Low-Density Lipoprotein-Mimicking Nanoparticles for Tumor-Targeted Theranostic Applications

被引:26
作者
Lee, Jeong Yu [1 ]
Kim, Jin-Ho [1 ,2 ,3 ]
Bae, Ki Hyun [4 ]
Oh, Mi Hwa [4 ]
Kim, Youngwook [2 ]
Kim, Jee Seon
Park, Tae Gwan [4 ]
Park, Keunchil [2 ,5 ]
Lee, Jung Hee [3 ,6 ]
Nam, Yoon Sung [1 ,4 ,7 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, Taejon 305701, South Korea
[2] Samsung Biomed Res Inst, Med Nanoelement Dev Ctr, Seoul 135710, South Korea
[3] Sungkyunkwan Univ, Dept Hlth Sci & Technol, Samsung Adv Inst Hlth Sci & Technol, Seoul 135710, South Korea
[4] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[5] Sungkyunkwan Univ, Div Hematol & Oncol, Samsung Med Ctr, Dept Med,Sch Med, Seoul 135710, South Korea
[6] Sungkyunkwan Univ, Samsung Med Ctr, Dept Radiol, Sch Med, Seoul 135710, South Korea
[7] Korea Adv Inst Sci & Technol, KAIST Inst NanoCentury KINC, KAIST Inst BioCentury KIB, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
low-density lipoproteins; nanoparticles; anti-cancer agents; self-assembly; imaging; MANGANESE OXIDE NANOPARTICLES; MAGNETIC-RESONANCE; DRUG-DELIVERY; IRON-OXIDE; IN-VIVO; SIRNA DELIVERY; CANCER-CELLS; PACLITAXEL; RECEPTOR; FORMULATION;
D O I
10.1002/smll.201303277
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study introduces multifunctional lipid nanoparticles (LNPs), mimicking the structure and compositions of low-density lipoproteins, for the tumor-targeted co-delivery of anti-cancer drugs and superparamagnetic nanocrystals. Paclitaxel (4.7 wt%) and iron oxide nanocrystals (6.8 wt%, 11 nm in diameter) are co-encapsulated within folate-functionalized LNPs, which contain a cluster of nanocrystals with an overall diameter of about 170 nm and a zeta potential of about -40 mV. The folate-functionalized LNPs enable the targeted detection of MCF-7, human breast adenocarcinoma expressing folate receptors, in T-2-weighted magnetic resonance images as well as the efficient intracellular delivery of paclitaxel. Paclitaxel-free LNPs show no significant cytotoxicity up to 0.2 mg mL(-1), indicating the excellent biocompatibility of the LNPs for intracellular drug delivery applications. The targeted anti-tumor activities of the LNPs in a mouse tumor model suggest that the low-density lipoprotein-mimetic LNPs can be an effective theranostic platform with excellent biocompatibility for the tumor-targeted co-delivery of various anti-cancer agents.
引用
收藏
页码:222 / 231
页数:10
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