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Published on: January 5, 2021
Melanoma-on-a-chip model for anticancer drug injecting delivery method
Pedro Herreros1, Ana López-Hernández1, Miguel Holgado2
1Group of Optics, Photonics and Biophotonics (GOFB), Center for Biomedical Technology, Universidad Politécnica de Madrid, Pozuelo de Alarcon, Spain; Group of Organ and Tissue on-a-Chip and In-Vitro Detection, Health Research Institute of the Hospital Clínico San Carlos, Madrid, Spain.
This study introduces a novel skin-on-a-chip model for melanoma research. The microfluidic device effectively models skin and delivers anticancer drugs, reducing melanoma cell populations.
Area of Science:
- Biomedical Engineering
- Oncology
- Drug Development
Background:
- Traditional skin models face challenges in pharmaceutical and cosmetic product development.
- Organ-on-a-chip systems, especially for skin, show promise but lack melanoma study integration.
- A need exists for advanced models to study melanoma and test anti-cancer therapies.
Purpose of the Study:
- To develop and validate a novel skin-on-a-chip device for melanoma research.
- To assess the efficacy of an anticancer drug (Gemcitabine) using this microfluidic model.
- To establish a high-fidelity platform for real-time drug testing and melanoma monitoring.
Main Methods:
- Designed a two-chamber microfluidic skin-on-a-chip device.
- Established a 3D co-culture of fibroblasts, keratinocytes, and melanoma cells.
- Administered the anticancer drug Gemcitabine via an integrated injection system.
Main Results:
- Observed a significant impact on co-culture cell distribution.
- Demonstrated a decrease in melanoma (cancerous) cell population post-Gemcitabine administration.
- Validated the chip's effectiveness for anti-melanoma therapy testing.
Conclusions:
- The developed skin-on-a-chip is an effective model for studying melanoma.
- The microfluidic platform facilitates real-time monitoring of anti-melanoma drug efficacy.
- This technology offers an enhanced fidelity alternative for drug development and melanoma research.

