Microtissues®

Summary

Published in Pharmacology Research & Perspectives (2024), this peer-reviewed study used 3D Petri Dish® micro-molds to form scaffold-free 3D microtissues. Full citation: Petzer, Melissa, et al. A549 Alveolar Carcinoma Spheroids as a Cytotoxicity Platform for Carboxyl‐ and Amine‐Polyethylene Glycol Gold Nanoparticles

🧬 Oncology

A549 Alveolar Carcinoma Spheroids as a Cytotoxicity Platform for Carboxyl‐ and Amine‐Polyethylene Glycol Gold Nanoparticles

Pharmacology Research & Perspectives 2024 Petzer, Melissa, et al
Cite as: Petzer, Melissa, et al. A549 Alveolar Carcinoma Spheroids as a Cytotoxicity Platform for Carboxyl‐ and Amine‐Polyethylene Glycol Gold Nanoparticles. Pharmacology Research & Perspectives (2024). doi:10.1002/prp2.70051 doi.org/10.1002/prp2.70051

Research Overview

Gold nanoparticles have distinctive physicochemical properties and can be functionalized as anticancer agents, and spheroids offer a more tissue-like test bed than monolayers. This study developed an A549 alveolar carcinoma spheroid model — generated in an agarose micro-mold — for cytotoxicity assessment and mechanistic evaluation of functionalized gold nanoparticles.

Spheroids were characterized over 21 days of culture for morphology, acid phosphatase activity, and protein content. Day-7 spheroids were then exposed for 72 hours to carboxyl-PEG- and amine-PEG-functionalized nanoparticles, with cytotoxicity read out by morphology, acid phosphatase activity, protein content, caspase-3/7 activity, and cell-cycle analysis.

Key Discoveries

  • A549 spheroids formed in an agarose micro-mold and characterized across 21 days of culture
  • Carboxyl-PEG and amine-PEG gold nanoparticles compared for 72-h cytotoxicity on day-7 spheroids
  • Multi-endpoint readout: morphology, acid phosphatase, protein, caspase-3/7, and cell cycle