Targeting functionalized nanoparticles towards 2D and 3D colorectal cancer models from cell lines and patient tumor biospecimens in microfluidics systems

• Grant number: 19/18471-6
• Support Opportunities: Scholarships abroad - Research Internship - Doctorate
• Start date: November 28, 2019
• End date: July 27, 2020
• Field of knowledge: Physical Sciences and Mathematics - Chemistry - Physical-Chemistry
• Principal Investigator: Mateus Borba Cardoso
• Grantee: Iris Renata Sousa Ribeiro
• Supervisor: Aleksander Skardal
• Host Institution: Centro Nacional de Pesquisa em Energia e Materiais (CNPEM). Campinas , SP, Brazil
• Institution abroad: Ohio State University, Columbus, United States
• Associated to the scholarship: 17/21318-0 - Targeting of functionalized nanoparticles in microfluidics systems containing multiple organoids, BP.DR

Abstract

Cancer is known for its high mortality rates and for treatments which are often related to undesirable secondary effects. Therefore, the development of alternative methods for treating this disease is of paramount significance. Thus, a powerful strategy is the use of multifunctional nanoparticles (NPs), which have been extensively investigated in the recent years. NPs functionalized with ligands are among the most promising therapeutic-based strategies since they enhance the drug targeting towards tumor cells while minimizing adverse effects. Despite its great potential, few NP-based systems have been approved by the Food and Drug Administration (FDA), especially because of the need of new platforms that mimic with high reliability the human body. As a consequence, the present project is intended to evaluate and compare the action of functionalized silica nanoparticles (SiO2NPs) with kinetic stabilizer (zwitterionic group) and tumor driver (folate group) in 2D and 3D cultures based on healthy and tumor human colon cells. These studies will be conducted in static and flow conditions, using an organ-on-a-chip platform, which consists of a microfluidic system incorporating synthetic in vitro tissues to simulate human physiology at the tissue and organ levels. Subsequently, experiments will be performed using patient colorectal tumor tissues in static and flow conditions, which provides a more reliable analysis on the behavior of NPs in tumors, opening doors for the advancement of personalized medicine.

Scientific publications

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

RIBEIRO, IRIS RENATA SOUSA; DA SILVA, RAQUEL FRENEDOSO; DOMINGUES, ROMENIA RAMOS; LEME, ADRIANA FRANCO PAES; CARDOSO, MATEUS BORBA. Dual-functionalized architecture enables stable and tumor cell-specific SiO2NPs 2 NPs in complex biological fluids. BEILSTEIN JOURNAL OF NANOTECHNOLOGY, v. 15, p. 15-pg., 2024-10-07. (17/21318-0, 21/12071-6, 15/25406-5, 19/18471-6)