4.8 Article

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

期刊

SMALL
卷 11, 期 2, 页码 222-231

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201303277

关键词

low-density lipoproteins; nanoparticles; anti-cancer agents; self-assembly; imaging

资金

  1. Korea Health Technology R&D Project, Ministry of Health Welfare [A111552]
  2. National Research Foundation (NRF) [2010-0029410]
  3. Converging Research Center - NRF of the Republic of Korea [2009-0082276]
  4. Korea Health Promotion Institute [A111552] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. Ministry of Science, ICT & Future Planning, Republic of Korea [KINC02] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2010-0029410, 2010-0027955] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

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.

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