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Citral-Loaded Self Nano-Emulsifying Drug Delivery System Suppresses Metastasis and Enhances Apoptosis in SW620 Colon
Mira Nadiah Mohd Izham1, Yazmin Hussin1, Nurul Elyani Mohamad2
1Department of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, Selangor, Malaysia.
Citral-loaded self-nano-emulsifying drug delivery systems (CIT-SNEDDS) effectively kill colon cancer cells by inducing apoptosis and inhibiting metastasis. Further studies are needed to explore CIT-SNEDDS as a potential colorectal cancer therapy.
Area of Science:
- Natural Product Chemistry
- Cancer Biology
- Drug Delivery Systems
Background:
- Colorectal cancer incidence is rising globally.
- Natural products like citral offer potential therapeutic avenues.
- Citral-loaded self-nano-emulsifying drug delivery systems (CIT-SNEDDS) show promise.
Purpose of the Study:
- To evaluate the apoptosis-inducing and anti-metastatic effects of CIT-SNEDDS on colon cancer cells.
- To assess the efficacy of CIT-SNEDDS compared to free citral and empty SNEDDS.
- To explore CIT-SNEDDS as a potential therapeutic agent for colorectal cancer.
Main Methods:
- Utilized Acridine Orange/Propidium Iodide and Annexin V assays to detect apoptosis.
- Performed cell cycle analysis via flow cytometry.
- Assessed anti-metastatic potential using scratch and trans-well assays on SW620 cells.
Main Results:
- CIT-SNEDDS significantly reduced colon cancer cell viability in a dose-dependent manner.
- Confirmed apoptosis induction and cell cycle arrest at S and G2/M phases by CIT-SNEDDS.
- Demonstrated significant inhibition of SW620 cell migration and invasion with CIT-SNEDDS treatment.
Conclusions:
- CIT-SNEDDS effectively induces apoptosis, disrupts the cell cycle, and inhibits cancer cell migration.
- These properties align with targeted cancer therapy goals.
- CIT-SNEDDS shows therapeutic potential for colorectal cancer, warranting further preclinical investigation.
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