GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent

Abstract. Nurcholis W, Khumaida N, Bintang M, Syukur M. 2021. GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent. Biodiversitas 22: 1179-1186. This work aimed to evaluate the bioactive compounds and anticancer activity in...

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Autores principales: Waras Nurcholis, NURUL KHUMAIDA, MARIA BINTANG, MUHAMAD SYUKUR
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Publicado: MBI & UNS Solo 2021
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spelling oai:doaj.org-article:3eb11594779a4ea393fdb61f2bdf57c12021-11-22T00:56:37ZGC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent1412-033X2085-472210.13057/biodiv/d220313https://doaj.org/article/3eb11594779a4ea393fdb61f2bdf57c12021-02-01T00:00:00Zhttps://smujo.id/biodiv/article/view/7900https://doaj.org/toc/1412-033Xhttps://doaj.org/toc/2085-4722Abstract. Nurcholis W, Khumaida N, Bintang M, Syukur M. 2021. GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent. Biodiversitas 22: 1179-1186. This work aimed to evaluate the bioactive compounds and anticancer activity in rhizome extract of ten Curcuma aeruginosa accessions to explore their pharmacological values. The GC-MS analysis was used to identify bioactive compounds. The cytotoxic activity was performed against MCF-7 (Human breastadeno carcinoma) and Vero cell lines using MTT assay. The GC-MS analysis revealed 71 of the compounds as sesquiterpenes (36), monoterpenes (20), phenolics (5), diterpenes (4), phenanthrene (1), tetrapeptides (1), oxazole (1), triazine (1), piperidine (1), and oxygenated hydrocarbons (1). The isocurcumenol was the most dominant metabolite in ethanol extract of C. aeruginosa rhizome, with the highest produced by KP accession (22.01%) followed MD accession (21.12%). However, camphor and ?-elemene were the metabolites produced by all accessions studied. In the Vero cell line as a normal cell, the cytotoxic activity varied from 13.28% (MD) to 45.17% (PW). Furthermore, the cytotoxic activity ranged from 1.16% (LC) to 49.70% (MD) against the MCF-7 cell line. The highest anticancer activity was produced in MD accessions; thus, it can be used as a source of quality raw materials for the pharmaceutical and food industry. Besides that, it can also be further developed to obtain superior varieties through plant breeding programs.Waras NurcholisNURUL KHUMAIDAMARIA BINTANGMUHAMAD SYUKURMBI & UNS Soloarticleagricultural biochemistry, bioactivities, chemometric analysis, profiling metabolite, volatile compoundsBiology (General)QH301-705.5ENBiodiversitas, Vol 22, Iss 3 (2021)
institution DOAJ
collection DOAJ
language EN
topic agricultural biochemistry, bioactivities, chemometric analysis, profiling metabolite, volatile compounds
Biology (General)
QH301-705.5
spellingShingle agricultural biochemistry, bioactivities, chemometric analysis, profiling metabolite, volatile compounds
Biology (General)
QH301-705.5
Waras Nurcholis
NURUL KHUMAIDA
MARIA BINTANG
MUHAMAD SYUKUR
GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent
description Abstract. Nurcholis W, Khumaida N, Bintang M, Syukur M. 2021. GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent. Biodiversitas 22: 1179-1186. This work aimed to evaluate the bioactive compounds and anticancer activity in rhizome extract of ten Curcuma aeruginosa accessions to explore their pharmacological values. The GC-MS analysis was used to identify bioactive compounds. The cytotoxic activity was performed against MCF-7 (Human breastadeno carcinoma) and Vero cell lines using MTT assay. The GC-MS analysis revealed 71 of the compounds as sesquiterpenes (36), monoterpenes (20), phenolics (5), diterpenes (4), phenanthrene (1), tetrapeptides (1), oxazole (1), triazine (1), piperidine (1), and oxygenated hydrocarbons (1). The isocurcumenol was the most dominant metabolite in ethanol extract of C. aeruginosa rhizome, with the highest produced by KP accession (22.01%) followed MD accession (21.12%). However, camphor and ?-elemene were the metabolites produced by all accessions studied. In the Vero cell line as a normal cell, the cytotoxic activity varied from 13.28% (MD) to 45.17% (PW). Furthermore, the cytotoxic activity ranged from 1.16% (LC) to 49.70% (MD) against the MCF-7 cell line. The highest anticancer activity was produced in MD accessions; thus, it can be used as a source of quality raw materials for the pharmaceutical and food industry. Besides that, it can also be further developed to obtain superior varieties through plant breeding programs.
format article
author Waras Nurcholis
NURUL KHUMAIDA
MARIA BINTANG
MUHAMAD SYUKUR
author_facet Waras Nurcholis
NURUL KHUMAIDA
MARIA BINTANG
MUHAMAD SYUKUR
author_sort Waras Nurcholis
title GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent
title_short GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent
title_full GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent
title_fullStr GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent
title_full_unstemmed GC-MS analysis of rhizome ethanol extracts from Curcuma aeruginosa accessions and their efficiency activities as anticancer agent
title_sort gc-ms analysis of rhizome ethanol extracts from curcuma aeruginosa accessions and their efficiency activities as anticancer agent
publisher MBI & UNS Solo
publishDate 2021
url https://doaj.org/article/3eb11594779a4ea393fdb61f2bdf57c1
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AT muhamadsyukur gcmsanalysisofrhizomeethanolextractsfromcurcumaaeruginosaaccessionsandtheirefficiencyactivitiesasanticanceragent
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