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叶酸修饰藜芦碱聚乙二醇-聚乳酸羟基乙酸共聚物纳米粒的初步药代动力学及体内抗肿瘤药效学研究。

Preliminary Study on Pharmacokinetics and Antitumor Pharmacodynamics of Folic Acid Modified Crebanine Polyethyleneglycol-Polylactic Acid Hydroxyacetic Acid Copolymer Nanoparticles.

机构信息

College of Traditional Chinese Medicine, Yunnan University of Chinese Medicine, Kunming, 650500, People's Republic of China.

The Key Laboratory of External Drug Delivery System and Preparation Technology in University of Yunnan Province, Kunming, 650500, People's Republic of China.

出版信息

Int J Nanomedicine. 2024 Oct 17;19:10513-10536. doi: 10.2147/IJN.S477027. eCollection 2024.

Abstract

PURPOSE

Liver cancer is associated significantly with morbidity and mortality. The combination of low-intensity ultrasound with nanomedicine delivery systems holds promise as an alternative for the treatment for liver cancer. This study focuses on the utilization of folic acid (FA) modified nanoparticles, which are loaded with fluorescent dye DiR and liquid fluorocarbon (PFP). These nanoparticles have the potential to enhance liver cancer targeting under ultrasound stimulation and future applications in vivo.

METHODS

The pharmacokinetics and tissue distribution of folic acid-modified Crebanine polyethylene glycol-polylactic acid copolymer nanoparticles (FA-Cre@PEG-PLGA NPs) were investigated. The pharmacokinetic parameters, liver targeting, and in vivo distribution were assessed. Additionally, the inhibitory impacts of FA-Cre@PEG-PLGA NPs in combination with ultrasonic irradiation on the proliferation and acute toxicity of H22 cells of mouse hepatoma were investigated in vitro. The tumor targeting and anti-tumor efficacy of FA-Cre@PEG-PLGA NPs were assessed utilizing a small animal in vivo imaging system and an in situ hepatocellular carcinoma transplantation model, respectively.

RESULTS

The pharmacokinetic studies and tissue distribution tests demonstrated that FA-Cre@PEG-PLGA NPs conspicuously prolonged the half-life and retention time of the drug in rats, and the liver targeting effect was pronounced. Additionally, the in vivo acute toxicity test indicated that FA-Cre@PEG-PLGA NPs had minimal adverse reactions and could fulfill the aim of attenuating the drug. The outcomes of the animal experiments further substantiated that FA-Cre@PEG-PLGA NPs had a longer retention time at the tumor site, a superior anti-tumor effect, and less damage to liver and kidney tissue.

CONCLUSION

The integration of FA-Cre@PEG-PLGA NPs with ultrasound irradiation demonstrated exceptional safety and potent anti-tumor efficacy in vivo, presenting a promising therapeutic strategy for the treatment of liver cancer through the combination of ultrasound technology with a nanomedicine delivery system.

摘要

目的

肝癌与发病率和死亡率密切相关。低强度超声与纳米医学输送系统的结合有望成为治疗肝癌的替代方法。本研究专注于使用叶酸(FA)修饰的纳米颗粒,这些纳米颗粒负载有荧光染料 DiR 和液态氟碳(PFP)。这些纳米颗粒有可能在超声刺激下增强肝癌靶向,并在未来的体内应用中发挥作用。

方法

研究了叶酸修饰的长春瑞滨聚乙二醇-聚乳酸共聚物纳米粒(FA-Cre@PEG-PLGA NPs)的药代动力学和组织分布。评估了药代动力学参数、肝靶向和体内分布。此外,还研究了 FA-Cre@PEG-PLGA NPs 与超声辐照联合对小鼠肝癌 H22 细胞增殖和急性毒性的体外抑制作用。利用小动物体内成像系统和原位肝癌移植模型评估了 FA-Cre@PEG-PLGA NPs 的肿瘤靶向和抗肿瘤疗效。

结果

药代动力学研究和组织分布试验表明,FA-Cre@PEG-PLGA NPs 显著延长了药物在大鼠体内的半衰期和保留时间,且肝靶向效果明显。此外,体内急性毒性试验表明,FA-Cre@PEG-PLGA NPs 不良反应极小,能够达到减毒的目的。动物实验的结果进一步证实,FA-Cre@PEG-PLGA NPs 在肿瘤部位的滞留时间更长,抗肿瘤效果更好,对肝、肾组织的损伤更小。

结论

FA-Cre@PEG-PLGA NPs 与超声辐照相结合,在体内显示出了优异的安全性和强大的抗肿瘤疗效,为通过将超声技术与纳米医学输送系统相结合治疗肝癌提供了一种有前途的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ff/11492913/901f95bbbb5d/IJN-19-10513-g0001.jpg

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