Mucuna pruriens (seed)
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=Supplementary Information= | =Supplementary Information= | ||
==Other Publications== | ==Other Publications== | ||
− | ===HPTLC L- | + | ===HPTLC L-dopa Estimation, Modi, ''et al.'', 2008=== |
− | '''Estimation of L-Dopa from Mucuna pruriens LINN and Formulations Containing M. pruriens by HPTLC Method,''' | + | '''Estimation of L-Dopa from ''Mucuna pruriens'' LINN and Formulations Containing ''M. pruriens'' by HPTLC Method,''' |
<blockquote>'''Abstract.''' | <blockquote>'''Abstract.''' | ||
− | A selective, precise, and accurate high-performance thin-layer chromatographic (HPTLC) method has been developed for the analysis of L-dopa in Mucuna pruriens seed extract and its formulations. The method involves densitometric evaluation of L-dopa after resolving it by HPTLC on silica gel plates with n-butanol–acetic acid–water (4.0+1.0+1.0, v/v) as the mobile phase. Densitometric analysis of L-dopa was carried out in the absorbance mode at 280 nm. The relationship between the concentration of L-dopa and corresponding peak areas was found to be linear in the range of 100 to 1200 ng/spot. The method was validated for precision (inter and intraday), repeatability, and accuracy. Mean recovery was 100.30%. The relative standard deviation (RSD) values of the precision were found to be in the range 0.64—1.52%. In conclusion, the proposed TLC method was found to be precise, specific and accurate and can be used for identification and quantitative determination of L-dopa in herbal extract and its formulations.<ref> | + | A selective, precise, and accurate high-performance thin-layer chromatographic (HPTLC) method has been developed for the analysis of L-dopa in ''Mucuna pruriens'' seed extract and its formulations. The method involves densitometric evaluation of L-dopa after resolving it by HPTLC on silica gel plates with n-butanol–acetic acid–water (4.0+1.0+1.0, v/v) as the mobile phase. Densitometric analysis of L-dopa was carried out in the absorbance mode at 280 nm. The relationship between the concentration of L-dopa and corresponding peak areas was found to be linear in the range of 100 to 1200 ng/spot. The method was validated for precision (inter and intraday), repeatability, and accuracy. Mean recovery was 100.30%. The relative standard deviation (RSD) values of the precision were found to be in the range 0.64—1.52%. In conclusion, the proposed TLC method was found to be precise, specific and accurate and can be used for identification and quantitative determination of L-dopa in herbal extract and its formulations.<ref> |
− | Modi, K.P., Patel, N.M., Goyal, R.K. 2008. Estimation of L-Dopa from Mucuna pruriens LINN and Formulations Containing M. pruriens by HPTLC Method ''Chemical and Pharmaceutical Bulletin'' 56(3), 357-359. http://doi.org/10.1248/cpb.56.357</ref></blockquote> | + | Modi, K.P., Patel, N.M., Goyal, R.K. 2008. Estimation of L-Dopa from ''Mucuna pruriens'' LINN and Formulations Containing ''M. pruriens'' by HPTLC Method ''Chemical and Pharmaceutical Bulletin'' 56(3), 357-359. http://doi.org/10.1248/cpb.56.357</ref></blockquote> |
+ | |||
+ | ===HPTLC L-dopa degradation, Pulikkalpura, ''et al.'', 2015=== | ||
+ | '''Levodopa in ''Mucuna pruriens'' and its degradation,''' | ||
+ | <blockquote>'''Abstract.''' | ||
+ | |||
+ | ''Mucuna pruriens'' is the best known natural source of L-dopa, the gold standard for treatment of Parkinsonism. ''M. pruriens'' varieties are protein rich supplements, and are used as food and fodder worldwide. Here, we report L-dopa contents in seeds of fifty six accessions of four ''M. pruriens'' varieties, ''M. pruriens'' var. ''pruriens'', ''M. pruriens'' var. ''hirsuta'', ''M. pruriens'' var. ''utilis'' and ''M. pruriens'' var. ''thekkadiensis'', quantified by HPTLC-densitometry. L-dopa contents varied between 0.58 to 6.42 (%, dr. wt.). High and low L-dopa yielding genotypes/chemotypes of ''M. pruriens'' could be multiplied for medicinal and nutritional purposes, respectively. HPTLC profiles of ''M. pruriens'' seeds on repeated extraction (24 h) in 1:1 formic acid-alcohol followed by development in butanol:acetic acid:water (4:1:1, v/v) showed consistent degradation of L-dopa (Rf 0.34 ± 0.02) into a second peak (Rf 0.41 ± 0.02). An average of 52.11% degradation of L-dopa was found in seeds of ''M. pruriens'' varieties. Since ''M. pruriens'' seeds and/or L-dopa are used for treatment of Parkinson’s disease and as an aphrodisiac both in modern and/or traditional systems of medicine, the finding of high level of L-dopa degradation (in pure form and in ''M. pruriens'' extracts) into damaging quinones and ROS is very significant.<ref> | ||
+ | Pulikkalpura, H. Kurup, R., Mathew, P.J., Baby, S. 2015. Levodopa in ''Mucuna pruriens'' and its degradation. ''Scientific Reports'' 5, 11078. http://doi.org/10.1038/srep11078</ref></blockquote> | ||
=Sources= | =Sources= | ||
<references /> | <references /> |
Latest revision as of 16:59, 12 April 2016
Contents |
Nomenclature
Mucuna pruriens (L.) DC. Fabaceae
Standardized common name (English): velvet bean
Ayurvedic name(s): atmagupta; kapikacchu
Botanical Voucher Specimen
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Organoleptic Characteristics
Macroscopic Characteristics
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Microscopic Characteristics
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High Performance Thin Layer Chromatographic Identification
Supplementary Information
Other Publications
HPTLC L-dopa Estimation, Modi, et al., 2008
Estimation of L-Dopa from Mucuna pruriens LINN and Formulations Containing M. pruriens by HPTLC Method,
Abstract. A selective, precise, and accurate high-performance thin-layer chromatographic (HPTLC) method has been developed for the analysis of L-dopa in Mucuna pruriens seed extract and its formulations. The method involves densitometric evaluation of L-dopa after resolving it by HPTLC on silica gel plates with n-butanol–acetic acid–water (4.0+1.0+1.0, v/v) as the mobile phase. Densitometric analysis of L-dopa was carried out in the absorbance mode at 280 nm. The relationship between the concentration of L-dopa and corresponding peak areas was found to be linear in the range of 100 to 1200 ng/spot. The method was validated for precision (inter and intraday), repeatability, and accuracy. Mean recovery was 100.30%. The relative standard deviation (RSD) values of the precision were found to be in the range 0.64—1.52%. In conclusion, the proposed TLC method was found to be precise, specific and accurate and can be used for identification and quantitative determination of L-dopa in herbal extract and its formulations.[7]
HPTLC L-dopa degradation, Pulikkalpura, et al., 2015
Levodopa in Mucuna pruriens and its degradation,
Abstract. Mucuna pruriens is the best known natural source of L-dopa, the gold standard for treatment of Parkinsonism. M. pruriens varieties are protein rich supplements, and are used as food and fodder worldwide. Here, we report L-dopa contents in seeds of fifty six accessions of four M. pruriens varieties, M. pruriens var. pruriens, M. pruriens var. hirsuta, M. pruriens var. utilis and M. pruriens var. thekkadiensis, quantified by HPTLC-densitometry. L-dopa contents varied between 0.58 to 6.42 (%, dr. wt.). High and low L-dopa yielding genotypes/chemotypes of M. pruriens could be multiplied for medicinal and nutritional purposes, respectively. HPTLC profiles of M. pruriens seeds on repeated extraction (24 h) in 1:1 formic acid-alcohol followed by development in butanol:acetic acid:water (4:1:1, v/v) showed consistent degradation of L-dopa (Rf 0.34 ± 0.02) into a second peak (Rf 0.41 ± 0.02). An average of 52.11% degradation of L-dopa was found in seeds of M. pruriens varieties. Since M. pruriens seeds and/or L-dopa are used for treatment of Parkinson’s disease and as an aphrodisiac both in modern and/or traditional systems of medicine, the finding of high level of L-dopa degradation (in pure form and in M. pruriens extracts) into damaging quinones and ROS is very significant.[8]
Sources
- ↑ Images courtesy of the C.V. Starr Virtual Herbarium of the New York Botanical Garden http://sciweb.nybg.org/science2/VirtualHerbarium.asp
- ↑ Images courtesy of the C.V. Starr Virtual Herbarium of the New York Botanical Garden http://sciweb.nybg.org/science2/VirtualHerbarium.asp
- ↑ Images courtesy of the C.V. Starr Virtual Herbarium of the New York Botanical Garden http://sciweb.nybg.org/science2/VirtualHerbarium.asp
- ↑ United States Dispensatory (1918)
- ↑ Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
- ↑ Elan M. Sudberg, Alkemist Laboratories http://www.alkemist.com
- ↑ Modi, K.P., Patel, N.M., Goyal, R.K. 2008. Estimation of L-Dopa from Mucuna pruriens LINN and Formulations Containing M. pruriens by HPTLC Method Chemical and Pharmaceutical Bulletin 56(3), 357-359. http://doi.org/10.1248/cpb.56.357
- ↑ Pulikkalpura, H. Kurup, R., Mathew, P.J., Baby, S. 2015. Levodopa in Mucuna pruriens and its degradation. Scientific Reports 5, 11078. http://doi.org/10.1038/srep11078