4.7 Article

In Vivo Evaluation of Porous Silicon and Porous Silicon Solid Lipid Nanocomposites for Passive Targeting and Imaging

期刊

MOLECULAR PHARMACEUTICS
卷 11, 期 8, 页码 2876-2886

出版社

AMER CHEMICAL SOC
DOI: 10.1021/mp500225b

关键词

porous silicon; solid lipid nanocomposite; F-18 radiolabeling; passive targeting; EPR effect; cancer

资金

  1. FinPharma Doctoral Program (FPDP, Drug Discovery section)
  2. University of Helsinki Funds
  3. Academy of Finland [252215, 256394, 136805, 272908]
  4. Biocentrum Helsinki
  5. European Research Council under the European Union [310892]
  6. Academy of Finland (AKA) [272908, 136805, 272908, 136805] Funding Source: Academy of Finland (AKA)

向作者/读者索取更多资源

The use of nanoparticle carriers for the sustained release of cytotoxic drugs in cancer therapy can result in fewer adverse effects and can thus be of great benefit for the patient. Recently, a novel nanocomposite, prepared by the encapsulation of THCPSi nanoparticles within solid lipids (SLN), was developed and characterized as a promising drug delivery carrier in vitro. The present study describes the in vivo evaluation of unmodified THCPSi nanopartides and THCPSi solid lipid nanocomposites (THCPSi-SLNCs) as potential drug delivery carriers for cancer therapy by using F-18 radiolabeling for the detection of the particle biodistribution in mice. Passive tumor targeting of F-18-THCPSis and F-18-THCPSi-SLNCs by the enhanced permeation and retention effect was investigated in a murine breast cancer model. Encapsulation of THCPSi nanoparticles with solid lipids improved their accumulation in tumors at a 7 week time point (tumor-to-liver ratio 0.10 +/- 0.08 and 0.24 +/- 0.0996 for F-18-THCPSis and F-18-THCPSi SLNCs, respectively).

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