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

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      93 163
      (Study of the identification of Shenronglutai pills by thin-layer chromatography
      CH. ZHAO (Zhao Chunxiang)*, G. ZHANG (Zhang Guijie), L. ZHANG (Zhang Li), L. XU (Xu Liangyan) (*Jilin Prov. Inst. Drug Cont., Cahngchun, Jilin 130062, P. R. China)

      J. Chinese Trad. Patent Med. (Zhongchengyao) 25 (8), 680-682 (2004). TLC on silica gel with 1) ethyl acetate - formic acid - water - methanol 35:10:15:2; 2) benzene - ethyl acetate 19:1; 3) chloroform - ethyl acetate - methanol - water; 4) petroleum ether; 5) petroleum ether - ethyl acetate 17:3; 6) chloroform - methanol - water 13:7:2; 7) ethyl acetate - formic acid - water 10:2:3. Detection 1) under daylight, 2) by spraying with 5 % H2SO4 in ethanol and heating at 105 ºC, 3) by spraying with 5 % p-dimethylaminobenzaldehyde in 10 % H2SO4 in ethanol and heating at 105 ºC, 4) by spraying with 2 % 2,4-dinitrophenylhydrazine in ethanol, 5) by spraying with 1 % vanillin - H2SO4 solution, 6) by spraying with 5 % FeCI3 in ethanol, 7) by spraying with 2 % AICI3 in ethanol and under UV 365 nm, 8) under UV light. Identification by fingerprint techniques.

      Classification: 32c
      94 027
      RP TLC evaluation of log P for higher fatty acids, hydroxy acids and their esters
      A. NIESTROJ, Alina PYKA*, J. SLIWIOK (*Department of Analytical Chemistry, Faculty of Pharmacy, Silesian Academy of Medicine, 4 Jagiellonska Street, 41-200 Sosnowiec, Poland)

      J. Planar Chromatogr. 17, 143-146 (2004). TLC of oleic, elaidic, palmitic, stearic, ricinoleic acid, methyl ricinoleate, alpha-hydroxypalmitic acid, methyl alpha-hydroxypalmitate, 12-hydroxystearic acid, methyl 12-hydroxystearate, 9,10-dihydroxystearic acid, methyl 9,10-dihydroxystearate on RP-18 with methanol - water 19:1 and 9:1. Detection with iodine vapor.

      Classification: 11a
      94 054
      Qualitative and quantitative HPTLC methods for quality control of Stephania tetranda
      Anne BLATTER, E. REICH* (*CAMAG Laboratory, Sonnenmattstr. 11, 4132 Muttenz, Switzerland)

      J. Liq. Chrom. Rel. Technol. 27, 2087-2100 (2004). HPTLC of tetrandrine on silica gel with toluene - ethyl acetate - methanol - 28 % ammonia 100:100:50:3. Detection under UV light at 366 nm, and under white light after reaction with iodine (yellowish zones). If the plate is subsequently derivatized with anisaldehyde solution, the alkaloids show a strong blue fluorescence under UV light at 366 nm. Quantitative determination at 210 nm. The calibration curve is linear for 50 - 112.5 ng tetrandine per zone. Also HPTLC of aristolochic acids (AAs) on silica gel with the upper phase of toluene - ethyl acetate - water - formic acid 20:10:1:1 and derivatization with tin(II) chloride (to be prepared freshly: dissolve 1 g tin(II) chloride•2H2O in 1.5 mL 36 % hydrochloric acid diluted with 8 mL water), followed by heating at 100 °C for 1 min and evaluation under UV light at 366 nm. The method allows detection of 1 ppm of AA.

      Classification: 32e
      94 078
      Validated HPTLC method for estimation of lamotrigine in tablets
      K. M. PATIL, A. K. AGGARWAL, S. L. BODHANKAR (Department of Pharmacology, Bharati Vidyapeeth Deemed University, Poona College of Pharmacy, Erandwane, Pune 411038, India)

      Indian J. Pharm. Sci. 66 (3), 283-286 (2004). TLC of lamotrigine in its tablet dosage form on silica gel with acetone - toluene - ammonia 14:6:1. Quantitative determination by absorbance measurement at 312 nm. The method was quantitatively evaluated in terms of linearity, accuracy, precision, repeatability, and specificity to prove its utility in the analysis of tablet dosage form.

      Classification: 32a
      94 103
      (Study of the quality standard for Qieban Zhiyang ointment
      H. ZHANG (Zhang Huizhong)*, M. PAN (Pan Mingyun), J. ZHANG (Zhang Jianli), SH. WANG (Wang Shushi), CH. LI (Li Chengshen) (* Liaoning Prov. Inst. TCM, Shenyang, Liaoning 110034, China)

      Chinese J. Trad. Patent Med. (Zhongchengyao) 26 (7), 597-600 (2004). TLC of Qieban Zhiyang ointment extracts on silica gel with 1) benzene - ethyl acetate 10:1; 2) petroleum ether (60-90 ºC) - ethyl formate - formic acid 15:5:1; 3) chloroform - methanol - ammonia 40:3:1; 4) benzene - chloroform - acetone 5:4:1; 5) chloroform - methanol 19:1. Detection 1) under UV 365 nm; 2) by exposing to ammonia vapor; 3) by spraying with potassium iodobismuthate solution; 4) under daylight. Identification by fingerprint technique. Quantification of icariine by HPLC.

      Classification: 32c
      95 034
      Planar chromatography of some 1-arylpiperazines behaving as dopaminergic ligands
      J. D. VELICKOVIC, D. ANDRIC, G. ROGLIC, Z. L. TESIC, Dusanka M. MILOJKOVIC-OPSENICA* (*Faculty of Chemistry, University of Belgrade, P. O. Box 158, 11001 Belgrade, Serbia and Montenegro)

      J. Planar Chromatogr. 17, 255-260 (2004). TLC of fourteen 1-arylpiperazine derivatives on silica gel with monocomponent and binary non-polar mobile phases and on RP-18 with binary mobile phases comprising mixtures of methanol, acetone, or dioxane (as organic modifiers) and water in a horizontal chamber after equilibration for 15 min. Detection under UV light at 254 nm.

      Classification: 23e, 32a
      95 062
      (Study of the quality standard for Qieyou Tangjiang extract) (Chinese)
      J. GAO (Gao Jiarong)*, J. ZHANG (Zhang Junru) (*No.1 Affiliated Hosp., Anhui Coll. TCM, Anhui, Hefei 230031, China)

      Chinese J. Trad. Pat. Med. (Zhongchengyao) 27(1), 94-96 (2005). HPTLC on silica gel with 1) n-butanol - glacial acid - water 19:5:5; 2) petroleum ether (30-60 ºC) - formic acetate - formic acid 15:5:1; 3) chloroform - ethyl acetate - methanol - formic acid 200:25:50:1. Detection 1) by spraying with 0.5 % ninhydrin in ethanol; 2) under UV 365 nm; 3) by spraying with vanillin - H2SO4 solution and heating. Identification by fingerprint technique. Quantification of emodin by densitometry at 440 nm. Validation of the method by investigation of linearity (0.1 µg - 0.5 µg, r = 0.998); precision (RSD = 3.8 %, n = 15 within plate and RSD = 3.2 %, n = 5 plate to plate); reproducibility of five time assay towards the same sample (RSD = 4.4 %); standard addition recovery (99.5 %, RSD = 2.2 %, n = 5). The results for some real life samples are given.

      Classification: 32c
      95 098
      (Study of the quality control of Kangbingdu oral liquid) (Chinese)
      J. ZHANG (Zhang Junping)*, X. HUANG (Huang Xiaolan), H. LE (Le Haiping) (*Nanchang Municip. Inst. Drug Cont., Nanchang, Jiangxi 330003, China)

      Chinese J. Trad. Pat. Med. (Zhongchengyao) 26 (9), App.12-14 (2004). TLC on silica gel with 1) n-butanol - glacial - water 19:5:5; 2) chloroform - methanol - glacial acetic acid - 17:2:1; 3) two fold development with benzene - acetone 9:1. Detection 1) by spraying with ninhydrin solution and heating at 105 ºC; 2) by spraying with 5 % vanillin solution and heating; 3) by spraying with a solution of 8 % vanillin in ethanol - H2SO4, and heating at 105 ºC. Identification by fingerprint technique. Quantification of phyllyrin by densitometry at 280 nm. The quantitative procedure is validated by investigating its linearity (1 - 5 µg/spot, r = 0.9998); precision (RSD = 0.36 % n = 5); repeatability (RSD = 2.92 % n = 5) and standard addition recovery (99.6 %, RSD = 2.4 %, n = 5), etc. The determination results are given for a group of real life samples.

      Classification: 32c
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