4.8 Article

Controlled and Tunable Loading and Release of Vesicles by Using Gigahertz Acoustics

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 1, 页码 159-163

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201810181

关键词

controlled loading; controlled release; gigahertz acoustic streaming; transient nanopores; vesicles

资金

  1. Natural Science Foundation of China (NSFC) [61674114, 91743110, 21861132001]
  2. National Key R&D Program of China [2017YFF0204600]
  3. 111 Project [B07014]
  4. Volkswagen Foundation (FlapChips project) [91-056]
  5. Fonds der Chemischen Industrie
  6. Deutsche Forschungsgemeinschaft [DFG SFB858]

向作者/读者索取更多资源

Controllable exchange of molecules between the interior and the external environment of vesicles is critical in drug delivery and micro/nano-reactors. While many approaches exist to trigger release from vesicles, controlled loading remains a challenge. Herein, we show that gigahertz acoustic streaming generated by a nanoelectromechanical resonator can control the loading and release of cargo into and from vesicles. Polymer-shelled vesicles showed loading and release of molecules both in solution and on a solid substrate. We observed deformation of individual giant unilamellar vesicles and propose that the shear stress generated by gigahertz acoustic streaming induces the formation of transient nanopores, with diameters on the order of 100 nm, in the vesicle membranes. This provides a non-invasive method to control material exchange across membranes of different types of vesicles, which could allow site-specific release of therapeutics and controlled loading into cells, as well as tunable microreactors.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Physics, Condensed Matter

Induced Forster resonance energy transfer by encapsulation of DNA-scaffold based probes inside a plant virus based protein cage

Mark V. de Ruiter, Nico J. Overeem, Gaurav Singhai, Jeroen J. L. M. Cornelissen

JOURNAL OF PHYSICS-CONDENSED MATTER (2018)

Article Chemistry, Multidisciplinary

Time-Dependent Binding of Molecules and Nanoparticles at Receptor-Modified Supported Lipid Bilayer Gradients in a Microfluidic Device

Nico J. Overeem, Pieter H. (Erik) Hamming, Jurriaan Huskens

CHEMISTRYSELECT (2020)

Review Chemistry, Multidisciplinary

A Dynamic, Supramolecular View on the Multivalent Interaction between Influenza Virus and Host Cell

Nico J. Overeem, Erhard van der Vries, Jurriaan Huskens

Summary: This review explores how influenza viruses navigate mucus and recognize host cells through multivalent interactions. The surface proteins of the influenza A virus facilitate specific binding to host cells, and the importance of these multivalent interactions in crossing mucus and entering host cells is discussed. Techniques to measure the avidity and receptor specificity of influenza viruses are also reviewed.
Article Chemistry, Multidisciplinary

Multivalent Affinity Profiling: Direct Visualization of the Superselective Binding of Influenza Viruses

Nico J. Overeem, P. H. (Erik) Hamming, Malte Tieke, Erhard van der Vries, Jurriaan Huskens

Summary: The method of multivalent affinity profiling (MAP) allows for quantitatively assessing the binding of influenza A virus (IAV) to receptor density gradients, determining the threshold receptor density, and visualizing and assessing the superselective binding of IAVs. The threshold receptor density increases with increasing flow rate, indicating that the superselective binding of IAV is influenced by shear force and experimental conditions. This method enables not only comparative studies of virus-receptor interactions but also fundamental studies on the mechanism of superselectivity.

ACS NANO (2021)

Article Nanoscience & Nanotechnology

Receptor Density-Dependent Motility of Influenza Virus Particles on Surface Gradients

P. H. Erik Hamming, Nico J. Overeem, Kevin Diestelhorst, Tren Fiers, Malte Tieke, Gael M. Vos, Geert-Jan P. H. Boons, Erhard van der Vries, Stephan Block, Jurriaan Huskens

Summary: Influenza viruses use surface motility to find or create locations for cell entry and enhance cellular uptake. The motility is expected to depend on the receptor density, and surface gradients with varying receptor densities can mimic the local variations on the cell surface. By tracking individual virus particles over surfaces with receptor density gradients, researchers found that surface mobility and the probability of sticking are significantly dependent on receptor density. The findings provide insights into how the virus locates high-receptor density patches for cell entry. Overall, the study scores 8 out of 10.

ACS APPLIED MATERIALS & INTERFACES (2023)

Article Chemistry, Multidisciplinary

Hierarchical Multivalent Effects Control Influenza Host Specificity

Nico J. Overeem, P. H. Erik Hamming, Oliver C. Grant, Daniele Di Iorio, Malte Tieke, M. Candelaria Bertolino, Zeshi Li, Gael Vos, Robert P. de Vries, Robert J. Woods, Nicholas B. Tito, Geert-Jan P. H. Boons, Erhard van der Vries, Jurriaan Huskens

ACS CENTRAL SCIENCE (2020)

Review Chemistry, Multidisciplinary

Influenza as a molecular walker

P. H. (Erik) Hamming, Nico J. Overeem, Jurriaan Huskens

CHEMICAL SCIENCE (2020)

暂无数据