Hydrodynamically driven self-assembly of giant vesicles of metal nanoparticles for remote-controlled release

Jie He; Zengjiang Wei; Lei Wang; Zuleykhan Tomova; Taarika Babu; Chaoyang Wang; Xiaojun Han; John T. Fourkas; Zhihong Nie

doi:10.1002/anie.201208425

Hydrodynamically driven self-assembly of giant vesicles of metal nanoparticles for remote-controlled release

Jie He^*
, Zengjiang Wei
, Lei Wang
, Zuleykhan Tomova
, Taarika Babu
, Chaoyang Wang
, Xiaojun Han
, John T. Fourkas
, Zhihong Nie

^*Corresponding author for this work

University of Maryland, College Park
South China University of Technology
School of Chemistry and Chemical Engineering, Harbin Institute of Technology

Research output: Contribution to journal › Article › peer-review

135 Scopus citations

Abstract

The hydrodynamics of laminar flow in a microfluidic device has been used to control the continuous self-assembly of gold nanoparticles (NPs) tethered with amphiphilic block copolymers. Spherical micelles, giant vesicles (500 nm-2.0 μm), or disk-like micelles could be formed by varying the flow rates of fluids. Such vesicles can release encapsulated hydrophilic species by using near-IR light (see picture).

Original language	English
Pages (from-to)	2463-2468
Number of pages	6
Journal	Angewandte Chemie - International Edition
Volume	52
Issue number	9
DOIs	https://doi.org/10.1002/anie.201208425
State	Published - 25 Feb 2013
Externally published	Yes

Keywords

giant vesicles
nanoparticles
photothermal effect
plasmonic properties
self-assembly

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10.1002/anie.201208425

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title = "Hydrodynamically driven self-assembly of giant vesicles of metal nanoparticles for remote-controlled release",

abstract = "The hydrodynamics of laminar flow in a microfluidic device has been used to control the continuous self-assembly of gold nanoparticles (NPs) tethered with amphiphilic block copolymers. Spherical micelles, giant vesicles (500 nm-2.0 μm), or disk-like micelles could be formed by varying the flow rates of fluids. Such vesicles can release encapsulated hydrophilic species by using near-IR light (see picture).",

keywords = "giant vesicles, nanoparticles, photothermal effect, plasmonic properties, self-assembly",

author = "Jie He and Zengjiang Wei and Lei Wang and Zuleykhan Tomova and Taarika Babu and Chaoyang Wang and Xiaojun Han and Fourkas, \{John T.\} and Zhihong Nie",

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T1 - Hydrodynamically driven self-assembly of giant vesicles of metal nanoparticles for remote-controlled release

AU - He, Jie

AU - Wei, Zengjiang

AU - Wang, Lei

AU - Tomova, Zuleykhan

AU - Babu, Taarika

AU - Wang, Chaoyang

AU - Han, Xiaojun

AU - Fourkas, John T.

AU - Nie, Zhihong

PY - 2013/2/25

Y1 - 2013/2/25

N2 - The hydrodynamics of laminar flow in a microfluidic device has been used to control the continuous self-assembly of gold nanoparticles (NPs) tethered with amphiphilic block copolymers. Spherical micelles, giant vesicles (500 nm-2.0 μm), or disk-like micelles could be formed by varying the flow rates of fluids. Such vesicles can release encapsulated hydrophilic species by using near-IR light (see picture).

AB - The hydrodynamics of laminar flow in a microfluidic device has been used to control the continuous self-assembly of gold nanoparticles (NPs) tethered with amphiphilic block copolymers. Spherical micelles, giant vesicles (500 nm-2.0 μm), or disk-like micelles could be formed by varying the flow rates of fluids. Such vesicles can release encapsulated hydrophilic species by using near-IR light (see picture).

KW - giant vesicles

KW - nanoparticles

KW - photothermal effect

KW - plasmonic properties

KW - self-assembly

UR - https://www.scopus.com/pages/publications/84874250364

U2 - 10.1002/anie.201208425

DO - 10.1002/anie.201208425

M3 - 文章

C2 - 23362104

AN - SCOPUS:84874250364

SN - 1433-7851

VL - 52

SP - 2463

EP - 2468

JO - Angewandte Chemie - International Edition

JF - Angewandte Chemie - International Edition

IS - 9

ER -

Hydrodynamically driven self-assembly of giant vesicles of metal nanoparticles for remote-controlled release

Abstract

Keywords

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