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Flexible Filaments for in Vivo Imaging and Delivery: Persistent Circulation of Filomicelles Opens the Dosage Window for Sustained Tumor Shrinkage
被引:245
作者:
Christian, David A.
Cai, Shenshen
Garbuzenko, Olga B.
[2
]
Harada, Takamasa
Zajac, Allison L.
Minko, Tamara
[2
]
Discher, Dennis E.
[1
]
机构:
[1] Univ Penn, CBE, Dept Chem & Biomol Engn, Philadelphia, PA 19104 USA
[2] Rutgers State Univ, Dept Pharmaceut, Piscataway, NJ 08854 USA
关键词:
Worm micelle;
optical imaging;
in vivo tracking;
tumor;
paclitaxel;
near infrared;
drug delivery;
block copolymer;
INFRARED-EMISSIVE POLYMERSOMES;
DRUG-DELIVERY;
WORM MICELLES;
PACLITAXEL;
PARAMETER;
DESIGN;
MODELS;
SHAPE;
D O I:
10.1021/mp900022m
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:
Shape effects of synthetic carriers are largely unexplored in vivo, although recent findings suggest that flexible filaments can persist in the circulation even if microns in length. Here, to better assess biodistribution, a near-infrared fluorophore (NIRF) was incorporated into such block copolymer "filomicelles", and both in vivo and ex vivo imaging show that the majority of these wormlike micelles remain in the circulation for at least a day after intravenous injection. NIRF imaging further suggests that filomicelles convect into a tumor and some fragments can penetrate into the tumor stroma. To assess a functional effect, the hydrophobic drug paclitaxel (tax) was loaded into both filomicelles and sonication-generated spherical micelles of the same copolymer. Intravenous injection of tax-loaded filomicelles nearly doubles the maximum tolerated dose of tax in normal mice compared to tax-loaded spherical micelles. In tumor-bearing mice, the higher dose of tax produces greater and more sustained tumor shrinkage and tumor cell apoptosis. These results thus begin to address mechanisms for how nonspherical carriers deliver both imaging agents and anticancer therapeutics to solid tumors.
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页码:1343 / 1352
页数:10
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