E-Lip-siRNA-sFlt1 对先兆子痫的治疗效果:靶向基因沉默和改善妊娠结局。

Nanomedicine (London, England) Pub Date : 2024-01-01 Epub Date: 2024-07-17 DOI:10.1080/17435889.2024.2368449
Jinhua Dong, Yingying Zhang, Jingsheng Zhou, Shuhui Mao, Jianfen Tang, Suping Li, Qiang Ma, Ling Ai, Wei Wang, Guanghao Zhu, Huijing Shao, Yingdi Meng, Huaiwen Chen, Danqing Chen
{"title":"E-Lip-siRNA-sFlt1 对先兆子痫的治疗效果:靶向基因沉默和改善妊娠结局。","authors":"Jinhua Dong, Yingying Zhang, Jingsheng Zhou, Shuhui Mao, Jianfen Tang, Suping Li, Qiang Ma, Ling Ai, Wei Wang, Guanghao Zhu, Huijing Shao, Yingdi Meng, Huaiwen Chen, Danqing Chen","doi":"10.1080/17435889.2024.2368449","DOIUrl":null,"url":null,"abstract":"<p><p><b>Aim:</b> To evaluate a liposome complex conjugated with anti-epidermal growth factor receptor (EGFR) antibodies for the treatment of pre-eclampsia (PE).<b>Methods:</b> In <i>in vitro</i> experiments, the transfection rate, silencing effect and cytotoxicity were determined. In the <i>in vivo</i> PE model, the siRNA distribution, mean arterial pressure, 24-h urine protein concentration, serum sFlt1 concentration, number of viable fetuses and placental weight were measured.<b>Results:</b> The nanomedicine effectively reduced the expression of sFIt1 and had a strong ability to target placental tissues. It could significantly reduce the symptoms of pre-eclampsia and improve pregnancy outcomes in PE model rats.<b>Conclusion:</b> The constructed nanomedicine can improve pregnancy outcomes in a rat model of pre-eclampsia and provides a new strategy for the treatment of pre-eclampsia.</p>","PeriodicalId":74240,"journal":{"name":"Nanomedicine (London, England)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11389737/pdf/","citationCount":"0","resultStr":"{\"title\":\"Therapeutic effect of E-Lip-siRNA-sFlt1 on pre-eclampsia: targeted gene silencing and improved pregnancy outcomes.\",\"authors\":\"Jinhua Dong, Yingying Zhang, Jingsheng Zhou, Shuhui Mao, Jianfen Tang, Suping Li, Qiang Ma, Ling Ai, Wei Wang, Guanghao Zhu, Huijing Shao, Yingdi Meng, Huaiwen Chen, Danqing Chen\",\"doi\":\"10.1080/17435889.2024.2368449\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Aim:</b> To evaluate a liposome complex conjugated with anti-epidermal growth factor receptor (EGFR) antibodies for the treatment of pre-eclampsia (PE).<b>Methods:</b> In <i>in vitro</i> experiments, the transfection rate, silencing effect and cytotoxicity were determined. In the <i>in vivo</i> PE model, the siRNA distribution, mean arterial pressure, 24-h urine protein concentration, serum sFlt1 concentration, number of viable fetuses and placental weight were measured.<b>Results:</b> The nanomedicine effectively reduced the expression of sFIt1 and had a strong ability to target placental tissues. It could significantly reduce the symptoms of pre-eclampsia and improve pregnancy outcomes in PE model rats.<b>Conclusion:</b> The constructed nanomedicine can improve pregnancy outcomes in a rat model of pre-eclampsia and provides a new strategy for the treatment of pre-eclampsia.</p>\",\"PeriodicalId\":74240,\"journal\":{\"name\":\"Nanomedicine (London, England)\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11389737/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanomedicine (London, England)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/17435889.2024.2368449\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanomedicine (London, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/17435889.2024.2368449","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/17 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的:评估一种与抗表皮生长因子受体(EGFR)抗体结合的脂质体复合物用于治疗子痫前期(PE)的效果。研究方法:在体外实验中,研究人员对脂质体复合物与抗表皮生长因子受体(EGFR)抗体的结合率进行了评估:在体外实验中,测定转染率、沉默效果和细胞毒性。在体内子痫模型中,测定 siRNA 分布、平均动脉压、24 小时尿蛋白浓度、血清 sFlt1 浓度、存活胎儿数和胎盘重量。结果显示纳米药物有效降低了 sFIt1 的表达,并具有很强的靶向胎盘组织的能力。它能明显减轻子痫前期症状,改善 PE 模型大鼠的妊娠结局。结论所构建的纳米药物可改善子痫前期模型大鼠的妊娠结局,为治疗子痫前期提供了一种新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic effect of E-Lip-siRNA-sFlt1 on pre-eclampsia: targeted gene silencing and improved pregnancy outcomes.

Aim: To evaluate a liposome complex conjugated with anti-epidermal growth factor receptor (EGFR) antibodies for the treatment of pre-eclampsia (PE).Methods: In in vitro experiments, the transfection rate, silencing effect and cytotoxicity were determined. In the in vivo PE model, the siRNA distribution, mean arterial pressure, 24-h urine protein concentration, serum sFlt1 concentration, number of viable fetuses and placental weight were measured.Results: The nanomedicine effectively reduced the expression of sFIt1 and had a strong ability to target placental tissues. It could significantly reduce the symptoms of pre-eclampsia and improve pregnancy outcomes in PE model rats.Conclusion: The constructed nanomedicine can improve pregnancy outcomes in a rat model of pre-eclampsia and provides a new strategy for the treatment of pre-eclampsia.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信