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.

      129 050
      Simultaneous quantification of brexpiprazole and sertraline HCl in synthetic mixture by thin‑layer chromatography method
      S. VAHORA, U. CHHALOTIYA*, H. KACHHIYA, J. TANDEL, D. SHAH (*Indukaka Ipcowala College of Pharmacy, Beyond GIDC, P.B. No. 53, Vitthal Udyognagar, Gujarat 388 121, India,

      J. Planar Chromatogr. 34, 549-557 (2021). HPTLC of brexpiprazole (1) and sertraline HCl (2) on silica gel with n-propanol - hexane - toluene - triethylamine 70:20:10:1. Quantitative determination by absorbance measurement at 254 nm. The hRF values for (1) and (2) were 36 and 47, respectively. Linearity was between 4500 and 15000 ng/zone for (1) and 90 and 300 ng/zone for (2). Interday and intra-day precisions were below 4 % (n=3). The LOD and LOQ were 163 and 495 ng/zone for (1) and 35 and 107 ng/zone for (2), respectively. Recovery was between 99.5 and 101.1 % for (1) and 99.4 and 102.0 % for (2).

      Classification: 17a, 23e
      128 037
      Rapid determination of histamine level in seafood using read-out strips based on high-performance thin layer chromatography modified with self-visualization nanomaterials
      Y. ZHANG (Zhang Yiming), J. YU (Yu Jinsheng), S. LAI (Lai Shuyu), J. SONG (Song JIan), X. WU (Wu Xiaomei), D. WANG (Wang Dingnan), L. PANG (Pang Lonjiang)*, T. CHAI (Chai Tinhting) (*School of Agriculture and Food Science, Zhejiang A & F University, Hangzhou, 311300, People’s Republic of China,

      Food Control. 122, 107816 (2021). HPTLC of histamine in fish samples on a silica gel read-out strip coated with a ninhydrin@TiO2 complex (0.1 M titanium butoxide and 5 % ninhydrin as precursors) as self-visualization nanomaterial in the histamine target zone (hRF value of 24). Samples were developed using n-butanol - acetone - ammonia 20:5:2. Detection after heating at 80 °C for 30 s. Linearity was between 15 and 320 mg/kg. The LOD for histamine was 5 mg/kg. 

      Classification: 17a
      127 005
      Utilization of a crown ether/amine‐type rotaxane as a probe for the versatile detection of anions and acids by Thin‐Layer Chromatography.
      S. MIYAGAWA, M. KIMURA, S. KAGAMI, T. KAWASAKI, Y. TOKUNAGA* (*Department of Materials Science and Engineering, University of Fukui, Bunkyo, Fukui, Japan;

      Chem. Asian J. 15(19), 3044-3049 (2020). The studied rotaxane combines a dibenzocrown of 8 ethers (DB24C8) with an axle chain (Ax) containing two amines, one of them in an aniline group, allowing stability of the rotaxane even when the other one is unprotonated. TLC on silica gel in 4 steps, with detection under UV light or after derivatization with phosphomolybdic acid in ethanol. (1) Before the synthesis of the rotaxane, unprotonated Ax was isolated by preparative TLC of the protonated Ax obtained by addition of HCl or toluenesulfonic acid (TsOH); the mobile phases were chloroform – methanol 10:1 and toluene – tetrahydrofurane 3:2, respectively. The isolated molecules were confirmed as totally unprotonated Ax by NMR, suggesting a complete loss of HCl and TsOH on the silica gel layer. (2) After synthesis, unprotonated rotaxane, pure vs. monoprotonated by the addition of 10 different acids (and purified by column chromatography CC), was applied on TLC plates and developed with dichloromethane – acetone – water 3:16:1; the hRF values were very different, depending on the counter-anions from the used acids. (3) The same behavior (except with sulfuric acid) was observed under the same conditions when CC was omitted (unprotonated rotaxane samples were mixed with each of the acids, or with two acids at the same time for acid-competitive TLC analysis). (4) When unprotonated rotaxane was applied under the same conditions as in step (3) with the sodium salts instead of the acids, the behavior was similar (except for the shapes of the spots, due to the salts in excess). The rotaxane can thus be used for the TLC separation and detection of sodium salts, by forming salts of protonated rotaxane with the anion afforded by these sodium salts. The rotaxane protonation seems to be promoted by the methanol of the spotting mixture; indeed, when step (3) was performed with the mobile phase chloroform – methanol 10:1, a second zone appeared because methanol formed a salt with the rotaxane (identified by NMR).

      Classification: 4e, 5a, 5b, 17a
      127 046
      Fate of tris(2‑chloroethyl)amine in water and alkaline environment determined by thin‑layer chromatography and gas chromatography–mass spectrometry
      T. ROZSYPAL (Nuclear, Biological and Chemical Defence Institute, University of Defence, Vita Nejedleho 691, 68203 Vyskov, Czech Republic,

      J. Planar Chromatogr. 33, 669-677 (2020). HPTLC of tris(2-chloroethyl)amine (HN-3) on silica gel with benzene - methanol - triethylamine 425:75:1. Detection by spraying with derivatization reagent (2mg/mL of KMnO4 with 4 mL of H3PO4). The method allowed to study the influence of pH on the degradation of HN-3 and the triethanolamine rate of appearance.

      Classification: 17a
      124 043
      A simple and rapid method for histamine analysis in fish and fishery products by TLC determination
      Z. TAO (Tao Zhihua)*, M. SATO, Y. HAN (Han Yali), Z. TAN (Tan Zhujun), T. TAMAGUCHI, T. NAKANO (*Department of Food and Biology Technology, Guangdong University of Technology, Guangzhou University Town, 100, Guangzhou, China,

      Food Control. 22, 1154-1157 (2011). TLC of histamine in fish and fishery products on cellulose with ammonia - ethanol 1:3. Detection by spraying with Pauly's reagent (equal mixture of 20 mM sulfanilic acid in a 1 M HCl solution and 200 mM sodium nitrite solution, followed by adding 10 % anhydrous sodium carbonate in a 5 % ethanol solution). Color intensity was recorded using a digital camera, followed by imaging processing. Linearity was between 30 and 1000 ng/zone for histamine. Intermediate precision was below 5 % (n=3). The LOD was 20 ppm (2 mg/100 g). Recovery rate was between 93 and 98 %.

      Classification: 17a
      124 042
      Quantitative TLC-SERS detection of histamine in seafood with support vector machine analysis
      A. TAN (Tan Ailing), Y. ZHAO (Zhao Yong), K. SIVASHANMUGAN, K. SQUIRE, A. WANG* (*School of Electrical Engineering and Computer Science, Oregon State University, Corvallis, OR, 97331, USA,

      Food Control. 103, 111-118 (2019). Thin layer chromatography in tandem with surface-enhanced Raman scattering (TLC-SERS) of histamine in tuna samples on diatomaceous earth plates with ethanol - ammonia 3:1. Detection by spraying with Pauly's reagent (equal mixture of 20 mM sulfanilic acid in a 1 M HCl solution and 200 mM sodium nitrite solution, followed by adding 10 % anhydrous sodium carbonate in a 5 % ethanol solution). Gold nanoparticles were deposited on the plate zone and measurements were performed using a Raman spectrometer with an excitation laser wavelength of 785 nm.

      Classification: 4e, 17a
      100 041
      Thin-Layer Chromatographic separation of cadaverine and ornithine, and spectrophotometric quantification
      H.A. KHAN (Department of Biochemistry, College of Science, Bld 5, King Saud University, P. O. Box 2455, Riyadh 11451, Saudi Arabia; khan_haseeb@yahoo. com)

      J. Planar Chromatogr. 20, 231-233 (2007). TLC of cadaverine and ornithine on calcium sulfate (and silica gel) with methanol. Detection by spraying with 0.2 % ethanolic solution of ninhydrin and then heating the plates at 110 °C for 15 min. Quantitation by scraping the spot from the plate and measuring the absorbance at 550 nm. The lower limit of detection was found to be 0.75 µg/zone of ornithine.

      Classification: 17a
      106 162
      Development and validation of a HPTLC method for simultaneous densitometric analysis of ranitidine hydrochloride and dicyclomine hydrochloride as the bulk drugs and in the tablet dosage form
      R. NANDA*, S. POTAWALE, V. BHAGWAT, R. DESHMUKH, P. DESHPANDE (*Dr. D. Y. Patil Institute of Pharmaceutical Sciences & Research, Pimpri, Pune 411018, India,,

      Journal of Pharmacy Research 3(8), 1997-1999 (2010). TLC on silica gel (plates pre-washed with methanol) with methanol - water - acetic acid 80:20:1. The hRf value of ranitidine HCl was 27 and of dicyclomine HCl was 67. Derivatization by exposure to iodine vapor. Densitometric evaluation at 410 nm. The method was linear in the range of 400-2400 ng/band for dicyclomine hydrochloride and 150-900 ng/band for ranitidine hydrochloride. The mean recovery was 98.8 ± 0.5 % for ranitidine HCl and 99.1 ± 0.8 % for dicyclomine HCl.

      Classification: 17a, 32a