• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

硒化镉量子点的生物积累对 Wistar 大鼠的生化和氧化损伤。

Bioaccumulation of CdSe Quantum Dots Show Biochemical and Oxidative Damage in Wistar Rats.

机构信息

Shaheed Rajguru College of Applied Sciences for Women, University of Delhi, New Delhi, India.

School of Physical Sciences, Jawaharlal Nehru University, New Delhi, India.

出版信息

Oxid Med Cell Longev. 2023 Apr 6;2023:7707452. doi: 10.1155/2023/7707452. eCollection 2023.

DOI:10.1155/2023/7707452
PMID:37064800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10101743/
Abstract

Cadmium selenium quantum dots (CdSe QDs) with modified surfaces exhibit superior dispersion stability and high fluorescence yield, making them desirable biological probes. The knowledge of cellular and biochemical toxicity has been lacking, and there is little information on the correlation between and data. The current study was carried out to assess the toxicity of CdSe QDs after intravenous injection in Wistar male rats (230 g). The rats were given a single dose of QDs of 10, 20, 40, and 80 mg/kg and were kept for 30 days. Following that, various biochemical assays, hematological parameters, and bioaccumulation studies were carried out. Functional as well as clinically significant changes were observed. There was a significant increase in WBC while the RBC decreased. This suggested that CdSe quantum dots had inflammatory effects on the treated rats. The various biochemical assays clearly showed that high dose induced hepatic injury. At a dose of 80 mg/kg, bioaccumulation studies revealed that the spleen (120 g/g), liver (78 g/g), and lungs (38 g/g) accumulated the most. In treated Wistar rats, the bioretention profile of QDs was in the following order: the spleen, liver, kidney, lungs, heart, brain, and testis. The accumulation of these QDs induced the generation of intracellular reactive oxygen species, resulting in an alteration in antioxidant activity. It is concluded that these QDs caused oxidative stress, which harmed cellular functions and, under certain conditions, caused partial brain, kidney, spleen, and liver dysfunction. This is one of the most comprehensive studies on the nanotoxicity of CdSe quantum dots.

摘要

镉硒量子点(CdSe QDs)经过表面修饰后,表现出卓越的分散稳定性和高荧光产率,是理想的生物探针。然而,关于其细胞和生化毒性的认识还很缺乏,并且关于与毒性数据的相关性的信息也很少。本研究旨在评估静脉注射 Wistar 雄性大鼠(230g)后 CdSe QDs 的毒性。大鼠单次给予 10、20、40 和 80mg/kg 的 QDs,并饲养 30 天。之后,进行了各种生化分析、血液学参数和生物累积研究。结果观察到了功能和临床相关的变化。白细胞计数显著增加,而红细胞计数减少。这表明 CdSe 量子点对处理后的大鼠具有炎症作用。各种生化分析清楚地表明,高剂量会导致肝损伤。在 80mg/kg 剂量下,生物累积研究表明脾脏(120g/g)、肝脏(78g/g)和肺部(38g/g)积累最多。在处理过的 Wistar 大鼠中,QDs 的生物保留特征如下:脾脏、肝脏、肾脏、肺部、心脏、大脑和睾丸。这些 QDs 的积累诱导了细胞内活性氧的产生,导致抗氧化活性发生改变。结论是,这些 QDs 引起了氧化应激,损害了细胞功能,在某些情况下导致了部分脑、肾、脾和肝功能障碍。这是关于 CdSe 量子点纳米毒性的最全面的研究之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/a4d49739e1f9/OMCL2023-7707452.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/77409f4a7696/OMCL2023-7707452.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/05aa13c78e0b/OMCL2023-7707452.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/b1f7484da559/OMCL2023-7707452.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/b80c2cc113fd/OMCL2023-7707452.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/dde11fc35a65/OMCL2023-7707452.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/4146fe1755d4/OMCL2023-7707452.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/d973092b5bcb/OMCL2023-7707452.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/a4d49739e1f9/OMCL2023-7707452.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/77409f4a7696/OMCL2023-7707452.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/05aa13c78e0b/OMCL2023-7707452.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/b1f7484da559/OMCL2023-7707452.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/b80c2cc113fd/OMCL2023-7707452.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/dde11fc35a65/OMCL2023-7707452.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/4146fe1755d4/OMCL2023-7707452.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/d973092b5bcb/OMCL2023-7707452.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/855a/10101743/a4d49739e1f9/OMCL2023-7707452.008.jpg

相似文献

1
Bioaccumulation of CdSe Quantum Dots Show Biochemical and Oxidative Damage in Wistar Rats.硒化镉量子点的生物积累对 Wistar 大鼠的生化和氧化损伤。
Oxid Med Cell Longev. 2023 Apr 6;2023:7707452. doi: 10.1155/2023/7707452. eCollection 2023.
2
CdSe/ZnS quantum dots exhibited nephrotoxicity through mediating oxidative damage and inflammatory response.硒化镉/硫化锌量子点通过介导氧化损伤和炎症反应表现出肾毒性。
Aging (Albany NY). 2020 Nov 16;13(8):12194-12206. doi: 10.18632/aging.103774.
3
The cytotoxicities in prokaryote and eukaryote varied for CdSe and CdSe/ZnS quantum dots and differed from cadmium ions.CdSe 和 CdSe/ZnS 量子点对原核生物和真核生物的细胞毒性与镉离子不同。
Ecotoxicol Environ Saf. 2019 Oct 15;181:336-344. doi: 10.1016/j.ecoenv.2019.06.027. Epub 2019 Jun 13.
4
Acute toxicity and tissue distribution of CdSe/CdS-MPA quantum dots after repeated intraperitoneal injection to mice.CdSe/CdS-MPA 量子点经腹腔重复注射后小鼠的急性毒性和组织分布。
J Appl Toxicol. 2013 Sep;33(9):940-50. doi: 10.1002/jat.2775. Epub 2012 Jun 25.
5
Transcriptome Profile Alteration with Cadmium Selenide/Zinc Sulfide Quantum Dots in .硒化镉/硫化锌量子点对 . 的转录组谱改变
Biomolecules. 2019 Oct 25;9(11):653. doi: 10.3390/biom9110653.
6
Genotoxicity of intraperitoneal injection of lipoamphiphile CdSe/ZnS quantum dots in rats.大鼠腹腔注射脂溶性CdSe/ZnS量子点的遗传毒性
Mutat Res Genet Toxicol Environ Mutagen. 2013 Dec 12;758(1-2):48-55. doi: 10.1016/j.mrgentox.2013.09.004. Epub 2013 Sep 20.
7
Toxicity assessment of repeated intravenous injections of arginine-glycine-aspartic acid peptide conjugated CdSeTe/ZnS quantum dots in mice.小鼠重复静脉注射精氨酸-甘氨酸-天冬氨酸肽偶联的CdSeTe/ZnS量子点的毒性评估
Int J Nanomedicine. 2014 Oct 17;9:4809-17. doi: 10.2147/IJN.S70092. eCollection 2014.
8
The interactions between CdSe quantum dots and yeast Saccharomyces cerevisiae: adhesion of quantum dots to the cell surface and the protection effect of ZnS shell.硒化镉量子点与酿酒酵母的相互作用:量子点与细胞表面的黏附及硫化锌壳的保护作用。
Chemosphere. 2014 Oct;112:92-9. doi: 10.1016/j.chemosphere.2014.03.071. Epub 2014 Apr 21.
9
Systematic evaluation of CdSe/ZnS quantum dots toxicity on the reproduction and offspring health in male BALB/c mice.系统评价 CdSe/ZnS 量子点对雄性 BALB/c 小鼠生殖及子代健康的毒性。
Ecotoxicol Environ Saf. 2021 Mar 15;211:111946. doi: 10.1016/j.ecoenv.2021.111946. Epub 2021 Jan 25.
10
Effects of CdSe and CdSe/ZnS Core/Shell Quantum Dots on Singlet Oxygen Production and Cell Toxicity.CdSe和CdSe/ZnS核壳量子点对单线态氧生成及细胞毒性的影响
J Nanosci Nanotechnol. 2018 Mar 1;18(3):1568-1576. doi: 10.1166/jnn.2018.15305.

引用本文的文献

1
Natural biomass-derived carbon quantum dots: a path to antioxidant, anticancer, antibiofilm, and bacterial bioimaging potential.天然生物质衍生的碳量子点:通往抗氧化、抗癌、抗生物膜及细菌生物成像潜力之路。
Mikrochim Acta. 2025 Apr 8;192(5):286. doi: 10.1007/s00604-025-07132-x.
2
Exploring In Vivo Pulmonary and Splenic Toxicity Profiles of Silicon Quantum Dots in Mice.探索硅量子点在小鼠体内的肺和脾毒性特征
Materials (Basel). 2024 Jun 6;17(11):2778. doi: 10.3390/ma17112778.
3
In Vivo Assessment of Hepatic and Kidney Toxicity Induced by Silicon Quantum Dots in Mice.

本文引用的文献

1
ZnO Quantum Dots Induced Oxidative Stress and Apoptosis in HeLa and HEK-293T Cell Lines.氧化锌量子点诱导HeLa和HEK-293T细胞系的氧化应激和细胞凋亡。
Front Pharmacol. 2020 Feb 27;11:131. doi: 10.3389/fphar.2020.00131. eCollection 2020.
2
Biodistribution, Clearance And Morphological Alterations Of Intravenously Administered Iron Oxide Nanoparticles In Male Wistar Rats.静脉注射氧化铁纳米颗粒在雄性 Wistar 大鼠体内的分布、清除和形态学改变。
Int J Nanomedicine. 2019 Dec 6;14:9677-9692. doi: 10.2147/IJN.S223142. eCollection 2019.
3
Probing the Cytotoxicity Of Semiconductor Quantum Dots.
硅量子点对小鼠肝肾毒性的体内评估
Nanomaterials (Basel). 2024 Mar 1;14(5):457. doi: 10.3390/nano14050457.
4
A Review of in vivo Toxicity of Quantum Dots in Animal Models.量子点在动物模型体内毒性的综述。
Int J Nanomedicine. 2023 Dec 29;18:8143-8168. doi: 10.2147/IJN.S434842. eCollection 2023.
5
Exploring the potential and safety of quantum dots in allergy diagnostics.探索量子点在过敏诊断中的潜力与安全性。
Microsyst Nanoeng. 2023 Nov 17;9:145. doi: 10.1038/s41378-023-00608-x. eCollection 2023.
探究半导体量子点的细胞毒性
Nano Lett. 2004 Jan 1;4(1):11-18. doi: 10.1021/nl0347334. Epub 2003 Dec 10.
4
Gold nanoparticles: Distribution, bioaccumulation and toxicity. In vitro and in vivo studies.金纳米粒子:分布、生物蓄积和毒性。体外和体内研究。
Nanomedicine. 2018 Jan;14(1):1-12. doi: 10.1016/j.nano.2017.08.011. Epub 2017 Sep 4.
5
Iron oxide nanoparticles induced cytotoxicity, oxidative stress and DNA damage in lymphocytes.氧化铁纳米颗粒诱导淋巴细胞细胞毒性、氧化应激和 DNA 损伤。
J Appl Toxicol. 2017 Oct;37(10):1232-1244. doi: 10.1002/jat.3485. Epub 2017 Jun 6.
6
Hemorheological characteristics of red blood cells exposed to surface functionalized graphene quantum dots.暴露于表面功能化石墨烯量子点的红细胞的血液流变学特性
Food Chem Toxicol. 2016 Nov;97:346-353. doi: 10.1016/j.fct.2016.09.034. Epub 2016 Oct 1.
7
Time-dependent biodistribution and excretion of silver nanoparticles in male Wistar rats.银纳米颗粒在雄性 Wistar 大鼠体内的时相分布和排泄。
J Appl Toxicol. 2012 Nov;32(11):920-8. doi: 10.1002/jat.2758. Epub 2012 Jun 13.
8
In vivo clearance and toxicity of monodisperse iron oxide nanocrystals.体内单分散氧化铁纳米晶体的清除和毒性。
ACS Nano. 2012 Jun 26;6(6):4947-54. doi: 10.1021/nn300456z. Epub 2012 Jun 5.
9
Nano-TiO2-induced apoptosis by oxidative stress-mediated DNA damage and activation of p53 in human embryonic kidney cells.纳米二氧化钛通过氧化应激介导的 DNA 损伤和 p53 的激活诱导人胚肾细胞凋亡。
Appl Biochem Biotechnol. 2012 Jun;167(4):791-808. doi: 10.1007/s12010-012-9699-3. Epub 2012 May 22.
10
DNA damage caused by metal nanoparticles: involvement of oxidative stress and activation of ATM.金属纳米颗粒引起的 DNA 损伤:氧化应激的参与和 ATM 的激活。
Chem Res Toxicol. 2012 Jul 16;25(7):1402-11. doi: 10.1021/tx200513t. Epub 2012 May 14.