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Multistage Nanoparticle Delivery System-A New Approach to Cancer Therapeutics
Abstract:
Traditional methods of tumor therapy have many limitations. Thus, cancer nanomedicine is developing rapidly as a new treatment for tumors. In the past decade, the literature in this field has almost doubled every two years. However, the therapeutic nanoparticle (NP) platforms that have been approved for cancer treatment have not achieved the expected results in clinical application. Cancer nanomedicine still faces many obstacles and challenges. An abnormal cancer vascular system and a thick interstitial matrix can impose physiological barriers. As a result, drug delivery in tumor tissue depends mainly on diffusion. The diffusion efficiency of large NPs is poor; they are trapped around the blood vessels. Smallmolecule drug conjugates (SMDCs), miniaturized biologic drug conjugates (mBDCs), and small NPs can pass through this barrier. However, poor aggregation in tumors, easy elimination, and poor pharmacokinetics (PK) limit their therapeutic effects. In recent years, a selective new multistage delivery system was proposed to solve the challenge of infiltration. By incorporating smaller NPs or molecular drugs into large controlled-release particles for multistep delivery to tumors, we can make full use of the advantageous pharmacokinetics, the accumulation of large particles in the tumor, and the deep infiltration of small particles. In addition to changing the particle size, the multistage NP delivery system can also change the shape, charge, flexibility, and surface coating of the NPs to enhance penetration. Based on recent multistage delivery system research, this review expounds on the main direction of multistage delivery considering the ways in which large particles are triggered to release small particles.
Insights
Cancer nanomedicine faces challenges with drug delivery. A new multistage nanoparticle system improves tumor infiltration by releasing smaller particles within the tumor for enhanced cancer therapy.
Area of Science:
- Oncology
- Nanomedicine
- Drug Delivery
Background:
- Traditional cancer therapies have limitations.
- Approved nanoparticle (NP) platforms show limited clinical success due to physiological barriers in tumors.
- Tumor drug delivery is hindered by abnormal vasculature and interstitial matrix, relying on inefficient diffusion.
Purpose of the Study:
- To review advancements in cancer nanomedicine, focusing on overcoming drug delivery challenges.
- To explore the potential of multistage nanoparticle delivery systems for improved tumor infiltration and therapeutic efficacy.
- To discuss strategies for triggering the release of smaller particles from larger carriers within tumors.
Main Methods:
- Review of recent literature on multistage nanoparticle delivery systems for cancer.
- Analysis of factors influencing nanoparticle penetration, including size, shape, charge, flexibility, and surface coating.
- Examination of triggered release mechanisms for multistage systems.
Main Results:
- Multistage NP delivery systems offer a solution to poor infiltration by combining the benefits of large particle accumulation and small particle deep penetration.
- Optimization of NP properties (size, shape, charge, flexibility, coating) enhances tumor penetration.
- Triggered release of smaller NPs or drugs from larger carriers improves drug delivery efficiency.
Conclusions:
- Multistage nanoparticle delivery systems represent a promising direction for enhancing cancer nanomedicine efficacy.
- Targeted release of therapeutic payloads within the tumor microenvironment is crucial for overcoming delivery barriers.
- Further research into triggered release mechanisms and NP property optimization is needed for clinical translation.

