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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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.

      100 123
      A HPTLC method for quantitative estimation of swetiamarin in marketed polyherbal antidiabetic formulations
      P.M. Patel, K.N. Patel, R.K. Goyel* (*Dept. of Pharmacognosy, L. M. College of Pharmacy, Ahemdabad, India)

      Indian J. Pharm. Sci. 69(3), 446 (2007). HPTLC of swetimarin (a phytoconstituent of Enieostemma Littorale) in chloroform extracts of a polyherbal antidiabetic commercial formulation on silica gel with benzene - methanol 4:1. Detection by spraying with 10 % methanolic sulphuric acid and heating at 130° C for 2 min. Evaluation by densitometry at 536 nm. The linearity range was 50-1500 ng/zone. Recovery was more than 96 %.

      Classification: 32e
      101 052
      OPLC comparison of methods for aqueous extraction of Sennae folium and Tilia flos plant samples
      Á.Z. DÁVID*, E. MINCSOVICS, K. PÁPAI, K. LUDÁNYI, I. ANTAL, I. KLEBOVICH (*Semmelweis University, Department of Pharmaceutics, Högyes Endre Street 7, 1092 Budapest, Hungary; dadam@gyok.sote.hu)

      J. Planar Chromatogr. 21, 119-123 (2008). TLC of aqueous Senna and Tilia extracts with sennoside A and B as standards on silica gel after immersion in acetonitrile - water 17:3, with 2-propanol - ethyl acetate - water 9:9:7 (for Senna extracts) and 2-butanone - ethyl acetate - formic acid - water 3:5:1:1. Detection under UV 254 nm. Although quantitative analysis was not performed, peak areas served for comparative evaluation.

      Classification: 32e
      102 111
      Effect of hydrolysis on the yield of hederagenin and high-performance thin-layer chromatography densitometric quantification of hederagenin in fruit pericarp of Sapindus spp
      J. KALOLA, S. ANANDJIWALA, H. SRINAVASA, M. RAJANI* (*B. V. Patel Pharmaceutical Education and Research Development Center, Pharmacognosy and Phytochemistry Department, Thaltej, Ahemdabad 380 054, Gujarat, India; rajanivenkat@hotmail.com)

      J. AOAC Int. 91, 1174-1178 (2008). HPTLC of hederagenin on silica gel with toluene - ethyl acetate - formic acid 7:3:5 in a twin-trough chamber. Detection with anisaldehyde - sulfuric acid reagent by dipping for 1 s and heating for 7 min at 100 °C. Quantitative determination by absorbance measurement at 595 nm.

      Classification: 32e
      103 111
      Mahanimbine in Murraya koenigi - Marker analysis and acetyl cholinesterase enzyme inhibition
      N.S. Kumar*, M. VEnkatesh, S. ponnusankar, P. venkatesh, A. Gantait, N. NeMA, S. Bhadra, D. Mukherjee, S. pamdit, P. MUKHERJEE (*School of Natural Product Studies, Dept. of Pharmaceutical Tech., Jadavpur University, Kolkata, India)

      Abstract No. 0983, IHCB (2009). HPTLC of mahanimbine (a carbazole alkaloid isolated from Murraya koenigi) on silica gel with petroleum ether - chloroform 13:7. The hRf value of mahanimbine was 60. Quantitative determination by absorbance measurement at 254 nm. The method was linear in the concentration range of 50-250 ng/spot. Enzyme inhibition activity of methanol, petroleum ether, and chloroform exctracts of the plant and of mahanimbine was evaluated using galantamine as standard inhibitor of the enzyme.

      Classification: 32e
      103 164
      (Study on the quality standard for Yangxue Fuzheng capsules) (Chinese)
      G. ZHANG (Zhang Guoxia)*, P. LI (Li Ping), B. HAN (Han Biao) (*No. 2 People’s Hosp., Lanzhou Univ., Lanzhou 330030, China)

      J. Chinese Trad. Patent Med. 29 (4), 536-540 (2007). TLC of Yangxue Fuzheng (a traditional Chinese patent medicine) capsule extracts on silica gel with 1) chloroform - methanol - water 13:7:2, 2) chloroform - ethyl acetate - methanol - water 15:40:22:10, 3) ethyl acetate - butanone - methanol - water 10:1:1:1, 4) chloroform - methanol 40:3, 5) petroleum ether (60-90 ºC) - ethyl acetate 1:1. Detection 1) under UV 365 nm, 2) in daylight after spraying with 10 % sulfuric acid in ethanol and heating at 105 ºC.

      Classification: 32e
      104 100
      Detection of the potential adulterant Teucrium chamaedrys in Scutellaria baicalensis raw material and extract by high-performance thin-layer chromatography
      T. HONG, M.L. JEONG, M. ZAHN, B.A. FAY, K. LEE, H. HWANGBO, E. PARK, M. KIM, W. MA* (*Unigen Inc., Quality Control/Quality Assurance Department, 2660 Willamette Dr, NE, Lacey, WA 98516, USA; WenwenM@unigen.net)

      J. AOAC Int. 92, 785-788 (2009). HPTLC of plant extracts and herbal preparations applied bandwise on silica gel with ethyl acetate - formic acid - acetic acid - water 100:11:11:25 after preconditioning for 5 min. Detection by immersion in natural products reagent (diphenylboric acid 2-aminoethylester) followed by polyethylene glycol 400 reagent for 2 s. After air-drying the plates were evaluated under UV 366 nm.

      Classification: 32e
      104 183
      (Study of the quality standard for Qingshen Jianfei pills) (Chinese)
      Y. QI (Qi Yanfei)*, Q. GONG (Gong Qing), M. LU (Lu Min) (*Zhejiang Provin. Inst. Food & Med., Hangzhou, Zhejiang 310004, China)

      J. Chinese Trad. & Herb. Med. 39 (12), 1818-1829 (2008). TLC of the extracts of the TCM drug on silica gel with 1) chloroform - methanol - acetone - ammonia 2:1:4:4; 2) chloroform - methanol - acetone - formic acid 32:8:4:7; 3) ethyl acetate - butanone - formic acid - water 10:1:1:1; 4) chloroform - methanol - water 13:7:2. Detection by evaluation under UV 365 nm and after spraying with 1) potassium iodobismuthate reagent; 2) a 1:1 mixture of 1 % potassium ferricyanide and 1 % FeCl3; 3) by spraying with 10 % sulfuric acid in ethanol followed by heating at 105 °C until coloration.

      Classification: 32c
      105 025
      Estimation of curcumin and 3-acetyl-11-keto-a-boswellic acid in a marketed herbal product rheumax using HPTLC
      P. KUSHWALI*, Sheeja EDWIN, K. VARSHNEY, E. JARALD, S. AHMAD, A. DAUA (*TIFACORE in Green Pharma, B. R. Nahata College of Pharma, Mhow-Neemuch Rd., Mandsaur (M.P.), India)

      International Seminar on Herbal Drug Research, PN-028 (2009). HPTLC of curcumin and 3-acetyl-11-keto-a-boswellic acid in the herbal product Rheumax (contains Curcuma longa, Boswellia serrata, Tinospora cordifolia and Vitex negundo) on silica gel with chloroform - methanol 37:3 for curcumin and n-hexane - ethyl acetate 1:1 for the acid. Quantitative determination by absorbance measurement at 430 nm for curcumin and 254 nm for the acid. The method was linear in the range of 100-500 ng/band for curcumin and 1500-4000 ng/band for the acid.

      Classification: 11a