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.

Page
      106 170
      Simultaneous estimation of nebivolol hydrochloride and s-amlodipine besylate by high-performance thin-layer chromatography
      A. SHARMA, B. PATEL, R. PATEL* (*Prof. Parul Institute of Pharmacy, Vaghodiya, Vadodara, Gujarat, India, drbhp@rediffmail.com)

      International Journal of Pharma and Bio Sciences 1(4), 339-345 (2010). TLC on silica gel (plates pre-washed with methanol) with chloroform - toluene - methanol - glacial acetic acid 50:20:30:1. The hRf value of s-amlodipine was 33 and of nebivolol 48. Densitometric evaluation at 271 nm. The linearity range was 500-2500 ng/zone for nebivolol and 250-1250 ng/zone for s-amlodipine. The method was suitable for routine analysis of the formulation.

      Classification: 32c
      107 140
      A validated densitometric TLC method for analysis of cefuroxime axetil and potassium clavulanate in combined tablet dosage forms
      M.R. SENGAR*, S.V. GANDHI, U.P. PATIL, V.S. RAJMANE, K.G. BOTHARA (*A.I.S.S.M.S. College of Pharm. Dep. of Pharm. Anal., Kennedy Road, Pune 411001, India)

      Acta Chromatographica 22 (1), 91-97 (2010), DOI:10.1556/AChrom.22.2010.1.7. TLC on silica gel with chloroform – methanol – toluene 4:3:3. The hRf value was 77 and 29 for cefuroxime axetil and potassium clavulanate, respectively. Quantification by densitometry at 225 nm. The linearity was in the range of 0.5–2.5 and 2–10 µg/band, respectively. Application of the method for analysis of the drugs in a pharmaceutical formulation with a recovery of 100.1 % for cefuroxime axetil and 99.9 % for potassium clavulanate.

      Classification: 32c
      114 083
      (Study on the method for qualitative and quantitative determination of bilirubin in compound paracetamol and chlorphenamine maleate granules) (Chinese)
      Y. MA (Ma Yuemin)*, CH. ZENG (Zeng Changqing), CH. HUANG (Huang Chunhui), X. SONG (Song Xiaoxiao) (*Shenzhen Inst. for Drug Contr., Guangdong, Shenzhen 518057, China)

      J. Chinese Modern Med. & Pharm. 20 (31), 54-56 (2013). Paracetamol and chlorphenamine maleate granule are an anti cold medicine effective for cold induced nasal congestion, headache, sore throat, fever, etc. Artificial bezoar is one of the main ingredients and bilirubin is the key effective component in the medicine. For quality control, TLC of the extracts and bilirubin on silica gel with isooctane – ethyl acetate – glacial acetic acid 11:5:3, detection under white light. Quantitative determination of bilirubin by UV spectrophotometry. Demonstration by applying to real life samples from three pharmaceutical factories indicated that the method was suited for the quality control of the medicine.

      Classification: 4e, 32c
      119 110
      Resolution of enantiomers of (RS)-baclofen by ligand-exchange thin-layer chromatography
      M. SINGH, P. MALIK, R. BHUSHAN* (*Dep. of Chem., Indian Inst. of Technol. Roorkee, Roorkee 247667, India, rbushfcy54@gmail.com)

      J. Chromatogr. Sci. 54 (5), 842-846 (2016). Development of a new chromatographic method for direct enantioresolution of (RS)-baclofen by ligand-exchange TLC, adopting two different approaches: (A) on plates prepared by mixing the ligand exchange reagents (LER) with silica gel slurry, development with different achiral solvents or solvents without chiral additive; (B) on silica gel without chiral selector and the LER consisting of Cu(II)–L-amino acid complex as chiral mobile phase additive. Preparation of LERs by using Cu(II) acetate and four L-amino acids (L-tryptophan, L-histidine, L-proline and L-phenylalanine). Detection by exposure to iodine vapor. Study of the effect of temperature and the mole ratio of Cu(II)-to-amino acid on enantioresolution. L-tryptophan proved to be a good ligand using a common mobile phase in each case.

      Classification: 32c, 38
      55 129
      Therapeutic drug monitoring by high performance thin-layer chromatography
      G. MALIKIN, S. LAM, A. KARMEN

      Chromatographia 18, 253-259 (1984). HPTLC of antiarrhythmic drugs on silica with benzene - ethyl acetate - methanol - triethylamine 7:6:1:1 and of chloramphenicol on silica with heptane - chloroform - methanol 6:12:3. Densitometry by absorbance at 265 nm or by fluorescence for the former and by absorbance at 280 nm for the latter. Method for monitoring of therapeutic drugs in blood serum. Comparison with EMIT and HPLC.

      Classification: 32c
      58 016
      Qualitative organic analysis, 1) Identification of drugs by principal component analysis of standardized thin-layer chromatographic data in four eluent systems
      G MUSUMARRA, G. SCARLATA, G. CIRMA, G. ROMANO, S. PALAZZO, S. CLEMENTI, G. GUILETTI

      J. Chromatogr. 350, 151-168 (1985). TLC on silica with four developing systems: 1) ethyl acetate - methanol - 30% NH3 85:10:5, 2) cyclohexane. - toluene - diethylamine 65:25:10, 3) ethyl acetate - chloroform 5:5, 4) acetone with the plate dipped in KOH solution. Detection by spraying with Dragendorff reagent and acidified iodoplatinate solution. A two-component model accounting for 73% of the total variance. Results of great practical importance in analytical toxicology.

      Classification: 2a, 32c
      61 224
      Nachweis von Prajmaliumbitartrat (Neo-Gilurytmal) im Urin durch Dünnschicht-Chromatographie
      E. NOVAKOVA, (Inst.für Toxikologie FUL UK, CS-12000 Praha 2, Katerinská 32, CSSR)

      (Detection of prajmaliumbitartrate (neo-gilurytmal) in urine by thin-layer chromatography). Pharmazie 42, 550-551 (1987). TLC of the antiarrhythmic prajmalin on silica with methanol - acetic acid - HCl 10:85:5, chloroform - ethanol - acetic acid 15:15:10 and toluene - ethanol - acetone - diethyl amine 30:20:20:1. Detection with Dragendorff’s reagent modified by Kaiser and Jori (addition of 1 g cersulfat and 1 mol/L, conc. nitric acid).

      Classification: 32c
      62 232
      Wasserbestimmung in Erythromycin nach Karl Fischer
      M. MÜLLER, (Dr. Karl Thomae GmbH, Analytik, Postfach 1755, 7950 Biberach an der Riss, FRG)

      (Water determination in Erythromycin by Karl Fischer method). Dtsch. Apoth. Ztg. 127, 2034-2036 (1987). TLC of Erythromycin on silica with ethyl acetate - isopropanol - methanol 80:30:20 after saturation with 15% ammonium acetate solution (pH 9.6). Detection by spraying with anisaldehyde - sulfuric acid and heating at 110°C.

      Classification: 32c
Page