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Optimization of Purification, Identification and Evaluation of the in Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones
In this study, an efficient purification method for the polyphenols of Pinus koraiensis pinecone (PPP) has been developed. AB-8 resin was verified to offer good adsorption and desorption ratio for PPP. Response surface methodology (RSM) indicated that the optimized purification parameters for PPP we...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272533/ https://www.ncbi.nlm.nih.gov/pubmed/26056816 http://dx.doi.org/10.3390/molecules200610450 |
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author | Yi, Juanjuan Wang, Zhenyu Bai, Haina Yu, Xiaojin Jing, Jing Zuo, Lili |
author_facet | Yi, Juanjuan Wang, Zhenyu Bai, Haina Yu, Xiaojin Jing, Jing Zuo, Lili |
author_sort | Yi, Juanjuan |
collection | PubMed |
description | In this study, an efficient purification method for the polyphenols of Pinus koraiensis pinecone (PPP) has been developed. AB-8 resin was verified to offer good adsorption and desorption ratio for PPP. Response surface methodology (RSM) indicated that the optimized purification parameters for PPP were 1.70 mg GAE/mL phenolic sample concentration, 22.00 mL sample volume, and 63.00% ethanol concentration. Under these conditions, the experimental purity of PPP was 27.93 ± 0.14% (n = 3), which matched well with the predicted purity of 28.17%. Next, the antiproliferative effects of PPP on seven cancer cell lines, including A375 (human skin melanoma cancer cell line), A549 (human lung cancer cell line), SH-SY5Y (human neuroblastoma cell line), LOVO (human colon cancer stem cell line), MCF-7 (human breast cancer cell line), HeLa (human cervical cancer line), and HT29 (human colon cancer line), were examined by MTT assays. The results indicated that PPP had the highest capacity for inhibiting LOVO cells growth with an EC(50) value of 0.317 ± 0.0476 mg/mL. Finally, Ultra-high performance liquid chromatography- tandem mass spectrometry (UPLC-MS) was used to tentatively identify twenty-four peaks in the purified PPP, of which five representative peaks were identified as catechin, methyl quercetin, o-vanillin, luteolin and coronaric acid. Our results demonstrate that Pinus koraiensis pinecone is a readily available source of polyphenols, and the purified PPP could be a promising natural antitumor agent for applications in functional foods. |
format | Online Article Text |
id | pubmed-6272533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62725332018-12-31 Optimization of Purification, Identification and Evaluation of the in Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones Yi, Juanjuan Wang, Zhenyu Bai, Haina Yu, Xiaojin Jing, Jing Zuo, Lili Molecules Article In this study, an efficient purification method for the polyphenols of Pinus koraiensis pinecone (PPP) has been developed. AB-8 resin was verified to offer good adsorption and desorption ratio for PPP. Response surface methodology (RSM) indicated that the optimized purification parameters for PPP were 1.70 mg GAE/mL phenolic sample concentration, 22.00 mL sample volume, and 63.00% ethanol concentration. Under these conditions, the experimental purity of PPP was 27.93 ± 0.14% (n = 3), which matched well with the predicted purity of 28.17%. Next, the antiproliferative effects of PPP on seven cancer cell lines, including A375 (human skin melanoma cancer cell line), A549 (human lung cancer cell line), SH-SY5Y (human neuroblastoma cell line), LOVO (human colon cancer stem cell line), MCF-7 (human breast cancer cell line), HeLa (human cervical cancer line), and HT29 (human colon cancer line), were examined by MTT assays. The results indicated that PPP had the highest capacity for inhibiting LOVO cells growth with an EC(50) value of 0.317 ± 0.0476 mg/mL. Finally, Ultra-high performance liquid chromatography- tandem mass spectrometry (UPLC-MS) was used to tentatively identify twenty-four peaks in the purified PPP, of which five representative peaks were identified as catechin, methyl quercetin, o-vanillin, luteolin and coronaric acid. Our results demonstrate that Pinus koraiensis pinecone is a readily available source of polyphenols, and the purified PPP could be a promising natural antitumor agent for applications in functional foods. MDPI 2015-06-05 /pmc/articles/PMC6272533/ /pubmed/26056816 http://dx.doi.org/10.3390/molecules200610450 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yi, Juanjuan Wang, Zhenyu Bai, Haina Yu, Xiaojin Jing, Jing Zuo, Lili Optimization of Purification, Identification and Evaluation of the in Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones |
title | Optimization of Purification, Identification and Evaluation of the in
Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones |
title_full | Optimization of Purification, Identification and Evaluation of the in
Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones |
title_fullStr | Optimization of Purification, Identification and Evaluation of the in
Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones |
title_full_unstemmed | Optimization of Purification, Identification and Evaluation of the in
Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones |
title_short | Optimization of Purification, Identification and Evaluation of the in
Vitro Antitumor Activity of Polyphenols from Pinus Koraiensis Pinecones |
title_sort | optimization of purification, identification and evaluation of the in
vitro antitumor activity of polyphenols from pinus koraiensis pinecones |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272533/ https://www.ncbi.nlm.nih.gov/pubmed/26056816 http://dx.doi.org/10.3390/molecules200610450 |
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