Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo

In this work, a pH-sensitive liposome–polymer nanoparticle (NP) composed of lipid, hyaluronic acid (HA) and poly(β-amino ester) (PBAE) was prepared using layer-by-layer (LbL) method for doxorubicin (DOX) targeted delivery and controlled release to enhance the cancer treatment efficacy. The NP with p...

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Main Authors: Wanfu Men, Peiyao Zhu, Siyuan Dong, Wenke Liu, Kun Zhou, Yu Bai, Xiangli Liu, Shulei Gong, Shuguang Zhang
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:Drug Delivery
Subjects:
Online Access:http://dx.doi.org/10.1080/10717544.2019.1709922
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spelling doaj-0b8b769111244d589b4070d0b9d3dbae2021-07-06T11:30:10ZengTaylor & Francis GroupDrug Delivery1071-75441521-04642020-01-0127118019010.1080/10717544.2019.17099221709922Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivoWanfu Men0Peiyao Zhu1Siyuan Dong2Wenke Liu3Kun Zhou4Yu Bai5Xiangli Liu6Shulei Gong7Shuguang Zhang8Department of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityDepartment of Thoracic Surgery, The First Affiliated Hospital of China Medical UniversityIn this work, a pH-sensitive liposome–polymer nanoparticle (NP) composed of lipid, hyaluronic acid (HA) and poly(β-amino ester) (PBAE) was prepared using layer-by-layer (LbL) method for doxorubicin (DOX) targeted delivery and controlled release to enhance the cancer treatment efficacy. The NP with pH-sensitivity and targeting effect was successfully prepared by validation of charge reversal and increase of hydrodynamic diameter after each deposition of functional layer. We further showed the DOX-loaded NP had higher drug loading capacity, suitable particle size, spherical morphology, good uniformity, and high serum stability for drug delivery. We confirmed that the drug release profile was triggered by low pH with sustained release manner in vitro. Confocal microscopy research demonstrated that the NP was able to effectively target and deliver DOX into human non-small cell lung carcinoma (A549) cells in comparison to free DOX. Moreover, the blank NP showed negligible cytotoxicity, and the DOX-loaded NP could efficiently induce the apoptosis of A549 cells as well as free DOX. Notably, in vivo experiment results showed that the DOX-loaded NPs effectively inhibited the growth of tumor, enhanced the survival of tumor-bearing mice and improved the therapeutic efficacy with reduced side-effect comparing with free drug. Therefore, the NP could be a potential intelligent anticancer drug delivery carrier for cancer chemotherapy, and the LbL method might be a useful strategy to prepare multi-functional platform for drug delivery.http://dx.doi.org/10.1080/10717544.2019.1709922drug deliverylayer-by-layernanoparticleph-sensitivityha-targetingcontrolled releasecancer therapy
collection DOAJ
language English
format Article
sources DOAJ
author Wanfu Men
Peiyao Zhu
Siyuan Dong
Wenke Liu
Kun Zhou
Yu Bai
Xiangli Liu
Shulei Gong
Shuguang Zhang
spellingShingle Wanfu Men
Peiyao Zhu
Siyuan Dong
Wenke Liu
Kun Zhou
Yu Bai
Xiangli Liu
Shulei Gong
Shuguang Zhang
Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo
Drug Delivery
drug delivery
layer-by-layer
nanoparticle
ph-sensitivity
ha-targeting
controlled release
cancer therapy
author_facet Wanfu Men
Peiyao Zhu
Siyuan Dong
Wenke Liu
Kun Zhou
Yu Bai
Xiangli Liu
Shulei Gong
Shuguang Zhang
author_sort Wanfu Men
title Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo
title_short Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo
title_full Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo
title_fullStr Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo
title_full_unstemmed Layer-by-layer pH-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo
title_sort layer-by-layer ph-sensitive nanoparticles for drug delivery and controlled release with improved therapeutic efficacy in vivo
publisher Taylor & Francis Group
series Drug Delivery
issn 1071-7544
1521-0464
publishDate 2020-01-01
description In this work, a pH-sensitive liposome–polymer nanoparticle (NP) composed of lipid, hyaluronic acid (HA) and poly(β-amino ester) (PBAE) was prepared using layer-by-layer (LbL) method for doxorubicin (DOX) targeted delivery and controlled release to enhance the cancer treatment efficacy. The NP with pH-sensitivity and targeting effect was successfully prepared by validation of charge reversal and increase of hydrodynamic diameter after each deposition of functional layer. We further showed the DOX-loaded NP had higher drug loading capacity, suitable particle size, spherical morphology, good uniformity, and high serum stability for drug delivery. We confirmed that the drug release profile was triggered by low pH with sustained release manner in vitro. Confocal microscopy research demonstrated that the NP was able to effectively target and deliver DOX into human non-small cell lung carcinoma (A549) cells in comparison to free DOX. Moreover, the blank NP showed negligible cytotoxicity, and the DOX-loaded NP could efficiently induce the apoptosis of A549 cells as well as free DOX. Notably, in vivo experiment results showed that the DOX-loaded NPs effectively inhibited the growth of tumor, enhanced the survival of tumor-bearing mice and improved the therapeutic efficacy with reduced side-effect comparing with free drug. Therefore, the NP could be a potential intelligent anticancer drug delivery carrier for cancer chemotherapy, and the LbL method might be a useful strategy to prepare multi-functional platform for drug delivery.
topic drug delivery
layer-by-layer
nanoparticle
ph-sensitivity
ha-targeting
controlled release
cancer therapy
url http://dx.doi.org/10.1080/10717544.2019.1709922
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