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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      69 068
      (Determination of amygdalin in seeds of plum, Prunus, by thin-layer chromatography
      H. SHEN* (Shen Hongmei), Ch. Qiao (Qiao Chuanzhou), ZH. SU (Su Zhongwu), (*Second Military Med. Coll., Shanghai, 20043 P.R. China)

      J. Chinese Herb Med. (Zhongcaoyao) 23, 16-17 (1992). TLC of amygdalin on silica with chloroform – methanol 2:1. Quantification by densitometry (absorbance at 208 nm).

      Classification: 8b, 32e
      69 105
      (Determination of taurocholic acid and hyodeoxycholic acid in Qingkailing injection by thin-layer chromatography
      J. ZHANG (Zhang Jianjun), SH. PO (Po Shaoying), H. XU (Xu Hangli), Z. CHEN (Chen Zengjie), (Exp. Pharm. Fact., Beijing Coll. Trad. Chin. Med., Beijing, 10013 P.R. China)

      Chinese J. Hosp. Pharm. (Zhongquo Yiyuan Yaoxue Zazhi) 11, 260-262 (1991). TLC of taurocholic acid and hyodeoxycholic acid on silica with cyclohexane – ethyl acetate – acetic acid 4:4:1. Quantification by densitometry at 400 nm.

      Classification: 13d, 32c
      69 159
      Assay and purity control of chlortetracycline and demeclocycline by TLC
      W. NAIDONG, C. HAUGLUSTAINE, E. ROETS, J. HOOGMARTENS, (Katholieke Univ. Leuven voor Farmaceutische Chemeie, Inst. voor Farm. Wetenschappen, Van Evenstraat, B-3000 Leuven, Belgium)

      J. Planar Chromatogr. 4, 63-68 (1991). TLC on silica with dichloromethane – methanol – water 60:35:5 for CTC and 59:35:6 for DMCTC; silica gel layer was previously sprayed with 10% ECTA solution adjusted to pH 8.0. The less important anhydro derivatives of CTC and DMCTC were better separated on silanized silica with methanol – acetonitrile – 0.5 m oxalic acid (pH 2.0) 1:1:6. Quantification by densitometry at 280 nm. Correlation with LC method r >0.9999; RSD for TLC for the assay of the main components <2%.

      Classification: 28a
      69 195
      (Determination of chloropromazine hydrochloride in injection by thin-layer chromatography
      Z. LI (Li Zengguang), T. SHI (Shi Tieguo), J. Wu (Wu Jitao), (Dep. Chem., Yangzhou Norm. Coll., Jiangsu, 225002 P.R. China)

      Chinese J. Pharm. Anal. (Yaowu Fenxi Zazhi) 12, 47-48 (1992). TLC of chloropromazine hydrochloride on silica with cyclohexane – acetone – diethylamine 8:1:1. Quantification by densitometry at 253 nm. Comparison of the results with those obtained by other methods. R.S.D., > 2.4%. Recovery, ~100%. The results are in good agreement with those from other methods.

      Classification: 32c
      70 028
      Fiber-optic remote sensor for in situ fluorometric quantification in thin-layer chromatography
      A. NAVAS DIAZ, (Fac. Sci., Univ. Malaga, Malaga, Spain 29071)

      Anal. Chim. Acta 255, 297-303 (1991). Description of a fiber-optic-based fluorescence instrument for in-situ quantitative scanning in TLC. TLC of phenothiazines on silica with chloroform - methanol 9:1. Enhancing the fluorescence signal by immersion in a mixture of Triton X-100 - chloroform 1:4. Detection limit 5.3 µM for acepromazine and 6.4 µM for propiomazine.

      Classification: 3f
      70 096
      (Separation of constituents in the dried venom of toads and determination of the resibufogenin by thin-layer chromatography
      Z. ZHANG (Zhang Zizhong), L. GAO (Gao Luxia), Q. LU (Lu Qingtao), (Shandong Coll. Tradit. Chin. Med., Jinan, 250014 P.R. China)

      Phytochemica Analysis 3, 160-164 (1992). TLC of norsesquiterpenes of bracken fern extracts on silica with dichloromethane - acetone 3:7. Detection under UV. Isolation of pterosin B by prep. TLC with the conditions indicated above. Elution of the compound from the plate with ethyl acetate. See also M. Saito et al., Phytochemistry 28, 1605-1611 (1989).

      Classification: 14
      70 171
      (Determination of phospholipid components in Danggui by thin-layer chromatography
      R. GUO (Guo Rong), J. LU (Lu Jinchao), Y. XU (Xu Yimin), (Nanjing Coll. Tradit. Chin. Med., Nanjing 210029, P.R. China)

      J. Trad. Chin. Med. (Zhongguo Zhongyao Zazhi) 16, 741-742 (1991). TLC of phospholipids on silica with chloroform - methanol - acetic acid - ethanol - water 50:8:12:2:1. Detection by spraying with ammonium molybdate reagent. Quantification by densitometry at 700 nm.

      Classification: 32e
      70 193
      Quantitative analysis of diazepam and related compounds in drug substance and tablet dosage form by HPTLC and scanning densitometry
      D.J. WHITE, J.T. STEWART, I.L. HONIGBERG*, (*Dept. of Medicinal Chem., College of Pharmacy, Univ. of Georgia, Athens, GA 30602, USA)

      J. Planar Chromatogr. 4, 413-415 (1991). HPTLC of diazepam, nordiazepam, ACMP, and MACB on silica with chloroform - ethyl acetate 3:1. Quantification by densitometry (absorbance at 354 nm). Plates were prewashed with chloroform - ethyl acetate 3:1 and aqueous NH3 - methanol 1:9, dried and activated for 15 min at 160°C in order to achieve uniform and low background signals.

      Classification: 32a
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