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通过液辅佐球磨法制备帕唑帕尼富马酸盐二钠甘草次酸纳米晶胶束。

Preparation of pazopanib-fumarate disodium glycyrrhizinate nanocrystalline micelles by liquid-assisted ball milling.

机构信息

Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, China.

Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, China; Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education, College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou 310014, China.

出版信息

Eur J Pharm Sci. 2023 Sep 1;188:106530. doi: 10.1016/j.ejps.2023.106530. Epub 2023 Jul 17.

Abstract

Pazopanib (PZ) is a multikinase inhibitor, which is mainly used in the treatment of soft tissue sarcoma and advanced renal cancer. However, because of its water insolubility, oral bioavailability is poor. At the same time, photo lability and high dose oral administration lead to severe hepatotoxicity, which is limited in clinical application. In this paper, the novel pazopanib-fumarate disodium glycyrrhizinate nanocrystalline micelles are successfully prepared by liquid-assisted ball milling. The prepared cocrystals and nanocrystalline micelle structures are systematically characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and Fourier Transform Infrared Spectrometer (FTIR) analysis. In vitro solubility and dissolution experiments show that the solubility and dissolution of nanocrystalline micelles are significantly improved under different simulated physiological conditions. The accelerated stabilization experiments show that the nanocrystalline micelles have good physical and chemical stability and showed excellent stability in water (Zeta potential was 62.39 mV). In addition, the in vivo bioavailability of nanocrystalline micelles is 3 times higher than that of PZ, and the therapeutic threshold (> 20 μg/mL) is up to 30 h. This new strategy provides a feasible solution to the undesirable properties of PZ.

摘要

帕唑帕尼(PZ)是一种多激酶抑制剂,主要用于软组织肉瘤和晚期肾癌的治疗。然而,由于其水溶性差,口服生物利用度低。同时,光不稳定性和高剂量口服给药导致严重的肝毒性,这在临床应用中受到限制。本文通过液辅助球磨成功制备了新型帕唑帕尼富马酸二钠甘草酸盐纳米晶胶束。通过 X 射线衍射(XRD)、差示扫描量热法(DSC)和傅里叶变换红外光谱(FTIR)分析对所制备的共晶和纳米晶胶束结构进行了系统表征。体外溶解度和溶解实验表明,在不同模拟生理条件下,纳米晶胶束的溶解度和溶解明显提高。加速稳定性实验表明,纳米晶胶束具有良好的物理化学稳定性,在水中表现出优异的稳定性(Zeta 电位为 62.39 mV)。此外,纳米晶胶束的体内生物利用度是 PZ 的 3 倍,治疗阈值(>20μg/mL)达到 30 h。这种新策略为改善 PZ 的不理想性质提供了可行的解决方案。

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