The application provides a
drug-loaded
nanoparticle Cor@PDA-PEG@CD11b and a preparation method and application thereof, the preparation method comprises the following steps: S1, mixing
cordycepin solution and PDA
aqueous solution, so that the
cordycepin and the PDA form a complex Cor@PDA through π-π stacking effect; S2, the obtained complex Cor@PDA is modified by PEG to prepare a complex Cor@PDA@PEG; S3, the obtained Cor@PDA@PEG is dispersed in a
buffer solution, and an anti-CD11
b antibody is added; after reacting for 24h,
centrifugation, washing, collecting the precipitate, and
drying, the Cor@PDA-PEG@CD11b is obtained. The
drug-loaded
nanoparticle Cor@PDA-PEG@CD11b prepared by the application provides a new idea and direction for the treatment of
sepsis-related
lung injury; through the characteristics of the PDA nanoparticles, the
cordycepin is released in a controlled manner, and the problem that the cordycepin is rapidly oxidized and inactivated after entering the body is avoided, the
bioavailability is improved, the specific antibodies on the surface of immune cells and the physiological characteristics are utilized, the immune cells are quickly and chemotactically recruited to the inflammatory
injury site in the early stage of acute
inflammation, the
drug is quickly and accurately targeted, and the
sepsis lung injury is reduced.