纳米晶载丹参酮IIA脂质体具有高载药量和稳定性,可有效逆转肝纤维化

IF 4.2 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Nanomedicine : nanotechnology, biology, and medicine Pub Date : 2024-11-27 DOI:10.1016/j.nano.2024.102797
Chunyan Cai BS , Kai Liu MMed , Dejun Yang BS , Jijiao Wu BS , Zhaolei Peng BS , Yulin Wang BS , Jingjing Xi BS , Fan Xie MMed , Xiaofang Li Ph.D
{"title":"纳米晶载丹参酮IIA脂质体具有高载药量和稳定性,可有效逆转肝纤维化","authors":"Chunyan Cai BS ,&nbsp;Kai Liu MMed ,&nbsp;Dejun Yang BS ,&nbsp;Jijiao Wu BS ,&nbsp;Zhaolei Peng BS ,&nbsp;Yulin Wang BS ,&nbsp;Jingjing Xi BS ,&nbsp;Fan Xie MMed ,&nbsp;Xiaofang Li Ph.D","doi":"10.1016/j.nano.2024.102797","DOIUrl":null,"url":null,"abstract":"<div><div>Tanshinone IIA (TSIIA) is a lipid-soluble pharmacological constituent extracted from the <em>Salvia miltiorrhiza</em> with anti-hepatic fibrosis properties. However, its clinical use has been limited due to its poor water solubility and oral bioavailability. In this paper, we constructed a drug delivery system consisting of a drug nanocrystal core and a liposome shell: TSIIA nanocrystals@liposome (TNC@Lipo). This combination can greatly improve the solubility and bioavailability of poorly water-soluble drugs. TNC@Lipo was prepared by ultrasonic method combined with antisolvent method. In order to obtain the optimal TNC, we optimized the formulation ratio and preparation process of TNC by single-factor experiments. The results showed that TNC@Lipo had higher drug loading (27.86 ± 1.55 %) and superior stability. And TNC@Lipo can significantly reversed CCl<sub>4</sub>-induced liver fibrosis in mice compared with free-TSIIA. In conclusion, this study provides a new approach for the clinical application of TSIIA.</div></div>","PeriodicalId":19050,"journal":{"name":"Nanomedicine : nanotechnology, biology, and medicine","volume":"63 ","pages":"Article 102797"},"PeriodicalIF":4.2000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The nanocrystal-loaded liposome of tanshinone IIA with high drug loading and stability towards efficient liver fibrosis reversion\",\"authors\":\"Chunyan Cai BS ,&nbsp;Kai Liu MMed ,&nbsp;Dejun Yang BS ,&nbsp;Jijiao Wu BS ,&nbsp;Zhaolei Peng BS ,&nbsp;Yulin Wang BS ,&nbsp;Jingjing Xi BS ,&nbsp;Fan Xie MMed ,&nbsp;Xiaofang Li Ph.D\",\"doi\":\"10.1016/j.nano.2024.102797\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Tanshinone IIA (TSIIA) is a lipid-soluble pharmacological constituent extracted from the <em>Salvia miltiorrhiza</em> with anti-hepatic fibrosis properties. However, its clinical use has been limited due to its poor water solubility and oral bioavailability. In this paper, we constructed a drug delivery system consisting of a drug nanocrystal core and a liposome shell: TSIIA nanocrystals@liposome (TNC@Lipo). This combination can greatly improve the solubility and bioavailability of poorly water-soluble drugs. TNC@Lipo was prepared by ultrasonic method combined with antisolvent method. In order to obtain the optimal TNC, we optimized the formulation ratio and preparation process of TNC by single-factor experiments. The results showed that TNC@Lipo had higher drug loading (27.86 ± 1.55 %) and superior stability. And TNC@Lipo can significantly reversed CCl<sub>4</sub>-induced liver fibrosis in mice compared with free-TSIIA. In conclusion, this study provides a new approach for the clinical application of TSIIA.</div></div>\",\"PeriodicalId\":19050,\"journal\":{\"name\":\"Nanomedicine : nanotechnology, biology, and medicine\",\"volume\":\"63 \",\"pages\":\"Article 102797\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-11-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nanomedicine : nanotechnology, biology, and medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1549963424000662\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanomedicine : nanotechnology, biology, and medicine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1549963424000662","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

摘要

丹参酮IIA (TSIIA)是从丹参中提取的一种具有抗肝纤维化特性的脂溶性药理成分。然而,由于其水溶性和口服生物利用度差,其临床应用受到限制。在本文中,我们构建了一个由药物纳米晶核和脂质体壳组成的药物传递系统:TSIIA nanocrystals@liposome (TNC@Lipo)。这种组合可以大大提高水溶性差的药物的溶解度和生物利用度。用超声波法结合抗溶剂法制备了TNC@Lipo。为了获得最佳的TNC,我们通过单因素实验优化了TNC的配方配比和制备工艺。结果表明,TNC@Lipo具有较高的载药量(27.86±1.55%)和较好的稳定性。与游离tsiia相比,TNC@Lipo能显著逆转ccl4诱导的小鼠肝纤维化。本研究为TSIIA的临床应用提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
The nanocrystal-loaded liposome of tanshinone IIA with high drug loading and stability towards efficient liver fibrosis reversion
Tanshinone IIA (TSIIA) is a lipid-soluble pharmacological constituent extracted from the Salvia miltiorrhiza with anti-hepatic fibrosis properties. However, its clinical use has been limited due to its poor water solubility and oral bioavailability. In this paper, we constructed a drug delivery system consisting of a drug nanocrystal core and a liposome shell: TSIIA nanocrystals@liposome (TNC@Lipo). This combination can greatly improve the solubility and bioavailability of poorly water-soluble drugs. TNC@Lipo was prepared by ultrasonic method combined with antisolvent method. In order to obtain the optimal TNC, we optimized the formulation ratio and preparation process of TNC by single-factor experiments. The results showed that TNC@Lipo had higher drug loading (27.86 ± 1.55 %) and superior stability. And TNC@Lipo can significantly reversed CCl4-induced liver fibrosis in mice compared with free-TSIIA. In conclusion, this study provides a new approach for the clinical application of TSIIA.
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
CiteScore
11.10
自引率
0.00%
发文量
133
审稿时长
42 days
期刊介绍: The mission of Nanomedicine: Nanotechnology, Biology, and Medicine (Nanomedicine: NBM) is to promote the emerging interdisciplinary field of nanomedicine. Nanomedicine: NBM is an international, peer-reviewed journal presenting novel, significant, and interdisciplinary theoretical and experimental results related to nanoscience and nanotechnology in the life and health sciences. Content includes basic, translational, and clinical research addressing diagnosis, treatment, monitoring, prediction, and prevention of diseases.
期刊最新文献
Determination diabetes mellitus disease markers in tear fluid by photothermal AFM-IR analysis Glutathione-responsive polypeptide nanogel encapsulates Shikonin for breast cancer therapy Exploiting novel placental homing peptides for targeted drug delivery in breast cancer Machine learning-driven Raman spectroscopy: A novel approach to lipid profiling in diabetic kidney disease Soluble microneedle acupuncture patches containing melittin liposomes for the percutaneous treatment of rheumatoid arthritis
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1