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An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency

We developed a smart nanofiber mesh (SNM) with anticancer abilities as well as injectability and fast recovery from irregular to non-compressible shapes. The mesh can be injected at the tumor site to modulate and control anticancer effects by loading the chemotherapeutic drug, paclitaxel (PTX), as w...

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Autores principales: Chen, Lili, Fujisawa, Nanami, Takanohashi, Masato, Ebara, Mitsuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669589/
https://www.ncbi.nlm.nih.gov/pubmed/36406225
http://dx.doi.org/10.3389/fbioe.2022.1046147
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author Chen, Lili
Fujisawa, Nanami
Takanohashi, Masato
Ebara, Mitsuhiro
author_facet Chen, Lili
Fujisawa, Nanami
Takanohashi, Masato
Ebara, Mitsuhiro
author_sort Chen, Lili
collection PubMed
description We developed a smart nanofiber mesh (SNM) with anticancer abilities as well as injectability and fast recovery from irregular to non-compressible shapes. The mesh can be injected at the tumor site to modulate and control anticancer effects by loading the chemotherapeutic drug, paclitaxel (PTX), as well as magnetic nanoparticles (MNPs). The storage modulus of the mesh decreases when applied with a certain shear strain, and the mesh can pass through a 14-gauge needle. Moreover, the fibrous morphology is maintained even after injection. In heat-generation measurements, the mesh achieved an effective temperature of mild hyperthermia (41–43°C) within 5 min of exposure to alternating magnetic field (AMF) irradiation. An electrospinning method was employed to fabricate the mesh using a copolymer of N-isopropylacrylamide (NIPAAm) and N-hydroxyethyl acrylamide (HMAAm), whose phase transition temperature was adjusted to a mildly hyperthermic temperature range. Pplyvinyl alcohol (PVA) was also incorporated to add shear-thinning property to the interactions between polymer chains derived from hydrogen bonding, The “on-off” switchable release of PTX from the mesh was detected by the drug release test. Approximately 73% of loaded PTX was released from the mesh after eight cycles, whereas only a tiny amount of PTX was released during the cooling phase. Furthermore, hyperthermia combined with chemotherapy after exposure to an AMF showed significantly reduced cancer cell survival compared to the control group. Subsequent investigations have proven that a new injectable local hyperthermia chemotherapy platform could be developed for cancer treatment using this SNM.
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spelling pubmed-96695892022-11-18 An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency Chen, Lili Fujisawa, Nanami Takanohashi, Masato Ebara, Mitsuhiro Front Bioeng Biotechnol Bioengineering and Biotechnology We developed a smart nanofiber mesh (SNM) with anticancer abilities as well as injectability and fast recovery from irregular to non-compressible shapes. The mesh can be injected at the tumor site to modulate and control anticancer effects by loading the chemotherapeutic drug, paclitaxel (PTX), as well as magnetic nanoparticles (MNPs). The storage modulus of the mesh decreases when applied with a certain shear strain, and the mesh can pass through a 14-gauge needle. Moreover, the fibrous morphology is maintained even after injection. In heat-generation measurements, the mesh achieved an effective temperature of mild hyperthermia (41–43°C) within 5 min of exposure to alternating magnetic field (AMF) irradiation. An electrospinning method was employed to fabricate the mesh using a copolymer of N-isopropylacrylamide (NIPAAm) and N-hydroxyethyl acrylamide (HMAAm), whose phase transition temperature was adjusted to a mildly hyperthermic temperature range. Pplyvinyl alcohol (PVA) was also incorporated to add shear-thinning property to the interactions between polymer chains derived from hydrogen bonding, The “on-off” switchable release of PTX from the mesh was detected by the drug release test. Approximately 73% of loaded PTX was released from the mesh after eight cycles, whereas only a tiny amount of PTX was released during the cooling phase. Furthermore, hyperthermia combined with chemotherapy after exposure to an AMF showed significantly reduced cancer cell survival compared to the control group. Subsequent investigations have proven that a new injectable local hyperthermia chemotherapy platform could be developed for cancer treatment using this SNM. Frontiers Media S.A. 2022-11-03 /pmc/articles/PMC9669589/ /pubmed/36406225 http://dx.doi.org/10.3389/fbioe.2022.1046147 Text en Copyright © 2022 Chen, Fujisawa, Takanohashi and Ebara. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Chen, Lili
Fujisawa, Nanami
Takanohashi, Masato
Ebara, Mitsuhiro
An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency
title An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency
title_full An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency
title_fullStr An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency
title_full_unstemmed An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency
title_short An injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency
title_sort injectable hyperthermic nanofiber mesh with switchable drug release to stimulate chemotherapy potency
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669589/
https://www.ncbi.nlm.nih.gov/pubmed/36406225
http://dx.doi.org/10.3389/fbioe.2022.1046147
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