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Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy

BACKGROUND: Improving the water solubility of hydrophobic photosensitizer and increasing its accumulation in tumor tissue are essential for in vivo photodynamic therapy (PDT). Considering commercialization or clinical application in future, it will be promising to achieve these purposes by developin...

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Autores principales: Son, Jihwan, Yi, Gawon, Kwak, Moon-Hwa, Yang, Seung Mok, Park, Jae Myung, Lee, Bo-In, Choi, Myung-Gyu, Koo, Heebeom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449946/
https://www.ncbi.nlm.nih.gov/pubmed/30953510
http://dx.doi.org/10.1186/s12951-019-0475-1
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author Son, Jihwan
Yi, Gawon
Kwak, Moon-Hwa
Yang, Seung Mok
Park, Jae Myung
Lee, Bo-In
Choi, Myung-Gyu
Koo, Heebeom
author_facet Son, Jihwan
Yi, Gawon
Kwak, Moon-Hwa
Yang, Seung Mok
Park, Jae Myung
Lee, Bo-In
Choi, Myung-Gyu
Koo, Heebeom
author_sort Son, Jihwan
collection PubMed
description BACKGROUND: Improving the water solubility of hydrophobic photosensitizer and increasing its accumulation in tumor tissue are essential for in vivo photodynamic therapy (PDT). Considering commercialization or clinical application in future, it will be promising to achieve these purposes by developing new agents with simple and non-toxic structure. RESULTS: We conjugated multiple chlorin e6 (Ce6) molecules to gelatin polymer, synthesizing two types of gelatin–Ce6 conjugates with different amounts of Ce6: gelatin–Ce6-2 and gelatin–Ce6-8. The resulting conjugates remained soluble in aqueous solutions for a longer time than hydrophobic Ce6. The conjugates could generate singlet oxygen and kill tumor cells upon laser irradiation. After intravenous injection into SCC-7 tumor-bearing mice, gelatin–Ce6-2 showed prolonged blood circulation and highly increased accumulation in tumor tissue as observed in real-time imaging in vivo. After laser irradiation, gelatin–Ce6-2 suppressed tumor growth completely and enabled improved PDT compared to free Ce6 and gelatin–Ce6-8. CONCLUSIONS: This work demonstrates that a simple structure based on photosensitizer and gelatin can highly improve water solubility and stability. Superior tumor tissue accumulation and increased therapeutic efficacy of gelatin–Ce6 during in vivo PDT showed its high potential for clinical application. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0475-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-64499462019-04-15 Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy Son, Jihwan Yi, Gawon Kwak, Moon-Hwa Yang, Seung Mok Park, Jae Myung Lee, Bo-In Choi, Myung-Gyu Koo, Heebeom J Nanobiotechnology Research BACKGROUND: Improving the water solubility of hydrophobic photosensitizer and increasing its accumulation in tumor tissue are essential for in vivo photodynamic therapy (PDT). Considering commercialization or clinical application in future, it will be promising to achieve these purposes by developing new agents with simple and non-toxic structure. RESULTS: We conjugated multiple chlorin e6 (Ce6) molecules to gelatin polymer, synthesizing two types of gelatin–Ce6 conjugates with different amounts of Ce6: gelatin–Ce6-2 and gelatin–Ce6-8. The resulting conjugates remained soluble in aqueous solutions for a longer time than hydrophobic Ce6. The conjugates could generate singlet oxygen and kill tumor cells upon laser irradiation. After intravenous injection into SCC-7 tumor-bearing mice, gelatin–Ce6-2 showed prolonged blood circulation and highly increased accumulation in tumor tissue as observed in real-time imaging in vivo. After laser irradiation, gelatin–Ce6-2 suppressed tumor growth completely and enabled improved PDT compared to free Ce6 and gelatin–Ce6-8. CONCLUSIONS: This work demonstrates that a simple structure based on photosensitizer and gelatin can highly improve water solubility and stability. Superior tumor tissue accumulation and increased therapeutic efficacy of gelatin–Ce6 during in vivo PDT showed its high potential for clinical application. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0475-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-05 /pmc/articles/PMC6449946/ /pubmed/30953510 http://dx.doi.org/10.1186/s12951-019-0475-1 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Son, Jihwan
Yi, Gawon
Kwak, Moon-Hwa
Yang, Seung Mok
Park, Jae Myung
Lee, Bo-In
Choi, Myung-Gyu
Koo, Heebeom
Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy
title Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy
title_full Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy
title_fullStr Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy
title_full_unstemmed Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy
title_short Gelatin–chlorin e6 conjugate for in vivo photodynamic therapy
title_sort gelatin–chlorin e6 conjugate for in vivo photodynamic therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449946/
https://www.ncbi.nlm.nih.gov/pubmed/30953510
http://dx.doi.org/10.1186/s12951-019-0475-1
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