Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug Delivery

In this study, hyaluronic acid (HA), a natural polysaccharide that can specifically bind to CD44 receptors, was conjugated onto laponite® (LAP) nanodisks for the encapsulation and specific delivery of the anti-cancer drug doxorubicin (DOX) to CD44-overexpressed cancer cells. The prepared LM-...

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Main Authors: Tingting Jiang, Guangxiang Chen, Xiangyang Shi, Rui Guo
Format: Article
Language:English
Published: MDPI AG 2019-01-01
Series:Polymers
Subjects:
LAP
Online Access:http://www.mdpi.com/2073-4360/11/1/137
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spelling doaj-c17bee8848b94db69b4612c3061927702020-11-25T00:46:10ZengMDPI AGPolymers2073-43602019-01-0111113710.3390/polym11010137polym11010137Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug DeliveryTingting Jiang0Guangxiang Chen1Xiangyang Shi2Rui Guo3Key Laboratory of Science & Technology of Eco-Textile, Ministry of Education, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, ChinaKey Laboratory of Science & Technology of Eco-Textile, Ministry of Education, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, ChinaKey Laboratory of Science & Technology of Eco-Textile, Ministry of Education, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, ChinaKey Laboratory of Science & Technology of Eco-Textile, Ministry of Education, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620, ChinaIn this study, hyaluronic acid (HA), a natural polysaccharide that can specifically bind to CD44 receptors, was conjugated onto laponite® (LAP) nanodisks for the encapsulation and specific delivery of the anti-cancer drug doxorubicin (DOX) to CD44-overexpressed cancer cells. The prepared LM-HA could encapsulate DOX efficiently and release drug in a continuous manner with pH-responsiveness. In vitro cell viability assay proved that LM-HA had good biocompatibility, and drug-loaded LM-HA/DOX exhibited targeted anti-tumor effects against HeLa cells with CD44 receptors overexpressed. In addition, the flow cytometric detection and confocal laser scanning microscope results confirmed that LM-HA/DOX could be specifically internalized by HeLa cells via CD44-mediated endocytosis. Therefore, the HA-modified LAP nanodisks with high drug loading efficiency, pH-sensitive drug release properties and CD44 targetability might be an efficient nanoplatform for cancer chemotherapy.http://www.mdpi.com/2073-4360/11/1/137LAPhyaluronic aciddoxorubicinCD44 receptor targeted
collection DOAJ
language English
format Article
sources DOAJ
author Tingting Jiang
Guangxiang Chen
Xiangyang Shi
Rui Guo
spellingShingle Tingting Jiang
Guangxiang Chen
Xiangyang Shi
Rui Guo
Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug Delivery
Polymers
LAP
hyaluronic acid
doxorubicin
CD44 receptor targeted
author_facet Tingting Jiang
Guangxiang Chen
Xiangyang Shi
Rui Guo
author_sort Tingting Jiang
title Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug Delivery
title_short Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug Delivery
title_full Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug Delivery
title_fullStr Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug Delivery
title_full_unstemmed Hyaluronic Acid-Decorated Laponite® Nanocomposites for Targeted Anticancer Drug Delivery
title_sort hyaluronic acid-decorated laponite® nanocomposites for targeted anticancer drug delivery
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2019-01-01
description In this study, hyaluronic acid (HA), a natural polysaccharide that can specifically bind to CD44 receptors, was conjugated onto laponite® (LAP) nanodisks for the encapsulation and specific delivery of the anti-cancer drug doxorubicin (DOX) to CD44-overexpressed cancer cells. The prepared LM-HA could encapsulate DOX efficiently and release drug in a continuous manner with pH-responsiveness. In vitro cell viability assay proved that LM-HA had good biocompatibility, and drug-loaded LM-HA/DOX exhibited targeted anti-tumor effects against HeLa cells with CD44 receptors overexpressed. In addition, the flow cytometric detection and confocal laser scanning microscope results confirmed that LM-HA/DOX could be specifically internalized by HeLa cells via CD44-mediated endocytosis. Therefore, the HA-modified LAP nanodisks with high drug loading efficiency, pH-sensitive drug release properties and CD44 targetability might be an efficient nanoplatform for cancer chemotherapy.
topic LAP
hyaluronic acid
doxorubicin
CD44 receptor targeted
url http://www.mdpi.com/2073-4360/11/1/137
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AT guangxiangchen hyaluronicaciddecoratedlaponitenanocompositesfortargetedanticancerdrugdelivery
AT xiangyangshi hyaluronicaciddecoratedlaponitenanocompositesfortargetedanticancerdrugdelivery
AT ruiguo hyaluronicaciddecoratedlaponitenanocompositesfortargetedanticancerdrugdelivery
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