WANG Xue-qing, DAI Jun-dong, ZHANG Qiang, ZHANG Tao, XIA Gui-min. Relative bioavailability of cyclosporine A-loaded hydroxypropyl methylcellulose phthalate nanoparticles for oral administration in ratsJ. Acta Pharmaceutica Sinica, 2004, 39(6): 463-466.
Citation: WANG Xue-qing, DAI Jun-dong, ZHANG Qiang, ZHANG Tao, XIA Gui-min. Relative bioavailability of cyclosporine A-loaded hydroxypropyl methylcellulose phthalate nanoparticles for oral administration in ratsJ. Acta Pharmaceutica Sinica, 2004, 39(6): 463-466.

Relative bioavailability of cyclosporine A-loaded hydroxypropyl methylcellulose phthalate nanoparticles for oral administration in rats

  • AimTo study the preparation of hydroxypropyl methylcellulose phthalate(HPMCP) nanoparticles and compare its pharmacokinetic characteristics with Neoral. MethodsHPMCP nanoparticles loaded cyclosporine A were prepared by solvent-nonsolvent method. CyA-HP50 nanoparticles, CyA-HP55 nanoparticles and Neoral were orally administered at the dosage of 15 mg·kg-1 to rats. The CyA concentration in blood were determined by HPLC. Pharmacokinetic parameters were calculated by 3P97 program. ResultsThe concentration-time data of the three preparations were best fit by two compartment model. The relative bioavailability of CyA-HP50 and CyA-HP55 nanoparticles calculated by the AUC0-72 were 82.3% and 119.6%, bioequivalent to the reference of Neoral. The relative bioavailability of CyA-HP55 nanoparticles was 145.3% of CyA-HP50 nanoparticles. Conclusion CyA HPMCP nanoparticles could be prepared easily and reproducibly. It was found that the oral absorption of CyA can be increased by using the HPMCP nanoparticles.
  • loading

Catalog

    Turn off MathJax
    Article Contents

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return