Systemically Delivered Magnetic Hyperthermia for Prostate Cancer Treatment

被引:41
作者
Albarqi, Hassan A. [1 ,2 ]
Demessie, Ananiya A. [1 ]
Sabei, Fahad Y. [1 ,3 ]
Moses, Abraham S. [1 ]
Hansen, Mikkel N. [4 ]
Dhagat, Pallavi [4 ]
Taratula, Olena R. [1 ]
Taratula, Oleh [1 ]
机构
[1] Oregon State Univ, Dept Pharmaceut Sci, Coll Pharm, Portland, OR 97201 USA
[2] Najran Univ, Dept Pharmaceut, Coll Pharm, Najran 61441, Saudi Arabia
[3] Jazan Univ, Dept Pharmaceut, Coll Pharm, Jazan 88723, Saudi Arabia
[4] Oregon State Univ, Sch Elect Engn & Comp Sci, Corvallis, OR 97331 USA
基金
美国国家卫生研究院;
关键词
nanoparticle; nanocluster; magnetic hyperthermia; alternating magnetic field; prostate cancer; IRON-OXIDE NANOPARTICLES; NANOMEDICINE PLATFORM; DRUG-DELIVERY; THERMOTHERAPY; NANOPLATFORM; DENDRIMER; THERAPY;
D O I
10.3390/pharmaceutics12111020
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Herein, we report a novel therapy for prostate cancer based on systemically delivered magnetic hyperthermia. Conventional magnetic hyperthermia is a form of thermal therapy where magnetic nanoparticles delivered to cancer sites via intratumoral administration produce heat in the presence of an alternating magnetic field (AMF). To employ this therapy for prostate cancer tumors that are challenging to inject intratumorally, we designed novel nanoclusters with enhanced heating efficiency that reach prostate cancer tumors after systemic administration and generate desirable intratumoral temperatures upon exposure to an AMF. Our nanoclusters are based on hydrophobic iron oxide nanoparticles doped with zinc and manganese. To overcome the challenges associated with the poor water solubility of the synthesized nanoparticles, the solvent evaporation approach was employed to encapsulate and cluster them within the hydrophobic core of PEG-PCL (methoxy poly(ethylene glycol)-b-poly(epsilon-caprolactone))-based polymeric nanoparticles. Animal studies demonstrated that, following intravenous injection into mice bearing prostate cancer grafts, the nanoclusters efficiently accumulated in cancer tumors within several hours and increased the intratumoral temperature above 42 degrees C upon exposure to an AMF. Finally, the systemically delivered magnetic hyperthermia significantly inhibited prostate cancer growth and did not exhibit any signs of toxicity.
引用
收藏
页码:1 / 14
页数:14
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