Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticles

The objective of this study is to compare the targeting ability of activated carbon nanoparticles and nanoliposomes, which are used as carriers for delivering docetaxel (DTX) to the metastatic lymph nodes. In this study, we first prepared the DTX-loaded activated carbon nanoparticles (DTX-AC-NPs) by...

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Main Authors: Tiantian Ye, Wen Xu, Tianyu Shi, Rui Yang, Xinggang Yang, Shujun Wang, Weisan Pan
Format: Article
Language:English
Published: Elsevier 2015-02-01
Series:Asian Journal of Pharmaceutical Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1818087614000543
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author Tiantian Ye
Wen Xu
Tianyu Shi
Rui Yang
Xinggang Yang
Shujun Wang
Weisan Pan
author_facet Tiantian Ye
Wen Xu
Tianyu Shi
Rui Yang
Xinggang Yang
Shujun Wang
Weisan Pan
author_sort Tiantian Ye
collection DOAJ
description The objective of this study is to compare the targeting ability of activated carbon nanoparticles and nanoliposomes, which are used as carriers for delivering docetaxel (DTX) to the metastatic lymph nodes. In this study, we first prepared the DTX-loaded activated carbon nanoparticles (DTX-AC-NPs) by modifying the activated carbon with nitric acid oxidation and absorbing DTX in the concentrated nitro-oxide nanocarbon. We then prepared DTX-loaded nanoliposomes (DTX-LPs) by the proliposome method. The physiochemical properties of DTX-AC-NPs and DTX-LPs were carefully evaluated in vitro. The metastatic lymph node uptake and the injection site retention were investigated by analyzing the DTX concentration in metastatic lymph nodes and injection sites. The result showed that DTX-AC-NPs and DTX-LPs with suitable and stable physicochemical properties could be used for in vivo lymph node targeting studies. DTX-AC-NPs significantly increased DTX-AUC(0–24) and prolonged DTX-retention in metastatic lymph nodes compared to DTX-LPs and non-modified activate carbon in vivo. This study demonstrated activated carbon nanoparticles may be potential intralymphatic drug delivery system to preferentially target regional metastatic lymph nodes.
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spelling doaj.art-707f1b3519834b53865ca8b2b33756732022-12-21T18:23:01ZengElsevierAsian Journal of Pharmaceutical Sciences1818-08762015-02-01101647210.1016/j.ajps.2014.08.004Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticlesTiantian Ye0Wen Xu1Tianyu Shi2Rui Yang3Xinggang Yang4Shujun Wang5Weisan Pan6Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, ChinaDepartment of R & D, Shenyang Green Pharmaceutical CO., LTD, 176 Shenbei Road, 110164, ChinaDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, ChinaDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, ChinaDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, ChinaDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, ChinaDepartment of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, ChinaThe objective of this study is to compare the targeting ability of activated carbon nanoparticles and nanoliposomes, which are used as carriers for delivering docetaxel (DTX) to the metastatic lymph nodes. In this study, we first prepared the DTX-loaded activated carbon nanoparticles (DTX-AC-NPs) by modifying the activated carbon with nitric acid oxidation and absorbing DTX in the concentrated nitro-oxide nanocarbon. We then prepared DTX-loaded nanoliposomes (DTX-LPs) by the proliposome method. The physiochemical properties of DTX-AC-NPs and DTX-LPs were carefully evaluated in vitro. The metastatic lymph node uptake and the injection site retention were investigated by analyzing the DTX concentration in metastatic lymph nodes and injection sites. The result showed that DTX-AC-NPs and DTX-LPs with suitable and stable physicochemical properties could be used for in vivo lymph node targeting studies. DTX-AC-NPs significantly increased DTX-AUC(0–24) and prolonged DTX-retention in metastatic lymph nodes compared to DTX-LPs and non-modified activate carbon in vivo. This study demonstrated activated carbon nanoparticles may be potential intralymphatic drug delivery system to preferentially target regional metastatic lymph nodes.http://www.sciencedirect.com/science/article/pii/S1818087614000543Activated carbon nanoparticleNanoliposomeDocetaxelMetastatic lymph nodeLymph node targeting
spellingShingle Tiantian Ye
Wen Xu
Tianyu Shi
Rui Yang
Xinggang Yang
Shujun Wang
Weisan Pan
Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticles
Asian Journal of Pharmaceutical Sciences
Activated carbon nanoparticle
Nanoliposome
Docetaxel
Metastatic lymph node
Lymph node targeting
title Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticles
title_full Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticles
title_fullStr Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticles
title_full_unstemmed Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticles
title_short Targeted delivery of docetaxel to the metastatic lymph nodes: A comparison study between nanoliposomes and activated carbon nanoparticles
title_sort targeted delivery of docetaxel to the metastatic lymph nodes a comparison study between nanoliposomes and activated carbon nanoparticles
topic Activated carbon nanoparticle
Nanoliposome
Docetaxel
Metastatic lymph node
Lymph node targeting
url http://www.sciencedirect.com/science/article/pii/S1818087614000543
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