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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      110 043
      TLC assay of L-carnitine in dietary supplements
      Monika DABROWSKA*, Emilia SIECZKA, M. STAREK (*Jagiellonian University Collegium Medicum, Department of Inorganic and Analytical Chemistry, 9 Medyczna St, 30-688, Poland, mtylka@cm-uj.krakow.pl)

      J. Planar Chromatogr. 25, 450-455 (2012). HPTLC of L-carnitine in dietary supplements on cellulose with methanol - water 5:1 + 1 drop glacial acetic acid. Detection by spraying with ninhydrin reagent. Quantitative determination by absorbance measurement at 420 nm. The hRf of L-carnitine was 65. Linearity was in the range of 10-40 µg/zone. Limits of detection and quantification were 3 and 8 µg/zone, respectively. Precision (%RSD) was below 1.6 %. Recovery was in the range of 99.5 and 103.6 %.

      Classification: 18a
      110 062
      Statistical correlation and simultaneous estimation of atazanavir sulfate and ritonavir in fixed dosage form by high performance liquid chromatography and high-performance thin-layer chromatography
      Anindita BEHERA*, K. SETHY, Dannana SANKAR, S. MITRA, S. SI (*School of Pharmaceutical Sciences, Siksha O Anusandhan University, Bharatpur, Ghatikia, Bhubaneswar - 751003, Orissa, India, anindita02@gmail.com)

      J. Liq. Chromatogr. Relat. Technol. 35, 1731-1749 (2012). HPTLC of atazanavir sulfate (1) and ritonavir (2) in fixed dosage on silica gel with toluene – methanol – glacial acetic acid – ethyl acetate 14:1:3:4. Quantitative determination by absorbance measurement at 254 nm. The hRf values of (1) and (2) were 50 and 63, respectively. Linearity was 30-300 ng/zone for (1) and 10-100 ng/zone for (2). The intermediate/inter-day/intra-day precision was 0.3 % for (1) and 0.7 % for (2) (n=6). The limit of detection and quantification was 16 and 49 ng/zone for (1) and 18 and 55 ng/zone for (2), respectively. Recovery (by standard addition) was 99.9 % for (1) and (2). The results were in accordance with those by a validated HPLC method.

      Classification: 32a
      110 101
      (Study of the method for the quality control of Fuyanshuan suppository) (Chinese)
      X. LIU (Liu Xiaochuan)*, X. LI (Li Xixiang), ZH. JIAO (Jiao Zhenghua), Q. GU (Gu Qiuli), L. WANG (Wang Lanxia) (*Gansu Provinc. Hosp. of TCM, Gansu, Lanzhou 730050, China)

      Chinese J. of Inform. on TCM 17 (12), 48-50 (2010). Fuyanshuan suppository is a herbal TCM preparation for heat clearing, detoxifying, eliminating stagnation, regulating the flow of vital energy and invigorating the circulation of blood. For quality control TLC of the extracts of the preparation 1) for Ajuga becumbens Thunb., on silica gel with cyclohexane - chloroform – ethyl acetate – glacial acetic acid 40:10:16:1, detection by spraying with 10 % sulfuric acid in ethanol and heating at 100 °C, evaluation under UV 366 nm or daylight; 2) for Lonicera japonica, on silica gel with chloroform – acetone – formic acid 3:2:1, detection by exposure to daylight for 10 min and viewing under UV 366 nm.

      Classification: 32e
      110 127
      Simultaneous determination of propanolol hydrochloride and flunarizine dihydrochloride in bulk and capsule using reversed-phase high-performance thin layer chromatography/densitometry
      A. PATIL, A. SHIRKHEDKAR*, S. SURANA, P. NAWALE (*R.C. Patel Institute Pharmaceutical Education and Research, Shirpur Dist., Dhule, India, atulshirkhedkar@rediffmail.com)

      J. Chil. Chem. Soc. 57, 1033-1035 (2012). HPTLC of propanolol hydrochloride (1) and flunarizine dihydrochloride (2) in combined dosage form on silica gel with methanol - toluene - ammonia 14:6:1. Quantitative determination by absorbance measurement at 267 nm. The hRf of compounds (1) and (2) were 63 and 48, respectively. Linearity was in the range of 800-4800 ng/zone for (1) and 200-1200 ng/zone for (2). Limits of detection and quantification were 25 and 75 ng/zone for (1) and 16 and 48 ng/zone for (2), respectively. Intermediate/intra-day/inter-day precision was below 2.0 % (n=6). Recovery for both (1) and (2) was between 99.3 and 100.9 %.

      Classification: 32a
      110 169
      Validated HPTLC method for simultaneous determination of loratadine and desloratadine in presence of co-formulated drug
      R. YOUSSEF*, E. KHAMIS, M. EL-SAYED, Mona MONEIM (*Faculty of Pharmacy, Department of Pharmaceutical Analytical Chemistry, University of Alexandria, El-Messalah, Alexandria 21521, Egypt, rmmy1973@yahoo.com)

      J. Planar Chromatogr. 25, 456-462 (2012). HPTLC of loratadine (1) and desloratadine (2) on silica gel with methanol + 1 drop ammonia. Quantitative determination by absorbance measurement at 254 nm. The hRf values of (1) and (2) were 76 and 20, respectively. Linearity was in the range of 250-850 ng/band for (1) and 100-1000 ng/band for (2). Limits of detection and quantification were 90 and 250 µg/band for (1) and 30 and 100 µg/band for (2), respectively. Intra- and inter-day precisions were found to be less than 2 %. Recoveries were between 97.8 and 101.5 % for both (1) and (2).

      Classification: 32a
      111 018
      Development of high-performance thin-layer chromatography (HPTLC) technique for evaluation of sunscreen photostability
      M. CHAVAN, A. VAIDYA* (*Unilever R & D India, 64 Main Road, Whitefield, Bangalore, India, ashish.vaidya@unilever.com)

      J. Planar Chromatogr. 25, 122-126 (2012). HPTLC of 4-tert-butyl, 4-methoxydibenzoylmethane along with a photostabilizer on silica gel, then exposed to solar simulated sunlight and developed with n-hexane - ethyl acetate 9:1. Detection under UV 366 nm. Quantitative determination of the amount of sunscreen left after solar exposure by absorbance measurement at 357 nm.

      Classification: 5b
      111 037
      Rapid test for content uniformity of coenzyme Q10 in soft gel capsules by HPTLC
      Anita ANKLI, D. HANDLOSER, Valeria WIDMER, E. REICH*, E. CENIVIVA (*CAMAG Laboratory, Sonnenmattstr. 11, 4132 Muttenz, Switzerland, lab@camag.com)

      CBS 107, 5-7 (2011). HPTLC of coenzyme Q10 in toluene extracts of soft gel capsules on silica gel (pre-washed by development from both sides with methanol) with toluene in the horizontal developing chamber from both sides. Detection under UV 254 nm. The hRf value of coenzyme Q10 is 20. Quantitative absorption measurement at 282 nm, evaluation via peak height. Linearity was in the range of 20-50 ng/band. Polynomial calibration ranged 20-150 ng/band. The parallel analysis of 60 samples (10 samples each from 6 batches) and 12 standards required only 86 min. The test for content uniformity was performed with 10 samples according to the European Pharmacopoeia and the USP 34 and the requirements were met.

      Classification: 20
      111 055
      Stability-indicating densitometric HPTLC method for qualitative and quantitative analysis of arbutin in commercial whitening creams
      S. ALQASOUMI, P. ALAM*, M. ABDEL (*Department of Pharmacognosy, College of Pharmacy, Salman Bin AbdulAziz University, P.O. Box 173, Al-Kharj 11942, Kingdom of Saudi Arabia, prawez_pharma@yahoo.com)

      J. Planar Chromatogr. 25, 168-173 (2012). HPTLC of arbutin in commercial whitening creams with methanol - chloroform - acetic acid 7:12:1. Quantitative determination by absorbance measurement at 254 nm. The hRf value of arbutin was 40. LOD and LOQ were found to be 42 and 112 ng/zone, respectively.

      Classification: 32a
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