» Articles » PMID: 24733684

Ultra-performance LC Separation and Quadrupole Time-of-flight MS Identification of Major Alkaloids in Plumula Nelumbinis

Overview
Journal Phytochem Anal
Publisher Wiley
Specialties Biology
Chemistry
Date 2014 Apr 16
PMID 24733684
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: As an essential medicine and tea source in many countries, Plumula Nelumbinis potentially exerts its major biological activities through its alkaloids. However, the activities of Plumula Nelumbinis are not fully understood due to the lack of studies on its chemical components.

Objective: To establish an ultra-performance liquid chromatography combined with diode-array detector (UPLC/DAD) method, coupled to an electrospray ionisation with quadrupole time-of-flight mass spectrometry (ESI/QTOF/MS) method, for the separation and identification of Plumula Nelumbinis alkaloids.

Methods: The eluant from an UPLC separation of an ethanol extract of Plumula Nelumbinis was directly infused into an ESI/QTOF/MS system. Both positive and negative ion modes of ESI with low and high collision energy (CE) were used to obtain sufficient MS information.

Results: Twenty-one alkaloids were tentatively identified based on their chromatographic characteristics, UV spectra, exact mass, MS fragments and literature reports. They consist of six bis-1-benzyltetrahydroisoquinoline, eleven benzyltetrahydroisoquinoline (including two glycoalkaloids and two quaternary ammoniums), two aporphine, one proaporphine and one indole alkaloids. Eleven were identified in Plumula Nelumbinis for the first time and seven were first reported in Nelumbo nucifera Gaertn. Five compounds, namely norcoclaurine-4'-O-glucoside, norcoclaurine-6-O-glucoside, isolotusine, 6-demethyl-4-demethylN-methylcoclaurine and N-norisoliensinine, were characterised and proposed as new compounds.

Conclusion: The established UPLC/DAD - ESI/QTOF/MS method is efficient for systematic identification of the alkaloids in Plumula Nelumbinis extract.

Citing Articles

Exploring Chemical Composition, Antioxidant, Enzyme Inhibitory and Cytotoxic Properties of Hausskn. & Bornm. from Turkey Flora: A Novel Source of Bioactive Agents to Design Functional Applications.

Yagi S, Zengin G, Uba A, Maciejewska-Turska M, Sieniawska E, Swiatek L Antioxidants (Basel). 2024; 13(6).

PMID: 38929082 PMC: 11200578. DOI: 10.3390/antiox13060643.


Visualization and identification of benzylisoquinoline alkaloids in various tissues.

Hao C, Yang W, Dong G, Yu Y, Liu Y, Zhang J Heliyon. 2023; 9(6):e16138.

PMID: 37251486 PMC: 10220311. DOI: 10.1016/j.heliyon.2023.e16138.


Elucidation of the (R)-enantiospecific benzylisoquinoline alkaloid biosynthetic pathways in sacred lotus (Nelumbo nucifera).

Menendez-Perdomo I, Facchini P Sci Rep. 2023; 13(1):2955.

PMID: 36805479 PMC: 9940101. DOI: 10.1038/s41598-023-29415-0.


sp. and as the Main Contributors to the Antibacterial Activity of the Medicinal Drink Horchata: A Study Based on the Antibacterial and Chemical Analysis of 21 Plants.

Fernandez-Soto P, Celi D, Tejera E, Alvarez-Suarez J, Machado A Molecules. 2023; 28(2).

PMID: 36677749 PMC: 9862262. DOI: 10.3390/molecules28020693.


Isoquinoline Alkaloids from Franch: Focus on Coptisine as a Potential Therapeutic Candidate against Gastric Cancer Cells.

Nakonieczna S, Grabarska A, Gawel K, Wroblewska-Luczka P, Czerwonka A, Stepulak A Int J Mol Sci. 2022; 23(18).

PMID: 36142236 PMC: 9499618. DOI: 10.3390/ijms231810330.


References
1.
Kashiwada Y, Aoshima A, Ikeshiro Y, Chen Y, Furukawa H, Itoigawa M . Anti-HIV benzylisoquinoline alkaloids and flavonoids from the leaves of Nelumbo nucifera, and structure-activity correlations with related alkaloids. Bioorg Med Chem. 2004; 13(2):443-8. DOI: 10.1016/j.bmc.2004.10.020. View

2.
. Isolation of lapachol from Diphysa robinoides. J Nat Prod. 1986; 49(3):547. DOI: 10.1021/np50045a035. View

3.
Chen Y, Fan G, Wu H, Wu Y, Mitchell A . Separation, identification and rapid determination of liensine, isoliensinine and neferine from embryo of the seed of Nelumbo nucifera Gaertn. by liquid chromatography coupled to diode array detector and tandem mass spectrometry. J Pharm Biomed Anal. 2006; 43(1):99-104. DOI: 10.1016/j.jpba.2006.06.016. View

4.
Agnihotri V, ElSohly H, Khan S, Jacob M, Joshi V, Smillie T . Constituents of leaves and their antimalarial and antifungal activity. Phytochem Lett. 2017; 1(2):89-93. PMC: 5690537. DOI: 10.1016/j.phytol.2008.03.003. View

5.
Lin Z, Wang H, Fu Q, An H, Liang Y, Zhang B . Simultaneous separation, identification and activity evaluation of three butyrylcholinesterase inhibitors from Plumula nelumbinis using on-line HPLC-UV coupled with ESI-IT-TOF-MS and BChE biochemical detection. Talanta. 2013; 110:180-9. DOI: 10.1016/j.talanta.2013.02.033. View