A fluorescence microscopic method for characterizing size, quantity, and oxidation of lipid droplets (LDs) in HepG2 cells was developed. LDs were induced by palmitic (PA), oleic (OA), or linoleic acids (LA), and stained with two fluorescent probes for neutral lipids and lipid peroxides. Each fatty acid increased the number of LDs and oxidized LDs (oxLDs) and the degree of LD oxidation time-dependently, as well as increased intracellular triglyceride hydroperoxides. LDs induced by LA without AAPH showed the most significant oxidation degree over PA and OA, especially in large LDs (area ≥3 µm 2 , oxLD/LD = 52.3±21.7%). Under this condition, two food-derived antioxidants were evaluated, and both of them significantly improved the LD characteristics. Moreover, chlorogenic acid reduced the quantity of large LDs by 74.0%−87.6% dose-dependently. The proposed method might provide a new approach to evaluate the effect of dietary antioxidants.