Nanoparticle Association with Brain Cells Is Augmented by Protein Coronas Formed in Cerebrospinal Fluid.

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Claire Rennie, Nabila Morshed, Matthew Faria, Lyndsey Collins-Praino, Andrew Care
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引用次数: 0

Abstract

Neuronanomedicine harnesses nanoparticle technology for the treatment of neurological disorders. An unavoidable consequence of nanoparticle delivery to biological systems is the formation of a protein corona on the nanoparticle surface. Despite the well-established influence of the protein corona on nanoparticle behavior and fate, as well as FDA approval of neuro-targeted nanotherapeutics, the effect of a physiologically relevant protein corona on nanoparticle-brain cell interactions is insufficiently explored. Indeed, less than 1% of protein corona studies have investigated protein coronas formed in cerebrospinal fluid (CSF), the fluid surrounding the brain. Herein, we utilize two clinically relevant polymeric nanoparticles (PLGA and PLGA-PEG) to evaluate the formation of serum and CSF protein coronas. LC-MS analysis revealed distinct protein compositions, with selective enrichment/depletion profiles. Enhanced association of CSF precoated particles with brain cells demonstrates the importance of selecting physiologically relevant biological fluids to more accurately study protein corona formation and subsequent nanoparticle-cell interactions, paving the way for improved nanoparticle engineering for in vivo applications.

脑脊液中形成的蛋白质冠状体增强了纳米颗粒与脑细胞的结合。
神经医学利用纳米粒子技术治疗神经系统疾病。纳米颗粒传递到生物系统的一个不可避免的后果是在纳米颗粒表面形成蛋白质电晕。尽管蛋白质冠对纳米颗粒行为和命运的影响已经确立,并且FDA批准了神经靶向纳米疗法,但生理学上相关的蛋白质冠对纳米颗粒-脑细胞相互作用的影响还没有得到充分的探索。事实上,只有不到1%的蛋白质冠状体研究调查了脑脊液(脑脊液)中形成的蛋白质冠状体。脑脊液是大脑周围的液体。在此,我们利用两种临床相关的聚合物纳米颗粒(PLGA和PLGA- peg)来评估血清和脑脊液蛋白冠状体的形成。LC-MS分析显示不同的蛋白质组成,具有选择性富集/耗尽谱。脑脊液预包覆颗粒与脑细胞的增强关联表明,选择生理相关的生物流体对于更准确地研究蛋白质电晕形成和随后的纳米颗粒-细胞相互作用的重要性,为改进体内应用的纳米颗粒工程铺平了道路。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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