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:

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      124 029
      Quantification of lupeol in polyherbal formulation by high-performance thin-layer chromatography method using design of experiments as a tool to assess optimization of method development and extraction efficiency
      V. PATEL, K. SOLANKI, K. PATEL*, T. GANDHI (*Anand Pharmacy College, Opp. Town Hall, Anand, Gujarat, India, kalpana_jpatel@yahoo.com)

      J. Planar Chromatogr. 32, 385-392 (2019). HPTLC of lupeol in formulations on silica gel with toluene - ethyl acetate 237:13. Detection by dipping into anisaldehyde–sulfuric acid reagent, followed by heating at 110 ºC for 10 min. Quantitative determination by absorbance measurement at 600 nm. The hRF value for lupeol was 42. Linearity was between 500 and 3000 ng/zone. Intermediate precision was below 1 % (n=3). The LOD and LOQ were 7 and 21 ng/zone, respectively. Recovery rate was between 99.5 and 101.5 %.

      Classification: 14
      124 009
      Protection of mouse brain from paracetamol-induced stress by Centella asiatica methanol extract
      G. VISWANATHAN, V. DAN, N. RADHAKRISHNAN, A. NAIR, A. NAIR, S. BABY* (*Phytochemistry and Phytopharmacology Division, Jawaharlal Nehru Tropical Botanic Garden and Research Institute, Pacha-Palode 695562, Thiruvananthapuram, Kerala, India, sabulal@jntbgri.res.in)

      J. Ethnopharmacol. 236, 474-483 (2019). HPTLC of asiaticoside and madecassoside in Centella asiatica on silica gel with butanol - ethyl acetate - water 4:1:5. Detection by spraying with anisaldehyde-sulfuric acid reagent, followed by heating at 105 ºC for 5 min. Qualitative identification under UV light at 580 nm.    
       

      Classification: 14
      124 039
      High-performance thin-layer chromatographic fingerprints of triterpenoids for distinguishing between Isodon lophanthoides and Isodon lophanthoides var. gerardianus
      C. LIN (Lin Chaozhan), F. LIU (Liu Fangle), R. ZHANG (Zhang Runjing), M. LIU (Liu Meiting), C. ZHU* (Zhu Chenchen), J. ZHAO (Zhao Jing), S. LI (Li Shaoping) (*Guangzhou University of Chinese Medicine, Institute of Clinical Pharmacology, Baiyun Rd, Guangzhou, China 510405, zhucc@gzucm.edu.cn)

      J. AOAC Int. 102, 714-719 (2019). HPTLC fingerprint of the aerial parts of Isodon lophanthoides (Buch. Ham. ex D. Don) Hara (IL) on silica gel with toluene - chloroform - ethyl acetate - formic acid 30:10:10:1. Detection by spraying with 10 % sulfuric acid in ethanol, followed by heating at 105 ºC. Among the 12 bands with good resolution, four ursane-type triterpenoids were recognized as ursolic acid (hRF 61), 2α-hydroxy-12-en-28-ursolic acid (hRF 25), 2α,19α-dihydroxy-12-en-28-ursolic acid (hRF 19), and 2α-O-β-D-glucoside-12-en-28-ursolic acid (hRF 3). The method allowed to distinguish Isodon lophanthoides from its substitute, I. lophanthoides var. gerardianus and was a prospect for the quality control of I. lophanthoidis herba.

      Classification: 14
      123 030
      Method validation and simultaneous quantification of five triterpenoids from Codonopsis ovata by High-Performance Thin-Layer Chromatography
      A. DAR*, P. SANGWAN, N. SINGH, A. KUMAR (*Bioorganic Chemistry Division, CSIR ‒ Indian, Institute of Integrative Medicine, Canal Road Jammu Tawi 180001, India, alamgirdar@skuastkashmir.ac.in)

      J. Planar Chromatogr. 32, 251-256 (2019). HPTLC of taraxerol (1), 3β-hydroxyoleanane-12-one (2), betulinic acid (3), ursolic acid (4), and oleanolic acid (5) in Codonopsis ovata on silica gel with n-hexane - ethyl acetate - formic acid 20:5:1. Detection by dipping into a ceric ammonium sulfate reagent, followed by heating at 105-110 ºC for 5 min. Quantitative determination by absorbance measurement at 366 nm. The hRF values for (1) to (5) were 74, 64, 51, 44 and 22, respectively. Linearity was between 100 and 600 ng/zone for (1) to (5). The intermediate precision was below 5 % (n=3). The LOD and LOQ were 30 and 60 ng/zone for (1) and (4), 60 and 90 ng/zone for (2), 60 and 100 ng/zone for (3) and 30 and 70 ng/zone for (5), respectively. Recovery rate ranged between 85.7 and 97.2 % for (1) to (5).

      Classification: 14
      123 032
      Chemotaxonomic differentiation of Clerodendrum species based on High-Performance Thin-Layer Chromatographic fingerprinting of key secondary metabolites and chemometric data analysis
      M. SRIVASTAVA, P. MISHRA, N. KUMAR, K. SHANKER* (*Analytical Chemistry Department, CSIR-Central Institute of Medicinal and Aromatic Plants, Lucknow 226015, India, kspklko@yahoo.com)

      J. Planar Chromatogr. 32, 211-222 (2019). HPTLC of 24β-ethylcholesta-5,22E,25-triene-3β-O-D-glucoside (1), clerodinin-A (2), 24β-ethylcholesta-5,22E,25-triene-3β-ol (3), and lupeol (4) in three closely related Clerodendrum species (C. inerme, C. multiforum, and C. viscosum) on silica gel with toluene - ethyl - acetate - methanol - acetic acid 13:6:2:1. Detection by dipping into anisaldehyde - sulfuric acid - acetic acid 1:5:95, followed by air drying for 10 min and heating at 135 °C for 7 min. Quantitative determination by absorbance measurement at 560 nm. The hRF values for (1) to (4) were 35, 82, 89 and 96, respectively. Linearity was between 100 and 500 ng/zone for (1) to (4). The intermediate precision was below 3 % (n=9). The LOD and LOQ were 20 and 70 ng/zone for (1), 40 and 150 ng/zone for (2), 40 and 120 ng/zone for (3) and 50 and 150 ng/zone for (4), respectivley. Recovery rate was between 99.0 and 101.0 % for (1) to (4).

      Classification: 14
      123 038
      Validated simultaneous High-Performance Thin-Layer Chromatographic analysis of ursolic acid, β-sitosterol, lupeol and quercetin in the methanolic fraction of Ichnocarpus frutescens
      J. DWIVEDI, A. GUPTA, S. VERMA, S. PALIWAL, A. RAWAT* (*Pharmacognosy & Ethnopharmacology Division, CSIR ‒ National Botanical Research Institute, Lucknow, India, pharmacognosy1@rediffmail.com)

      J. Planar Chromatogr. 32, 103-108 (2019). HPTLC of ursolic acid (1), β-sitosterol (2), lupeol (3) and quercetin (4) in the aerial parts of Ichnocarpus frutescens on silica gel with toluene - ethyl acetate - formic acid 80:20:1. Quantitative determination by absorbance measurement at 500 nm for (1), 550 nm for (2), 650 nm for (3) and 310 nm for (4). The hRF values for (1) to (4) were 66, 70, 75 and 42, respectively. Linearity was between 100 and 600 ng/zone for (1) to (4). The intermediate precision was below 2 % (n=3). The LOD and LOQ were 60 and 182 ng for (1), 80 and 242 ng for (2), 50 and 151 ng for (3) and 45 and 137 ng for (4), respectivley. Recovery rate was between 96.9 and 100.1 % for (1) to (4).

      Classification: 8a, 14
      123 045
      A fast isolation method for glycyrrhizic acid, the bioactive marker of Glycyrrhiza glabra, and its quantitative evaluation in some single and multiherbal formulations using High-Performance Thin-Layer Chromatography
      U. MALLAVADHANI*, Y. APARNA, S. MOHAPATRA, D. MANE (*Centre for Natural Products & Traditional Knowledge, CSIR ‒ Indian Institute of Chemical Technology, Hyderabad 500007, India, mallavadhani@iict.res.in)

      J. Planar Chromatogr. 32, 81-87 (2019). HPTLC of glycyrrhizic acid in Glycyrrhiza glabra on silica gel with n-butanol - acetic acid - water 7:2:1. Quantitative determination by absorbance measurement at 260 nm. The hRF value of glycyrrhizic acid was 33. Linearity was between 0.2 and 2.5 µg/zone. The intermediate precision was below 6 % (n=3). The LOD and LOQ were 160 and 487 ng/zone. Recovery rate was 98.8 %.

      Classification: 14
      123 048
      Assessment of environmental quantitative variation of diosgenin in Fenugreek seeds via High-Performance Thin-Layer Chromatography method
      A. FOUDAH, P. ALAM, A. AL FURAIH, M. SALKINI, M. ABDEL-KADER* (*Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, P.O. Box 173, Al-Kharj 11942, Saudi Arabia, mpharm101@hotmail.com)

      J. Planar Chromatogr. 32, 89-93 (2019). HPTLC of diosgenin in the seeds of Fenugreek (Trigonella foenum-graecum) on silica gel with hexane - acetone 4:1. Detection by dipping into an anisaldehyde–sulfuric acid reagent, followed by heating at 105 °C for 10 min. Quantitative determination by absorbance measurement at 430 nm. The hRF value of diosgenin was 30. Linearity was between 50 and 400 ng/zone. The intermediate precision was below 2 % (n=6). The LOD and LOQ for diosgenin were 9 and 19 ng/zone. Recovery was between 98.0 and 99.2 %.

      Classification: 14