Synthesis of chloro-substituted analogs of Thiazole orange – Fluorophores for flow cytometric analyses

► Synthesis of chloro-containing analogs of Thiazole orange has been reported. ► Spectral properties of the dyes in presence of dsDNA have been investigated. ► The ability of dyes to stain live or apoptotic cells were examined by flow cytometry. ► The dyes are suitable for detection of apoptosis at...

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Veröffentlicht in:Journal of photochemistry and photobiology. B, Biology Biology, 2011-06, Vol.103 (3), p.215-221
Hauptverfasser: Kaloyanova, S., Ivanova, I., Tchorbanov, A., Dimitrova, P., Deligeorgiev, T.
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container_issue 3
container_start_page 215
container_title Journal of photochemistry and photobiology. B, Biology
container_volume 103
creator Kaloyanova, S.
Ivanova, I.
Tchorbanov, A.
Dimitrova, P.
Deligeorgiev, T.
description ► Synthesis of chloro-containing analogs of Thiazole orange has been reported. ► Spectral properties of the dyes in presence of dsDNA have been investigated. ► The ability of dyes to stain live or apoptotic cells were examined by flow cytometry. ► The dyes are suitable for detection of apoptosis at low concentrations (1 × 10 −11 M). Synthesis, absorption and fluorescence properties of a series of asymmetrical monomethine cyanine dyes, chloro-containing analogs of Thiazole orange, are reported. Their staining ability was studied by flow cytometry. The saturating concentrations of each dye that gives a stable staining intensity have been determined. The ability of dyes B9, B11, B13 to stain live macrophages and apoptotic splenocytes was investigated. Positive signal in nucleus of adherent macrophages detected by fluorescent microscopy showed good specificity of B9, B11 and B13 dyes for DNA. In apoptotic assay cells positive for Annexin V were stained more brightly with the dyes B9, B11 and B13 than with propidium iodide. Despite that B13 showed high DNA selectivity it induces apoptosis of splenocytes and it is not suitable for detection of dead cells. The other synthesized chloro-containing analogs of Thiazole orange B9 and B11 can be successfully used for flow cytometric analyses of DNA content in live cells and for analyses of cell apoptosis.
doi_str_mv 10.1016/j.jphotobiol.2011.03.012
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Synthesis, absorption and fluorescence properties of a series of asymmetrical monomethine cyanine dyes, chloro-containing analogs of Thiazole orange, are reported. Their staining ability was studied by flow cytometry. The saturating concentrations of each dye that gives a stable staining intensity have been determined. The ability of dyes B9, B11, B13 to stain live macrophages and apoptotic splenocytes was investigated. Positive signal in nucleus of adherent macrophages detected by fluorescent microscopy showed good specificity of B9, B11 and B13 dyes for DNA. In apoptotic assay cells positive for Annexin V were stained more brightly with the dyes B9, B11 and B13 than with propidium iodide. Despite that B13 showed high DNA selectivity it induces apoptosis of splenocytes and it is not suitable for detection of dead cells. 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B, Biology</title><addtitle>J Photochem Photobiol B</addtitle><description>► Synthesis of chloro-containing analogs of Thiazole orange has been reported. ► Spectral properties of the dyes in presence of dsDNA have been investigated. ► The ability of dyes to stain live or apoptotic cells were examined by flow cytometry. ► The dyes are suitable for detection of apoptosis at low concentrations (1 × 10 −11 M). Synthesis, absorption and fluorescence properties of a series of asymmetrical monomethine cyanine dyes, chloro-containing analogs of Thiazole orange, are reported. Their staining ability was studied by flow cytometry. The saturating concentrations of each dye that gives a stable staining intensity have been determined. The ability of dyes B9, B11, B13 to stain live macrophages and apoptotic splenocytes was investigated. Positive signal in nucleus of adherent macrophages detected by fluorescent microscopy showed good specificity of B9, B11 and B13 dyes for DNA. 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Ivanova, I. ; Tchorbanov, A. ; Dimitrova, P. ; Deligeorgiev, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-3cf75b512d9ceeccd8ac70311bee1e29149165fd566a6bc88fc3e71421b2e46a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>absorption</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Benzothiazoles - chemical synthesis</topic><topic>Benzothiazoles - chemistry</topic><topic>Benzothiazoles - pharmacology</topic><topic>DNA</topic><topic>DNA - analysis</topic><topic>DNA - metabolism</topic><topic>DNA-binding dye</topic><topic>Flow cytometry</topic><topic>Flow Cytometry - methods</topic><topic>Fluorescence</topic><topic>fluorescence microscopy</topic><topic>fluorescent dyes</topic><topic>Fluorescent Dyes - chemical synthesis</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fluorescent Dyes - pharmacology</topic><topic>Hydrocarbons, Chlorinated - chemical synthesis</topic><topic>Hydrocarbons, Chlorinated - chemistry</topic><topic>Hydrocarbons, Chlorinated - pharmacology</topic><topic>macrophages</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Microscopy, Fluorescence - methods</topic><topic>photobiology</topic><topic>photochemistry</topic><topic>propidium</topic><topic>Propidium - chemistry</topic><topic>Propidium - pharmacology</topic><topic>Quinolines - chemical synthesis</topic><topic>Quinolines - chemistry</topic><topic>Quinolines - pharmacology</topic><topic>Spleen - cytology</topic><topic>Spleen - metabolism</topic><topic>splenocytes</topic><topic>Thiazole orange analogs</topic><topic>thiazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaloyanova, S.</creatorcontrib><creatorcontrib>Ivanova, I.</creatorcontrib><creatorcontrib>Tchorbanov, A.</creatorcontrib><creatorcontrib>Dimitrova, P.</creatorcontrib><creatorcontrib>Deligeorgiev, T.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of photochemistry and photobiology. B, Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaloyanova, S.</au><au>Ivanova, I.</au><au>Tchorbanov, A.</au><au>Dimitrova, P.</au><au>Deligeorgiev, T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of chloro-substituted analogs of Thiazole orange – Fluorophores for flow cytometric analyses</atitle><jtitle>Journal of photochemistry and photobiology. B, Biology</jtitle><addtitle>J Photochem Photobiol B</addtitle><date>2011-06-02</date><risdate>2011</risdate><volume>103</volume><issue>3</issue><spage>215</spage><epage>221</epage><pages>215-221</pages><issn>1011-1344</issn><eissn>1873-2682</eissn><abstract>► Synthesis of chloro-containing analogs of Thiazole orange has been reported. ► Spectral properties of the dyes in presence of dsDNA have been investigated. ► The ability of dyes to stain live or apoptotic cells were examined by flow cytometry. ► The dyes are suitable for detection of apoptosis at low concentrations (1 × 10 −11 M). Synthesis, absorption and fluorescence properties of a series of asymmetrical monomethine cyanine dyes, chloro-containing analogs of Thiazole orange, are reported. Their staining ability was studied by flow cytometry. The saturating concentrations of each dye that gives a stable staining intensity have been determined. The ability of dyes B9, B11, B13 to stain live macrophages and apoptotic splenocytes was investigated. Positive signal in nucleus of adherent macrophages detected by fluorescent microscopy showed good specificity of B9, B11 and B13 dyes for DNA. In apoptotic assay cells positive for Annexin V were stained more brightly with the dyes B9, B11 and B13 than with propidium iodide. Despite that B13 showed high DNA selectivity it induces apoptosis of splenocytes and it is not suitable for detection of dead cells. The other synthesized chloro-containing analogs of Thiazole orange B9 and B11 can be successfully used for flow cytometric analyses of DNA content in live cells and for analyses of cell apoptosis.</abstract><cop>Switzerland</cop><pub>Elsevier B.V</pub><pmid>21482132</pmid><doi>10.1016/j.jphotobiol.2011.03.012</doi><tpages>7</tpages></addata></record>
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subjects absorption
Animals
Apoptosis
Apoptosis - drug effects
Benzothiazoles - chemical synthesis
Benzothiazoles - chemistry
Benzothiazoles - pharmacology
DNA
DNA - analysis
DNA - metabolism
DNA-binding dye
Flow cytometry
Flow Cytometry - methods
Fluorescence
fluorescence microscopy
fluorescent dyes
Fluorescent Dyes - chemical synthesis
Fluorescent Dyes - chemistry
Fluorescent Dyes - pharmacology
Hydrocarbons, Chlorinated - chemical synthesis
Hydrocarbons, Chlorinated - chemistry
Hydrocarbons, Chlorinated - pharmacology
macrophages
Mice
Mice, Inbred ICR
Microscopy, Fluorescence - methods
photobiology
photochemistry
propidium
Propidium - chemistry
Propidium - pharmacology
Quinolines - chemical synthesis
Quinolines - chemistry
Quinolines - pharmacology
Spleen - cytology
Spleen - metabolism
splenocytes
Thiazole orange analogs
thiazoles
title Synthesis of chloro-substituted analogs of Thiazole orange – Fluorophores for flow cytometric analyses
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