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Published on: June 23, 2020
Targeting Tumor Cells with Nanoparticles for Enhanced Co-Drug Delivery in Cancer Treatment
Wen-Ying Huang1, Chih-Ho Lai2, Shin-Lei Peng3
1Department of Applied Cosmetology, Hung-Kuang University, Taichung 433304, Taiwan.
Abstract:
Gastric cancer (GC) is a fatal malignant tumor, and effective therapies to attenuate its progression are lacking. Nanoparticle (NP)-based solutions may enable the design of novel treatments to eliminate GC. Refined, receptor-targetable NPs can selectively target cancer cells and improve the cellular uptake of drugs. To overcome the current limitations and enhance the therapeutic effects, epigallocatechin-3-gallate (EGCG) and low-concentration doxorubicin (DX) were encapsulated in fucoidan and d-alpha-tocopherylpoly (ethylene glycol) succinate-conjugated hyaluronic acid-based NPs for targeting P-selectin-and cluster of differentiation (CD)44-expressing gastric tumors. The EGCG/DX-loaded NPs bound to GC cells and released bioactive combination drugs, demonstrating better anti-cancer effects than the EGCG/DX combination solution. In vivo assays in an orthotopic gastric tumor mouse model showed that the EGCG/DX-loaded NPs significantly increased the activity of gastric tumors without inducing organ injury. Overall, our EGCG/DX-NP system exerted a beneficial effect on GC treatment and may facilitate the development of nanomedicine-based combination chemotherapy against GC in the future.
Insights
New nanoparticles loaded with epigallocatechin-3-gallate (EGCG) and doxorubicin (DX) show promise for gastric cancer (GC) treatment. This novel nanomedicine effectively targets GC cells, enhancing anti-cancer effects and reducing organ injury in preclinical models.
Area of Science:
- Biomedical Engineering
- Nanomedicine
- Oncology
Background:
- Gastric cancer (GC) remains a significant global health challenge with limited effective therapeutic options.
- Nanoparticle (NP)-based drug delivery systems offer a promising avenue for developing novel GC treatments.
- Targeted NPs can enhance drug delivery to cancer cells, improving therapeutic efficacy and reducing side effects.
Purpose of the Study:
- To develop and evaluate a novel nanoparticle system for targeted gastric cancer therapy.
- To investigate the synergistic anti-cancer effects of epigallocatechin-3-gallate (EGCG) and doxorubicin (DX) delivered via nanoparticles.
- To assess the in vivo efficacy and safety of the developed EGCG/DX-loaded NPs in a gastric tumor mouse model.
Main Methods:
- Encapsulation of EGCG and low-concentration DX into fucoidan and hyaluronic acid-based NPs conjugated with d-alpha-tocopherylpoly (ethylene glycol) succinate.
- Targeting of P-selectin and CD44 receptors expressed on gastric cancer cells.
- In vitro evaluation of NP binding, cellular uptake, and anti-cancer effects compared to free drug combinations.
- In vivo assessment of therapeutic efficacy and organ toxicity in an orthotopic gastric tumor mouse model.
Main Results:
- The developed EGCG/DX-loaded NPs effectively targeted and bound to gastric cancer cells, enhancing cellular uptake.
- The NP-based drug delivery demonstrated superior anti-cancer effects compared to the free EGCG/DX combination solution.
- In vivo studies showed significant inhibition of gastric tumor progression with no observed organ injury.
Conclusions:
- The EGCG/DX-NP system represents a promising nanomedicine-based approach for gastric cancer treatment.
- This novel system enhances combination chemotherapy efficacy through targeted delivery and synergistic drug action.
- Further development of this nanomedicine platform could lead to improved therapeutic strategies for gastric cancer.
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