Carbon
dots (CDs) with exciting photoluminescence characteristics,
mild toxicity, and good biocompatibility are the research hotspots
in biomedical application. Here, a compact antibacterial activity
of CDs from levofloxacin hydrochloride is reported. The obtained CDs
with an average size of 1.27 nm have fascinating antibacterial properties
against both gram-positive and negative bacteria, with minimum inhibitory
concentrations (MICs) of 64, 128, 64, and 128 μg/mL for Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa), Staphylococcus
aureus (S. aureus),
and Bacillus subtilis (B. subtilis). The antibacterial processes of CDs
from extracellular to intracellular were demonstrated, including physical/chemical
binding to membrane, wrapping on the surface, destruction of the cell
membrane, and promoting reactive oxygen species (ROS) production into
the cell without additional light or oxidant. Surprisingly, CDs exert
moderate cytotoxicity on mammalian cells at the equivalent bactericidal
concentration, in which the cell viability is more than 80% at 100
μg/mL of CDs. The investigation of antibacterial CDs may provide
a useful avenue for further exploiting CD-based nano-bactericides
in biomedical applications.