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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      109 090
      Thin layer chromatographic method for the determination of flurbiprofen
      V. JAGATHI*, V. RAJESH, D. RAMESH, G. DEVALARAO (*K.V.S.R. Siddhartha College Pharmaceutical Sciences, Siddhartha Nagar, Vijayawada, A.P., India)

      Research Journal of Pharmaceutical, Biological and Chemical Sciences 2(1), 108-110 (2011). TLC of flurbiprofen in raw material and tablet dosage form on silica gel with chloroform - methanol - 25 % ammonia 45:5:3. Quantitative evaluation by absorbance measurement at 247 nm. The method was linear in the range of 50-600 ng/band. The sample was subjected to different stress conditions and all the degradation products were well resolved from the main compound. The method can therefore be used for stability studies.

      Classification: 32a
      109 109
      Comparison of TLC fingerprint profile of different extracts of Embelia ribes
      Vandana, S. ARORA* (*Chitkara College of Pharmacy, Rajpura (PNB), India)

      International Journal of PharmTech Research 2(4), 2438-2440 (2010). TLC of methanolic extracts of powdered dry fruits of Embelia ribes on silica gel with toluene - acetone - acetic acid 18:2:1. Detection with anisaldehyde-sulphuric acid reagent. The hRf values of the four major bands were 13, 27, 32, and 60.

      Classification: 32e
      109 128
      Adenosine A1 receptor binding activity of methoxy flavonoids from Orthosiphon stamineus
      N.D. YULIANA, A. KHATIB*, A.M. R. LINK-STRUENSEE, A.P. IJZERMAN, F. RUNGKAT-ZAKARIA, Y.H. CHOI, R. VERPOORTE (*Division of Pharmacognosy, Section Metabolomics, Institute of Biology, Leiden University, Einsteinweg 55, 2333 CC Leiden, The Netherlands; alfikhatib@hotmail.com)

      Planta Med. 75, 132-136 (2009). Analytical and preparative TLC of 3’-hydroxy-4’,5,6,7-tetramethoxyflavone, 3’,5-dihydroxy-4’,6,7-trimethoxy-flavone (eupatorin), and 3’,4’,5,6,7-pentamethoxyflavonene (sinensetin) and methanolic plant extracts of Orthosiphon stamineus on silica gel with chloroform - ethyl acetate 7:3, and chloroform - ethyl acetate - acetic acid 30:70:1. Detection by spraying with anisaldehyde-sulfuric acid followed by heating.

      Classification: 32e
      110 038
      (Development of a procedure for thin-layer chromatography of soybean saponin) (Chinese)
      H. LI (Li He)*, B. SONG (Song Bing), SH. ZHENG (Zheng Shimei), X. DING (Ding Xiaoying), Y. MA (Ma Yunchao), P. WANG (Wang Peiwu) (*Siping Munic. Administr. of Agr. Economy, Siping, Jilin Prov. 136000 China)

      Anhui Agri. Sci. Bull. 18 (1), 43-45 (2012). Soybean saponin is a component of soybean which has physiological activities and is composed of a variety of monomers. Presentation of a procedure for the separation of saponin extracted from soybean using ethanol. TLC on silica gel with 1) chloroform – ethyl acetate – methanol – water 15:40:22:10; 2) chloroform – ethyl acetate – methanol – water 3:4:2:1; 3) chloroform – ethyl acetate – methanol – water – acetic acid 3:4:2:1:0.05; 4) chloroform – ethyl acetate – methanol – water – acetic acid 30:80:40:20:1. Detection by spraying with 10 % sulfuric acid in ethanol and heating at 95 ºC until the zones are clearly visualized. Detection under UV 366 nm. The results showed that the mobile phase 1 gave the optimum separation of the soybean saponin.

      Classification: 14
      110 067
      (Preparation of Qichai Hugan pills and its quality control) (Chinese)
      J. CHANG (Chang Jimei)*, J. CHANG (Chang Juan) (*Affiliated Hosp. with Xinxiang Med. Coll., Henan, Xinxiang 453003, China)

      Chinese J. Prac. Med. 7 (3), 251-252 (2012). Presentation of a procedure for preparation and quality control of Qichai Hugan pills. TLC of the extracts 1) for Astragalus mongholicus, on silica gel with the lower phase of chloroform - ethyl acetate - methanol - water 10:20:11:5, detection by spraying with 10 % sulfuric acid in ethanol and heating at 105 °C for 5 min and viewing under daylight and UV 366 nm; 2) for the root of Chinese thorowax, on silica gel with the lower phase of chloroform - methanol - water 7:3:1, detection by spraying with a solution of p-dimethylaminobenzaldehyde - sulfuric acid - ethanol 1:2:18 followed by heating at 105 °C and viewing under daylight; 3) for the fruit of Chinese wolfberry, on silica gel with toluene – ethyl acetate - formic acid 15:5:2, detection under UV 366 nm; 4) for the root of red-rooted salvia, on silica gel with chloroform - acetone - formic acid 60:5:2, detection by spraying with a solution of 2 % ferric chloride - 1 % potassium ferricyanide 1:1 and viewing under daylight.

      Classification: 32e
      110 083
      Quantification of bergenin from Mallotus philippinensis by HPTLC–MS and study on different extraction methods
      K. HARIBABU, M. AJITHA, B. RAMESH, K. SURESH*, J. RAO (*Natural Product Chemistry Division, Indian Institute of Chemical Technology, Hyderabad-500 007, India, suresh@iict.res.in)

      J. Planar Chromatogr. 25, 445-449 (2012). HPTLC of bergenin in the stem-bark and roots of Mallotus phillippensis on silica gel with ethyl acetate - methanol - acetic acid - formic acid 16:2:1:1. Quantitative determination by absorbance measurement at 284 nm and by TLC-MS using the TLC-MS Interface. The hRf of bergenin was 49. Linearity was in the range of 100-600 ng/zone. Limits of detection and quantification were 29, 37 and 98 ng/zone, respectively. Intermediate intra-day/inter-day precision was 1.1 % (n=6). Recovery was between 96.6 and 98.9 %.

      Classification: 32e
      110 100
      (Study on the method for the determination of glucosamine sulfate potassium chloride by thin-layer chromatography (Chinese)
      M. LIU (Liu Min), ZH. XIE (Xie Zhigang), H. YIN (Yin Hongping), M. WANG (Wang Min)* (*Coll. of life sci. & technol., China Pharm. Univ., Jiangsu, Nanjing 210009, China)

      J. Strait Pharm. 24 (5), 36-38 (2012). Glucosamine sulfate is a kind of glycosaminoglycan, which, as a medicine, is able to stimulate cartilage cells, to supplement the cartilage matrix and to inhibit matrix metalloproteinase expression, thus to promote the repair of cartilage. For better quality control of the medicine a method is presented for the analysis of the related substances in glucosamine sulfate potassium chloride. TLC on silica gel with dichloromethane – methanol – ammonia 2:2:1, detection by exposure to iodine vapors for 30 min and evaluation in daylight. The LOD was 25 µg/mL. Investigation of the stability of the medicines by analysis of a sample submitted to typical stress conditions such as acid, alkali, water bath, hydrogen peroxide, high temperature and UV light. Degradation occurred only for the samples treated with alkali and in the water bath.

      Classification: 32c
      110 119
      Berberine and sanguinarine quantitation in Argemone mexicana L
      Miriam MONFORTE, Cecilia GUIZAR, J. RUBIO, Mildred CARRILLO, F. VAZQUEZ* (*Escuela de Nutrición, Departamento de Ciencias de la Salud, Universidad Anáhuac del Mayab, Km 15.5 Carretera Mérida-Progreso, Mérida Yucatán, Mexico, felipe@cicy.mx)

      (Papaveraceae) tissues by TLC–in situ fluorography. J. Planar Chromatogr. 25, 358-360 (2012). TLC of berberine and sanguinarine on silica gel with n-butanol - water - ammonia 8:1:1. Detection by densitometry in fluorescence mode at 325 nm. The hRf of berberine and sanguinarine were 29 and 95, respectively.

      Classification: 32e
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