Acid‐Activatable Transmorphic Peptide‐Based Nanomaterials for Photodynamic Therapy

Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH‐responsive transformable peptide‐based nanoparticles for photodynamic therapy (PDT) with prolonged tumor retention times. The self‐assembled peptide–porphyrin nanoparticles transformed into...

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Published inAngewandte Chemie International Edition Vol. 59; no. 46; pp. 20582 - 20588
Main Authors Sun, Bingbing, Chang, Rui, Cao, Shoupeng, Yuan, Chengqian, Zhao, Luyang, Yang, Haowen, Li, Junbai, Yan, Xuehai, Hest, Jan C. M.
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 09.11.2020
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John Wiley and Sons Inc
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Abstract Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH‐responsive transformable peptide‐based nanoparticles for photodynamic therapy (PDT) with prolonged tumor retention times. The self‐assembled peptide–porphyrin nanoparticles transformed into nanofibers when exposed to the acidic tumor microenvironment, which was mainly driven by enhanced intermolecular hydrogen bond formation between the protonated molecules. The nanoparticle transformation into fibrils improved their singlet oxygen generation ability and enabled high accumulation and long‐term retention at tumor sites. Strong fluorescent signals of these nanomaterials were detected in tumor tissue up to 7 days after administration. Moreover, the peptide assemblies exhibited excellent anti‐tumor efficacy via PDT in vivo. This in situ fibrillar transformation strategy could be utilized to design effective stimuli‐responsive biomaterials for long‐term imaging and therapy. Fibrillar‐transformable peptide‐porphyrin (PWG) nanoparticles activated by the acidic inter‐ and intracellular tumor microenvironment were developed for photodynamic therapy (PDT). The transformation of nanoparticles into nanofibers improved their singlet oxygen generation ability and enabled high accumulation and long‐term retention at tumor sites, resulting in excellent anti‐tumor efficacy via PDT in vivo.
AbstractList Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH-responsive transformable peptide-based nanoparticles for photodynamic therapy (PDT) with prolonged tumor retention times. The self-assembled peptide-porphyrin nanoparticles transformed into nanofibers when exposed to the acidic tumor microenvironment, which was mainly driven by enhanced intermolecular hydrogen bond formation between the protonated molecules. The nanoparticle transformation into fibrils improved their singlet oxygen generation ability and enabled high accumulation and long-term retention at tumor sites. Strong fluorescent signals of these nanomaterials were detected in tumor tissue up to 7 days after administration. Moreover, the peptide assemblies exhibited excellent anti-tumor efficacy via PDT in vivo. This in situ fibrillar transformation strategy could be utilized to design effective stimuli-responsive biomaterials for long-term imaging and therapy.Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH-responsive transformable peptide-based nanoparticles for photodynamic therapy (PDT) with prolonged tumor retention times. The self-assembled peptide-porphyrin nanoparticles transformed into nanofibers when exposed to the acidic tumor microenvironment, which was mainly driven by enhanced intermolecular hydrogen bond formation between the protonated molecules. The nanoparticle transformation into fibrils improved their singlet oxygen generation ability and enabled high accumulation and long-term retention at tumor sites. Strong fluorescent signals of these nanomaterials were detected in tumor tissue up to 7 days after administration. Moreover, the peptide assemblies exhibited excellent anti-tumor efficacy via PDT in vivo. This in situ fibrillar transformation strategy could be utilized to design effective stimuli-responsive biomaterials for long-term imaging and therapy.
Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH‐responsive transformable peptide‐based nanoparticles for photodynamic therapy (PDT) with prolonged tumor retention times. The self‐assembled peptide–porphyrin nanoparticles transformed into nanofibers when exposed to the acidic tumor microenvironment, which was mainly driven by enhanced intermolecular hydrogen bond formation between the protonated molecules. The nanoparticle transformation into fibrils improved their singlet oxygen generation ability and enabled high accumulation and long‐term retention at tumor sites. Strong fluorescent signals of these nanomaterials were detected in tumor tissue up to 7 days after administration. Moreover, the peptide assemblies exhibited excellent anti‐tumor efficacy via PDT in vivo. This in situ fibrillar transformation strategy could be utilized to design effective stimuli‐responsive biomaterials for long‐term imaging and therapy. Fibrillar‐transformable peptide‐porphyrin (PWG) nanoparticles activated by the acidic inter‐ and intracellular tumor microenvironment were developed for photodynamic therapy (PDT). The transformation of nanoparticles into nanofibers improved their singlet oxygen generation ability and enabled high accumulation and long‐term retention at tumor sites, resulting in excellent anti‐tumor efficacy via PDT in vivo.
Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH-responsive transformable peptide-based nanoparticles for photodynamic therapy (PDT) with prolonged tumor retention times. The self-assembled peptide-porphyrin nanoparticles transformed into nanofibers when exposed to the acidic tumor microenvironment, which was mainly driven by enhanced intermolecular hydrogen bond formation between the protonated molecules. The nanoparticle transformation into fibrils improved their singlet oxygen generation ability and enabled high accumulation and long-term retention at tumor sites. Strong fluorescent signals of these nanomaterials were detected in tumor tissue up to 7 days after administration. Moreover, the peptide assemblies exhibited excellent anti-tumor efficacy via PDT in vivo. This in situ fibrillar transformation strategy could be utilized to design effective stimuli-responsive biomaterials for long-term imaging and therapy.
Author Yan, Xuehai
Cao, Shoupeng
Sun, Bingbing
Chang, Rui
Yuan, Chengqian
Zhao, Luyang
Yang, Haowen
Li, Junbai
Hest, Jan C. M.
AuthorAffiliation 4 Laboratory of Immunoengineering Department of Biomedical Engineering Institute for Complex Molecular Systems Eindhoven University of Technology 5600 MB Eindhoven The Netherlands
1 Bio-Organic Chemistry Institute of Complex Molecular Systems Department of Biomedical Engineering Eindhoven University of Technology P. O. Box 513 5600 MB Eindhoven The Netherlands
2 State Key Laboratory of Biochemical Engineering Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 China
3 Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China
AuthorAffiliation_xml – name: 1 Bio-Organic Chemistry Institute of Complex Molecular Systems Department of Biomedical Engineering Eindhoven University of Technology P. O. Box 513 5600 MB Eindhoven The Netherlands
– name: 2 State Key Laboratory of Biochemical Engineering Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 China
– name: 4 Laboratory of Immunoengineering Department of Biomedical Engineering Institute for Complex Molecular Systems Eindhoven University of Technology 5600 MB Eindhoven The Netherlands
– name: 3 Beijing National Laboratory for Molecular Sciences CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics Institute of Chemistry Chinese Academy of Sciences Beijing 100190 China
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  organization: Eindhoven University of Technology
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32687653$$D View this record in MEDLINE/PubMed
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Issue 46
Keywords self-assembly
NANOPARTICLES
fibrillar transformation
photodynamic therapy
RETENTION
PH
peptides
photosensitizers
PI-PI-STACKING
ELECTROSTATIC REPULSION
COMBINATION
CANCER
Language English
License Attribution-NonCommercial
2020 The Authors. Published by Wiley-VCH GmbH.
This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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Snippet Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH‐responsive transformable peptide‐based...
Inspired by the dynamic morphology control of molecular assemblies in biological systems, we have developed pH-responsive transformable peptide-based...
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StartPage 20582
SubjectTerms Acids - chemistry
Assemblies
Biomaterials
Biomedical materials
Chemistry
Chemistry, Multidisciplinary
fibrillar transformation
Fibrils
Fluorescence
Humans
Hydrogen bonds
Hydrogen-Ion Concentration
Morphology
Nanofibers
Nanomaterials
Nanoparticles
Nanostructures - chemistry
Nanotechnology
Peptides
Peptides - chemistry
Photochemotherapy - methods
Photodynamic therapy
photosensitizers
Photosensitizing Agents - chemistry
Physical Sciences
Porphyrins
Porphyrins - chemistry
Retention
Science & Technology
self-assembly
Singlet oxygen
Spectrum Analysis - methods
Tumor Microenvironment
Tumors
Title Acid‐Activatable Transmorphic Peptide‐Based Nanomaterials for Photodynamic Therapy
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202008708
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000566420900001
https://www.ncbi.nlm.nih.gov/pubmed/32687653
https://www.proquest.com/docview/2456381402
https://www.proquest.com/docview/2425896769
https://pubmed.ncbi.nlm.nih.gov/PMC7693186
Volume 59
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