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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      93 110
      Content uniformity test of cinchocaine hydrochloride
      H. JEHLE*, I. MESAROS, S. SIGGERT, B. WOCHNER, D. KLEIBER, N. SINNER (*Quality Control Non-Sterile Products, Altana Pharma AG, Byk-Gulden-Str. 2, D-78467 Konstanz, Germany, Harald.jehle@altanapharma.com)

      CBS 92, 1-3 (2004). HPTLC of cinchocaine hydrochloride from suppositories on silica gel with 1-butanol - toluene - ethanol - water - 100 % acetic acid 10:8:7:4:1 over 30 mm followed by heating at 110 °C for 10 min. Quantitative determination by fluorescence measurement at 313/>400 nm.Precision is 2 % and recovery 101 %.

      Classification: 23e, 32a
      93 129
      HPTLC applied to the post-production quality assurance of etoposide infusion solutions
      E. REICH* (Ed.) (*CAMAG, Sonnenmattstr. 11, 4132 Muttenz, Switzerland)

      CBS 86, 6 (2001). HPTLC of etoposide solution (in 5 % dextrose or 0.9% NaCl) on silica gel in horizontal development chamber in sandwich configuration with diethyl ether - dichloromethane - methanol 24:20:1. Quantitative determination by absorbance measurement at 290 nm.

      Classification: 32a
      93 150
      (Quick identification of snake bile in Shedan Chuanbeiye syrup
      ZH. XIE (Xie Zhimin)*, M. WANG (Wang Minchun), Y. Wang (Wang Yunxia), X. WANG (Wang Xinli) (*Xi'an Inst. Drug Cont., Xi'an, 710054, P. R. China)

      J. Chinese Trad. Patent Med. (Zhongchengyao) 25 (7), 583-584 (2004). TLC on silica gel with benzene - ethyl acetate - methanol - glacial acetic acid - water 16:10:8:4:3. Detection under daylight or UV light. Identification by finger print technique. TLC screening of many other animal's bile, such as duck bile, chicken bile, cow bile, sheep bile, pig bile and fish bile, etc. Discussion of the possibility of replacing snake bile with some other animal's bile containing similar components.

      Classification: 4d, 32c
      94 034
      From visual evaluation according to the pharmacopoeia to exact analytical results
      H. HOFMAN (STADA R&D GmbH, Analytical Development, Sladastrasse 2, D-61118 Bad Vilbel, Germany, herbert.hofmann@stada.de)

      CBS 93, 5-7 (2004). HPTLC of N,N-diethylethane-1,2-diamine in metoclopramide finished products on silica gel with 32 % ammonia - methanol - dichloromethane 3:15:80 over 40 mm with chamber saturation. Detection by dipping in 0.2 % ethanolic ninhydrin solution for 1 s, followed by drying at 120 °C for 5 min. Quantitative determination by absorbance measurement at 480 nm and evaluation of peak area with polynomial regression. The correlation coefficient of the calibration curve is 0.9995, the residual standard deviation 2.19 %. Intermediate precision is 1.65 %. Recovery for 0.2-1.0 % impurity is 100.5 %. Limit of quantitation is 0.05 % impurity.

      Classification: 17a, 32a
      94 070
      Densitometric determination of naproxen, and of naproxen methyl ester, its impurity, in pharmaceutical preparations
      J. KRZEK*, M. STAREK (*Jagiellonian University, Collegium Medicum, Department of Inorganic and Analytical Chemistry, 9 Medyczna Str., 30-688 Kraków, Poland)

      J. Planar Chromatogr. 17, 137-142 (2004). TLC of naproxen in pharmaceutical preparations (Naprosyn, Apranax, Aleve, Naproxen) on silica gel with cyclohexane - chloroform - methanol 12:6:1. Quantitative determination at 223 nm. Limit of detection for naproxen is 30 ng. Recovery and repeatability were satisfactory.

      Classification: 32a
      94 092
      Simultaneous determination of pioglitazone and glimepiride by high-performance thin-layer chromatography
      R. T. SANE MENON, S. INAMDAR*, M. MOTE, A. MENEZES (*TDM laboratories, Plot No. 194, Scheme No. 6, Road No. 15, Sion (E), Koliwada, Mumbai-22, India)

      J. Planar Chromatogr. 17, 154-156 (2004). HPTLC of pioglitazone hydrochloride ((±)-5-{p-[2-(5-ethyl-2-pyridyl)-ethoxy]benzyl}-2,4-thiazolidinedione hydrochloride) and glimepiride (trans-3-ethyl-2,5-dihydroxy-4-methyl-N-[2-[4-[[[[(4-methylcyclohexyl)amino]-carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide)and atorvastatin as internal standard on silica gel after pre-washing in a twin-trough chamber after pre-saturation with toluene - methanol - ethyl acetate - formic acid 70:20:15:0.1. Evaluation by densitometry at 235 nm.

      Classification: 32a
      95 009
      Fluorescence evaluation using the Kubelka-Munk formula
      B. SPANGENBERG*, M. WEYANDT-SPANGENBERG (*University of Applied Sciences Offenburg, Badstrasse 24, 77652 Offenburg, Germany)

      J. Planar Chromatogr. 17, 164-168 (2004). HPTLC of flupirtine maleate on silica gel with ethyl acetate - methanol - 25 % ammonia 17:2:1 in a saturated developing chamber. Then the developed plate must be dipped for 2 s in 1:3 paraffin - hexane. Dipping increases the fluorescence tenfold and preserves the fluorescence stability for hours. Presentation of a new formula for transforming fluorescence measurements in accordance with Kubelka-Munk theory. The fluorescence signals, the absorption signals, and data from a selected reference are combined in one expression. Only diode-array techniques can measure all the required data simultaneously. The fluorescence calibration curve was linear over the range 300 to 5000 ng per spot.

      Classification: 3f, 32a
      95 063
      (Study of the quality standard for Yijing Bushen granules) (Chinese)
      CH. GUO (Guo Changqiang)*, J. LIU (Liu Jinxing), M. ZHANG (Zhang Min), Y. LI (Li Yan), CH. ZHOU (Zhou Chuanguo) (*Shandong Acad. TCM, Jinan, Shangdong 250014, China)

      Chinese J. Trad. Pat. Med. (Zhongchengyao) 26 (9), 716-719 (2004). TLC on silica gel with 1) ethyl acetate - chloroform - formic acid 3:2:1; 2) chloroform - methanol 7:2; 3) petroleum ether (60-90 ºC) - ethyl acetate 7:3. Detection 1) under UV 365 nm; 2) by spraying with 10 % H2SO4 in ethanol and heating at 105 ºC for 5 min; 3) by spraying with vanillin - H2SO4 solution. Identification by fingerprint technique. Quantification of icarrin by HPLC.

      Classification: 32c
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