Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer Therapy

We have designed imidazolium and piperazinium salts of pyropheophorbide-a in order to develop effective photosensitizers which have good solubility in polar and non polar media and to reveal the possible influences of the piperazine and imidazole moieties on the biological activities of pyropheophor...

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Main Authors: Young Key Shim, Narangerel Badraa, Gerelt-Ireedui Sengee
Format: Article
Language:English
Published: MDPI AG 2008-08-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/9/8/1407/
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spelling doaj-0872ea8927f542c48c1d9c38a46988032020-11-25T01:01:14ZengMDPI AGInternational Journal of Molecular Sciences1422-00672008-08-019814071415Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer TherapyYoung Key ShimNarangerel BadraaGerelt-Ireedui SengeeWe have designed imidazolium and piperazinium salts of pyropheophorbide-a in order to develop effective photosensitizers which have good solubility in polar and non polar media and to reveal the possible influences of the piperazine and imidazole moieties on the biological activities of pyropheophorbide-a. The phototoxicity of those pyropheophorbide-a salts against A549 cells was studied in vitro and compared with that of pyropheophorbide-a. The result showed that complexing piperazine and imidazole into pyropheophorbide-a decreases its dark toxicity without greatly decreasing phototoxicity and, enhances its phototoxicity without greatly increasing dark toxicity, respectively. This work not only describes novel amphiphilic salt complexes of pyropheophobide-a which retain the biological activities of the parent compound pyropheophorbide-a and could be effective candidate for PDT, but also reveals the possibility of developing effective photosensitizers by complexing imidazole and piperazine into other hydrophobic photosensitizers.http://www.mdpi.com/1422-0067/9/8/1407/piperazinium saltsimidazolium saltspyropheophorbide-aphotodynamic therapy.
collection DOAJ
language English
format Article
sources DOAJ
author Young Key Shim
Narangerel Badraa
Gerelt-Ireedui Sengee
spellingShingle Young Key Shim
Narangerel Badraa
Gerelt-Ireedui Sengee
Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer Therapy
International Journal of Molecular Sciences
piperazinium salts
imidazolium salts
pyropheophorbide-a
photodynamic therapy.
author_facet Young Key Shim
Narangerel Badraa
Gerelt-Ireedui Sengee
author_sort Young Key Shim
title Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer Therapy
title_short Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer Therapy
title_full Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer Therapy
title_fullStr Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer Therapy
title_full_unstemmed Synthesis and Biological Evaluation of New Imidazolium and Piperazinium Salts of Pyropheophorbide-a for Photodynamic Cancer Therapy
title_sort synthesis and biological evaluation of new imidazolium and piperazinium salts of pyropheophorbide-a for photodynamic cancer therapy
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2008-08-01
description We have designed imidazolium and piperazinium salts of pyropheophorbide-a in order to develop effective photosensitizers which have good solubility in polar and non polar media and to reveal the possible influences of the piperazine and imidazole moieties on the biological activities of pyropheophorbide-a. The phototoxicity of those pyropheophorbide-a salts against A549 cells was studied in vitro and compared with that of pyropheophorbide-a. The result showed that complexing piperazine and imidazole into pyropheophorbide-a decreases its dark toxicity without greatly decreasing phototoxicity and, enhances its phototoxicity without greatly increasing dark toxicity, respectively. This work not only describes novel amphiphilic salt complexes of pyropheophobide-a which retain the biological activities of the parent compound pyropheophorbide-a and could be effective candidate for PDT, but also reveals the possibility of developing effective photosensitizers by complexing imidazole and piperazine into other hydrophobic photosensitizers.
topic piperazinium salts
imidazolium salts
pyropheophorbide-a
photodynamic therapy.
url http://www.mdpi.com/1422-0067/9/8/1407/
work_keys_str_mv AT youngkeyshim synthesisandbiologicalevaluationofnewimidazoliumandpiperaziniumsaltsofpyropheophorbideaforphotodynamiccancertherapy
AT narangerelbadraa synthesisandbiologicalevaluationofnewimidazoliumandpiperaziniumsaltsofpyropheophorbideaforphotodynamiccancertherapy
AT gereltireeduisengee synthesisandbiologicalevaluationofnewimidazoliumandpiperaziniumsaltsofpyropheophorbideaforphotodynamiccancertherapy
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