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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      104 166
      Simultaneous determination of alprazolam and fluoxetine hydrochloride in tablet formulations hy high-performance column liquid chromatography and high-performance thin-layer chromatography
      R.B. PATEL*, M.R. PATEL, M.B. SHANKAR, K.K. BHATT (*Sardar Patel Univrsity, A. R. College of Pharmacy & G. H. Patel Institute of Pharmacy, Vallabh Vidyanagar 388120, Gujarat, India; rashmru@gmail.com)

      J. AOAC Int. 92, 1082-1087 (2009). HPTLC of alprazolam and fluoxetine hydrochloride in pure powder and formulations on silica gel with acetone - toluene - ammonia 12:7:1 in a twin trough chamber saturated for 30 min. Quantitative determination by absorbance measurement at 230 nm. There was no significant difference in the determined content of alprazolam and fluoxetine by HPTLC and HPLC methods (assay results compared by applying the paired t-test).

      Classification: 32a
      104 197
      Development and validation of analytical method on HPTLC for the determination of ivabradine hydrochloride as bulk drug and in pharmaceutical formulations
      Sunita SEERAPU*, B. SRINIVASAN (*Delhi Institute of Pharmaceutical Sciences and Research (DIPSAR), New Delhi, India)

      Abstract No. F-275, 61st IPC (2009). HPTLC of ivabradine HCl on silica gel with methanol - chloroform 1:1. The hRf value was 59. Quantitative determination by absorbance measurement at 285 nm. Linearity was in the range of 100-800 ng/spot with r2=0.9989 (via peak area).

      Classification: 32a
      104 230
      Stability-indicating HPTLC determination of tadalafil in API and in its pharmaceutical dosage form
      P. WAVHAL*, J. SANGSHETTI, A. SARKATE, P. WAKTE, D. SHINDE (*Dept. of Chemical Technology, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad, Maharashtra, India)

      Abstract No. F-257, 61st IPC (2009). HPTLC of tadalafil on silica gel with n-hexane - ethyl acetate - acetonitrile 14:3:3. The hRf value was 65. Quantitative determination by absorbance measurement at 215 nm. The method was linear in the range of 10-60 ng/band. The drug was subjected to different stress conditions (acid, alkali, oxidative, photodegradation, thermal) and showed degradation under all stress conditions. Degradation products and excipients of the formulation were well separated from the main component.

      Classification: 32a
      105 088
      Validated instrumental planar chromatographic method for quantification of fluphenazine hydrochloride in injections
      Sigrid MENNICKENT*, J. CONTRERAS, C. REYES, M. VEGA, M. DE DIEGO (*Department of Pharmacy, Faculty of Pharmacy, University of Concepción, P. O. Box 237, Concepción, Chile; smennick@udec.cl)

      J. Planar Chromatogr. 23, 75-78 (2010). HPTLC of fluphenazine hydrochloride on silica gel (prewashed with methanol) with methanol - water 9:1 in a saturated twin-trough chamber. Quantitative determination by absorbance measurement at 306 nm. Linearity was in the range of 100 to 500 ng/µL with a correlation coefficient of 0.998. LOD and LOQ were 1.45 and 4.40 ng/zone, respectively. Intra-assay and inter-assay precision, expressed as relative standard deviation (RSD), were in the range 0.73-1.77 % (n = 3) and 1.18-1.86 % (n = 9), respectively. Recovery of fluphenazine hydrochloride was between 98.3 and 101.5 %, with RSD not higher than 1.87 %. The method was selective for fluphenazine hydrochloride and the preservatives in the injections.

      Classification: 32a
      106 141
      HPTLC determination of cefpodoxime proxetil and potassium clavulanate in combined tablet dosage form
      S. GANDHI*, P. DESHPANDE, U. PATIL, P. MUNDHE, P. R. DESHMUKH (*Dept. of Pharmaceutical Analysis, AISSMS College of Pharmacy, Kennedy Rd., Pune, India)

      The Pharma Review 149-150 (2010). TLC on silica gel with chloroform - methanol - toluene 4:3. The hRf value was 16 and 66 for potassium clavulanate and cefpodoxime proxetil respectively. Densitometric analysis was carried out at 215 nm. The method was linear in the range of 500-2500 and 2000-10000 ng/band for cefpodoxime proxetil and potassium clavulanate respectively. The recoveries are in the range of 99.1-100.7 %.

      Classification: 32a
      108 077
      Chemical fingerprint of Potentilla species by using HPTLC method
      A. BAZYLKO, M. TOMCZYK*, A. FLAZINSKA, A. LEGAS (*Department of Pharmacognosy, Faculty of Pharmacy, Medical University of Bialystok, ul. Mickiewicza 2 a, 15-230 Bialystok, Poland; tomczy@umweb.edu.pl)

      J. Planar Chromatogr. 24, 441-444 (2011). HPTLC of plant extracts and 17 polyphenolic compounds (apigenin, apigenin-7-glucoside, ellagic acid, hyperoside, isoquercitrin, kaempferol, kaempferol-3-glucoside, kaempferol-3-glucuronide, luteolin, luteolin-7-glucoside, methyl brevifolincarboxylate, myricetin, quercetin, quercetin-3-glucuronide, rutin, tiliroside, ellagic acid 3,3’-di-O-methyl ether 4-xylopyranoside) on silica gel (prewashed with methanol) with toluene - ethyl formate - formic acid 7:5:1 in an automatic developing chamber set with a twin-trough chamber at 22 °C and a relative humidity of 48 %. Detection under UV light at 254 and 366 nm, and at 366 nm after spraying with 1.0 % methanolic diphenylborinic acid 2-aminoethylester.

      Classification: 32a
      109 073
      A stability indicating HPTLC method for the analysis of irinotecan in bulk drug and marketed injectables
      N. AKHTAR, S. TALEGAONKAR*, R. KHAR, A. ZEENAT, M. JAGGI (*Dept. of Pharmaceutics, Faculty of Pharmacy, Hamdard University, New Delhi 110 062, India, stalegaonkar@gmail.com)

      J. Liq. Chromatogr. Relat. Technol. 34, 1502-1517 (2011). HPTLC of irinotecan in bulk drug and injectable formulations on silica gel with acetone - ethyl acetate 17:3 + 1 drop acetic acid. Quantitative determination by absorbance measurement at 366 nm. The hRf of irinotecan was 31. Linearity was 50-500 ng/zone. The LOD and LOQ was found to be 10 and 33 ng/zone. The intra-day precision was 4.3 % (n = 6) and inter-day precision over three different days was 3.1 %. Intra-day and inter-day accuracy were 96.9-100.3 % and 96.5-98.7 %, respectively. Recovery (by standard addition) ranged from 94.6-101.4 %.

      Classification: 32a
      109 118
      Separation and determination of four oxicams in pharmaceutical formulations by thin-layer chromatographic-densitometric method
      Malgorzata STAREK (Department of Inorganic and Analytical Chemistry, Collegium Medicum, Jagiellonian University, 9 Medyczna Str., 30-688 Kraków, Poland; mstarek@interia.pl)

      J. Planar Chromatogr. 24, 367-372 (2011). TLC of piroxicam, meloxicam, tenoxicam, and isoxicam on silica gel with ethyl acetate - ethanol - toluene 6:3:1 + 2 drops of 25 % ammonia. Quantitative determination by densitometry in absorbance mode at 360 nm. Linearity was between 50-500 ng/zone. The hRf value was 53 for piroxicam, 78 for meloxicam, 61 for tenoxicam, and 82 for isoxicam. LOD were 10, 30, 10, and 20 ng/zone and LOQ were 20, 80, 40, and 40 ng/zone for piroxicam, meloxicam, tenoxicam, and isoxicam, respectively. The recovery was in the range of 93.2-102.9 % with %RSD of less than 1 %. The inter- and intra-day precision (%RSD) was between 0.3-0.8 %.

      Classification: 32a
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