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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      107 133
      Validated HPTLC method for quantification of epicatechin in extracts of leaves of Cassia fistula Linn
      D.H. NAGORE*, V.K. GHOSH, M.J. PATIL, A.M. WAHILE (*Tulip Lab Pvt. Ltd. F-20/21 MIDC Ranjangaon, Tal-Shirur, Pune 412220, India)

      Acta Chromatographica 22 (2), 259-265 (2010), DOI:10.1556/AChrom.22.2010.2.8. Description of a new, simple, precise, and accurate method for quantification of (-)-epicatechin in the leaves of Cassia fistula by HPTLC on silica gel with toluene – ethyl acetate – formic acid – methanol 205:3:1:1. Quantification by densitometry at 280 nm. The linearity was in the range of 200–800 ng/band. Method precision was 1.4 %RSD and instrumental precision 1.1 %RSD. Recovery was 98.1 % and specificity regarding matrix was given.

      Classification: 32e
      108 073
      Catechol alkenyls from Semecarpus anacardium
      H. ADHAMI, T. LINDER, H. KAEHLIG, D. SCHUSTER, M. ZEHL, Liselotte KRENN* (*Department of Pharmacognosy, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria, liselotte.krenn@univie.ac.at)

      J. Ethnopharmacol. 139, 142-148 (2012). HPTLC of 1,2-dihydroxy-3-pentadec-8-enylbenzene (A) and 1,2-dihydroxy-3-pentadeca-8,11-dienylbenzene (B) in the fruits of Semecarpus anacardium L. f. (Anacardiaceae) on RP-18 with acetonitrile - water 199:1. Detection by spraying with anisaldehyde - sulfuric acid reagent. The hRf values of (A) and (B) were 31 and 42, respectively. The method was combined with ESI-MS and NMR for compound identification.

      Classification: 32e
      108 095
      A new monoterpene alkaloid and other constituents of Plumeria acutifolia
      E.M. HASSAN*, A.A. SHAHAT, N.A. IBRAHIM, A.J. VLIETINCK, S. APERS, L. PIETERS (*Department of Medicinal and Aromatic Plants, National Research Centre, 12311 Dokki, Cairo, Egypt; emadnrc@yahoo.com)

      Planta Med. 74, 1749-1750 (2008). Analytical and preparative TLC of a new monoterpene alkaloid plumerianine, (R)-4’-{(S)-1-hydroxyethyl)-5,6-dihydro-5’H-spiro[cyclopenta[c]pyridine-7,2’-furan}-5’-one, the iridoid 15-demethylplumeride, lupeol, uvaol, and ursolic acid on silica gel with toluene - ethyl acetate 8:2 or 8:3 and chloroform - methanol 9:1. Detection by spraying with vanillin-sulfuric acid reagent.

      Classification: 32e
      108 118
      Simultaneous quantification of two bioactive lupane triterpenoids from Diospyros melanoxylon stem bark
      K.K. ROUT, R.K. SINGH*, S.K. MISHRA (*Department of Chemistry, North Orissa University, Sriramchandra Vihar, Baripada, Mayurbhanjy-757003, Orissa, India; rajeshks2001@yahoo.com)

      J. Planar Chromatogr. 24, 376-380 (2011). HPTLC of stem bark extracts from D. melanoxylon and lupeol and betulin on silica gel, prewashed with methanol, with ethyl acetate - hexane 9:41 with chamber saturation for 3 min at 29 +/- 4 °C and 65 +/- 5 % relative humidity. The hRf value was 46 and 25 for lupeol and betulin, respectively. Quantitative determination by densitometry in absorption mode at 560 nm for lupeol and 510 nm for betulin. Detection by derivatization with 5 % methanol-sulfuric acid reagent. The LOD and LOQ was 40 and 100 ng/zone for lupeol and 50 and 100 ng/zone for betulin, respectively. The instrument precision and repeatability (n = 6) were 0.8 and 1.3 % for lupeol and 1.1 and 1.2 % for betulin, respectively. The linearity range was 100-500 ng/zone for both lupeol and betulin. The intra-day and inter-day precision was 1.1-1.7 % and 1.3-2.0 % for lupeol and 0.8-1.9 % and 1.9-2.2 % for betulin.

      Classification: 32e
      108 144
      Limonoids and quinoline alkaloids from Dictamnus dasycarpus
      J. YANG (Yang Jun-Li), L. LIU (Liu Lei-Lei), Y. SHI* (Shi Yan-Ping) (*Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, People’s Republic of China; shiyp@licp.cas.cn)

      Planta Med. 77, 271-276 (2011). Analytical and preparative TLC of limonoids and quinoline alkaloids (1’,2’-didehydro-7,8-dimethoxyplatydesmine, 3-chloro-8,9-dimethoxygeibalansine, dasylactone A, dasylactone B, dictamnine, 7,8-dimethoxymyrtopsine, isofraxinellone, fraxinellone, obacunone, limonoic acid, rutaevine, and rutaevine acetate) on silica gel with chloroform - methanol 30:1, 10:1 and 6:1. Detection under UV 254 nm and by spraying with 98 % sulfuric acid - ethanol 1:19 followed by heating.

      Classification: 32e
      109 092
      Standardization of marketed Adulsa syrup containing vasaka by high-performance thin-layer chromatography
      Vandana KADLAG*, Veena KASTURE, Seema GOSAVI, Rasika BHALKE (*Dept. of Pharmaceutical Chemistry, MGV’S College of Pharmacy, Panchavati, Nashik, (MS), India)

      Asian Journal of Chemistry 23(5), 1917-1921 (2011). TLC of concentrated methanolic extracts of a polyherbal ayurvedic syrup formulation (containing vasaka as main ingredient) on silica gel with methanol - toluene - dioxane - 25 % ammonia 2:2:5:1. The hRf value of vasicine was 74. Quantitative evaluation by absorbance measurement at 254 nm using vasicine as marker for standardization of the formulation. The method was found to be linear in the range of 4-12 ng/band. Isolation of vasicine from Adhatoda varica is also described.

      Classification: 32e
      109 117
      Identification of 11 marker compounds simultaneously in herb Lancea tibetica by using high-performance thin-layer chromatography
      Z.-H. SONG (Song Zong-Hua), Z.-Z. QIAN (Qian Zhong-Zhi), C. S. RUMALLA, T. J. SMILLIE, I. A. KHAN* (*National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences and Department of Pharmacognosy, School of Pharmacy, University of Mississippi, University, MS 38677, USA; ikhan@olemiss.edu)

      J. Planar Chromatogr. 24, 312-315 (2011) HPTLC of methanolic extracts of L. tibetica on silica gel (prewashed with methanol) with hexane - ethyl acetate - formic acid 12:7:1 for three furofuranolignans (sylvatesmin, (+)-piperrtol, horsfieldin), beta-sitosterol, and oleanolic acid, and with chloroform - methanol - water - formic acid 70:25:4:2 for four furofuranolignans (phillyrin, tibeticoside A, lantibeside C, and lantibeside), verbascoside and isoverbascoside in a twin-trough chamber with saturation for 20 min. Detection by immersion in ethanolic sulfuric acid for 2 s followed by heating for 5 min at 100 °C. The hRf values were 17, 25, 29, 51, 60, 70, 66, 49, 46, 19, and 21 for sylvatesmin, (+)-piperrtol, horsfieldin, oleanolic acid, beta-sitosterol, phyllirin, tibeticoside A, lantibeside C, lantiboside, verbascoside and isoverbascoside, respectively.

      Classification: 32e
      110 073
      (Study on the identification of Compound Kuhuang lotion by thin-layer chromatography) (Chinese)
      M. FANG (Fang Mingyu) (Hebei Provincial Tangshan Fengnan Hosp., Dep. Of TCM, Hebei, Fengnan 063300, China)

      Hebei J. Trad. Chinese Med. 34 (3), 433-434 (2012). Compound Kuhuang lotion is a TCM preparation used clinically for clearing heat and eliminating dampness, eliminating stagnations of blood, and relieving pains. Description of a method for the quality control of the preparation. TLC of the extracts of the preparations on silica gel 1) for Rheum officinale and the standards emodin, rhein, chrysophanol and aloe emodin, with petroleum ether (60-90 ºC) – ethyl acetate – formic acid 15:5:1, detection in daylight; 2) for Radix Sophorae flavescentis and the standard matrine, with ethyl acetate – propanone – benzene – ammonia 30:10:30:1, detection by spraying with a solution of potassium iodobismuthate – water – hydrochloric acid 10:200:1, detection in daylight; 3) for Golden Cypress and the standard berberine, with benzene – ethyl acetate – methanol – isoamyl alcohol – water 20:10:5:5:1, detection at UV 366 nm.

      Classification: 32e
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