PEGylated Phospholipid Micelle-Encapsulated Near-Infrared PbS Quantum Dots for in vitro and in vivo Bioimaging

被引:65
作者
Hu, Rui [1 ,2 ]
Law, Wing-Cheung [2 ]
Lin, Guimiao [1 ]
Ye, Ling [3 ]
Liu, Jianwei [3 ]
Liu, Jing [3 ]
Reynolds, Jessica L. [4 ]
Yong, Ken-Tye [1 ]
机构
[1] Nanyang Technol Univ, Sch Elect & Elect Engn, Singapore 639798, Singapore
[2] SUNY Buffalo, Inst Lasers Photon & Biophoton, Buffalo, NY 14260 USA
[3] Chinese Peoples Liberat Army Gen Hosp, Inst Gerontol & Geriatr, Beijing 100853, Peoples R China
[4] SUNY Buffalo, Innovat Ctr, Dept Med, Div Allergy Immunol & Rheumatol, Buffalo, NY 14203 USA
来源
THERANOSTICS | 2012年 / 2卷 / 07期
关键词
Phospholipid; Micelle encapsulation; quantum dots; bioimaging; PEG; TETRAZOLIUM FORMAZAN ASSAY; FLUORESCENT PROTEIN; NANOCRYSTALS; DELIVERY; BILAYERS; THERAPY; FOLATE; AGENTS; DRUGS; LIGHT;
D O I
10.7150/thno.4275
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Surface modification and functionalization of bioconjugated quantum dots (QDs) has drawn great attention for the past few years due to their wide applications in biomedical research. In this contribution, we demonstrate the use of PEGylated phospholipid micelles to encapsulate near infrared emitting ultra-small lead sulfide (PbS) QDs for in vitro and in vivo imaging. The cytotoxicity of the micelle-encapsulated QDs formulation was evaluated using MTS assay and histological analysis studies. We have found that upon encapsulating the QDs with phospholipid micelle, the toxicity of the PbS QDs is reduced, from which we envision that the PEGylated phospholipid micelle-encapsulated PbS QDs formulation can be used as theranostics probes for some selected applications in cell imaging and small animals study.
引用
收藏
页码:723 / 733
页数:11
相关论文
共 45 条
[21]   Optical imaging in drug discovery and diagnostic applications [J].
Licha, K ;
Olbrich, C .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (08) :1087-1108
[22]   Polyethylene glycol-diacyllipid micelles demonstrate increased acculumation in subcutaneous tumors in mice [J].
Lukyanov, AN ;
Gao, ZG ;
Mazzola, L ;
Torchilin, VP .
PHARMACEUTICAL RESEARCH, 2002, 19 (10) :1424-1429
[23]   Mechanism of Bioactive Transfer through Liposomal Bilayers [J].
Maherani, Behnoush ;
Arab-Tehrany, Elmira ;
Linder, Michel .
CURRENT DRUG TARGETS, 2011, 12 (04) :531-545
[24]   Quantum dot bioconjugates for imaging, labelling and sensing [J].
Medintz, IL ;
Uyeda, HT ;
Goldman, ER ;
Mattoussi, H .
NATURE MATERIALS, 2005, 4 (06) :435-446
[25]   Quantum dots for live cells, in vivo imaging, and diagnostics [J].
Michalet, X ;
Pinaud, FF ;
Bentolila, LA ;
Tsay, JM ;
Doose, S ;
Li, JJ ;
Sundaresan, G ;
Wu, AM ;
Gambhir, SS ;
Weiss, S .
SCIENCE, 2005, 307 (5709) :538-544
[26]   Synthesis and characterization of monodisperse nanocrystals and close-packed nanocrystal assemblies [J].
Murray, CB ;
Kagan, CR ;
Bawendi, MG .
ANNUAL REVIEW OF MATERIALS SCIENCE, 2000, 30 :545-610
[27]   Fluorescence intermittency in single cadmium selenide nanocrystals [J].
Nirmal, M ;
Dabbousi, BO ;
Bawendi, MG ;
Macklin, JJ ;
Trautman, JK ;
Harris, TD ;
Brus, LE .
NATURE, 1996, 383 (6603) :802-804
[28]   Fluorescence imaging with near-infrared light: new technological advances that enable in vivo molecular imaging [J].
Ntziachristos, V ;
Bremer, C ;
Weissleder, R .
EUROPEAN RADIOLOGY, 2003, 13 (01) :195-208
[29]  
Prasad PN, 2004, QUANTUM CONFINED MAT, P79
[30]  
Prasad PN, 2004, BIOIMAGING PRINCIPLE, P203