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Bridging Smart Nanosystems with Clinically Relevant Models and Advanced Imaging for Precision Drug Delivery

Advanced science (Weinheim, Baden-Wurttemberg, Germany)(2024)

German Ctr Lung Res DZL | Univ Hlth & Rehabil Sci | Cent South Univ

Cited 7|Views13
Abstract
AbstractIntracellular delivery of nano‐drug‐carriers (NDC) to specific cells, diseased regions, or solid tumors has entered the era of precision medicine that requires systematic knowledge of nano‐biological interactions from multidisciplinary perspectives. To this end, this review first provides an overview of membrane‐disruption methods such as electroporation, sonoporation, photoporation, microfluidic delivery, and microinjection with the merits of high‐throughput and enhanced efficiency for in vitro NDC delivery. The impact of NDC characteristics including particle size, shape, charge, hydrophobicity, and elasticity on cellular uptake are elaborated and several types of NDC systems aiming for hierarchical targeting and delivery in vivo are reviewed. Emerging in vitro or ex vivo human/animal‐derived pathophysiological models are further explored and highly recommended for use in NDC studies since they might mimic in vivo delivery features and fill the translational gaps from animals to humans. The exploration of modern microscopy techniques for precise nanoparticle (NP) tracking at the cellular, organ, and organismal levels informs the tailored development of NDCs for in vivo application and clinical translation. Overall, the review integrates the latest insights into smart nanosystem engineering, physiological models, imaging‐based validation tools, all directed towards enhancing the precise and efficient intracellular delivery of NDCs.
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advanced imaging,intracellular delivery,nano-bio interaction,nano-drug-carries,physiological models
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要点】:本文综述了利用智能纳米系统结合临床相关模型和高级成像技术,以提高纳米药物载体(NDC)精准递送效率的方法和模型,突出了跨学科研究的重要性。

方法】:文章详细介绍了电穿孔、声穿孔、光穿孔、微流体递送和微注射等膜破裂方法,并探讨了NDC的特性如粒子大小、形状、电荷、疏水性和弹性对细胞摄取的影响。

实验】:文章回顾了多种体外或离体的人/动物来源的病理生理模型以及现代显微技术用于纳米粒子(NP)在细胞、器官和生物体水平上的精确追踪,但未具体提及实验数据集名称。