The invention discloses a mouse peritoneal
macrophage phagocytosis experiment method. The method comprises the following steps: step 1,
reagent preparation and SPF-level Kunming mouse preparation; 2, macrophage induction: injecting a 6% soluble
starch solution into the
abdominal cavity of the mouse; 3, inducing phagocytic reaction, namely injecting 1% chicken
erythrocyte suspension into the
abdominal cavity 48 hours after injecting the 6% soluble
starch solution; 4, collecting a sample, injecting the 1% chicken
red blood cell suspension for 30 minutes, and taking
peritoneal fluid; 5, preparing and
dyeing a smear, and clearly distinguishing
cell morphology; and 6, carrying out microscopic examination and quantitative analysis, and evaluating the activity of the macrophages by counting the phagocytic percentage and the
phagocytic index. The method solves the problems of disordered parameters, difficulty in
dyeing identification, extensive results and the like in a traditional method, is simpler and more convenient to operate and higher in result stability, and can provide reliable
technical support for immunological research,
drug development and
disease assessment so as to guarantee the accuracy of experimental data.