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Updated: Mar 15, 2026

Porous Silicon Microparticles for Delivery of siRNA Therapeutics
Published on: January 15, 2015
Codelivery of anticancer drugs and siRNA by mesoporous silica nanoparticles
Mohammad Yahya Hanafi-Bojd1, Legha Ansari2, Bizhan Malaekeh-Nikouei3
1Cellular & Molecular Research Center, Department of Pharmacology, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran.
Abstract:
The most common method for cancer treatment is chemotherapy. Multidrug resistance (MDR) is one of the major obstacles in chemotherapeutic treatment of many human cancers. One strategy to overcome this challenge is the delivery of anticancer drugs and siRNA simultaneously using nanoparticles. Mesoporous silica nanoparticles are one of the most popular nanoparticles for cargo delivery because of their intrinsic porosity. This paper highlights recent advances in codelivery of chemotherapeutic and siRNA with mesoporous silica nanoparticles for cancer therapy. In addition, synthesis and functionalization approaches of these nanoparticles are summarized. This review presents insight into the utilization of nanoparticles and combination therapy to achieve more promising results in chemotherapy.
Insights
This review explores using mesoporous silica nanoparticles for codelivering chemotherapy drugs and siRNA to combat cancer multidrug resistance (MDR). This approach enhances cancer treatment efficacy by overcoming resistance to conventional therapies.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Chemotherapy is a primary cancer treatment, but multidrug resistance (MDR) limits its effectiveness.
- Nanoparticles offer a promising strategy for overcoming MDR in cancer therapy.
- Mesoporous silica nanoparticles (MSNs) are widely used for drug delivery due to their porous structure.
Purpose of the Study:
- To review recent advancements in using MSNs for codelivering chemotherapeutic drugs and small interfering RNA (siRNA) for cancer treatment.
- To summarize synthesis and functionalization methods for MSNs in cancer therapy.
- To provide insights into nanoparticle-based combination therapy for improved chemotherapy outcomes.
Main Methods:
- Review of recent scientific literature on mesoporous silica nanoparticles for cancer therapy.
- Analysis of studies focusing on simultaneous delivery of chemotherapeutic agents and siRNA.
- Summary of MSN synthesis and surface modification techniques.
Main Results:
- MSNs enable efficient codelivery of chemotherapeutic drugs and siRNA, enhancing anticancer efficacy.
- Functionalization of MSNs can improve targeting and controlled release of therapeutic agents.
- Combination therapy using MSNs demonstrates potential to overcome multidrug resistance.
Conclusions:
- Mesoporous silica nanoparticles are effective carriers for codelivering chemotherapy and siRNA to combat cancer.
- Nanoparticle-based combination therapy represents a promising strategy to enhance cancer treatment outcomes.
- Further research into MSN synthesis and functionalization can optimize their clinical application in oncology.
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