The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles

Hongjun Gao,2# Jinjian Liu,1# Cuihong Yang,1 Tangjian Cheng,2 Liping Chu,1 Hongyan Xu,1 Aimin Meng,1 Saijun Fan,1 Linqi Shi,2 Jianfeng Liu11Tianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Science & Pekin...

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Autores principales: Gao H, Liu J, Yang C, Cheng T, Chu L, Xu H, Meng A, Fan S, Shi L
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Publicado: Dove Medical Press 2013
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spelling oai:doaj.org-article:18ecbfa10fb84ababef16ac8616d69fc2021-12-02T02:47:47ZThe impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles1176-91141178-2013https://doaj.org/article/18ecbfa10fb84ababef16ac8616d69fc2013-11-01T00:00:00Zhttp://www.dovepress.com/the-impact-of-pegylation-patterns-on-the-in-vivo-biodistribution-of-mi-a14877https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Hongjun Gao,2# Jinjian Liu,1# Cuihong Yang,1 Tangjian Cheng,2 Liping Chu,1 Hongyan Xu,1 Aimin Meng,1 Saijun Fan,1 Linqi Shi,2 Jianfeng Liu11Tianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Science & Peking Union Medical College, Tianjin, People's Republic of China; 2Key Laboratory of Functional Polymer Materials, Ministry of Education, and Institute of Polymer Chemistry, Nankai University, Tianjin, People’s Republic of China #These two authors contributed equally in the present workAbstract: Polyethylene glycol (PEG)-ylation is a widely used strategy to fabricate nanocarriers with a long blood circulation time. Further elaboration of the contribution of the surface PEGylation pattern to biodistribution is highly desirable. We fabricated a series of polyion complex (PIC) micelles PEGylated with different ratios (PEG2k and PEG550). The plasma protein adsorption, murine macrophage uptake, and in vivo biodistribution with iodine-125 as the tracer were systematically studied to elucidate the impact of PEGylation patterns on the biodistribution of micelles. We demonstrated that the PEGylated micelles with short hydrophilic PEG chains mixed on the surface were cleared quickly by the reticuloendothelial system (RES), and the single PEG2k PEGylated micelles could efficiently prolong the blood circulation time and increase their deposition in tumor sites. The present study extends the understanding of the PEGylation strategy to further advance the development of ideal nanocarriers for drug delivery and imaging applications.Keywords: drug delivery, PEGylation, mixed shell micelles, macrophage uptake, in vivo biodistributionGao HLiu JYang CCheng TChu LXu HMeng AFan SShi LLiu JDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2013, Iss Issue 1, Pp 4229-4246 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Gao H
Liu J
Yang C
Cheng T
Chu L
Xu H
Meng A
Fan S
Shi L
Liu J
The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles
description Hongjun Gao,2# Jinjian Liu,1# Cuihong Yang,1 Tangjian Cheng,2 Liping Chu,1 Hongyan Xu,1 Aimin Meng,1 Saijun Fan,1 Linqi Shi,2 Jianfeng Liu11Tianjin Key Laboratory of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Science & Peking Union Medical College, Tianjin, People's Republic of China; 2Key Laboratory of Functional Polymer Materials, Ministry of Education, and Institute of Polymer Chemistry, Nankai University, Tianjin, People’s Republic of China #These two authors contributed equally in the present workAbstract: Polyethylene glycol (PEG)-ylation is a widely used strategy to fabricate nanocarriers with a long blood circulation time. Further elaboration of the contribution of the surface PEGylation pattern to biodistribution is highly desirable. We fabricated a series of polyion complex (PIC) micelles PEGylated with different ratios (PEG2k and PEG550). The plasma protein adsorption, murine macrophage uptake, and in vivo biodistribution with iodine-125 as the tracer were systematically studied to elucidate the impact of PEGylation patterns on the biodistribution of micelles. We demonstrated that the PEGylated micelles with short hydrophilic PEG chains mixed on the surface were cleared quickly by the reticuloendothelial system (RES), and the single PEG2k PEGylated micelles could efficiently prolong the blood circulation time and increase their deposition in tumor sites. The present study extends the understanding of the PEGylation strategy to further advance the development of ideal nanocarriers for drug delivery and imaging applications.Keywords: drug delivery, PEGylation, mixed shell micelles, macrophage uptake, in vivo biodistribution
format article
author Gao H
Liu J
Yang C
Cheng T
Chu L
Xu H
Meng A
Fan S
Shi L
Liu J
author_facet Gao H
Liu J
Yang C
Cheng T
Chu L
Xu H
Meng A
Fan S
Shi L
Liu J
author_sort Gao H
title The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles
title_short The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles
title_full The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles
title_fullStr The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles
title_full_unstemmed The impact of PEGylation patterns on the in vivo biodistribution of mixed shell micelles
title_sort impact of pegylation patterns on the in vivo biodistribution of mixed shell micelles
publisher Dove Medical Press
publishDate 2013
url https://doaj.org/article/18ecbfa10fb84ababef16ac8616d69fc
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