Glycyrrhizic Acid-Based Liposome for Tumor-Targeted Delivery of Cantharidin

CTD公司 毒性 斑蝥素 脂质体 药物输送 内吞作用 化学 药理学 医学 受体 生物化学 海洋学 有机化学 地质学
作者
Yuxiang Wang,Wen‐Zhen Wang,Hailu Yao,Jingjing Wang,Fenghe Yang,Yu Zhang,Guanhua Du,Guang Han
出处
期刊:ACS applied nano materials [American Chemical Society]
卷期号:7 (1): 1030-1044 被引量:8
标识
DOI:10.1021/acsanm.3c05019
摘要

Cantharidin (CTD), an effective ingredient derived from poisonous traditional Chinese medicine Mylabris, shows unique efficacy against hepatocellular carcinoma (HCC), but severe toxicity hinders its clinical application. Liposomes (LPs) are considered to be a platform for the effective delivery of chemotherapeutic agents. Nevertheless, the application of cholesterol, which is usually used to stabilize the structure of LPs, has been compromised due to various drawbacks. Glycyrrhizic acid (GA) has the ability to improve the properties of the phospholipid bilayer in addition to its targeting and hepatoprotective effects. Here, we develop a GA LP loaded with CTD (CTD–GA–LP) utilizing GA as a cholesterol replacement to effectively overcome the obstacles faced by common LPs and to enhance the efficacy of CTD and reduce its toxicity. In the study, CTD–GA–LP was prepared by the ethanol injection method and comprised a homogeneous spherical shape with an evenly distributed particle size, showing a particle size and polydispersity index of 76.12 ± 4.01 nm and 0.18 ± 0.02, respectively. CTD–GA–LP exhibited a better drug loading capacity and stability than CTD–C–LP. An in vitro study showed that CTD–GA–LP can selectively target tumor cells and significantly improve cellular absorption by the GA-receptor-mediated endocytosis pathway to achieve active targeted delivery of drugs. Compared with CTD–C–LP, CTD–GA–LP exhibited notably higher toxicity to the growth of HepG2 cells and low toxicity to L-02 hepatocytes. Using a H22 tumor-bearing mice model, CTD–GA–LP was proved to be able to promote the accumulation of CTD in the tumor tissue and possessed the most pronounced tumor inhibitory rate. Also, CTD–GA–LP reduced the accumulation of CTD in normal organs and prolonged the survival time of tumor-bearing mice. In conclusion, CTD–GA–LP provides an attractive and potential strategy for the treatment of HCC and is very useful for improving the effectiveness and safety of CTD.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
onessscan完成签到,获得积分10
1秒前
甜梨完成签到 ,获得积分10
1秒前
parny完成签到 ,获得积分10
2秒前
大糖糕僧完成签到,获得积分10
2秒前
无情的聪健应助Tail采纳,获得20
2秒前
2秒前
未顾完成签到,获得积分10
2秒前
要减肥的湘云完成签到,获得积分10
3秒前
liu完成签到,获得积分10
3秒前
nuantong1shy完成签到,获得积分10
3秒前
xiaoyi完成签到,获得积分10
3秒前
Somnolence咩完成签到,获得积分10
3秒前
4秒前
科研通AI6.2应助仙峰水龙采纳,获得10
4秒前
上冬发布了新的文献求助10
4秒前
田田田完成签到,获得积分10
4秒前
陈琛琛完成签到,获得积分20
5秒前
DCH完成签到,获得积分10
5秒前
wang5945发布了新的文献求助10
5秒前
科研通AI2S应助壮观远航采纳,获得10
5秒前
江小雪完成签到,获得积分10
6秒前
wang完成签到 ,获得积分10
6秒前
周先森完成签到,获得积分10
6秒前
shining完成签到,获得积分10
7秒前
故意的语海完成签到,获得积分10
7秒前
wxhy发布了新的文献求助10
7秒前
Copyright应助西西弗斯采纳,获得10
8秒前
esin完成签到,获得积分10
8秒前
Wang发布了新的文献求助10
8秒前
传奇3应助小七采纳,获得10
9秒前
liuj完成签到,获得积分10
9秒前
JoymeansU完成签到,获得积分10
10秒前
kuikui1100完成签到,获得积分10
10秒前
底层特律应助元谷雪采纳,获得10
11秒前
zhuan完成签到,获得积分10
11秒前
wind完成签到 ,获得积分10
12秒前
13秒前
小麻豆完成签到,获得积分10
14秒前
Tail完成签到,获得积分10
14秒前
缓慢语雪完成签到,获得积分10
14秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
2026年中国辛酸癸酸聚乙二醇甘油酯行业市场现状调查及投资机会研判报告 1000
2026年中国辛酸癸酸聚乙二醇甘油酯行业市场规模及竞争格局分析报告 1000
48V Low-voltage Power Distribution Network (PDN) Architecture Industry Report, 2024 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
Introducing the Learning Sciences 600
Resiliency Scale for Adolescents--Chinese Version 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7324270
求助须知:如何正确求助?哪些是违规求助? 8939674
关于积分的说明 18953378
捐赠科研通 6980973
什么是DOI,文献DOI怎么找? 3215354
关于科研通互助平台的介绍 2382758
邀请新用户注册赠送积分活动 2194644