Abstract
A tumor targeted mesoporous silica nanoparticles (MSN)-based drug delivery system (DDS) was developed for inhalation treatment of lung cancer. The system was capable of effectively delivering inside cancer cells anticancer drugs (doxorubicin and cisplatin) combined with two types of siRNA targeted to MRP1 and BCL2 mRNA for suppression of pump and nonpump cellular resistance in non-small cell lung carcinoma, respectively. Targeting of MSN to cancer cells was achieved by the conjugation of LHRH peptide on the surface of MSN via poly(ethylene glycol) spacer. The delivered anticancer drugs and siRNA preserved their specific activity leading to the cell death induction and inhibition of targeted mRNA. Suppression of cellular resistance by siRNA effectively delivered inside cancer cells and substantially enhanced the cytotoxicity of anticancer drugs. Local delivery of MSN by inhalation led to the preferential accumulation of nanoparticles in the mouse lungs, prevented the escape of MSN into the systemic circulation, and limited their accumulation in other organs. The experimental data confirm that the developed DDS satisfies the major prerequisites for effective treatment of non-small cell lung carcinoma. Therefore, the proposed cancer-targeted MSN-based system for complex delivery of drugs and siRNA has high potential in the effective treatment of lung cancer.
Original language | English (US) |
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Pages (from-to) | 900-914 |
Number of pages | 15 |
Journal | Journal of Drug Targeting |
Volume | 19 |
Issue number | 10 |
DOIs | |
State | Published - Dec 2011 |
All Science Journal Classification (ASJC) codes
- Pharmaceutical Science
Keywords
- Body distribution
- Cisplatin
- Doxorubicin
- Drug resistance
- Lung cancer
- Luteinizing hormone-releasing hormone receptor (LHRHR)
- Mesoporous silica nanoparticles
- Pulmonary delivery
- SiRNA