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
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      94 102
      (Study of the quality Standard for Shangbiao oil
      W. ZENG (Zeng Weijie), N. CAI (Cai Naman), Q. WU (Wu Qunsong), J. ZHU (Zhu Jishi) (Guangdong Chaozhou Inst. Drug Cont., Chaozhou, Guangdong 521011, China)

      Chinese J. Trad. Patent Med. (Zhongchengyao) 26 (6), 452-455 (2004). TLC of Shangbiao oil extracts on silica gel with 1) n-heptane-ethyl acetate 17:3; 2) n-heptane - ethyl acetate 9:1; 3). Detection 1) by spraying with 2,4-dinitro-phenylhydrazine solution in ethanol; 2) by spraying with 5 % vanillin-H2SO4 solution and heating at 110 ºC for 5 min. Identification by fingerprint techniques. Quantification of menthol and camphor by GC.

      Classification: 32c
      95 072
      (Separation and purification of the active fraction of Sinisan powder with macroporous resins) (Chinese)
      CH. LI (Li Chuncheng), X. YANG (Yang Xinghao)*, J. CUI (Cui Jinghao, Y. WANG (Wang Yanfei), J. ZHU (Zhu Jia) (*Pharm. R & D Centre, Nanjing Normal Univ., Nanjing 210097, China)

      Chinese J. Trad. Pat. Med. (Zhongchengyao) 27(1), 84-87 (2005). TLC screening of Sinisan powder extracts, purified with macroporous resins, on silica gel with 1) n-butanol - ammonia - ethanol 7:3:1; 2) chloroform - methanol 7:1. Detection 1) by spraying with 5 % AICI3 in ethanol 2) by spraying with 5 % vanillin - H2SO4 solution. Identification by fingerprint technique. Screening of purification conditions by evaluation of the content of the active principle, and yield of the purified products. Type HP20 macroporous resin has been concluded to be the optimum for active fraction of the recipe in purification efficiency.

      Classification: 32c
      96 047
      Application of HPTLC to the analysis of horminone in Sphacele chamaedryoides (Balbis) Briq
      E. Pastene*, J. Alarcón, M. Avello, M. Nail, A. Urbina, D. Sepúlveda, M. Vega (*Universidad de Concepción, Barrio Universitario c/n. P. O. Box 237, Concepción, Chile)

      J. Planar Chromatogr. 18, 221-223 (2005). HPTLC of horminone on silica gel in a twin-trough chamber with hexane - dioxane 9:1. Absorbance measurement at 271 nm. For fluorescence analysis the plates were dipped in 1 % diphenylboryloxyethylamine in ethyl acetete for 2 s, followed by drying and dipping in a solution of 5 % PEG 8000 in dichloromethane for 2 s. After 15 min fluorescent zones of horminone were scanned at 366/>400 nm. Use of the fluorescence reagent successfully reduced the limits of detection and quantification to 0.75 ng/spot and 1.51 ng/spot, respectively. Linearity range was from 60-300 ng/spot.

      Classification: 15a
      96 141
      High-performance thin layer chromatography method for quantitative determination of four major anthraquinone derivatives in Rheum emodi
      N.P. SINGH, A.P. GUPTA, A.K. SINHA*, P.S. AHUJA (*Natural Plant Products Division, Institute of Himalayan Bioresource Technology, Post Box No. 6, Palampur 176061, Himachal Pradesh, India)

      J. Chromatogr. A 1077 (2), 202-206 (2005). HPTLC of physcion, chrysophanol, emodin and chrysophanol glycoside in Rheum emodi on RP-18 with methanol - water - formic acid 80:19:1. Quantitative determination by absorbance measurement at 445 nm. The calibration curves were linear in the range of 20-100 ng for physcion, 80-400 ng for chrysophanol and emodin, and 200-1000 ng for chrysophanol glycoside. The method was found to be reproducible and convenient for quantitative analysis of anthraquinone derivatives in the methanolic extract of rhizomes of Rheum emodi collected from three different locations of Western Himalaya, India.

      Classification: 32e
      97 041
      Cytotoxic alkaloids from the roots of Tylophora atrofolliculata
      X. HUANG (Xueshi Huang), S. GAO (Song Gao), L. FAN (Lishua Fan), S. YU* (Shishan Yu), X. LIANG (Xiaotian Liang) (*Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Xiannongtan Street, Beijing 100050, China; yushishan@imm.ac.cn)

      Planta Med. 70, 441-445 (2004). Preparative TLC of tylophoridicine E and F on silica gel with dichloromethane - methanol - ammonia 100:10:1 or 120:10:1. Detection with Dragendorff reagent.

      Classification: 22
      97 080
      Antifungal properties of surangin B, a coumarin from Mammea longifolia
      Y. DENG (Yanshen Deng), R. A. NICHOLSON (Department of Biological Sciences, Simon Fraser University, 8888ZUniversity Drive, Burnaby, British Columbia, V5A 1S6, Canada; nicholso.@sfu.ca)

      Planta Med. 71, 364-365 (2005). Analytical TLC of surangin B on silica gel with chloroform - toluene 1:1 and toluene - acetone 9:1. Detection under UV light at 254 nm.

      Classification: 32e
      97 110
      Determination of chenodeoxycholic acid in Hedan tablets by thin-layer chromatography (Chinese)
      Q. JIANG (Jiang Qing)*, R, YIN (Yin Rongli), Y. HU (Hu Youdan), L. ZHONG (Zhong Ling), (*Chengdu University TCM, Sichuan, Chengdu 611730, China)
      J. Chinese Trad. Patent Med. (Zhongchengyao) 27 (7), 854-856 (2005). TLC of chenodeoxycholic acid in Hedan tablets on silica gel with n-hexane - ethyl acetate - acetic acid - methanol 20:25:2:3. Detection by spraying with 10 % H2SO4 in ethanol followed by heating at 105 ºC until the spots are visualized. Quantification of chenodeoxycholic acid by densitometry at 375 nm. Validation of the procedure by investigation of its linearity range (0.47 - 2.33 µg/spot, R = 0.9992); of its repeatability (3.3 %, n = 5); of its precision (3.9 %, n = 5 within plate and 4.7 % n= 5 plate-to-plate); and its standard addition recovery (98.4%, RSD = 2.5 %, n = 5).
      Classification: 32c
      97 142
      Quantification of valerenic acid in Valeriana jatamansi and Valeriana officinalis by HPTLC
      N. SINGH*, A.P. GUPTA, B. SINGH, V. K. KAUL (*Department of Natural Plant Products, Institute of Himalayan Bioresource Technology, P. O. Box No. 6, Palampur, 176061 (HP), India)

      Chromatographia 63 (3-4), 209-213 (2006). HPTLC of valerenic acid in Valeriana jatamansi and Valeriana officinalis on silica gel with hexane - ethyl acetate - acetic acid 160:40:1. Detection with anisaldehyde-sulphuric acid reagent. Quantitative determination by absorbance measurement at 700 nm. The calibration curves were linear in the range of 500 ng - 2.5 µg/zone.

      Classification: 32e