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
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      73 073
      Determination of pteroic acid by high-performance thin-layer chromatography
      R. BARTELS, L. BOCK*, (*Borstel Res. Inst., Parkallee 4a, D-23845 Borstel, Germany)

      Contribution to the investigation of 7,8-dihydropteroate synthase. J. Chromatogr. 659, 185-189 (1994). Evaluation of the 7,8-dihydropteroate synthase reaction via determination of the stable pteroic acid from oxidation of the enzymatic product dihydropteroic acid. TLC on amino-bonded silica with a solution of 52% acetonitrile in 100 mM tris-HCl buffer (pH 8.6). Quantification by densitometry. Detection limit: at levels down to 0.5 ng/µL.

      Classification: 20
      75 070
      Curcumin, a major component of food spice turmeric (Curcuma longa) inhibits aggregation and alters eicosanoid metabolism in human blood platelets
      K.C. SRIVASTAVA, A. BORDIA, S.K. VERMA, (Dept. of Environmental Med., Inst. of Community Health, Odense, Denmark)

      Prostaglandins Leukotr Essent Fatty Acids 52, 223-227 (1995). TLC of hydroxy derivatives of arachidonic acid (12-hydroxyheptadecatrienoic acid and 12-hydroxyeicosatetraenoic acid), thromboxane B2, prostaglandins and phospholipids on silica with the upper organic phase of ethyl acetate - isooctane - acetic acid - water 11:5:2:10 or hexane - ether - acetic acid 80:30:1. Detection by exposure to iodine vapor. After marking the spots were scraped off and counted for radioactivity in a liquid scintillation counter.

      Classification: 11a, 11b
      78 057
      (Simultaneous separation of the metablins of amino acids, organic acids and nucleosides in clinical chemistry by two-dimensional thin-layer chromatography
      Y. WU (Wu Youguang), B. KUANG (Kuang Bohai), F. LONG (Long Fei), (Jiangxi Med. Coll., Nanchang 330006, P.R. China)

      Chromatogr. (Sepu) 14, 259-263 (1996). Two dimensional TLC of 30 amino acids, 40 organic acids and 20 nucleosides and related compounds on cellulose - silica with 1) isopropanol - ethyl acetate - acetone - methanol - para-amyl alcohol - NH3 - water 9:3:3:1:1:3:3, butanol - isopropanol - acetone - formic acid - water 18:8:8:3:6, 2) tert-butanol - ethanol - NH3 - water 5:6:1:3, isopentanol - petrol ether - ethanol - formic acid - propionic acid - water 45:100:25:20:1:1, 3) isopropanol - ethyl acetate - methanol - NH3 - water 5:3:1:3:1, isopropanol - saturated (NH4)2SO4 - water 4:77:19, for both direction, respectively. Detection under UV 254 nm, by spraying with 0.1 % acridine in ethanol, by spraying with ninhydrin-cadmium acetate reagent. Detection limit 10-10 - 10-11 mol, 2x10-8 - 5x10-8 mol, and 1x10-8 - 3x10-8 mol, respectively.

      Classification: 11, 18a
      94 049
      Selective separation and determination of cephalosporins by TLC on stannic oxide layers
      S. A. NABI*, E. LAIQ, A. ISLAM (*Anal. Res. Lab., Dep. Chem., Aligarh Muslim Univ., Aligarh-202002, India)

      Acta Chromatographica 14, 92-101 (2004). Study of the chromatographic behavior of some cephalosporins on synthetic inorganic ion-exchange (stannic oxide) layers with citrate and borate buffers as mobile phases. Separation of cephalosporins in synthetic mixtures and quantification by spectrophotometry. Quantitative determination of cephalosporins in blood serum samples from patients. Statistical discussion of recovery, accuracy, and reproducibility of the method.

      Classification: 32f
      99 085
      Densitometric determination of tadalafil citrate in tablets
      H. B. TAMPUBOLON, E. SUMARLIK, S. D. SAPUTRA, S. CHOLIFAH, W. F. KARTINASARI; G. INDRAYANTO* (*Assessment Service Unit, Faculty of Pharmacy, Airlangga University, Jl. Dharmawangsa dalam, Surabaya 60286, Indonesia; gunawanindrayanto@yahoo.com)

      J. Liq. Chromatogr. & Relat. Technol. 29, 2753-2765 (2006). TLC of tadalafil [6R,12aR)-2,3,6,7,12a-hexahydro-2-methyl-6-[3,4-(methylenedioxy)phenyl]pyrazino-[1’,2’:1,6]pyrido[3,4-b]indole-1,4-dione] on silica gel with n-hexane - ethyl acetate - methanol 4:3:1. Quantitative determination by absorbance measurement at 285 nm.

      Classification: 32a
      100 082
      TLC of quaternary pyridinium aldoximes, antidotes of organophosphorus esterase inhibitors
      T. CSERMELY, G. PETROIANU, K. KUCA, J. FÜRÉSZ, F. DARVAS, Z. GULYÁS, R. LAUFER, Huba KALÁSZ* (*Department of Pharmacology and Pharmacotherapy, Semmelweis University, 1089 Budapest, Nagyvárad tér 4, Hungary; huba.kalasz@gmail.com)

      J. Planar Chromatogr. 20, 39-42 (2007). Displacement TLC of quaternary pyridinium aldoximes (e. g. pralidoxime and obidoxime) on silica gel impregnated with paraffin oil by continous development with 10 % paraffin oil in n-hexane for 18 h with water - acetone - hydrochloric acid 8:1:1. Detection under UV light at 254 nm.

      Classification: 32a
      103 069
      Two-dimensional ultra-thin-layer chromatography and atmospheric pressure matrix-assisted laser desorption/ionization mass spectrometry in bioanalysis
      P.K. SALO, S. VILMUNEN, H. SALOMIES, R.A. KETOLA, R. KOSTIAINEN* (*Faculty of Pharmacy, Division of Pharmaceutical Chemistry, and Drug Discovery and Development Technology Center, University of Helsinki, Helsinki, Finland; risto.kostiainen@helsinki.fi)

      Anal. Chem. 79, 2101-2108 (2007). TLC of benzodiazepines (midazolam, diazepam, lorazepam, oxazepam, N-desalkyl-flurazepam, triazolam, nitrazepam) on monolithic UTLC phase (prewashed with methanol) with dichloromethane - acetone 93:7 for one-dimensional and toluene - acetone - ethanol - 25 % ammonia 70:20:3:1 for two-dimensional separation in a saturated chamber. Developing distance 2 cm; separation time for 1-D chromatography 2-6 min, for 2-D 4-12 min. Quantitative determination by absorbance measurement at 254 nm; for visual detection the analytes were derivatized by spraying with Dragendorff reagent. Identification of the separated compounds by AP-MALDI-MS. The limits of detection were in the picomole range and thus low enough for bioanalysis.

      Classification: 23e
      108 043
      Validated HPTLC method for simultaneous quantitation of cefixime and ofloxacin in bulk drug and in pharmaceutical formulation
      Janhavi RAO*, Kamini SETHY, Savita TADAV (*Dept. of Pharmaceutical Chemistry, Bharati Vidyapeeth Deemed University, Poona College of Pharmacy, Erandwane Pune, Maharashatra, India)

      Pharmacie Globale (IJCP) 4(05), 1-4 (2011). TLC of cefixime and ofloxacin in combined tablet dosage formulation on silica gel with n-butanol - 25% ammonia - water - DMSO 8:3:1:2. The hRf value of cefixime was 55 and of ofloxacin 65. Quantitative evaluation by absorbance measurement at 297 nm. The method was linear in the range of 30-180 ng/band for both drugs.

      Classification: 11a