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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      129 037
      Simultaneous determination of epimers (+)‑catechin and (‒)‑epicatechin in Onosma bracteatum Wall. using high‑performance thin‑layer chromatography‒mass spectrometry method
      A. RAJPARA, N. GANDHI, V. BHATT, M. SHAH* (*Department of Pharmacognosy, L. M. College of Pharmacy, Navrangpura, Ahmedabad 380009, Gujarat, India, mbshah2007@rediffmail.com)

      J. Planar Chromatogr. 35, 89-95 (2022). HPTLC of epimers (+)‑catechin (1) and (-)‑epicatechin (2) in Onosma bracteatum on silica gel with diisopropyl ether - ethyl acetate - formic acid 90:2:7. Detection by spraying with p-toluenesulfonic acid reagent, followed by heating at 110 °C. Quantitative determination by absorbance measurement at 280 nm. The hRF values for (1) and (2) were 47 and 37, respectively. Linearity was between 1000 and 5000 ng/zone for (1) and (2). Interday and intra-day precisions were below 2 % (n=3). The LOD and LOQ were 284 and 863 ng/zone for (1) and 183 and 611 ng/zone for (2). Average recovery was 98.9 % for (1) and 99.0 % for (2).

      Classification: 38
      129 038
      High‑performance thin‑layer chromatography‑based method development for the analysis of 4‑methoxy‑2‑nitroaniline as potential genotoxic impurity
      P. MINIYAR*, P. CHAVAN, S. PATIL, A. THOMAS, S. CHITLANGE (*STES’s Sinhgad Institute of Pharmaceutical Sciences, Savitribai Phule Pune University, Lonavala 410401, India, miniyarpankaj@gmail.com)

      J. Planar Chromatogr. 35, 73-81 (2022). HPTLC of omeprazole (1) and its impurity 4‑methoxy‑2‑nitroaniline (1) on silica gel with methanol - n-hexane - ethyl acetate 1:10:11. Quantitative determination by absorbance measurement at 291 and 223 nm for (1) and (2), respectively. The hRF values for (1) and (2) were 25 and 89, respectively. Linearity was between 100 and 500 ng/zone for (1) and 10 and 50 ng/zone for (2). Interday and intra-day precisions were below 1 % (n=3). The LOD and LOQ were 3.2 and 9.8 ng/zone for (1) and 0.41 and 1.25 ng/zone for (2), respectively. Recovery was in the range of 98-102 % for (2).

      Classification: 32a
      129 041
      Inherent stability testing of empagliflozin in the presence of metformin HCl by HPTLC and characterization of degradation products of empagliflozin by LC–ESI–QTOF–MS/MS
      V. VICHARE*, V. CHOUDHARI, V. TAMBE, S. DHOLE (*PES Modern College of Pharmacy (for Ladies), Moshi, Pune, Maharashtra, India, vicharevijaya11@gmail.com)

      J. Planar Chromatogr. 35, 61-71 (2022). HPTLC of empagliflozin (1) in the presence of metformin HCl (2) on silica gel with toluene - methanol - ammonia - glacial acetic acid 72:26:1:1. Quantitative determination by absorbance measurement at 230 nm. The hRF values for (1) and (2) were 15 and 48, respectively. Linearity was between 11 and 112 ng/zone for (1) and 85 and 850 ng/zone for (2). Interday and intra-day precisions were below 2 % (n=3). The LOD and LOQ were 0.6 and 1,7 ng/zone for (1) and 5 and 15 ng/zone for (2), respectively. Recovery was found to be in the range of 99.4-101.0 % for (1) and 100.3-101.4 % for (2). Degradation products were characterized by liquid chromatography coupled with electrospray ionizationquadrupole-time of flighttandem mass spectrometry (LCESIQTOFMS/MS).

      Classification: 8b, 17c
      129 042
      A validated high‑performance thin‑layer chromatography method for the simultaneous quantification of 6‑gingerol, guggulsterone E and guggulsterone Z in coded formulation AYUSH SG‑5 prepared for rheumatoid arthritis
      V. KUMAR*, V. KUSHWAHA, Y. GANDHI, S. MISHRA, V. CHARDE, C. JAGTAP, G. BABU, A. SINGH, R. SINGH, N. SRIKANTH (*Chemistry Section, Department of Chemistry, Central Ayurveda Research Institute, Jhansi, Uttar Pradesh 284003, India, vijaychem99@gmail.com)

      J. Planar Chromatogr. 35, 23-33 (2022). HPTLC of 6‑gingerol (1), guggulsterone (2) E and guggulsterone Z (3) on silica gel with toluene - acetone 9:1. Quantitative determination by absorbance measurement at 280 nm. The hRF values for (1) and (2) were 15, 19 and 25, respectively. Linearity was between 100 and 1200 ng/zone for (1) to (3). Interday and intra-day precisions were below 3 % (n=5). The LOD and LOQ were 100 and 400 ng/zone for (1) to (3), respectively. Recovery was between 95.4 and 101.05 %. 

      Classification: 7
      129 043
      β‑Cyclodextrin‑based chiral nanocomposite for thin‑layer chromatographic detection of enantiomers of fluoxetine
      S. BHARDWAJ, V. VASHISTHA* (*Department of Chemistry, GLA University, Mathura, UP 281406, India, vinod.vashistha@gla.ac.in)

      J. Planar Chromatogr. 35, 83-88 (2022). HPTLC of enantiomers of (RS)-fluoxetine on silica gel impregnated with a nanocomposite of β-cyclodextrin and 3D graphene (G/β-CD NC) with methanol - acetonitrile - water 4:3:1. Detection by exposure to iodine vapor. Average precision was below 2 %. LOD and LOQ were 1.8 and 5.4 mg/mL, respectively. Recovery was between 86 and 94 %.

      Classification: 38
      129 045
      Comparative validated chromatographic methods for the simultaneous determination of caffeine, codeine, paracetamol along with the related compound "p‑aminophenol" in tablets
      R. FEKRY, K. KELANI, Y. FAYEZ, M. TANTAWY* (*Analytical Chemistry Department, Faculty of Pharmacy, Modern University for Technology and Information, El‑hadaba El‑Wosta, Mokatam, 5th District, Cairo, Egypt, matantawy@hotmail.com)

      J. Planar Chromatogr. 35, 51-59 (2022). HPTLC of codeine (1), paracetamol (2), p-aminophenol (3) and caffeine (4) on silica gel with chloroform - methanol - acetone - ammonia 80:10:20:1. Quantitative determination by absorbance measurement at 220 nm. The hRF values for (1) to (4) were 24, 38, 46 and 61, respectively. Linearity was between 0.3 and 120 µg/zone for (1) and (4) and 1 and 20 µg/zone for (2) and (3). Interday and intra-day precisions were below 1 % (n=3). The LOD and LOQ were 0.06 and 0.21 µg/zone for (1), 0.23 and 0.7 µg/zone for (2), 0.24 and 0.82 µg/zone for (3) and 0.07 and 0.82 µg/zone for (4), respectively. Average recovery was 101.4 % for (1), 100.1 % for (2), 98.9 % for (3) and 98.3 % for (4).

      Classification: 23
      129 046
      A validated high‑performance thin‑layer chromatography method for the simultaneous determination of quercetin and gallic acid in Annona reticulata L.
      K. PATHAK*, R. DAS, N. GOGOI, R. SAIKIA, H. SARMA, A. DAS (*Department of Pharmaceutical Sciences, Faculty of Science and Engineering, Dibrugarh University, Dibrugarh, Assam 786004, India, kalyakster@gmail.com)

      J. Planar Chromatogr. 35, 35-41 (2022). HPTLC of quercetin (1) and gallic acid (2) in the leaves of Annona reticulata on silica gel with toluene - ethyl acetate - formic acid 45:50:8. Quantitative determination by absorbance measurement at 367 nm. The hRF values for (1) and (2) were 71 and 63, respectively. Linearity was between 200 and 1000 ng/zone for (1) and 200 and 1200 ng/zone for (2). Interday and intra-day precisions were below 2 % (n=5). The LOD and LOQ were 21 and 65 ng/zone for (1) and 15 and 55 ng/zone for (2), respectively. Recovery was between 98.0 and 99.1 % for (1) and 99.3 and 100.3 % for (2).

      Classification: 8a
      129 047
      Stimulation quantification of four natural lipase inhibitors from Alismatis Rhizoma by high‑performance thin‑layer chromatography method
      F. YANG (Yang Fei), M. KIM, L. GU (Gu Lihua), L. LI (Li Linnan), L. YANG (Yang Li), Z. WANG* (Wang Zhentao) (*Shanghai R&D Centre for Standardization of Chinese Medicines, Shanghai, China, ztwang@shutcm.edu.cn)

      J. Planar Chromatogr. 35, 3-12 (2022). HPTLC of alisol B 23-acetate (1), alisol B (2), alisol A (3) and alisol C 23-acetate (4) in the rhizomes of Alisma orientale on silica gel with cyclohexane - ethyl acetate 1:1. The hRF values for (1), (4), (2) and (3) were 62, 42, 28 and 9, respectively Quantitative determination by absorbance measurement at 254 nm for (1) and 208 nm for (2), (3) and (4). Linearity was between 125 and 2000 μg/zone for (1) and 83 and 2000 μg/zone for (2), (3) and (4). Interday and intra-day precisions were below 1 % (n=3). Average recovery was 94.2 % for (1), 90.3 % for (2), 97.0 % for (3) and 90.2 % for (4).

      Classification: 14
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