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用于可控药物递送的基于液滴的纳米凝胶微流控合成:通过气动驱动的流动聚焦结调整纳米材料特性

Droplet-based microfluidic synthesis of nanogels for controlled drug delivery: tailoring nanomaterial properties pneumatically actuated flow-focusing junction.

作者信息

Giannitelli Sara Maria, Limiti Emanuele, Mozetic Pamela, Pinelli Filippo, Han Xiaoyu, Abbruzzese Franca, Basoli Francesco, Del Rio Danila, Scialla Stefano, Rossi Filippo, Trombetta Marcella, Rosanò Laura, Gigli Giuseppe, Zhang Zhenyu Jason, Mauri Emanuele, Rainer Alberto

机构信息

Department of Engineering, Università Campus Bio-Medico di Roma, via Álvaro del Portillo 21, 00128 Rome, Italy.

Division of Neuroscience, Institute of Experimental Neurology, San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.

出版信息

Nanoscale. 2022 Aug 11;14(31):11415-11428. doi: 10.1039/d2nr00827k.

DOI:10.1039/d2nr00827k
PMID:35903969
Abstract

Conventional batch syntheses of polymer-based nanoparticles show considerable shortcomings in terms of scarce control over nanomaterials morphology and limited lot-to-lot reproducibility. Droplet-based microfluidics represents a valuable strategy to overcome these constraints, exploiting the formation of nanoparticles within discrete microdroplets. In this work, we synthesized nanogels (NGs) composed of hyaluronic acid and polyethyleneimine using a microfluidic flow-focusing device endowed with a pressure-driven micro-actuator. The actuator achieves real-time modulation of the junction orifice width, thereby regulating the microdroplet diameter and, as a result, the NG size. Acting on process parameters, NG hydrodynamic diameter could be tuned in the range 92-190 nm while preserving an extremely low polydispersity (0.015); those values are hardly achievable in batch syntheses and underline the strength of our toolbox for the continuous in-flow synthesis of nanocarriers. Furthermore, NGs were validated as a drug delivery system in a representative case study still lacking an effective therapeutic treatment: ovarian cancer. Using doxorubicin as a chemotherapeutic agent, we show that NG-mediated release of the drug results in an enhanced antiblastic effect . the non-encapsulated administration route even at sublethal dosages, highlighting the wide applicability of our microfluidics-enabled nanomaterials in healthcare scenarios.

摘要

基于聚合物的纳米颗粒的传统批量合成在对纳米材料形态的控制不足以及批次间再现性有限方面存在相当大的缺点。基于微滴的微流控技术是克服这些限制的一种有价值的策略,它利用离散微滴中纳米颗粒的形成。在这项工作中,我们使用配备压力驱动微致动器的微流控流动聚焦装置合成了由透明质酸和聚乙烯亚胺组成的纳米凝胶(NGs)。该致动器实现了对连接孔宽度的实时调制,从而调节微滴直径,进而调节NG尺寸。通过控制工艺参数,NG的流体动力学直径可在92 - 190 nm范围内调节,同时保持极低的多分散性(0.015);这些值在批量合成中很难实现,并突出了我们用于纳米载体连续流入合成的工具箱的优势。此外,在一个仍缺乏有效治疗方法的代表性案例研究——卵巢癌中,NGs被验证为一种药物递送系统。使用阿霉素作为化疗药物,我们表明NG介导的药物释放导致增强的抗增殖作用,即使在亚致死剂量下,非封装给药途径也有此效果,突出了我们基于微流控技术的纳米材料在医疗保健场景中的广泛适用性。

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