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A tumor-targeted polymer theranostics platform for positron emission tomography and fluorescence imagingElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nr03306k
Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on 89 Zr-labeled N -(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates. A set of polymers differing in molecular weight with either low dispersity or high dispersity were des...
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creator | Koziolová, Eva Goel, Shreya Chytil, Petr Janoušková, Olga Barnhart, Todd E Cai, Weibo Etrych, Tomáš |
description | Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on
89
Zr-labeled
N
-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates. A set of polymers differing in molecular weight with either low dispersity or high dispersity were designed and synthesized and their biodistribution
in vivo
was successfully and precisely observed over 72 h. Moreover, the feasibility of two imaging techniques, fluorescence imaging (FI) and positron emission tomography (PET), was compared using labeled polymer conjugates. Both methods gave comparable results thus showing the enhanced diagnostic potential of the prepared polymer-dye or polymer-chelator-
89
Zr constructs. The
in vivo
and
ex vivo
PET/FI studies indicated that the dispersity and molecular weight of the linear HPMA polymers have a significant influence on the pharmacokinetics of the polymer conjugates. The higher molecular weight and narrower distribution of molecular weights of the polymer carriers improve their pharmacokinetic profile for highly prolonged blood circulation and enhanced tumor uptake. Moreover, the same polymer carrier with the anticancer drug doxorubicin bound by a pH-sensitive hydrazone bond showed higher cytotoxicity and cellular uptake
in vitro
. Therefore, HPMA copolymers with low dispersity and a molecular weight near the limit of renal filtration can be used as highly efficient polymer carriers of tumor-targeted therapeutics or for theranostics with minimal side effects.
Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on
89
Zr-labeled
N
-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates. |
doi_str_mv | 10.1039/c7nr03306k |
format | article |
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89
Zr-labeled
N
-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates. A set of polymers differing in molecular weight with either low dispersity or high dispersity were designed and synthesized and their biodistribution
in vivo
was successfully and precisely observed over 72 h. Moreover, the feasibility of two imaging techniques, fluorescence imaging (FI) and positron emission tomography (PET), was compared using labeled polymer conjugates. Both methods gave comparable results thus showing the enhanced diagnostic potential of the prepared polymer-dye or polymer-chelator-
89
Zr constructs. The
in vivo
and
ex vivo
PET/FI studies indicated that the dispersity and molecular weight of the linear HPMA polymers have a significant influence on the pharmacokinetics of the polymer conjugates. The higher molecular weight and narrower distribution of molecular weights of the polymer carriers improve their pharmacokinetic profile for highly prolonged blood circulation and enhanced tumor uptake. Moreover, the same polymer carrier with the anticancer drug doxorubicin bound by a pH-sensitive hydrazone bond showed higher cytotoxicity and cellular uptake
in vitro
. Therefore, HPMA copolymers with low dispersity and a molecular weight near the limit of renal filtration can be used as highly efficient polymer carriers of tumor-targeted therapeutics or for theranostics with minimal side effects.
Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on
89
Zr-labeled
N
-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates.</description><identifier>ISSN: 2040-3364</identifier><identifier>EISSN: 2040-3372</identifier><identifier>DOI: 10.1039/c7nr03306k</identifier><language>eng</language><creationdate>2017-08</creationdate><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Koziolová, Eva</creatorcontrib><creatorcontrib>Goel, Shreya</creatorcontrib><creatorcontrib>Chytil, Petr</creatorcontrib><creatorcontrib>Janoušková, Olga</creatorcontrib><creatorcontrib>Barnhart, Todd E</creatorcontrib><creatorcontrib>Cai, Weibo</creatorcontrib><creatorcontrib>Etrych, Tomáš</creatorcontrib><title>A tumor-targeted polymer theranostics platform for positron emission tomography and fluorescence imagingElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nr03306k</title><description>Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on
89
Zr-labeled
N
-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates. A set of polymers differing in molecular weight with either low dispersity or high dispersity were designed and synthesized and their biodistribution
in vivo
was successfully and precisely observed over 72 h. Moreover, the feasibility of two imaging techniques, fluorescence imaging (FI) and positron emission tomography (PET), was compared using labeled polymer conjugates. Both methods gave comparable results thus showing the enhanced diagnostic potential of the prepared polymer-dye or polymer-chelator-
89
Zr constructs. The
in vivo
and
ex vivo
PET/FI studies indicated that the dispersity and molecular weight of the linear HPMA polymers have a significant influence on the pharmacokinetics of the polymer conjugates. The higher molecular weight and narrower distribution of molecular weights of the polymer carriers improve their pharmacokinetic profile for highly prolonged blood circulation and enhanced tumor uptake. Moreover, the same polymer carrier with the anticancer drug doxorubicin bound by a pH-sensitive hydrazone bond showed higher cytotoxicity and cellular uptake
in vitro
. Therefore, HPMA copolymers with low dispersity and a molecular weight near the limit of renal filtration can be used as highly efficient polymer carriers of tumor-targeted therapeutics or for theranostics with minimal side effects.
Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on
89
Zr-labeled
N
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89
Zr-labeled
N
-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates. A set of polymers differing in molecular weight with either low dispersity or high dispersity were designed and synthesized and their biodistribution
in vivo
was successfully and precisely observed over 72 h. Moreover, the feasibility of two imaging techniques, fluorescence imaging (FI) and positron emission tomography (PET), was compared using labeled polymer conjugates. Both methods gave comparable results thus showing the enhanced diagnostic potential of the prepared polymer-dye or polymer-chelator-
89
Zr constructs. The
in vivo
and
ex vivo
PET/FI studies indicated that the dispersity and molecular weight of the linear HPMA polymers have a significant influence on the pharmacokinetics of the polymer conjugates. The higher molecular weight and narrower distribution of molecular weights of the polymer carriers improve their pharmacokinetic profile for highly prolonged blood circulation and enhanced tumor uptake. Moreover, the same polymer carrier with the anticancer drug doxorubicin bound by a pH-sensitive hydrazone bond showed higher cytotoxicity and cellular uptake
in vitro
. Therefore, HPMA copolymers with low dispersity and a molecular weight near the limit of renal filtration can be used as highly efficient polymer carriers of tumor-targeted therapeutics or for theranostics with minimal side effects.
Here, we describe a novel polymer platform suitable for efficient diagnostics and potential theranostics based on
89
Zr-labeled
N
-(2-hydroxypropyl)methacrylamide (HPMA)-based copolymer conjugates.</abstract><doi>10.1039/c7nr03306k</doi><tpages>13</tpages></addata></record> |
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
title | A tumor-targeted polymer theranostics platform for positron emission tomography and fluorescence imagingElectronic supplementary information (ESI) available. See DOI: 10.1039/c7nr03306k |
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