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Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles

Semiconductiong polymer nanoparticles (Pdots) have a wide range of applications in biomedical fields including biomolecular probes, tumor imaging, and therapy. However, there are few systematic studies on the biological effects and biocompatibility of Pdots in vitro and in vivo. The physicochemical...

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Autores principales: Guo, Wanni, Chen, Mingjian, Yang, Yuxin, Ge, Guili, Tang, Le, He, Shuyi, Zeng, Zhaoyang, Li, Xiaoling, Li, Guiyuan, Xiong, Wei, Wu, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003845/
https://www.ncbi.nlm.nih.gov/pubmed/36903280
http://dx.doi.org/10.3390/molecules28052034
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author Guo, Wanni
Chen, Mingjian
Yang, Yuxin
Ge, Guili
Tang, Le
He, Shuyi
Zeng, Zhaoyang
Li, Xiaoling
Li, Guiyuan
Xiong, Wei
Wu, Steven
author_facet Guo, Wanni
Chen, Mingjian
Yang, Yuxin
Ge, Guili
Tang, Le
He, Shuyi
Zeng, Zhaoyang
Li, Xiaoling
Li, Guiyuan
Xiong, Wei
Wu, Steven
author_sort Guo, Wanni
collection PubMed
description Semiconductiong polymer nanoparticles (Pdots) have a wide range of applications in biomedical fields including biomolecular probes, tumor imaging, and therapy. However, there are few systematic studies on the biological effects and biocompatibility of Pdots in vitro and in vivo. The physicochemical properties of Pdots, such as surface modification, are very important in biomedical applications. Focusing on the central issue of the biological effects of Pdots, we systematically investigated the biological effects and biocompatibility of Pdots with different surface modifications and revealed the interactions between Pdots and organisms at the cellular and animal levels. The surfaces of Pdots were modified with different functional groups, including thiol, carboxyl, and amino groups, named Pdots@SH, Pdots@COOH, and Pdots@NH(2), respectively. Extracellular studies showed that the modification of sulfhydryl, carboxyl, and amino groups had no significant effect on the physicochemical properties of Pdots, except that the amino modification affected the stability of Pdots to a certain extent. At the cellular level, Pdots@NH(2) reduced cellular uptake capacity and increased cytotoxicity due to their instability in solution. At the in vivo level, the body circulation and metabolic clearance of Pdots@SH and Pdots@COOH were superior to those of Pdots@NH(2). The four kinds of Pdots had no obvious effect on the blood indexes of mice and histopathological lesions in the main tissues and organs. This study provides important data for the biological effects and safety assessment of Pdots with different surface modifications, which pave the way for their potential biomedical applications.
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spelling pubmed-100038452023-03-11 Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles Guo, Wanni Chen, Mingjian Yang, Yuxin Ge, Guili Tang, Le He, Shuyi Zeng, Zhaoyang Li, Xiaoling Li, Guiyuan Xiong, Wei Wu, Steven Molecules Article Semiconductiong polymer nanoparticles (Pdots) have a wide range of applications in biomedical fields including biomolecular probes, tumor imaging, and therapy. However, there are few systematic studies on the biological effects and biocompatibility of Pdots in vitro and in vivo. The physicochemical properties of Pdots, such as surface modification, are very important in biomedical applications. Focusing on the central issue of the biological effects of Pdots, we systematically investigated the biological effects and biocompatibility of Pdots with different surface modifications and revealed the interactions between Pdots and organisms at the cellular and animal levels. The surfaces of Pdots were modified with different functional groups, including thiol, carboxyl, and amino groups, named Pdots@SH, Pdots@COOH, and Pdots@NH(2), respectively. Extracellular studies showed that the modification of sulfhydryl, carboxyl, and amino groups had no significant effect on the physicochemical properties of Pdots, except that the amino modification affected the stability of Pdots to a certain extent. At the cellular level, Pdots@NH(2) reduced cellular uptake capacity and increased cytotoxicity due to their instability in solution. At the in vivo level, the body circulation and metabolic clearance of Pdots@SH and Pdots@COOH were superior to those of Pdots@NH(2). The four kinds of Pdots had no obvious effect on the blood indexes of mice and histopathological lesions in the main tissues and organs. This study provides important data for the biological effects and safety assessment of Pdots with different surface modifications, which pave the way for their potential biomedical applications. MDPI 2023-02-21 /pmc/articles/PMC10003845/ /pubmed/36903280 http://dx.doi.org/10.3390/molecules28052034 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Guo, Wanni
Chen, Mingjian
Yang, Yuxin
Ge, Guili
Tang, Le
He, Shuyi
Zeng, Zhaoyang
Li, Xiaoling
Li, Guiyuan
Xiong, Wei
Wu, Steven
Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles
title Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles
title_full Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles
title_fullStr Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles
title_full_unstemmed Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles
title_short Biocompatibility and Biological Effects of Surface-Modified Conjugated Polymer Nanoparticles
title_sort biocompatibility and biological effects of surface-modified conjugated polymer nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003845/
https://www.ncbi.nlm.nih.gov/pubmed/36903280
http://dx.doi.org/10.3390/molecules28052034
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