Cargando…

Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2

Previous reports from our laboratory have shown that a bifunctional agent obtained by conjugating a photosensitizer (HPPH) to a cyanine dye (CD) can be used for fluorescence image-guided treatment of tumor by photodynamic therapy (PDT). However, the resulting HPPH-CD conjugate showed a significant d...

Descripción completa

Detalles Bibliográficos
Autores principales: James, Nadine S., Ohulchanskyy, Tymish Y., Chen, Yihui, Joshi, Penny, Zheng, Xiang, Goswami, Lalit N., Pandey, Ravindra K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767117/
https://www.ncbi.nlm.nih.gov/pubmed/24019855
http://dx.doi.org/10.7150/thno.5923
_version_ 1782283627408654336
author James, Nadine S.
Ohulchanskyy, Tymish Y.
Chen, Yihui
Joshi, Penny
Zheng, Xiang
Goswami, Lalit N.
Pandey, Ravindra K.
author_facet James, Nadine S.
Ohulchanskyy, Tymish Y.
Chen, Yihui
Joshi, Penny
Zheng, Xiang
Goswami, Lalit N.
Pandey, Ravindra K.
author_sort James, Nadine S.
collection PubMed
description Previous reports from our laboratory have shown that a bifunctional agent obtained by conjugating a photosensitizer (HPPH) to a cyanine dye (CD) can be used for fluorescence image-guided treatment of tumor by photodynamic therapy (PDT). However, the resulting HPPH-CD conjugate showed a significant difference between the tumor-imaging and therapeutic doses. It was demonstrated that the singlet oxygen ((1)O(2)(*), a key cytotoxic agent in PDT) produced by the conjugate upon excitation of the HPPH moiety was partially quenched by the CD-moiety; this resulted in a reduced PDT response when compared to HPPH-PDT under similar treatment parameters. To improve the therapeutic potential of the conjugate, we synthesized a series of dual functional agents in which one or two HPPH moieties were separately conjugated to three different dyes (Cypate, modified IR820 or modified IR783). The newly synthesized conjugates were compared with our lead compound HPPH-CD in terms of photophysical properties, in vitro and in vivo PDT efficacy, tumor uptake and imaging potential. Among the analogs investigated, the conjugate, in which two HPPH moieties were linked to the modified IR820 produced enhanced tumor uptake and tumor contrast in both Colon 26 (a murine Colon carcinoma) and U87 (a human glioblastoma) cell lines. The long-term PDT efficacy (cure) of this conjugate in BALB/c mice, bearing Colon 26 tumors was also enhanced; however, its efficacy in Nude mice bearing U87 tumors was slightly reduced. It was also found that in all the conjugates the singlet oxygen generation and, consequently, PDT efficacy were compromised by a competing pathway, whereby an electronic excitation of HPPH, the energy donor, is deactivated through an electronic excitation energy transfer (Forster Resonance Energy Transfer, FRET) to the CD fluorophore, the energy acceptor, resulting in overall reduction of the singlet oxygen production. Conjugates with increased FRET showed reduced singlet oxygen production and PDT efficacy. Among the conjugates investigated, the bifunctional agent in which two HPPH moieties were linked to the benzoindole-based cyanine dye 11 showed superiority over the lead candidate 9 (mono HPPH-cyanine dye).
format Online
Article
Text
id pubmed-3767117
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-37671172013-09-09 Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2 James, Nadine S. Ohulchanskyy, Tymish Y. Chen, Yihui Joshi, Penny Zheng, Xiang Goswami, Lalit N. Pandey, Ravindra K. Theranostics Research Paper Previous reports from our laboratory have shown that a bifunctional agent obtained by conjugating a photosensitizer (HPPH) to a cyanine dye (CD) can be used for fluorescence image-guided treatment of tumor by photodynamic therapy (PDT). However, the resulting HPPH-CD conjugate showed a significant difference between the tumor-imaging and therapeutic doses. It was demonstrated that the singlet oxygen ((1)O(2)(*), a key cytotoxic agent in PDT) produced by the conjugate upon excitation of the HPPH moiety was partially quenched by the CD-moiety; this resulted in a reduced PDT response when compared to HPPH-PDT under similar treatment parameters. To improve the therapeutic potential of the conjugate, we synthesized a series of dual functional agents in which one or two HPPH moieties were separately conjugated to three different dyes (Cypate, modified IR820 or modified IR783). The newly synthesized conjugates were compared with our lead compound HPPH-CD in terms of photophysical properties, in vitro and in vivo PDT efficacy, tumor uptake and imaging potential. Among the analogs investigated, the conjugate, in which two HPPH moieties were linked to the modified IR820 produced enhanced tumor uptake and tumor contrast in both Colon 26 (a murine Colon carcinoma) and U87 (a human glioblastoma) cell lines. The long-term PDT efficacy (cure) of this conjugate in BALB/c mice, bearing Colon 26 tumors was also enhanced; however, its efficacy in Nude mice bearing U87 tumors was slightly reduced. It was also found that in all the conjugates the singlet oxygen generation and, consequently, PDT efficacy were compromised by a competing pathway, whereby an electronic excitation of HPPH, the energy donor, is deactivated through an electronic excitation energy transfer (Forster Resonance Energy Transfer, FRET) to the CD fluorophore, the energy acceptor, resulting in overall reduction of the singlet oxygen production. Conjugates with increased FRET showed reduced singlet oxygen production and PDT efficacy. Among the conjugates investigated, the bifunctional agent in which two HPPH moieties were linked to the benzoindole-based cyanine dye 11 showed superiority over the lead candidate 9 (mono HPPH-cyanine dye). Ivyspring International Publisher 2013-08-21 /pmc/articles/PMC3767117/ /pubmed/24019855 http://dx.doi.org/10.7150/thno.5923 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
James, Nadine S.
Ohulchanskyy, Tymish Y.
Chen, Yihui
Joshi, Penny
Zheng, Xiang
Goswami, Lalit N.
Pandey, Ravindra K.
Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2
title Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2
title_full Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2
title_fullStr Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2
title_full_unstemmed Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2
title_short Comparative Tumor Imaging and PDT Efficacy of HPPH Conjugated in the Mono- and Di-Forms to Various Polymethine Cyanine Dyes: Part - 2
title_sort comparative tumor imaging and pdt efficacy of hpph conjugated in the mono- and di-forms to various polymethine cyanine dyes: part - 2
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767117/
https://www.ncbi.nlm.nih.gov/pubmed/24019855
http://dx.doi.org/10.7150/thno.5923
work_keys_str_mv AT jamesnadines comparativetumorimagingandpdtefficacyofhpphconjugatedinthemonoanddiformstovariouspolymethinecyaninedyespart2
AT ohulchanskyytymishy comparativetumorimagingandpdtefficacyofhpphconjugatedinthemonoanddiformstovariouspolymethinecyaninedyespart2
AT chenyihui comparativetumorimagingandpdtefficacyofhpphconjugatedinthemonoanddiformstovariouspolymethinecyaninedyespart2
AT joshipenny comparativetumorimagingandpdtefficacyofhpphconjugatedinthemonoanddiformstovariouspolymethinecyaninedyespart2
AT zhengxiang comparativetumorimagingandpdtefficacyofhpphconjugatedinthemonoanddiformstovariouspolymethinecyaninedyespart2
AT goswamilalitn comparativetumorimagingandpdtefficacyofhpphconjugatedinthemonoanddiformstovariouspolymethinecyaninedyespart2
AT pandeyravindrak comparativetumorimagingandpdtefficacyofhpphconjugatedinthemonoanddiformstovariouspolymethinecyaninedyespart2