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聚合物量子点对怀孕小鼠和胎儿的生物相容性研究。

The biocompatibility studies of polymer dots on pregnant mice and fetuses.

作者信息

Wu Na, Zhang Zheng, Zhou Jie, Sun Zezhou, Deng Yueyue, Lin Guimiao, Ying Ming, Wang Xiaomei, Yong Ken-Tye, Wu Changfeng, Xu Gaixia

机构信息

Key laboratory of Optoelectronic Devices and System of The Ministry of Education/Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen Guangdong Province 518060, China.

State key laboratory on integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University Changchun, Jinlin 130012, China.

出版信息

Nanotheranostics. 2017 Jun 9;1(3):261-271. doi: 10.7150/ntno.18964. eCollection 2017.

DOI:10.7150/ntno.18964
PMID:29071192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5646735/
Abstract

Semiconducting polymer dots (Pdots) are small nanoparticles consisting primarily of fluorescent pi-conjugated polymers which show superior optical properties for biological imaging and biosensors. It is necessary to explore systematically the toxicity of Pdots on animals before extensive biomedical applications. The reproductive system is very sensitive to the external invasion and essential for species reproduction as well. In this work, we used the pregnant mice to investigate the reproductive toxicity of Pdots. The changes in body weight of each maternal mouse were recorded every two days. The main organs were collected and analyzed as soon as all the pregnant mice were sacrificed on the 15 embryonic day. Distributions of Pdots on maternal major organs and tissues were examined in frozen tissue sections. Hematoxylin and eosin (H&E) staining was performed to investigate the histopathological changes of maternal organs. The blood chemistry test was applied to study the effects of Pdots on organ functions. Female hormones were evaluated by immunoassays. The amniotic fluid was inspected for assessing their penetration ability of Pdots. Levels of placenta growth related factors were detected by RT-PCR to evaluate the function of placenta. These results showed that Pdots were mainly accumulated in liver and spleen, and no apparent impact was observed on maternal body weight and organs coefficients. Histopathological images also showed normal tissue morphology compared with the untreated group. The female hormones levels did not show significant difference among the three groups as well. Trace amount of Pdots could get into the amniotic fluid but did not change the placental functions and the early development of fetus. Our results demonstrated that Pdots have excellent biocompatibility and no reproductive toxicity under the dosages used in this work, which means that Pdots have great potential in preclinical applications in the future.

摘要

半导体聚合物点(Pdots)是主要由荧光π共轭聚合物组成的小纳米颗粒,在生物成像和生物传感器方面表现出优异的光学特性。在广泛的生物医学应用之前,有必要系统地探索Pdots对动物的毒性。生殖系统对外来入侵非常敏感,对物种繁殖也至关重要。在这项工作中,我们使用怀孕小鼠来研究Pdots的生殖毒性。每两天记录每只母鼠的体重变化。在胚胎第15天处死所有怀孕小鼠后,立即收集并分析主要器官。在冷冻组织切片中检查Pdots在母鼠主要器官和组织上的分布。进行苏木精和伊红(H&E)染色以研究母鼠器官的组织病理学变化。应用血液化学检测来研究Pdots对器官功能的影响。通过免疫测定评估雌性激素。检查羊水以评估Pdots的渗透能力。通过RT-PCR检测胎盘生长相关因子的水平以评估胎盘的功能。这些结果表明,Pdots主要积聚在肝脏和脾脏中,对母鼠体重和器官系数未观察到明显影响。组织病理学图像也显示与未处理组相比组织形态正常。三组之间的雌性激素水平也没有显著差异。微量的Pdots可以进入羊水,但不会改变胎盘功能和胎儿的早期发育。我们的结果表明,在本工作所用剂量下,Pdots具有优异的生物相容性且无生殖毒性,这意味着Pdots在未来的临床前应用中具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/af6db828e529/ntnov01p0261g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/917f27444782/ntnov01p0261g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/757debe7dba9/ntnov01p0261g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/d84357851169/ntnov01p0261g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/3000e6feb0e2/ntnov01p0261g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/41b5785d2220/ntnov01p0261g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/fd9bc72d7f72/ntnov01p0261g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/af6db828e529/ntnov01p0261g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/917f27444782/ntnov01p0261g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/757debe7dba9/ntnov01p0261g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/d84357851169/ntnov01p0261g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/3000e6feb0e2/ntnov01p0261g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/41b5785d2220/ntnov01p0261g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/fd9bc72d7f72/ntnov01p0261g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44b1/5646735/af6db828e529/ntnov01p0261g007.jpg

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