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.

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      127 026
      Comparison of phytochemical composition of Ginkgo biloba extracts using a combination of non-targeted and targeted analytical approaches
      B. COLLINS*, S. KERNS, K. AILLON, G. MUELLER, C. RIDER, C. RIDER, E. DEROSE, R. LONDON, J. HARNLY, S. WAIDYANATHA (*Division of the National Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA, bradley.collins@nih.gov)

      Anal. Bioanal. Chem. 412, 6789-3809 (2020). HPTLC of Ginkgo biloba extracts on silica gel with ethyl acetate - acetic acid - formic acid - water 100:11:11:26 (1) or toluene - ethyl acetate - formic acid 7:3:1 (2). Detection under UV light at 366 nm or by spraying with  natural product reagent (NPR) and polyethylene glycol (PEG). The method allowed to distinguish between characteristic and uncharacteristic unfinished product samples based on the presence or absence of bands corresponding to caffeic acid, rutin, hyperoside, chlorogenic acid, and genistein standards.

      Classification: 7, 8a
      127 031
      Determination of mono- and diacylglycerols from E 471 food emulsifiers in aerosol whipping cream by high-performance thin-layer chromatography–fluorescence detection
      Claudia OELLIG*, M. BLANKART, J. HINRICHS, W. SCHWACK, M. GRANVOGL (*Department of Food Chemistry and Analytical Chemistry (170a),
      Institute of Food Chemistry, University of Hohenheim, Garbenstrasse 28, 70599 Stuttgart, Germany, claudia.oellig@uni-hohenheim.de)

      Anal. Bioanal. Chem. 412, 7441-7451 (2020). HPTLC of mono- (1) and diacylglycerol (2) emulsifiers (E 471) in whipping creams on primuline impregnated silica gel with n-pentane - n-hexane - diethyl ether 9:9:22. Quantitative determination by fluorescence measurement at UV 366/> 400 nm. The hRF values for (1) and (2) were 10 and 52, respectively. Linearity was between 1.5 and 20 ng/zone for (1) and (2). Intermediate precision was below 7 % (n=4). The LOD and LOQ were 1.8 and 5.7 ng for (1) and (2). Recovery was between 95 and 105 % for (1) and 86 and 95 % for (2).

      Classification: 11a
      127 035
      Stability assessment of tamsulosin and tadalafil co-formulated in capsules by two validated chromatographic methods
      M. REZK, E. MOETY, M. WADIE*, M. TANTAWY (*Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, KasrEl-Aini Street, ET-11562, Cairo, Egypt, mina.wa.yousif@pharma.cu.edu.eg)

      J. Sep. Sci. 44, 530-538 (2021). HPTLC of tamsulosin (1) and tadalafil (2) in presence of their degradation products (2) and (3) on silica gel with ethyl acetate - toluene - methanol - ammonia 20:10:20:3. Quantitative determination by absorbance measurement at 280 nm. The hRF values for (1) to (4) were 55, 68, 14 and 24, respectively. Linearity was between 0.5 and 25 µg/zone for (1) and (2). Intermediate precision was below 2 % (n=3). Average recovery was 99.7 % for (1) and 100.3 % for (2).

      Classification: 23e, 32a
      127 037
      Methods for quantification of imidocarb dipropionate; application for the determination of its residues in bovine meat and milk samples
      G. SEDIK*, D. NAGUIB, F. MORSY, H. ZAAZAA (*Cairo University, Faculty of Pharmacy, Analytical Chemistry Department, Cairo, Egypt, ghada.sedik@pharma.cu.edu.eg)

      J. AOAC Int. 103, 980-988 (2020). HPTLC of imidocarb dipropionate and its forced induced degradation products in bovine meat and milk on silica gel with ethyl acetate - methanol - ammonia - water 85:10:5:2. Quantitative determination by absorbance measurement at 254 nm. Linearity was between 100 and 1800 ng/zone. Intermediate precision was below 1 % (n=3). The LOD and LOQ were 17 and 52 ng/zone, respectively. Average recovery was 100.8 %. The HPTLC method showed comparable results to a validated HPLC method for resolution and determination of imidocarb in the presence of its degradation products.

      Classification: 28a
      127 038
      Chromatographic methods for the determination of aminexil, pyridoxine, and niacinamide in a novel cosmetic hair preparation
      M. REZK, H. ESSAM, E. AMER, D. YOUSSIF (*National Organization for Drug Control and Research, Wezaret El-Zeraa st., Dokki, Giza, Egypt, dmsy1982@yahoo.com)

      J. AOAC Int. 103, 1167-1172 (2020). HPTLC of aminexil (1), niacinamide (2) and pyridoxine HCl (3) on silica gel with propanol - toluene - 33 % ammonia solution
      20:30:1. Quantitative determination by absorbance measurement at 270 nm. Linearity was between 0.25 and 1.25 µg/zone for (1), 2 and 7 µg/zone for (2) and 3 and 7 µg/zone for (3). Intermediate precision was below 2 % (n=3). The LOD and LOQ were 20 and 60 ng/zone for (1), 180 and 540 ng/zone for (2) and 140 and 430 ng/zone for (3), respectively. Average recovery was 100.1 % for (1) and (2) and 101.1 % for (3). 

      Classification: 23
      127 039
      HPTLC fingerprinting, photopigments, and nutrient analysis of Selinum tenuifolium along the altitudinal gradient
      R. SRIVASTAVA, P. DIXIT, L. SINGH, N. NAGPOORE, S. PANDEY, P. VERMA, V. RAWAT, G. SAXENA* (Department of Botany, University of Lucknow, Lucknow, Uttar Pradesh, India, gaurigupta72@yahoo.com)

      J. Liq. Chromatogr. Relat. Technol. 44, 87-94 (2021). HPTLC fingerprinting of Selinum
      tenuifolium
      on silica gel with toluene - ethyl acetate - formic acid 13:11:2. Detection under UV light at 254 nm and 366 nm. The hRF values for gallic acid and ferulic acid were 36 and 58, respectively. 

       

      Classification: 7, 32e
      127 040
      Analytical determinations of haloperidol and its combinations in pharmaceutical dosage forms and biological matrices
      S. KUMAR, C. NALINI* (*of Pharmaceutical Analysis, C.L. Baid Metha College of Pharmacy, The Tamil Nadu Dr. M.G.R. Medical University, Chennai 600096, India, nalini_cn@yahoo.co.in)

      J. Liq. Chromatogr. Relat. Technol. 44, 33-51 (2021). Review of analytical techniques for the determination of haloperidol, including TLC and HPTLC. Methods for the quantification of haloperidol in plasma samples and dosage forms using reverse phase TLC and silica gel HPTLC plates were discussed. In addition, methods for the study of lipophilicity of haloperidol were described. 

      Classification: 1b
      127 044
      Organ‑based chemo‑profiling of Echinops echinatus Roxb. using high‑performance thin‑layer chromatography (HPTLC) technique
      N. BHATT*, R. GUPTA, Y. BANSAL (*Department of Botany, Punjabi University, Patiala, Punjab, India, bhattnusrat91@gmail.com)

      J. Planar Chromatogr. 34, 173-181 (2021). HPTLC of caffeic acid (1), chlorogenic acid (2), quercetin (3), oleanolic acid (4), lupeol (5), betulinic acid (6), β-Sitosterol (7), campesterol (8) and ergosterol (9) in samples of Echinops echinatus on silica gel with toluene - ethyl acetate - formic acid - methanol 30:30:8:3 for (1) and (2), toluene - ethyl acetate - formic acid 5:4:1 for (3), toluene - methanol 9:1 for (4), petroleum ether - ethyl acetate - toluene 7:2:1 for (5) and (6), toluene - ethyl acetate 9:1 for (7) and toluene - methanol - formic acid for (8) and (9). Quantitative determination by absorbance measurement at 254 nm for (1) to (3), 540 nm for (4) to (6) and 530 nm for (7) to (9). The hRF values for (1) to (9) were 69, 80, 60, 30, 68, 55, 26, 67 and 75, respectively. Linearity was between 2 and 12 µg/mL for (1) to (9). Intermediate precision was below 2 % (n=6). The LOD and LOQ were 38 and 119 ng/zone for (1), 18 and 57 ng/zone for (2), 364 and 1100 ng/zone for (3), 11 and 32 ng/zone for (4), 40 and 123 ng/zone for (5), 15 and 46 ng/zone for (6), 8 and 23 ng/zone for (7), 52 and 159 ng/zone for (8) and 527 and 1598 ng/zone for (9), respectively. Recovery was between 95.7 and 99.6 % for (1) to (9). 

      Classification: 8a, 13c, 14
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