Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery

Inhalation administration, compared with intravenous administration, significantly enhances chemotherapeutic drug exposure to the lung tissue and may increase the therapeutic effect for pulmonary anticancer. However, further identification of cancer cells after lung deposition of inhaled drugs is ne...

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Main Authors: Rui Chen, Liu Xu, Qin Fan, Man Li, Jingjing Wang, Li Wu, Weidong Li, Jinao Duan, Zhipeng Chen
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Drug Delivery
Subjects:
Online Access:http://dx.doi.org/10.1080/10717544.2017.1365395
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spelling doaj-3bef994722524545a5e52c2f88abb3202020-11-25T03:29:07ZengTaylor & Francis GroupDrug Delivery1071-75441521-04642017-01-012411191120310.1080/10717544.2017.13653951365395Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug deliveryRui Chen0Liu Xu1Qin Fan2Man Li3Jingjing Wang4Li Wu5Weidong Li6Jinao Duan7Zhipeng Chen8Nanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineNanjing University of Chinese MedicineInhalation administration, compared with intravenous administration, significantly enhances chemotherapeutic drug exposure to the lung tissue and may increase the therapeutic effect for pulmonary anticancer. However, further identification of cancer cells after lung deposition of inhaled drugs is necessary to avoid side effects on normal lung tissue and to maximize drug efficacy. Moreover, as the action site of the major drug was intracellular organelles, drug target to the specific organelle is the final key for accurate drug delivery. Here, we designed a novel multifunctional nanoparticles (MNPs) for pulmonary antitumor and the material was well-designed for hierarchical target involved lung tissue target, cancer cell target, and mitochondrial target. The biodistribution in vivo determined by UHPLC–MS/MS method was employed to verify the drug concentration overwhelmingly increasing in lung tissue through inhaled administration compared with intravenous administration. Cellular uptake assay using A549 cells proved the efficient receptor-mediated cell endocytosis. Confocal laser scanning microscopy observation showed the location of MNPs in cells was mitochondria. All results confirmed the intelligent material can progressively play hierarchical target functions, which could induce more cell apoptosis related to mitochondrial damage. It provides a smart and efficient nanocarrier platform for hierarchical targeting of pulmonary anticancer drug. So far, this kind of material for pulmonary mitochondrial-target has not been seen in other reports.http://dx.doi.org/10.1080/10717544.2017.1365395inhaled administrationhierarchical targetmitochondriadrug deliverypulmonary anticancer drug
collection DOAJ
language English
format Article
sources DOAJ
author Rui Chen
Liu Xu
Qin Fan
Man Li
Jingjing Wang
Li Wu
Weidong Li
Jinao Duan
Zhipeng Chen
spellingShingle Rui Chen
Liu Xu
Qin Fan
Man Li
Jingjing Wang
Li Wu
Weidong Li
Jinao Duan
Zhipeng Chen
Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery
Drug Delivery
inhaled administration
hierarchical target
mitochondria
drug delivery
pulmonary anticancer drug
author_facet Rui Chen
Liu Xu
Qin Fan
Man Li
Jingjing Wang
Li Wu
Weidong Li
Jinao Duan
Zhipeng Chen
author_sort Rui Chen
title Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery
title_short Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery
title_full Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery
title_fullStr Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery
title_full_unstemmed Hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery
title_sort hierarchical pulmonary target nanoparticles via inhaled administration for anticancer drug delivery
publisher Taylor & Francis Group
series Drug Delivery
issn 1071-7544
1521-0464
publishDate 2017-01-01
description Inhalation administration, compared with intravenous administration, significantly enhances chemotherapeutic drug exposure to the lung tissue and may increase the therapeutic effect for pulmonary anticancer. However, further identification of cancer cells after lung deposition of inhaled drugs is necessary to avoid side effects on normal lung tissue and to maximize drug efficacy. Moreover, as the action site of the major drug was intracellular organelles, drug target to the specific organelle is the final key for accurate drug delivery. Here, we designed a novel multifunctional nanoparticles (MNPs) for pulmonary antitumor and the material was well-designed for hierarchical target involved lung tissue target, cancer cell target, and mitochondrial target. The biodistribution in vivo determined by UHPLC–MS/MS method was employed to verify the drug concentration overwhelmingly increasing in lung tissue through inhaled administration compared with intravenous administration. Cellular uptake assay using A549 cells proved the efficient receptor-mediated cell endocytosis. Confocal laser scanning microscopy observation showed the location of MNPs in cells was mitochondria. All results confirmed the intelligent material can progressively play hierarchical target functions, which could induce more cell apoptosis related to mitochondrial damage. It provides a smart and efficient nanocarrier platform for hierarchical targeting of pulmonary anticancer drug. So far, this kind of material for pulmonary mitochondrial-target has not been seen in other reports.
topic inhaled administration
hierarchical target
mitochondria
drug delivery
pulmonary anticancer drug
url http://dx.doi.org/10.1080/10717544.2017.1365395
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