pH-responsive water soluble smart vesicles containing a bis(styryl)benzene derivative for two-photon microscopy imaging

被引:11
|
作者
Nag, Okhil Kumar [2 ]
Lim, Chang Su [1 ]
Bao Lam Nguyen [2 ,3 ]
Kim, Boram [2 ]
Jang, Jihye [2 ]
Han, Ji Hee [1 ]
Cho, Bong Rae [1 ]
Woo, Han Young [2 ]
机构
[1] Korea Univ, Dept Chem, Seoul 136701, South Korea
[2] Pusan Natl Univ, Dept Cognomechatron WCU Engn, Miryang 627706, South Korea
[3] Inst Appl Mat Sci, Ho Chi Minh City, Vietnam
基金
新加坡国家研究基金会;
关键词
AGGREGATION-ENHANCED FLUORESCENCE; MODIFIED SILICA NANOPARTICLES; ABSORPTION; EXCITATION; COMPLEXES; POLYMER; SULFATE; SURFACTANT; PROBES; CHROMOPHORES;
D O I
10.1039/c1jm14693a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report self-assembled polymeric nanovesicles composed of 1,4-bis{4'-[N,N-bis(6 ''-trimethylammoniumhexyl)amino]styryl}benzene tetrabromide (C1), poly[(ethylene oxide)-block-(sodium 2-acrylamido-2-methyl-1-propane sulfonate)] (E-m-A(n)), and hexadecyltrimethylammonium bromide (C-16). Transmission electron microscopy (TEM) micrographs confirm the vesicular bilayer structures and atomic force microscopy (AFM) images show that the C1/E-m-A(n)/C-16 complexes form spherical nanostructures with a particle size ranging from 40 to 80 nm. The encapsulation of C1 inside the nanovesicles enhances similar to 2-fold the fluorescence quantum yield (eta) and two-photon action cross-section (eta delta, where delta is the two-photon absorption cross-section), and allows internalization into the cells, as revealed by the bright two-photon microscopy (TPM) images of human cervical epithelioid carcinoma (HeLa) cells labeled with the nanovesicles. Moreover, nanovesicles containing a chemotherapeutic drug and a neutral molecule can also be prepared. Furthermore, the C1/vesicular complex is disassembled under acidic conditions, highlighting its potential as a pH-responsive smart nanocarrier for the intracellular drug delivery. These results suggest a new possibility of using nanovesicles as efficient two-photon probes for TPM imaging and possibly as nanocarriers for intracellular drug delivery.
引用
收藏
页码:1977 / 1984
页数:8
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