Discovery of 2-deoxy glucose surfaced mixed layer dendrimer: a smart neuron targeted systemic drug delivery system for brain diseases

药物输送 树枝状大分子 靶向给药 药品 输送系统 化学 纳米技术 医学 药理学 材料科学 生物化学
作者
Anubhav Dhull,Zhi Zhang,Rishi Sharma,Aqib Iqbal Dar,Anu Rani,Jing Wei,Shamila Gopalakrishnan,Amanda Ghannam,Victoria Hahn,Anunay J. Pulukuri,Stefanie Tasevski,Sara Moughni,Boyang Jason Wu,Anjali Sharma
出处
期刊:Theranostics [Ivyspring International Publisher]
卷期号:14 (8): 3221-3245 被引量:1
标识
DOI:10.7150/thno.95476
摘要

The availability of non-invasive drug delivery systems capable of efficiently transporting bioactive molecules across the blood-brain barrier to specific cells at the injury site in the brain is currently limited.Delivering drugs to neurons presents an even more formidable challenge due to their lower numbers and less phagocytic nature compared to other brain cells.Additionally, the diverse types of neurons, each performing specific functions, necessitate precise targeting of those implicated in the disease.Moreover, the complex synthetic design of drug delivery systems often hinders their clinical translation.The production of nanomaterials at an industrial scale with high reproducibility and purity is particularly challenging.However, overcoming this challenge is possible by designing nanomaterials through a straightforward, facile, and easily reproducible synthetic process.Methods: In this study, we have developed a third-generation 2-deoxy-glucose functionalized mixed layer dendrimer (2DG-D) utilizing biocompatible and cost-effective materials via a highly facile convergent approach, employing copper-catalyzed click chemistry.We further evaluated the systemic neuronal targeting and biodistribution of 2DG-D, and brain delivery of a neuroprotective agent pioglitazone (Pio) in a pediatric traumatic brain injury (TBI) model. Results:The 2DG-D exhibits favorable characteristics including high water solubility, biocompatibility, biological stability, nanoscale size, and a substantial number of end groups suitable for drug conjugation.Upon systemic administration in a pediatric mouse model of traumatic brain injury (TBI), the 2DG-D localizes in neurons at the injured brain site, clears rapidly from off-target locations, effectively delivers Pio, ameliorates neuroinflammation, and improves behavioral outcomes.Conclusions: The promising in vivo results coupled with a convenient synthetic approach for the construction of 2DG-D makes it a potential nanoplatform for addressing brain diseases.

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