Selection of elite germplasms for industrially viable medicinal crop Bacopa monnieri for bacoside A production: An HPTLC-coupled chemotaxonomic study

2020 ◽  
Vol 158 ◽  
pp. 112975
Author(s):  
Abhijit Dey ◽  
Alok Kumar Hazra ◽  
Samapika Nandy ◽  
Prabhjot Kaur ◽  
Devendra Kumar Pandey
2017 ◽  
Vol 133 (2) ◽  
pp. 203-214 ◽  
Author(s):  
J. Leonard ◽  
Bishwanath Seth ◽  
Binod B. Sahu ◽  
V. R. Singh ◽  
Nivedita Patra

2013 ◽  
Vol 35 (7) ◽  
pp. 1121-1125 ◽  
Author(s):  
Poojadevi Sharma ◽  
Sheetal Yadav ◽  
Anshu Srivastava ◽  
Neeta Shrivastava

2017 ◽  
Vol 98 ◽  
pp. 76-81 ◽  
Author(s):  
Cinthya Christopher ◽  
Anil John Johnson ◽  
Paravanparampil Jacob Mathew ◽  
Sabulal Baby

2019 ◽  
Vol 57 (10) ◽  
pp. 920-930 ◽  
Author(s):  
Sunayna Choudhary ◽  
Indu Pal Kaur ◽  
Jai Malik

Abstract The use of herbs as medicine is an ancient form of healthcare known to mankind. Standardization of herbal medicines is however a challenging task and is the major bottleneck in their acceptance as the primary therapeutic option. The aim of this study was to develop and validate a simple, rapid HPLC method for standardizing the mixture of extracts of three Medhya Rasayanas (neurotonic), Convolvulus pluricaulis, Withania somnifera and Bacopa monnieri. Simultaneous estimation of the respective bioactive markers of these plants viz., scopoletin, withaferin A, bacoside A 3, bacopaside II, jujubogenin and bacosaponin C has been reported for the first time. The method was developed using Waters Hybrid X-Bridge shield with BEH technology 2.5 μm, 4.6 × 75 mm column and validated according to ICH guidelines. The 20 minutes run time makes the method eco-friendly. The method was linear over a range of 12.5–400 ng/10 μL for scopoletin and 62.5–2,000 ng/10 μL for withaferin A, bacoside A 3, bacopaside II, jujubogenin and bacosaponin C with detection limits of 8.0, 48.3, 30.4, 40.7, 15.6 and 18.9 ng/10 μL and quantification limits of 24.5, 146.5, 92.2, 123.4, 47.4 and 57.4 ng/10 μL, respectively. The correlation coefficient for each analyte was >0.999. The intra-day and inter-day precision was <2%. These results confirmed the precision, accuracy and robustness of the proposed method.


2010 ◽  
Vol 24 (8) ◽  
pp. 1217-1222 ◽  
Author(s):  
R. Sharath ◽  
B.G. Harish ◽  
V. Krishna ◽  
B.N. Sathyanarayana ◽  
H.M. Kumara Swamy

Fitoterapia ◽  
2010 ◽  
Vol 81 (5) ◽  
pp. 315-322 ◽  
Author(s):  
Jobin Mathew ◽  
Jes Paul ◽  
M.S. Nandhu ◽  
C.S. Paulose

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Rupali Gupta ◽  
Akanksha Singh ◽  
Madhumita Srivastava ◽  
Vivek Singh ◽  
M. M. Gupta ◽  
...  

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