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.

      127 041
      Simultaneous estimation of azilsartan medoxomil and chlorthalidone by chromatography method using design of experiment and quality risk management based quality by design approach
      P. PRAJAPATI*, S. PATEL, A. MISHRA (*Department of Quality Assurance, Maliba Pharmacy College, Uka Tarsadia University, Tarsadi, Mahuva, Surat, Gujarat 394350, India, pintu.prajapati@utu.ac.in)

      J. Planar Chromatogr. 33, 631-646 (2020). HPTLC of azilsartan medoxomil (1) and chlorthalidone (2) on silica gel with toluene - methanol - ethyl acetate - formic acid 35:10:5:1. Quantitative determination by absorbance measurement at 241 nm. The hRF values for (1) and (2) were 55 and 36. Linearity was between 800 and 4000 ng/zone for (1) and 250 and 1250 ng/zone for (2), respectively. Intermediate precision was below 2 % (n=3). The LOD and LOQ were 15 and 44 ng/zone for (1) and 10 and 32 ng/zone for (2). Recovery was between 100.8 and 101.7 % for (1) and 99.4 and 101.0 % for (2).

      Classification: 23e, 32a
      126 011
      Quality risk assessment and DoE-based analytical quality by design approach to stability-indicating assay method for acidic degradation kinetic study of apremilast
      P. PRAJAPATI*, H. PATEL, S. SHAH (*Maliba Pharmacy College, Maliba Campus, Uka Tarsadia University, Bardoli, Gujarat 394350, India, pintu.prajapati@utu.ac.in)

      J. Planar Chromatogr. 33, 231-244 (2020). HPTLC of apremilast on silica gel with toluene - methanol - ethyl acetate 7:2:1. Quantitative determination by absorbance measurement at 241 nm. The hRF value for apremilast was 63. Linearity was between 200 and 1000 ng/zone. Inter-day and intra-day precision were below 1 % (n=3). The LOD and LOQ were 4 and 13 ng, respectively. Recovery rate was between 99.7 and 100.0 %. Apremilast was subjected to acidic, alkaline, oxidative, dry heat, neutral, and photolytic degradation conditions. The method was implemented using a quality risk management and quality by design approach for regulatory requirements.

      Classification: 23e
      106 123
      Validation high performance thin layer chromatographic determination and content uniformity test for rosiglitazone tablets
      S. WALODE*, H. CHAUDHARI, M. SARASWAT, A. KASTURE, S. WADODKAR (*Sinhgad Institute of Pharmaceutical Science, Kusgaon (BK), Lonavala, Pune 410401, India)

      Indian J. Pharm. Sci. 72(2), 249-252 (2010). HPTLC of rosiglitazone on silica gel with methanol - toluene - chloroform - triethyl amine 2:161:1. Caffeine was used as internal standard. The hRf value of rosiglitazone was 31 and of caffeine 52. Densitometric evaluation at 264 nm. The method was linear in the range of 5-50 µg/band with average recovery of 99.8-100.2 %. The method was suitable for content uniformity testing according to USP and could be used for stability studies as well.

      Classification: 23e
      107 096
      Development and validation of HPTLC and derivative spectroscopic method for simultaneous estimation of nebivolol and hydrochlorothiazide in combined dosage form
      J. SHAH*, H. PATEL, S. PATEL, S. PANCHOLI (*Dept. of Pharmaceutical Analysis, Babaria Institute of Pharmacy, Vadodara-Mumbai NH#8, Varnama, Vadodara 391240, Gujarat, India)

      62nd Indian Pharmaceutical Congress Abstract No. F-258 (2010). TLC of nebivolol HCl and hydrochlorothiazide on silica gel with methanol – chloroform – toluene – triethylamine 10:25:14:1. Quantitative determination by absorbance measurement at 284 nm. The hRf value of nebivolol was 78 and of hydrochlorthiazide 41. The method was linear in the range of 5-100 ng/band and 20-140 ng/band for nebivolol HCl and hydrochlorothiazide, respectively. Recovery was in the range of 98.8-100.0 % for both drugs.

      Classification: 23e
      116 027
      Validation of ethnomedicinal potential of Tinospora cordifolia for anticancer and immunomodulatory activities and quantification of bioactive molecules by HPTLC
      M. BALA, K. PRATAP, P. VERMA, B. SINGH, Y. PADWAD* (*Regulatory Research Centre, Department of Biotechnology, CSIR-Institute of Himalayan Bioresource, Palampur, Himachal Pradesh, 176061, India, yogendra@ihbt.res.in)

      J. Ethnopharmacol. 175, 131-137 (2015). HPTLC of 11-hydroxymustakone (1), N-formylannonain (2) and yangambin (3) in Tinospora cordifolia on silica gel with chloroform - ethyl acetate - methanol 130:80:3. Detection by dipping into anisaldehyde sulfuric acid reagent, followed by heating at 100 °C for 5 min. Quantitative determination by absorbance measurement at 366 nm. LOD and LOQ were 75 and 225 ng/zone for (1), 150 and 450 ng/zone for (2) and 30 and 90 ng/zone for (3), respectively. The intermediate precision was below 3 % (n=3). Recovery for (1) to (3) was in the range of 99-108 %.

      Classification: 8b, 23e
      61 262
      Separation of methyl-substituted benz[C]acridines by reversed-phase high-performance thin-layer chromatography
      K. KAMATA*, N. MOTOHASI, (Tokyo Metropolitan Research Lab. of Public Health, 24-1, Hyakunincho 3-chome, Shinjuku-Ku, Tokyo 160, Japan)

      J. Chromatogr. 396, 437-440 (1987). Reversed-phase TLC on RP-18 silica with 1. methanol, 2. ethanol, 3. acetonitrile, 4. acetone, 5. ethyl acetate, and 6. chloroform. Detection under UV 254 nm. (More than 40 solvent systems were tested.)

      Classification: 23e, 37b
      67 038
      Identification and quantification of complex mixtures and their constituents by the combination of TLC with FTIR in situ measurement
      K.A. KOVAR, H.K. ENSSLIN, R. FREY, S. RIENAS, S. WOLFF, (Pharm. Inst. der Univ. Tübingen, Auf der Morgenstelle 8, D-W-7400 Tübingen 1, FRG)

      Proc. 6th Int. Symp. Instrum. Planar Chromatogr., (Interlaken 1991), Inst. Chromatogr., Bad Dürkheim, FRG, 185-193 (1991).Various benzodiazepines, some designer drugs e.g. MDA, MDMA, MDE, and sodium edetate (EDTA), were detected by FTIR scanning of the separated peaks on TLC plates. Automated multiple development (AMD) has been used for the separation of closely related substances. Using caffeine as an example, 3 different evaluation procedures were described.

      Keywords:
      Classification: 4e, 23e, 32a
      75 023
      2-Trichloromethyl-benzimidazole as a selective chromogenic reagent for the detection of some azoles on thin-layer plates
      L. KONOPSKI*, E. PAWLOWSKA, (*Inst. Industr. Org. Chem., Annopol 6, 03-236 Warsaw, Poland)

      J. Chromatogr. 669, 275-276 (1994). Discussion of the extension of the title compound to five-membered heteroaromatic rings containing 1-4 nitrogen atoms, as a selective chromogenic reagent. 22 compounds were examined. Discussion also of the reaction mechanisms.

      Keywords:
      Classification: 3e, 23e