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...
Gespeichert in:
Veröffentlicht in: | Yao hsüeh hsüeh pao 2010-12, Vol.45 (12), p.1545-1549 |
---|---|
Hauptverfasser: | , , , , , , , , |
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 |