Structural identification and quality study on isomers of a novel anticancer photosensitiser photocyanine

Our work focuses on the quality control and structural identification of Photocyanine as a cancer therapeutic photosensitizer. Photocyanine is a mixture which contains four ZnPcS2P2 type substituted Phthalocyanine isomers. In order to obtain the single component from Photocyanine, the mixture of fou...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Yao hsüeh hsüeh pao 2010-12, Vol.45 (12), p.1545-1549
Hauptverfasser: Yang, Bei-bei, Yao, Hui-sheng, Liu, Hong, Jiang, Zhou, Wang, Jian, He, Wen-yi, Wang, Yan, Chen, Nai-sheng, Huang, Jin-ling
Format: Artikel
Sprache:chi
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1549
container_issue 12
container_start_page 1545
container_title Yao hsüeh hsüeh pao
container_volume 45
creator Yang, Bei-bei
Yao, Hui-sheng
Liu, Hong
Jiang, Zhou
Wang, Jian
He, Wen-yi
Wang, Yan
Chen, Nai-sheng
Huang, Jin-ling
description Our work focuses on the quality control and structural identification of Photocyanine as a cancer therapeutic photosensitizer. Photocyanine is a mixture which contains four ZnPcS2P2 type substituted Phthalocyanine isomers. In order to obtain the single component from Photocyanine, the mixture of four isomers possessing the similar structures and chemical property had been isolated and purified. An HPLC method with a mixture of methanol-acetonitrile-ion-pair buffer as the mobile phase was applied to isolate the four isomers by means of a semi-preparative C18 column. To remove the salts which were mixed in the preparative product, a SPE C18 column was used to separate the salts by elution with water and then the marker component was eluted by methanol. Subsequently, a column of Sephadex LH-20 gel was applied to elute the crudes with methanol to desalination. The purity of the isolated compound was measured by TLC and four different isomers of phthalocyanine were obtained. The chemical structures of them were el
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_854377783</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>854377783</sourcerecordid><originalsourceid>FETCH-LOGICAL-p125t-7ae040706097595058d70b810805773795dc915f502d470424d41e47502789dd3</originalsourceid><addsrcrecordid>eNo1kE1LAzEYhHNQbK3-BcnN08KbTeKbHKX4BQUP6nlJN1mM7CbbfAj99y7YnoYZnpnDXJA1SMYboRBW5DrnHwDBNFdXZNUyLpnQck38R0m1LzWZkXrrQvGD703xMVATLD1UM_pypLlUe6RL6HOcXMo0DtTQEH_duHBlqYTeJTp_xxKzC9kXn8--P5rgg7shl4MZs7s96YZ8PT99bl-b3fvL2_Zx18yslaVB40AAwgNolFqCVBZhrxgokIgctbS9ZnKQ0FqBIFphBXMCF49KW8s35P5_d07xUF0u3eRz78bRBBdr7pQUHBEVX8i7E1n3k7PdnPxk0rE7v8P_ADaiYHo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>854377783</pqid></control><display><type>article</type><title>Structural identification and quality study on isomers of a novel anticancer photosensitiser photocyanine</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Yang, Bei-bei ; Yao, Hui-sheng ; Liu, Hong ; Jiang, Zhou ; Wang, Jian ; He, Wen-yi ; Wang, Yan ; Chen, Nai-sheng ; Huang, Jin-ling</creator><creatorcontrib>Yang, Bei-bei ; Yao, Hui-sheng ; Liu, Hong ; Jiang, Zhou ; Wang, Jian ; He, Wen-yi ; Wang, Yan ; Chen, Nai-sheng ; Huang, Jin-ling</creatorcontrib><description>Our work focuses on the quality control and structural identification of Photocyanine as a cancer therapeutic photosensitizer. Photocyanine is a mixture which contains four ZnPcS2P2 type substituted Phthalocyanine isomers. In order to obtain the single component from Photocyanine, the mixture of four isomers possessing the similar structures and chemical property had been isolated and purified. An HPLC method with a mixture of methanol-acetonitrile-ion-pair buffer as the mobile phase was applied to isolate the four isomers by means of a semi-preparative C18 column. To remove the salts which were mixed in the preparative product, a SPE C18 column was used to separate the salts by elution with water and then the marker component was eluted by methanol. Subsequently, a column of Sephadex LH-20 gel was applied to elute the crudes with methanol to desalination. The purity of the isolated compound was measured by TLC and four different isomers of phthalocyanine were obtained. The chemical structures of them were el</description><identifier>ISSN: 0513-4870</identifier><identifier>PMID: 21351495</identifier><language>chi</language><publisher>China</publisher><subject>Antineoplastic Agents - analysis ; Antineoplastic Agents - chemistry ; Chromatography, High Pressure Liquid - methods ; Indoles - analysis ; Indoles - chemistry ; Isomerism ; Molecular Structure ; Organometallic Compounds - analysis ; Organometallic Compounds - chemistry ; Photochemotherapy ; Photosensitizing Agents - analysis ; Photosensitizing Agents - chemistry ; Quality Control</subject><ispartof>Yao hsüeh hsüeh pao, 2010-12, Vol.45 (12), p.1545-1549</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21351495$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Bei-bei</creatorcontrib><creatorcontrib>Yao, Hui-sheng</creatorcontrib><creatorcontrib>Liu, Hong</creatorcontrib><creatorcontrib>Jiang, Zhou</creatorcontrib><creatorcontrib>Wang, Jian</creatorcontrib><creatorcontrib>He, Wen-yi</creatorcontrib><creatorcontrib>Wang, Yan</creatorcontrib><creatorcontrib>Chen, Nai-sheng</creatorcontrib><creatorcontrib>Huang, Jin-ling</creatorcontrib><title>Structural identification and quality study on isomers of a novel anticancer photosensitiser photocyanine</title><title>Yao hsüeh hsüeh pao</title><addtitle>Yao Xue Xue Bao</addtitle><description>Our work focuses on the quality control and structural identification of Photocyanine as a cancer therapeutic photosensitizer. Photocyanine is a mixture which contains four ZnPcS2P2 type substituted Phthalocyanine isomers. In order to obtain the single component from Photocyanine, the mixture of four isomers possessing the similar structures and chemical property had been isolated and purified. An HPLC method with a mixture of methanol-acetonitrile-ion-pair buffer as the mobile phase was applied to isolate the four isomers by means of a semi-preparative C18 column. To remove the salts which were mixed in the preparative product, a SPE C18 column was used to separate the salts by elution with water and then the marker component was eluted by methanol. Subsequently, a column of Sephadex LH-20 gel was applied to elute the crudes with methanol to desalination. The purity of the isolated compound was measured by TLC and four different isomers of phthalocyanine were obtained. The chemical structures of them were el</description><subject>Antineoplastic Agents - analysis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Indoles - analysis</subject><subject>Indoles - chemistry</subject><subject>Isomerism</subject><subject>Molecular Structure</subject><subject>Organometallic Compounds - analysis</subject><subject>Organometallic Compounds - chemistry</subject><subject>Photochemotherapy</subject><subject>Photosensitizing Agents - analysis</subject><subject>Photosensitizing Agents - chemistry</subject><subject>Quality Control</subject><issn>0513-4870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE1LAzEYhHNQbK3-BcnN08KbTeKbHKX4BQUP6nlJN1mM7CbbfAj99y7YnoYZnpnDXJA1SMYboRBW5DrnHwDBNFdXZNUyLpnQck38R0m1LzWZkXrrQvGD703xMVATLD1UM_pypLlUe6RL6HOcXMo0DtTQEH_duHBlqYTeJTp_xxKzC9kXn8--P5rgg7shl4MZs7s96YZ8PT99bl-b3fvL2_Zx18yslaVB40AAwgNolFqCVBZhrxgokIgctbS9ZnKQ0FqBIFphBXMCF49KW8s35P5_d07xUF0u3eRz78bRBBdr7pQUHBEVX8i7E1n3k7PdnPxk0rE7v8P_ADaiYHo</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Yang, Bei-bei</creator><creator>Yao, Hui-sheng</creator><creator>Liu, Hong</creator><creator>Jiang, Zhou</creator><creator>Wang, Jian</creator><creator>He, Wen-yi</creator><creator>Wang, Yan</creator><creator>Chen, Nai-sheng</creator><creator>Huang, Jin-ling</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201012</creationdate><title>Structural identification and quality study on isomers of a novel anticancer photosensitiser photocyanine</title><author>Yang, Bei-bei ; Yao, Hui-sheng ; Liu, Hong ; Jiang, Zhou ; Wang, Jian ; He, Wen-yi ; Wang, Yan ; Chen, Nai-sheng ; Huang, Jin-ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p125t-7ae040706097595058d70b810805773795dc915f502d470424d41e47502789dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi</language><creationdate>2010</creationdate><topic>Antineoplastic Agents - analysis</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Chromatography, High Pressure Liquid - methods</topic><topic>Indoles - analysis</topic><topic>Indoles - chemistry</topic><topic>Isomerism</topic><topic>Molecular Structure</topic><topic>Organometallic Compounds - analysis</topic><topic>Organometallic Compounds - chemistry</topic><topic>Photochemotherapy</topic><topic>Photosensitizing Agents - analysis</topic><topic>Photosensitizing Agents - chemistry</topic><topic>Quality Control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Bei-bei</creatorcontrib><creatorcontrib>Yao, Hui-sheng</creatorcontrib><creatorcontrib>Liu, Hong</creatorcontrib><creatorcontrib>Jiang, Zhou</creatorcontrib><creatorcontrib>Wang, Jian</creatorcontrib><creatorcontrib>He, Wen-yi</creatorcontrib><creatorcontrib>Wang, Yan</creatorcontrib><creatorcontrib>Chen, Nai-sheng</creatorcontrib><creatorcontrib>Huang, Jin-ling</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Yao hsüeh hsüeh pao</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Bei-bei</au><au>Yao, Hui-sheng</au><au>Liu, Hong</au><au>Jiang, Zhou</au><au>Wang, Jian</au><au>He, Wen-yi</au><au>Wang, Yan</au><au>Chen, Nai-sheng</au><au>Huang, Jin-ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural identification and quality study on isomers of a novel anticancer photosensitiser photocyanine</atitle><jtitle>Yao hsüeh hsüeh pao</jtitle><addtitle>Yao Xue Xue Bao</addtitle><date>2010-12</date><risdate>2010</risdate><volume>45</volume><issue>12</issue><spage>1545</spage><epage>1549</epage><pages>1545-1549</pages><issn>0513-4870</issn><abstract>Our work focuses on the quality control and structural identification of Photocyanine as a cancer therapeutic photosensitizer. Photocyanine is a mixture which contains four ZnPcS2P2 type substituted Phthalocyanine isomers. In order to obtain the single component from Photocyanine, the mixture of four isomers possessing the similar structures and chemical property had been isolated and purified. An HPLC method with a mixture of methanol-acetonitrile-ion-pair buffer as the mobile phase was applied to isolate the four isomers by means of a semi-preparative C18 column. To remove the salts which were mixed in the preparative product, a SPE C18 column was used to separate the salts by elution with water and then the marker component was eluted by methanol. Subsequently, a column of Sephadex LH-20 gel was applied to elute the crudes with methanol to desalination. The purity of the isolated compound was measured by TLC and four different isomers of phthalocyanine were obtained. The chemical structures of them were el</abstract><cop>China</cop><pmid>21351495</pmid><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0513-4870
ispartof Yao hsüeh hsüeh pao, 2010-12, Vol.45 (12), p.1545-1549
issn 0513-4870
language chi
recordid cdi_proquest_miscellaneous_854377783
source MEDLINE; Alma/SFX Local Collection
subjects Antineoplastic Agents - analysis
Antineoplastic Agents - chemistry
Chromatography, High Pressure Liquid - methods
Indoles - analysis
Indoles - chemistry
Isomerism
Molecular Structure
Organometallic Compounds - analysis
Organometallic Compounds - chemistry
Photochemotherapy
Photosensitizing Agents - analysis
Photosensitizing Agents - chemistry
Quality Control
title Structural identification and quality study on isomers of a novel anticancer photosensitiser photocyanine
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T16%3A54%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structural%20identification%20and%20quality%20study%20on%20isomers%20of%20a%20novel%20anticancer%20photosensitiser%20photocyanine&rft.jtitle=Yao%20hs%C3%BCeh%20hs%C3%BCeh%20pao&rft.au=Yang,%20Bei-bei&rft.date=2010-12&rft.volume=45&rft.issue=12&rft.spage=1545&rft.epage=1549&rft.pages=1545-1549&rft.issn=0513-4870&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E854377783%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=854377783&rft_id=info:pmid/21351495&rfr_iscdi=true