羧酸和胺修饰Pluronic f127热响应纳米凝胶作为脑药物传递的智能载体。

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2025-05-07 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S507362
Abegaz Tizazu Andrgie, Cheng-Han Liao, Tsung-Yun Wu, Hsueh-Hui Yang, Horng-Jyh Harn, Shinn-Zong Lin, Yu-Shuan Chen, Hsieh-Chih Tsai
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引用次数: 0

摘要

血脑屏障(BBB)是调节循环系统和大脑之间物质交换的重要保护屏障,限制药物进入脑组织。在整个BBB开发新的交付策略具有挑战性,但至关重要。多功能纳米凝胶是一种很有前途的药物载体,可以将治疗药物输送到脑组织的预定目标区域。方法:采用羧酸修饰和胺修饰的Pluronic F127 (ADF127和EDF127)热响应纳米凝胶体系作为脑组织药物纳米载体。在37°C的磷酸盐缓冲盐水(pH 7.4)中,体外观察纳米凝胶对3-丁基苯酞(BP)的释放曲线。此外,利用荧光成像观察dir标记纳米凝胶在重要器官中的积累。结果:ADF127相对持续释放血压(27%),Pluronic F127在前4 h内快速释放血压(39%)。使用C57BL/6JNarl小鼠模型的体内研究表明,静脉注射BP负载共聚纳米凝胶显示出快速的BP分布到肝脏,脾脏,心脏和肾脏。脑内DiR荧光强度依次为Pluronic F127 < ADF127 < EDF127共聚纳米凝胶。虽然DiR在脑组织中的荧光强度相对低于其他重要器官,但DiR标记的EDF127共聚纳米凝胶的荧光强度高出约10倍。结论:带正电荷的药物载体纳米材料具有更高的血脑屏障转移倾向,显著扩大了带正电荷的EDF127纳米凝胶作为纳米载体在体内脑组织治疗和成像中的适用性。因此,羧酸和胺修饰的Pluronic F127纳米凝胶(EDF127和ADF127)通过血脑屏障的通透性增加,也将为脑组织治疗和成像提供一种很有前景的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carboxylic Acid- and Amine-Modified Pluronic F127-Based Thermoresponsive Nanogels as Smart Carriers for Brain Drug Delivery.

Introduction: The blood-brain barrier (BBB) is a critical protective barrier that regulates the exchange of substances between the circulatory system and brain, restricting the access of drugs to brain tissues. Developing novel delivery strategies across the BBB is challenging but crucial. Multifunctional nanogels are promising drug carriers for delivering therapeutic agents to their intended target areas in the brain tissue.

Methods: This study introduced carboxylic acid- and amine-modified Pluronic F127 (ADF127 and EDF127)-based thermoresponsive nanogel systems as drug nanocarriers for brain tissues. The release profiles of 3-butylidenephthalide (BP) from the nanogels were investigated in vitro in phosphate-buffered saline (pH 7.4) at 37 °C for 48 h. Additionally, the accumulation of DiR-labeled nanogels in vital organs was observed using fluorescence imaging.

Results: A relatively sustained BP release (27%) from ADF127, followed by rapid BP release (39%) from Pluronic F127 within the first 4 h were observed. In vivo studies using the C57BL/6JNarl mouse model showed that intravenously administered BP-loaded copolymeric nanogels exhibited a rapid BP distribution to the liver, spleen, heart, and kidney. DiR fluorescence intensity in the brain increased in the order Pluronic F127 < ADF127 < EDF127 copolymeric nanogels. Although the fluorescence intensity of DiR in the brain tissue was relatively lower than those in other vital organs, the DiR-labeled EDF127 copolymeric nanogels showed approximately 10-fold higher fluorescence intensity.

Conclusion: Positively charged drug carrier nanomaterials demonstrate a higher propensity for transfer through the BBB, significantly expanding the applicability of positively charged EDF127 nanogels as nanocarriers for in vivo brain tissue treatment and imaging. Therefore, owing to their increased permeability across the BBB, carboxylic acid- and amine-modified Pluronic F127 nanogels (EDF127 and ADF127) will also offer a promising approach for brain tissue treatment and imaging.

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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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