Cargando…
In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice
The boron nitride (BN) nanoparticles, as the structural analogues of graphene, are the potential biomedicine materials because of the excellent biocompatibility, but their solubility and biosafety are the biggest obstacle for the clinic application. Here, we first synthesized the highly soluble BN n...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675755/ https://www.ncbi.nlm.nih.gov/pubmed/26659609 http://dx.doi.org/10.1186/s11671-015-1172-0 |
_version_ | 1782405053908254720 |
---|---|
author | Liu, Bo Qi, Wei Tian, Longlong Li, Zhan Miao, Guoying An, Wenzhen Liu, Dan Lin, Jing Zhang, Xiaoyong Wu, Wangsuo |
author_facet | Liu, Bo Qi, Wei Tian, Longlong Li, Zhan Miao, Guoying An, Wenzhen Liu, Dan Lin, Jing Zhang, Xiaoyong Wu, Wangsuo |
author_sort | Liu, Bo |
collection | PubMed |
description | The boron nitride (BN) nanoparticles, as the structural analogues of graphene, are the potential biomedicine materials because of the excellent biocompatibility, but their solubility and biosafety are the biggest obstacle for the clinic application. Here, we first synthesized the highly soluble BN nanoparticles coated by PEG (BN-PEG) with smaller size (~10 nm), then studied their biodistribution in vivo through radioisotope (Tc(99m)O(4)(−)) labeling, and the results showed that BN-PEG nanoparticles mainly accumulated in the liver, lung, and spleen with the less uptake by the brain. Moreover, the pathological changes induced by BN-PEG could be significantly observed in the sections of the liver, lung, spleen, and heart, which can be also supported by the test of biochemical indexes in serum. More importantly, we first observed the biodistribution of BN-PEG in the heart tissues with high toxicity, which would give a warning about the cardiovascular disease, and provide some opportunities for the drug delivery and treatment. |
format | Online Article Text |
id | pubmed-4675755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-46757552015-12-20 In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice Liu, Bo Qi, Wei Tian, Longlong Li, Zhan Miao, Guoying An, Wenzhen Liu, Dan Lin, Jing Zhang, Xiaoyong Wu, Wangsuo Nanoscale Res Lett Nano Express The boron nitride (BN) nanoparticles, as the structural analogues of graphene, are the potential biomedicine materials because of the excellent biocompatibility, but their solubility and biosafety are the biggest obstacle for the clinic application. Here, we first synthesized the highly soluble BN nanoparticles coated by PEG (BN-PEG) with smaller size (~10 nm), then studied their biodistribution in vivo through radioisotope (Tc(99m)O(4)(−)) labeling, and the results showed that BN-PEG nanoparticles mainly accumulated in the liver, lung, and spleen with the less uptake by the brain. Moreover, the pathological changes induced by BN-PEG could be significantly observed in the sections of the liver, lung, spleen, and heart, which can be also supported by the test of biochemical indexes in serum. More importantly, we first observed the biodistribution of BN-PEG in the heart tissues with high toxicity, which would give a warning about the cardiovascular disease, and provide some opportunities for the drug delivery and treatment. Springer US 2015-12-10 /pmc/articles/PMC4675755/ /pubmed/26659609 http://dx.doi.org/10.1186/s11671-015-1172-0 Text en © Liu et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Nano Express Liu, Bo Qi, Wei Tian, Longlong Li, Zhan Miao, Guoying An, Wenzhen Liu, Dan Lin, Jing Zhang, Xiaoyong Wu, Wangsuo In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice |
title | In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice |
title_full | In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice |
title_fullStr | In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice |
title_full_unstemmed | In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice |
title_short | In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice |
title_sort | in vivo biodistribution and toxicity of highly soluble peg-coated boron nitride in mice |
topic | Nano Express |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675755/ https://www.ncbi.nlm.nih.gov/pubmed/26659609 http://dx.doi.org/10.1186/s11671-015-1172-0 |
work_keys_str_mv | AT liubo invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT qiwei invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT tianlonglong invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT lizhan invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT miaoguoying invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT anwenzhen invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT liudan invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT linjing invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT zhangxiaoyong invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice AT wuwangsuo invivobiodistributionandtoxicityofhighlysolublepegcoatedboronnitrideinmice |