Fusogenic Viral Protein-Based Near-Infrared Active Nanocarriers for Biomedical Imaging

被引:2
作者
Bishnoi, Suman [1 ]
Kumari, Anshu [1 ,2 ]
Rehman, Sheeba [1 ]
Minz, Aliva [3 ]
Senapati, Shantibhusan [3 ]
Nayak, Debasis [1 ]
Gupta, Sharad [1 ,4 ]
机构
[1] Indian Inst Technol Indore, Dept Biosci & Biomed Engn, Indore 453552, India
[2] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[3] Inst Life Sci, Bhubaneswar 751023, Odisha, India
[4] Jawaharlal Nehru Univ, Sch Biotechnol, New Delhi 110067, India
关键词
VSV-G; ICG; VNPs; NIR imaging; NAVNs; VESICULAR STOMATITIS-VIRUS; INDOCYANINE-GREEN; FLUORESCENCE PROPERTIES; NANOPARTICLES; CELLS; NANOMATERIALS; MEMBRANE; DELIVERY; FUSION; DRUG;
D O I
10.1021/acsbiomaterials.1c00267
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
An effective drug delivery system (DDS) relies on an efficient cellular uptake and faster intracellular delivery of theranostic agents, bypassing the endosomal mediated degradation of the payload. The use of viral nanoparticles (VNPs) permits such advancement, as the viruses are naturally evolved to infiltrate the host cells to deliver their genetic material. As a proof of concept, we bioengineered the vesicular stomatitis virus glycoprotein (VSV-G)-based near-infrared (NIR) active viral nanoconstructs (NAVNs) encapsulating indocyanine green dye (ICG) for NIR bioimaging. NAVNs are spherical in size and have the intrinsic cellular-fusogenic properties of VSV-G. Further, the NIR imaging displaying higher fluorescence intensity in NAVNs treated cells suggests enhanced cellular uptake and delivery of ICG by NAVNs compared to the free form of ICG. The overall study highlights the effectiveness of VSV-G-based VNPs as an efficient delivery system for NIR fluorescence imaging.
引用
收藏
页码:3351 / 3360
页数:10
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