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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      132 029
      Red, green, and blue model-based assessment and principles of white analytical chemistry to robust stability-indicating chromatographic estimation of thiocolchicoside and diclofenac sodium
      P. PRAJAPATI*, V. PULUSU, S. SHAH (*Maliba Pharmacy College, Department of Quality Assurance, Maliba Campus, Bardoli-Mahuva Rd, Tarsadi, Mahuva, Surat, India, pintu21083@gmail.com)

      J. AOAC Int. 106, 1374-1388 (2023). HPTLC of diclofenac sodium (1) and thiocolchicoside (2) on silica gel with n-heptane - methyl acetate - ethanol 7:1:2. Quantitative determination by absorbance measurement at 278 nm. The hRF values for (1) and (2) were 79 and 12, respectively. Linearity was between was in the range of 100-500 ng/zone for (1) and 20-100 ng/zone for (2). Intermediate precisions were below 2 % (n=3). 

      Classification: 32a
      132 031
      A green reversed phase HPLC and HPTLC methods and their validation for simultaneous estimation of remogliflozin, vildgliptin and metformin in fixed dose combination formulation
      K. SETHY, G. KRISHNA, R. KATTA (*Department of Pharmaceutical Chemistry, School of Pharmacy, Centurion University of Technology and Management, Bhubaneswar, Odisha, India, gopalmedchem@gmail.com)

      J. Liq. Chromatogr. Relat. Technol. doi:10.1080/10826076.2023.2284721 (2023). HPTLC of remogliflozin (1), vildgliptin (2) and metformin (3) on silica gel with phosphate buffer - acetonitrile - glacial acetic acid 15:35:1. Quantitative determination by absorbance measurement at 205 nm. The hRF values for (1) to (3) were 78, 60 and 36, respectively. Linearity was in the range of 50-100 ng/zone for (1) to (3). Intermediate precisions were below 2 % (n=6). LOD and LOQ were 5 and 16 ng/zone for (1), 3 and 8 ng/zone for (2) and 47 and 142 ng/zone for (3). Recovery was between 98 and 102 %.

      Classification: 32a
      132 035
      Application of TLC-smartphone method for the analysis of carbamazepine in plasma
      M. ALI SOUSSI*, Y. MALLEK, W. AYED, S. LIOUANE, W. DOUKI (*Toxicology Laboratory, Fattouma Bourguiba University Hospital, Monastir, Tunisia, mohamedalisoussi@yahoo.fr)

      J. Liq. Chromatogr. Relat. Technol. 46, 335-342 (2023). HPTLC of carbamazepine in plasma on silica gel with cyclohexane - chloroform - acetic acid 2:2:1. Detection under UV light at 254 nm, followed by photographing with a smartphone. Images were processed using the JustTLC software. The hRF value for carbamazepine was 78. Linearity was in the range of 5-10 μg/mL. Intermediate precisions were below 2 % (n=3). LOD and LOQ were 0.94 and 2.8 μg/mLAverage recovery was 98 %.

      Classification: 32a
      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
      132 041
      Development and validation of a simple thin‑layer chromatography–smartphone method for plasma paracetamol quantification
      R. FERCHIOU, M. ALI SOUSSI*, D. GHEDIRA, D. FERCHIOU, W. DOUKI, M. NAJJAR (*Biochemistry‑Toxicology Laboratory, Fattouma Bourguiba University Hospital, Monastir, Tunisia, mohamedalisoussi@yahoo.fr)

      J. Planar Chromatogr. 36, 251-256 (2023). HPTLC of paracetamol in plasma on silica gel with acetone - hexane - ammonia 40:50:1. Quantitative determination by absorbance measurement at 254 nm. The hRF value for stigmasterol was 33. Linearity was in the range of 80-180 μg/mL. Intermediate precisions were below 5 % (n=3). LOD and LOQ were 9 and 27 μg/mL, respectively. Recovery was between 99.6 and 106.8 %.

      Classification: 32d
      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
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