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
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      97 154
      A simple and sensitive HPTLC method for the determination of content uniformity of atorvastatin calcium tablets
      Savita YADAV, Deepali MHASKE, A. KAKAD, B. PATIL, S. KADAM, S. DHANESHWAR* (*Dept. of Quality Assurance Techniques, Bharati Vidyapeeth Deemed University, Poona College of Pharmacy, Erandwane, Pune 411038, India)

      Indian J. Pharm. Sci. 67 (2), 182-186 (2005). HPTLC of atorvastatin calcium in its commercial single component tablet formulations (10 mg/tablet), on silica gel with benzene-methanol 7:3. The Rf value was 0.46. Quantitative determination by absorbance measurement at 281 nm. The method was validated in terms of linearity (200-600 ng/spot), precision (intraday variation: 0.25 - 1.01 %, interday variation: 0.21 - 0.88 %), accuracy and specificity. The LOD for atorvastatin calcium was 40 ng/spot, the LOQ was 200 ng/spot. The proposed method was successfully applied to determine atorvastatin calcium content of 10 individual tablet units of two market formulations after extracting atorvastatin calcium with methanol. All formulations were compliant with USP specifications (RSD less than or equal to 6 %) of the content uniformity test. The proposed HPTLC method can analyse ten or more formulation units simultaneously on a single plate and provides a faster and cost effective quality control tool for routine analysis of atorvastatin calcium formulation.

      Classification: 32a
      98 041
      Cardiolipin, its preferential deacylation in mammalian myocardia
      F. M. HELMY (Dept. of Biol. Sci., Delaware State Univ., Dover, DE, USA)

      Mini review and chromatographic-computional analysis. Acta Chrom. 17, 9-19 (2006). Comparative correlative TLC analysis conducted on whole-tissue homogenate of control and in-vitro-incubated samples of mammalian myocardia and bullfrog cardiac muscle and thigh skeletal muscle. The focus in the study was on TLC-densitometric analysis of the endogenous cardiolipin of control samples and their respective incubated samples to identify the products, e. g. lysocardiolipin, formed during in-vitro incubation. TLC of the chloroform-methanol extracts (2:1) obtained after the incubation from the freeze-dried tissues homogenate on silica gel with 1-propanol - chloroform - ethyl acetate - methanol - water 50:50:50:21:18. Visualization with thionine reagent, densitometry at 600 nm.

      Classification: 11c
      98 081
      (Determination of fulvotomentoside A in Lonicera Fulvotomentosa Hsu et S
      X. JIA (Jia Xiansheng)*, H. WU (Wu Hongfei), Q. MAO (Mao Qing) (*Guiyang Coll. TCM, Guiyang 550002, China)

      C. Cheng by thin-layer chromatography) (Chinese). Chinese J. Pharm. Anal. (Yaowu Fenxi Zazhi) 25 (6), 719- 721 (2005). TLC of fulvotomentoside A on silica gel with chloroform - methanol - water 61:32:5. Detection by spraying with 10 % H2SO4 in ethanol followed by heating at 105 ºC for 5 min. Quantitative determination by densitometry at 518 nm. The procedure was validated regarding linearity range (1.20 - 7.20 µg/spot, r = 0.998), repeatability (0.51 %, n = 5), precision (0.21 %, n = 5 within plate and 0.87 % n= 5 plate-to-plate), and recovery (99.7 %, RSD = 2.45 %, n = 5). The results are given for three batches of real life samples.

      Classification: 32c
      98 109
      Determination of salicylamide in pharmaceutical tablets by high-performance thin-layer chromatography with ultraviolet absorption densitometry
      C. SULLIVAN, J. SHERMA* (*Dept. Of Chem., Lafayette Coll., Easton, PA 18042-1782, USA)

      Acta Chrom. 16, 153-163 (2006). HPTLC of salicylamide in diuretic tablets and pain-relief tablets on silica gel with concentrating zones (pre-washed with dichloromethane - acetone 1:1) with dichloromethane – acetone 4:1. Quantification by densitometry at 254 nm. The method is suitable for routine quality-control analysis of pharmaceuticals containing salicylamide.

      Classification: 32a
      99 036
      A validated quantitative thin-layer chromatographic method for estimation of diosgenin in various plant samples, extract, and market formulation
      P. D. TRIVEDI, K. PUNDARIKASHUDU*, S. RATHNAM, K. S. SHAH (* L. J. Institute of Pharmacy, Near Nagdev Kalyan Mandir, Sanand Cross Roads, Ahmedabad 382210 Gujarat, India; kil_pundarik@yahoo.co.in)

      J. AOAC Int. 90, 358-363 (2007). TLC of diosgenin on silica gel with n-hexane - ethyl acetate 4:1 with chamber saturation for 15 min. Detection by dipping into a modified anisaldehyde-sulfuric acid reagent (0.1 % anisaldehyde in 2 % sulfuric acid) in order to reduce charring and background interference, followed by drying for 10 min under hot air and heating at 105 °C for 10 min. Quantitative determination by absorbance measurement at 428 nm.

      Classification: 14
      99 107
      Development and validation of three stability-indicating methods for determination of bisacodyl in pure form and pharmaceutical preparations
      Fadia H. METWALLY*, M. ABDELKAWY, I. A.NAGUIB (*Cairo University, Faculty of Pharmacy, Analytical Chemistry Department, Kasr El-Aini St, 11562, Cairo, Egypt, fadiahm@yahoo.com)

      J. AOAC Int. 90, 113-127 (2007). TLC of bisacodyl [4,4’-(2-pyridylmethylene)-bisphenol diacetate], monoacetyl bisacodyl and desacetyl bisacodyl on silica gel with chloroform - acetone 9:1. Quantitative absorbance measurement at 223 nm. Concentration range for bisacodyl was 0.2 - 1.4 µg/band, mean recovery was 100.4 +/- 1.9 %.

      Classification: 32a
      99 148
      Comparison of spectrodensitograms of the selected drugs on different chromatographic sorbents
      Alina PYKA*, M. BABUSKA, A. DZIADEK, D. GURAK (*Department of Analytical Chemistry, Faculty of Pharmacy, Silesian Academy of Medicine, 4 Jagiellonska Street, PL-41-200, Sosnowiec, Poland; alinapyka@wp.pl or apyka@slam.katowice.pl)

      J. Liq. Chromatogr. & Relat. Technol. 30, 1385-1400 (2007). TLC of alpha-tocopherol acetate, alpha-tocopherol, cholecalciferol, estradiol, testosterone, and hydrocortisone on silica gel, silica gel and kieselguhr, and aluminium oxide after prewashing with methanol; TLC of lipophilic vitamins on silica gel with toluene, and on RP-18 with methanol both with chamber saturation. Densitometric measurement at UV 254 nm. The resulting densitograms of the compounds studied indicate that applied sorbents have an influence on the wavelength of the obtained fundamental absorption band and the additional absorption bands, as well as on their intensity values.

      Classification: 32a
      100 023
      Densitometric determination of flavonoids in methanolic and aqueous extracts of Epilobii angustifolii herba by use of HPTLC
      Agnieszka BAZYLKO*, A.K. KISS, J. KOWALSKI (*Department of Pharmacognosy, Faculty of Pharmacy, Medical University of Warsaw, 1 Banach Street, 02-097 Warsaw, Poland; oklyzab@farm.amwaw.edu.pl)

      J. Planar Chromatogr. 20, 53-56 (2007). HPTLC of flavonoids (quercetin glucuronide, hyperoside, isoquercitrin, quercetin galloyl galactoside, quercitrin) on silica gel with ethyl acetate - formic acid - water 136:5:6 in a horizontal chamber. Densitometric quantitfication of flavonoids at 350 nm.

      Classification: 8a
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