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

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      132 038
      Validation of a high‑performance thin‑layer chromatography method for the quantitative determination of trehalulose
      M. MELLO, C. JACOBS, M. ISLAM, L. LIM, Cornelia LOCHER* (*Division of Pharmacy, School of Allied Health, University of Western Australia, Crawley, WA 6009, Australia, connie.locher@uwa.edu.au)

      J. Planar Chromatogr. 36, 201-210 (2023). HPTLC of trehalulose on silica gel with 1-butanol - 2-propanol - 5 mg/mL aqueous boric acid solution 3:5:1. Detection by spraying with aniline - diphenylamine - phosphoric acid reagent, followed by heating to 115 °C for 10 min. Plates were analyzed under white light using three sets of images: remission white, transmission white and remission–transmission white. The hRF value for trehalose was 5 (1) to (3) were 38, 24 and 50, respectively. Linearity was in the range of 100-800 ng/zone. Intermediate precisions were below 2 % (n=3). LOD and LOQ were 20 and 61 ng/zone, respectively. Mean recovery was 102.3 %.

      Classification: 10a
      132 039
      Thin‑layer chromatography quantification of ibuprofen using digital imaging
      C. ANTON, F. ECKER, Myriam MUNKER* (*Department of Food Technology, Fulda University of Applied Sciences, Leipziger Straße 123, 36037 Fulda, Germany, myriam.braun-muenker@lt.hs-fulda.de)

      J. Planar Chromatogr. 36, 257-263 (2023). HPTLC of ibuprofen on silica gel with acetic acid - ethyl acetate - n-hexane 5:24:71. Quantitative determination by absorbance measurement at 254 nm. Digital images were taken with a smartphone in a dark room under UV light. Image analysis was performed using the processing software Fiji. Linearity was in the range of 3-5 mg/mL. LOD and LOQ were 0.9 and 2.9 mg/mL, respectively. Mean recovery was 99.9 %.

      Classification: 32a
      132 040
      Quality by design approach for the quantitative determination of andrographolide, gallic acid and quercetin from polyherbal tablets by instrumental thin‑layer chromatography
      M. JADHAV, P. TATKE* (*Department of Pharmaceutical Chemistry, C. U. Shah College of Pharmacy, S.N.D.T. Women’s University, Santacruz (W), Mumbai, Maharashtra 400049, India, drpratimatatke@gmail.com)

      J. Planar Chromatogr. 36, 279-294 (2023). HPTLC of andrographolide (1), gallic acid (2) and quercetin (3) in polyherbal tablets on silica gel with toluene - ethyl acetate - methanol - formic acid 86:60:20:1. Quantitative determination by absorbance measurement at 247 nm. The hRF values for (1) to (3) were 38, 24 and 50, respectively. Linearity was in the range of 400-2400 ng/zone for (1) and 200-1200 ng/zone for (2) and (3). Intermediate precisions were below 1 % (n=3). LOD and LOQ were 48 and 101 ng/zone for (1), 27 and 86 ng/zone for (2) and 19 and 78 ng/zone for (3), respectively. Recovery was between 98.5 and 99.4 %.

      Classification: 7, 14
      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
      132 043
      Thin layer chromatography‒spectrodensitometric determination of a three‑component mixture of propyphenazone, caffeine, ergotamine tartrate, and two of their impurities with application to tablets, spiked human plasma, and green profile assessment
      M. RAGAB*, N. RAMADAN, N. EL-RAGEHY, B. EL-ZEANY (*Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El‑Aini St., Cairo ET‑11562, Egypt, mona.abdelhafez@pharma.cu.edu.eg)

      J. Planar Chromatogr. 36, 295-305 (2023). HPTLC of propyphenazone (1), caffeine (2) and ergotamine tartrate (3) in tablets and spiked human plasma on silica gel with methanol - ethyl acetate - glacial acetic acid 10:90:1. Quantitative determination by absorbance measurement at 210 nm. The hRF values for (1) to (3) were 84, 56 and 18, respectively. Linearity was in the range of 0.1-12 μg/zone for (1) and 0.1-10 μg/zone for (2) and (3). Intermediate precisions were below 2 % (n=3). Average recovery was 101.4 % for (1), 99.2 % for (2) and 101.1 % for (3).

      Classification: 32a
      132 045
      Analytical method development, validation and studies of degradation behavior of erlotinib hydrochloride in bulk and tablet formulation by thin‑layer chromatography
      H. VARU, R. JADAV, A. BAPODRA, M. AMBASANA* (*Department of Chemistry and Forensic Science, Bhakta Kavi Narsinh Mehta University, Junagadh, Gujarat, India, ambasanamrunal@gmail.com)

      J. Planar Chromatogr. 36, 307-313 (2023). HPTLC of erlotinib in bulk and tablet formulation on silica gel with ethyl acetate - toluene - glacial acetic acid 35:15:1. Quantitative determination by absorbance measurement at 246 nm. The hRF value for erlotinib was 39. Linearity was in the range of 200-800 ng/zone. Intermediate precisions were below 1 % (n=3). LOD and LOQ were 5 and 15 ng/zone, respectively. Average recovery was 100.1 %.

      Classification: 32a
      132 047
      Box‒Behnken design‑assisted development of an eco‑friendly thin‑layer chromatography‒densitometry method for the quantification of amlodipine besylate, metoprolol succinate, and telmisartan in synthetic mixture using AGREE tool
      K. PATEL*, P. MACWAN, A. PRAJAPATI, H. PATEL, R. PARMAR (*Department of Pharmaceutical Quality Assurance, Anand Pharmacy College, Anand, Gujarat, India, kalpana_jpatel@yahoo.com)

      J. Planar Chromatogr. 36, 265-277 (2023). HPTLC of amlodipine besylate (1), metoprolol succinate (2) and telmisartan (3) in a synthetic mixture on silica gel with toluene - isopropanol - methanol - triethylamine 30:10:5:1. Quantitative determination by absorbance measurement at 233 nm. The hRF values for (1) to (3) were 48, 36 and 15, respectively. Linearity was in the range of 500-2500 ng/zone for (1), 400-2000 ng/zone for (2) and 100-500 ng/zone for (3). Intermediate precisions were below 2 % (n=6). LOD and LOQ were 51 and 154 ng/zone for (1), 161 and 488 ng/zone for (2) and 26 and 79 ng/zone for (3), respectively. Mean recovery was 98.9 % for (1), 99.4 % for (2) and 100.2 % for (3).

      Classification: 32a
      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
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