (6). Intermediate precisions were below 2 % (n=3). LOD and LOQ were 26 and 79 ng/zone for (1), 22 and 80 ng/zone for (2), 21 and 64 ng/zone for (3), 31 and 94 ng/zone for (4), 10 and 102 ng/zone for (5), 65 and 197 ng/zone for (6) and 22 and 66 ng/zone for (7), respectively. Average recovery was between 99.1 and 103.1 % for (1) to (7).

      Classification: 7
      132 042
      Isolation, identification, and quantification of stigmasterol in Hygrophila schulli plant by a validated high‑performance thin‑layer chromatography‒densitometric method
      N. TAKALE, T. KOTHAWALE, B. GHULE*, N. KOTAGALE (*Department of Pharmacognosy, Government College of Pharmacy, Kathora Naka, Amravati, Maharashtra State 444604, India, ghulebv@rediffmail.com)

      J. Planar Chromatogr. 36, 223-235 (2023). HPTLC of stigmasterol in Hygrophila schulli on silica gel with toluene - methanol 9:1. Detection by spraying with anisaldehyde - sulfuric acid reagent, followed y heating at 105 °C for 4-5 min. Quantitative determination by absorbance measurement at 520 nm. The hRF value for stigmasterol was 47. Linearity was in the range of 100-500 ng/zone. Intermediate precisions were below 2 % (n=6). LOD and LOQ were 7 and 21 ng/zone, respectively. Recovery was between 98.9 and 99.2 %.

      Classification: 14
      132 048
      Development of thin‑layer chromatography‒densitometry for the quantification of lecithin6 in dietary supplements
      M. STAREK*, K. HOMA, J. STEPINSKA, M. DABROWSKA (*Department of Inorganic and Analytical Chemistry, Faculty of Pharmacy, Jagiellonian University Medical College, 9 Medyczna St, 30‑688 Kraków, Poland, m.starek@uj.edu.pl)

      J. Planar Chromatogr. 36, 99-110 (2023). HPTLC of lecithin in dietary supplements on silica gel with chloroform - methanol - glacial acetic acid 15:30:2. Detection by spraying with 0.5 % ammonium molybdate solution in a mixture of ethanol and sulfuric acid 1:9, followed by heating at 100 °C for 5 min. Quantitative determination by absorbance measurement at 360 nm. The hRF value for lecithin was 23. Linearity was in the range of 0.23-3.21 mg/mL. Intermediate precisions were below 2 % (n=6). LOD and LOQ were 0.09 and 0.26 mg/mL, respectively. Recovery was between 97 and 99 %.

      Classification: 11c
      132 049
      Development of betulin as phytochemical reference standard for the analysis of Hygrophila schulli plant by a validated high‑performance thin‑layer chromatography method
      N. TAKALE, S. WADIBHASME, B. GHULE*, N. KOTAGALE (*Department of Pharmacognosy, Government College of Pharmacy, Kathora Naka, Amravati, Maharashtra 444604, India, ghulebv@rediffmail.com)

      J. Planar Chromatogr. 36, 111-120 (2023). HPTLC of betulin in Hygrophila schulli on silica gel with toluene - methanol 8:1. Quantitative determination by absorbance measurement at 366 nm. The hRF value for betulin was 49. Linearity was in the range of 200-1000 ng/zone. Intermediate precisions were below 2 % (n=6). LOD and LOQ were 33 and 102 ng/zone, respectively. Average recovery was 98.0 %.

      Classification: 14
      132 050
      A validated high‑performance thin‑layer chromatography method for the quantification of genistein in the hydroalcoholic extract of Flemingia procumbens Roxb.
      S. CHAUDHARY*, E. KHARLYNGDOH, J. SHUKLA, P. BHARDWAJ, P. MUKHERJEE (*Institute of Bioresources and Sustainable Development (IBSD), Department of Biotechnology, Govt of India, Imphal, Manipur 795001, India, naturalproductm@gmail.com)

      J. Planar Chromatogr. 36, 121-127 (2023). HPTLC of genistein in Flemingia procumbens on silica gel with toluene - ethyl acetate - acetone - formic acid 20:4:2:1. Quantitative determination by absorbance measurement at 271 nm. The hRF value for genistein was 49. Linearity was in the range of 50-300 ng/zone. Intermediate precisions were below 2 % (n=6). LOD and LOQ were 2 and 71 ng/zone, respectively. Average recovery was 99.6 %.

      Classification: 8a
      132 051
      Development and validation of a high‑performance thin‑layer chromatography method for the simultaneous estimation of four cardioprotective triterpenoids in Terminalia arjuna W. & A. bark and a fermented polyherbal biomedicine
      S. HALDAR, A. ASH, S. MOHAPATRA*, R. SINGH, C. KATIYAR (*Corporate Analytical Design Excellence, Emami Limited, Kolkata 700056, India, satyabrata.mohapatra@emamigroup.com)

      J. Planar Chromatogr. 36, 129-136 (2023). HPTLC of arjunic acid (1), arjungenin (2), arjunetin (3) and arjunglucoside-I (4) in the bark of Terminalia arjuna on silica gel with ethyl acetate - toluene - tetrahydrofuran - acetic acid 10:5:4:1. Detection by spraying with anisaldehyde–sulfuric acid reagent. Quantitative determination by absorbance measurement at 598 nm. The hRF values for (1) to (4) were 64, 39, 24 and 16, respectively. Linearity was in the range of 200-800 ng/zone. Intermediate precisions were below 3 % (n=3). LOD and LOQ were 25 and 75 ng/zone for (1) and (2), 13 and 39 ng/zone for (3) and 13 and 18 ng/zone for (4). Average recoveries for (1) to (4) were 96.2 %, 102.6 %, 98.2 % and 97.9 %, respectively.

      Classification: 14
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