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Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy

Rationale: The combination of photosensitizers, oxygen supply agents, and adjuvant therapy drugs in a single nano-drug delivery system for photodynamic therapy (PDT) has been showing great promises to overcome the inherent challenges of PDT for tumor treatment. However, the complicated preparation o...

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Autores principales: Gong, Guidong, Pan, Jiezhou, He, Yunxiang, Shang, Jiaojiao, Wang, Xiaoling, Zhang, Yaoyao, Zhang, Guolin, Wang, Fei, Zhao, Gang, Guo, Junling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899564/
https://www.ncbi.nlm.nih.gov/pubmed/35265197
http://dx.doi.org/10.7150/thno.68563
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author Gong, Guidong
Pan, Jiezhou
He, Yunxiang
Shang, Jiaojiao
Wang, Xiaoling
Zhang, Yaoyao
Zhang, Guolin
Wang, Fei
Zhao, Gang
Guo, Junling
author_facet Gong, Guidong
Pan, Jiezhou
He, Yunxiang
Shang, Jiaojiao
Wang, Xiaoling
Zhang, Yaoyao
Zhang, Guolin
Wang, Fei
Zhao, Gang
Guo, Junling
author_sort Gong, Guidong
collection PubMed
description Rationale: The combination of photosensitizers, oxygen supply agents, and adjuvant therapy drugs in a single nano-drug delivery system for photodynamic therapy (PDT) has been showing great promises to overcome the inherent challenges of PDT for tumor treatment. However, the complicated preparation of integrating multiple components hampers their further developments. Here, we describe a self-assembly nanomicelle with rationally designed building blocks, which shows a high efficiency of synergistic chemo-photodynamic therapy in the animal modal. Methods: The nanomicelle was prepared by a coordination-driven self-assembly based on a rationally designed ferrocene cyclopalladated compound coupled with photosensitizers and hyaluronic acid (referred to as FCP-Tph/HA). The morphology, targeting drug delivery, pharmacokinetics, hemolysis, and multimodal synergistic therapy of FCP-Tph/HA were investigated. Results: The formation of nanomicelles presents a low hemolysis rate and a prolonged blood circulation time. FCP-Tph/HA possesses an enhanced antitumor effect in vitro through the specific binding of HA to CD44 and combining chemotherapy with oxygen self-supplying PDT. Simultaneously, the nanomicelle facilitates a significantly improved antitumor efficacy (>90% tumor regression) on a breast cancer model in vivo. Conclusion: Our results present a modular self-assembled nanomicellar platform with synergistic chemo-photodynamic therapy for challenging PDT-based tumor treatment.
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spelling pubmed-88995642022-03-08 Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy Gong, Guidong Pan, Jiezhou He, Yunxiang Shang, Jiaojiao Wang, Xiaoling Zhang, Yaoyao Zhang, Guolin Wang, Fei Zhao, Gang Guo, Junling Theranostics Research Paper Rationale: The combination of photosensitizers, oxygen supply agents, and adjuvant therapy drugs in a single nano-drug delivery system for photodynamic therapy (PDT) has been showing great promises to overcome the inherent challenges of PDT for tumor treatment. However, the complicated preparation of integrating multiple components hampers their further developments. Here, we describe a self-assembly nanomicelle with rationally designed building blocks, which shows a high efficiency of synergistic chemo-photodynamic therapy in the animal modal. Methods: The nanomicelle was prepared by a coordination-driven self-assembly based on a rationally designed ferrocene cyclopalladated compound coupled with photosensitizers and hyaluronic acid (referred to as FCP-Tph/HA). The morphology, targeting drug delivery, pharmacokinetics, hemolysis, and multimodal synergistic therapy of FCP-Tph/HA were investigated. Results: The formation of nanomicelles presents a low hemolysis rate and a prolonged blood circulation time. FCP-Tph/HA possesses an enhanced antitumor effect in vitro through the specific binding of HA to CD44 and combining chemotherapy with oxygen self-supplying PDT. Simultaneously, the nanomicelle facilitates a significantly improved antitumor efficacy (>90% tumor regression) on a breast cancer model in vivo. Conclusion: Our results present a modular self-assembled nanomicellar platform with synergistic chemo-photodynamic therapy for challenging PDT-based tumor treatment. Ivyspring International Publisher 2022-01-31 /pmc/articles/PMC8899564/ /pubmed/35265197 http://dx.doi.org/10.7150/thno.68563 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Gong, Guidong
Pan, Jiezhou
He, Yunxiang
Shang, Jiaojiao
Wang, Xiaoling
Zhang, Yaoyao
Zhang, Guolin
Wang, Fei
Zhao, Gang
Guo, Junling
Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy
title Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy
title_full Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy
title_fullStr Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy
title_full_unstemmed Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy
title_short Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy
title_sort self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergistic chemo-photodynamic therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899564/
https://www.ncbi.nlm.nih.gov/pubmed/35265197
http://dx.doi.org/10.7150/thno.68563
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