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Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency

In this study, we report a novel kind of targeting with paclitaxel (PTX)-loaded silk fibroin nanoparticles conjugated with iRGD–EGFR nanobody recombinant protein (anti-EGFR-iRGD). The new nanoparticles (called A-PTX-SF-NPs) were prepared using the carbodiimide-mediated coupling procedure and their c...

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Autores principales: Bian, Xinyu, Wu, Puyuan, Sha, Huizi, Qian, Hanqing, Wang, Qing, Cheng, Lei, Yang, Yang, Yang, Mi, Liu, Baorui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892850/
https://www.ncbi.nlm.nih.gov/pubmed/27313461
http://dx.doi.org/10.2147/OTT.S100678
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author Bian, Xinyu
Wu, Puyuan
Sha, Huizi
Qian, Hanqing
Wang, Qing
Cheng, Lei
Yang, Yang
Yang, Mi
Liu, Baorui
author_facet Bian, Xinyu
Wu, Puyuan
Sha, Huizi
Qian, Hanqing
Wang, Qing
Cheng, Lei
Yang, Yang
Yang, Mi
Liu, Baorui
author_sort Bian, Xinyu
collection PubMed
description In this study, we report a novel kind of targeting with paclitaxel (PTX)-loaded silk fibroin nanoparticles conjugated with iRGD–EGFR nanobody recombinant protein (anti-EGFR-iRGD). The new nanoparticles (called A-PTX-SF-NPs) were prepared using the carbodiimide-mediated coupling procedure and their characteristics were evaluated. The cellular cytotoxicity and cellular uptake of A-PTX-SF-NPs were also investigated. The results in vivo suggested that NPs conjugated with the recombinant protein exhibited more targeting and anti-neoplastic property in cells with high EGFR expression. In the in vivo antitumor efficacy assay, the A-PTX-SF-NPs group showed slower tumor growth and smaller tumor volumes than PTX-SF-NPs in a HeLa xenograft mouse model. A real-time near-infrared fluorescence imaging study showed that A-PTX-SF-NPs could target the tumor more effectively. These results suggest that the anticancer activity and tumor targeting of A-PTX-SF-NPs were superior to those of PTX-SF-NPs and may have the potential to be used for targeted delivery for tumor therapies.
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spelling pubmed-48928502016-06-16 Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency Bian, Xinyu Wu, Puyuan Sha, Huizi Qian, Hanqing Wang, Qing Cheng, Lei Yang, Yang Yang, Mi Liu, Baorui Onco Targets Ther Original Research In this study, we report a novel kind of targeting with paclitaxel (PTX)-loaded silk fibroin nanoparticles conjugated with iRGD–EGFR nanobody recombinant protein (anti-EGFR-iRGD). The new nanoparticles (called A-PTX-SF-NPs) were prepared using the carbodiimide-mediated coupling procedure and their characteristics were evaluated. The cellular cytotoxicity and cellular uptake of A-PTX-SF-NPs were also investigated. The results in vivo suggested that NPs conjugated with the recombinant protein exhibited more targeting and anti-neoplastic property in cells with high EGFR expression. In the in vivo antitumor efficacy assay, the A-PTX-SF-NPs group showed slower tumor growth and smaller tumor volumes than PTX-SF-NPs in a HeLa xenograft mouse model. A real-time near-infrared fluorescence imaging study showed that A-PTX-SF-NPs could target the tumor more effectively. These results suggest that the anticancer activity and tumor targeting of A-PTX-SF-NPs were superior to those of PTX-SF-NPs and may have the potential to be used for targeted delivery for tumor therapies. Dove Medical Press 2016-05-27 /pmc/articles/PMC4892850/ /pubmed/27313461 http://dx.doi.org/10.2147/OTT.S100678 Text en © 2016 Bian et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Bian, Xinyu
Wu, Puyuan
Sha, Huizi
Qian, Hanqing
Wang, Qing
Cheng, Lei
Yang, Yang
Yang, Mi
Liu, Baorui
Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency
title Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency
title_full Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency
title_fullStr Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency
title_full_unstemmed Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency
title_short Anti-EGFR-iRGD recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency
title_sort anti-egfr-irgd recombinant protein conjugated silk fibroin nanoparticles for enhanced tumor targeting and antitumor efficiency
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892850/
https://www.ncbi.nlm.nih.gov/pubmed/27313461
http://dx.doi.org/10.2147/OTT.S100678
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