The invention discloses an oral
solid lipid nano-particle preparation of
calcitonin, which is a
particle suspension containing 0.01 percent
sodium cholate in a water phase, wherein lipid nano-particles comprise an active medicament component and a lipid material forming the particles. Simultaneously, the preparation method comprises the following steps: dissolving or melting a medicament and a carrier in an
organic solvent phase together; quickly infusing the organic phase into the water phase stirred at a low temperature to form a lipid nano-particle dispersion liquid; standing, melting and performing high-speed
centrifugal separation on the lipid nano-particle dispersion liquid to obtain a nano-
particle deposition; and dispersing the deposition to obtain a target oral
calcitonin lipid nano-particle dispersion liquid. The oral
solid lipid nano-particle preparation uses the lipid material as a structural matrix material, and the oral
solid lipid nano-particle preparation of the
calcitonin is prepared through reasonable component proportion to prevent the medicament from leaking in an
aqueous medium and release the medicament in
modes of
in vivo esterase degradation and the like, thus the aim that the medicament contained in a nano-carrier can adjust the serum
calcium concentration more reasonably and more safely through biomembranes of mammals is achieved.