Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells

This study was designed to determine the cytotoxic effects of kenaf seed oil (Hibiscus cannabinus) variety V36 extracted using supercritical carbon dioxide fluid extraction (SFE) with different combinations of pressure (bars) and temperature (°C). Extracted oils were tested on human promyelocytic HL...

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Main Authors: Foo, Jhi Biau, Saiful Yazan, Latifah, Chan, Kim Wei, Md. Tahir, Paridah, Ismail, Maznah
Format: Article
Language:English
Published: Academic Journals 2011
Online Access:http://psasir.upm.edu.my/id/eprint/23891/1/238911.pdf
http://psasir.upm.edu.my/id/eprint/23891/
http://www.academicjournals.org/journal/AJB/article-abstract/7142EF734148
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spelling my.upm.eprints.238912017-11-16T01:41:38Z http://psasir.upm.edu.my/id/eprint/23891/ Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells Foo, Jhi Biau Saiful Yazan, Latifah Chan, Kim Wei Md. Tahir, Paridah Ismail, Maznah This study was designed to determine the cytotoxic effects of kenaf seed oil (Hibiscus cannabinus) variety V36 extracted using supercritical carbon dioxide fluid extraction (SFE) with different combinations of pressure (bars) and temperature (°C). Extracted oils were tested on human promyelocytic HL-60, murine myelomonocytic WEHI-3B and human chronic myelogenous K562 leukemic cell lines. The yield of kenaf seed oil extracted by SFE ranged from 11 to 13% (w/w). Oils were found to be cytotoxic towards all the leukemia cell lines in a dose-dependent manner with no effects on normal cells (3T3). Oil from SFE at 600 bar 40°C (V600/40) was more cytotoxic towards HL-60, WEHI-3B and K562 when compared with other kenaf seed oils (extracted with different parameters) with the IC50 values of 178.78±10.52, 189.43±11.63 and 213.33±15.45 μg/ml, respectively. V600/40-treated leukemia cells exhibited typical characteristics of apoptosis such as nuclear fragmentation, chromatin condensation, nuclear margination, membrane blebbing and cellular shrinkage, as viewed under inverted light microscope and fluorescence microscope. Cell cycle analysis using flow cytometry revealed that, V600/40 induced G1 phase cell cycle arrest and significantly increased (P < 0.05) the sub- G1 apoptotic population in the leukemia cells. In conclusion, kenaf seed oil V600/40 induced apoptosis via G1 phase cell cycle arrest in HL-60, WEHI-3B and K562 leukemia cell lines. Academic Journals 2011-06-15 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/23891/1/238911.pdf Foo, Jhi Biau and Saiful Yazan, Latifah and Chan, Kim Wei and Md. Tahir, Paridah and Ismail, Maznah (2011) Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells. African Journal of Biotechnology, 10 (27). art. no. 7142EF734148. pp. 5389-5397. ISSN 1684–5315 http://www.academicjournals.org/journal/AJB/article-abstract/7142EF734148 10.5897/AJB11.120
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description This study was designed to determine the cytotoxic effects of kenaf seed oil (Hibiscus cannabinus) variety V36 extracted using supercritical carbon dioxide fluid extraction (SFE) with different combinations of pressure (bars) and temperature (°C). Extracted oils were tested on human promyelocytic HL-60, murine myelomonocytic WEHI-3B and human chronic myelogenous K562 leukemic cell lines. The yield of kenaf seed oil extracted by SFE ranged from 11 to 13% (w/w). Oils were found to be cytotoxic towards all the leukemia cell lines in a dose-dependent manner with no effects on normal cells (3T3). Oil from SFE at 600 bar 40°C (V600/40) was more cytotoxic towards HL-60, WEHI-3B and K562 when compared with other kenaf seed oils (extracted with different parameters) with the IC50 values of 178.78±10.52, 189.43±11.63 and 213.33±15.45 μg/ml, respectively. V600/40-treated leukemia cells exhibited typical characteristics of apoptosis such as nuclear fragmentation, chromatin condensation, nuclear margination, membrane blebbing and cellular shrinkage, as viewed under inverted light microscope and fluorescence microscope. Cell cycle analysis using flow cytometry revealed that, V600/40 induced G1 phase cell cycle arrest and significantly increased (P < 0.05) the sub- G1 apoptotic population in the leukemia cells. In conclusion, kenaf seed oil V600/40 induced apoptosis via G1 phase cell cycle arrest in HL-60, WEHI-3B and K562 leukemia cell lines.
format Article
author Foo, Jhi Biau
Saiful Yazan, Latifah
Chan, Kim Wei
Md. Tahir, Paridah
Ismail, Maznah
spellingShingle Foo, Jhi Biau
Saiful Yazan, Latifah
Chan, Kim Wei
Md. Tahir, Paridah
Ismail, Maznah
Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells
author_facet Foo, Jhi Biau
Saiful Yazan, Latifah
Chan, Kim Wei
Md. Tahir, Paridah
Ismail, Maznah
author_sort Foo, Jhi Biau
title Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells
title_short Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells
title_full Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells
title_fullStr Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells
title_full_unstemmed Kenaf seed oil from supercritical carbon dioxide fluid extraction induced G1 phase cell cycle arrest and apoptosis in leukemia cells
title_sort kenaf seed oil from supercritical carbon dioxide fluid extraction induced g1 phase cell cycle arrest and apoptosis in leukemia cells
publisher Academic Journals
publishDate 2011
url http://psasir.upm.edu.my/id/eprint/23891/1/238911.pdf
http://psasir.upm.edu.my/id/eprint/23891/
http://www.academicjournals.org/journal/AJB/article-abstract/7142EF734148
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score 13.160551