Codelivery of an Optimal Drug/siRNA Combination Using Mesoporous Silica Nanoparticles To Overcome Drug Resistance in Breast Cancer in Vitro and in Vivo
California NanoSystems Institute · University of California, Los Angeles
Abstract
We used a multifunctional mesoporous silica nanoparticle (MSNP) carrier to overcome doxorubicin (Dox) resistance in a multidrug resistant (MDR) human breast cancer xenograft by codelivering Dox and siRNA that targets the P-glycoprotein (Pgp) drug exporter. The Pgp siRNA selection from among a series of drug resistance targets was achieved by performing high throughput screening in a MDR breast cancer cell line, MCF-7/MDR. Following the establishment of a MCF-7/MDR xenograft model in nude mice, we demonstrated that a 50 nm MSNP, functionalized by a polyethyleneimine-polyethylene glycol (PEI-PEG) copolymer, provides protected delivery of stably bound Dox and Pgp siRNA to the tumor site. The effective…
Citation impact
- FWCI
- 34.75
- Percentile
- 100%
- References
- 46
Authors
11- HMHuan MengCorresponding
California NanoSystems Institute, University of California, Los Angeles
- WXWilson X. Mai
California NanoSystems Institute, University of California, Los Angeles
- HZHaiyuan Zhang
California NanoSystems Institute, University of California, Los Angeles
- MXMin Xue
California NanoSystems Institute, University of California, Los Angeles
- TXTian Xia
California NanoSystems Institute, University of California, Los Angeles
Topics & keywords
- Nanocarriers
- Doxorubicin
- In vivo
- Multiple drug resistance
- Tumor microenvironment
- Cancer research
- Drug delivery
- P-glycoprotein
- Good health and well-being