Open Access
International Journal of Nanomedicine, volume Volume 13, pages 439-453
Development of biocompatible and VEGF-targeted paclitaxel nanodrugs on albumin and graphene oxide dual-carrier for photothermal-triggered drug delivery in vitro and in vivo
Publication type: Journal Article
Publication date: 2018-01-16
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 8
ISSN: 11769114, 11782013
PubMed ID:
29403275
Organic Chemistry
Drug Discovery
General Medicine
Biophysics
Pharmaceutical Science
Bioengineering
Biomaterials
Abstract
In this study, we performed the characterization and synthesis of biocompatible and targeted albumin and graphene oxide (GO) dual-carrier paclitaxel (PTX) nanoparticles for photothermal-triggered tumor therapy. PTX absorbed on GO nanosheets as cores were coated with human serum albumin (HSA), following surface conjugation with monoclonal antibodies (mAb) against vascular endothelial growth factor (VEGF; denoted as mAbVEGF) via polyethylene glycol linker to form targeted nanoparticles (PTX-GHP-VEGF). The spherical nanoparticles were 191±5 nm in size with good stability and biocompatibility. GO functioned as the first carrier and a near infrared absorber that can generate photothermal effects under 5-minute 808-nm laser irradiation to thermal trigger the release of PTX from the second carrier HSA nanoparticles. The mechanism of thermal-triggered drug release was also investigated preliminarily, in which the heat generated by GO induced swelling of PTX-GHP-VEGF nanoparticles which released the drugs. In vitro studies found that PTX-GHP-VEGF can efficiently target human SW-13 adrenocortical carcinoma cells as evaluated by confocal fluorescence microscopy as well as transmission electron microscopy, and showed an obvious thermal-triggered antitumor effect, mediated by apoptosis. Moreover, PTX-GHP-VEGF combined with near infrared irradiation showed specific tumor suppression effects with high survival rate after 100 days of treatment. PTX-GHP-VEGF also demonstrated high biosafety with no adverse effects on normal tissues and organs. These results highlight the remarkable potential of PTX-GHP-VEGF in photothermal controllable tumor treatment.
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Deng W. et al. Development of biocompatible and VEGF-targeted paclitaxel nanodrugs on albumin and graphene oxide dual-carrier for photothermal-triggered drug delivery in vitro and in vivo // International Journal of Nanomedicine. 2018. Vol. Volume 13. pp. 439-453.
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Deng W., QIU J., Wang S., Yuan Z., Jia Y., TAN H., Lu J., Zheng R. Development of biocompatible and VEGF-targeted paclitaxel nanodrugs on albumin and graphene oxide dual-carrier for photothermal-triggered drug delivery in vitro and in vivo // International Journal of Nanomedicine. 2018. Vol. Volume 13. pp. 439-453.
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TY - JOUR
DO - 10.2147/IJN.S150977
UR - https://doi.org/10.2147%2FIJN.S150977
TI - Development of biocompatible and VEGF-targeted paclitaxel nanodrugs on albumin and graphene oxide dual-carrier for photothermal-triggered drug delivery in vitro and in vivo
T2 - International Journal of Nanomedicine
AU - Deng, Wentao
AU - QIU, JUHUI
AU - Wang, Shaoting
AU - Yuan, Zhi
AU - Jia, Yuefeng
AU - TAN, HAILIN
AU - Lu, Jiru
AU - Zheng, Ruqiang
PY - 2018
DA - 2018/01/16 00:00:00
PB - Dove Medical Press
SP - 439-453
VL - Volume 13
PMID - 29403275
SN - 1176-9114
SN - 1178-2013
ER -
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@article{2018_Deng,
author = {Wentao Deng and JUHUI QIU and Shaoting Wang and Zhi Yuan and Yuefeng Jia and HAILIN TAN and Jiru Lu and Ruqiang Zheng},
title = {Development of biocompatible and VEGF-targeted paclitaxel nanodrugs on albumin and graphene oxide dual-carrier for photothermal-triggered drug delivery in vitro and in vivo},
journal = {International Journal of Nanomedicine},
year = {2018},
volume = {Volume 13},
publisher = {Dove Medical Press},
month = {jan},
url = {https://doi.org/10.2147%2FIJN.S150977},
pages = {439--453},
doi = {10.2147/IJN.S150977}
}