Inhibitory Effect of Tanshinone IIA Nanomicelles on Tumor Growth and Angiogenesis in Mice with Cervical Carcinoma Transplantation

体内 移植 流式细胞术 赫拉 体外 癌症研究 材料科学 分散性 血管生成 药理学 分子生物学 生物物理学 化学 生物化学 生物 医学 内科学 高分子化学 生物技术
作者
Ruihua Hu,Aimin Chen
出处
期刊:Science of Advanced Materials [American Scientific Publishers]
卷期号:15 (3): 319-329 被引量:1
标识
DOI:10.1166/sam.2023.4445
摘要

In recent years, traditional Chinese medicine (TCM), represented by tanshinone (Tas) and ganoderan polysaccharides, has attracted the attention of many scientists due to its mild effect of inhibiting tumors. In this research, poly-gamma-glutamic acid ( γ -PGA) was degraded into small molecule γ -PGA fragments by high-temperature acidolysis, and L-phenylalanine ethylester (L-PAE) was combined with small molecule γ -PGA fragments to generate γ -PGA-LA by dehydration condensation. The material was mixed with fat-soluble Tas IIA to form PL-Tas IIA nanomicelles (NMs). In addition to physical characterization, the in vitro biological activity of the material was detected to establish a tumor-bearing nude mouse model, which was inoculated with cervical cancer HeLa cells. The nude mouse models were grouped, and the effect of NMs on the growth of transplanted tumors was observed by intraperitoneal injection. The results revealed that the nanoparticle size was approximately 139.6±3.8 nm, and it had a good EPR effect, which was conducive to passive targeted therapy of tumors. The polydispersity coefficient and zeta potential were 0.138±0.005 and 33.6±1.6 mV, respectively. The NM was cocultured with the cells under various concentration conditions, and the cell survival rate was more than 85%. The tumor cell uptake performance of the NM was ideal, and the cell uptake ratio reached 71.62% at 60 min, as determined by flow cytometry. An in vivo tumor test demonstrated that PL-Tas IIA had a favorite tumor inhibition effect. The tumor-bearing nude mouse model showed that the prepared NMs can inhibit tumor growth, induce angiogenesis of xenografts, and further induce tumor cell apoptosis, further verifying that the prepared NMs can inhibit cervical cancer tumor growth.

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