Programming model methodology for data of drug release in vitro;

OBJECTIVE To prepare thymopentin microspheres and investigate the drug release in vitro.

Several characteristics of c hitosan nanoparticles such as morphology,particle size,zeta potential,drug entra pment efficiency and drug release in vitro were evaluated.

Preparation and in vitro dissolution of the solid dispersions of cinnamon oil;

Preparation and in vitro dissolution of glipizide sustained-release pellet capsules;

Preparation and in vitro dissolution of diclofenac sodium sustained-release tablets;

Preparation of diclofenac sodium liposomes by active loading method and its release in vitro;

Influence of gel vehicles on release in vitro and transdermal resorption of integerrimine;

Preparation of irinotecan hydrochloride containing liposomes by ammonium sulfate gradient method and its release in vitro

Study on preparation and in vitro release characteristics of Bitongning Patch;

Preparation and in vitro release of Niacin sustained-release tablets;

A study on the preparation and in vitro release models of doxorubicin-nanoparticles;

A mathematic model was proposed based on the experimental results and theoretical analysis of in vitro drug release.

OBJECTIVE To prepare praziquantel implants and investigate the in vitro drug release.