Chinese Journal of Tissue Engineering Research

Previous Articles     Next Articles

Release effect of epirubicin hydrochloride nano-targeted delivery

Tang Jia-ming, Zhao Xiu-hua, Zu Yuan-gang   

  1. Key Laboratory of Forest Plant Ecology of Ministry of Education, Northeast Forestry University, Harbin  150040, Heilongjiang Province, China
  • Received:2013-02-18 Revised:2013-03-02 Online:2013-05-21 Published:2013-05-21
  • Contact: Zu Yuan-gang, Professor, Key Laboratory of Forest Plant Ecology of Ministry of Education, Northeast Forestry University, Harbin 150040, Heilongjiang Province, China zygorl@yahoo.com.cn
  • About author:Tang Jia-ming★, Studying for master’s degree, Key Laboratory of Forest Plant Ecology of Ministry of Education, Northeast Forestry University, Harbin 150040, Heilongjiang Province, China tjmorl@yahoo.com.cn
  • Supported by:

    Nonprofit Industry Scientific Research Special Projects, No. 201204601*; Agricultural Science and Technology Achievement Transformation Foundation, No. 2011GB23600016*; Postdoctoral Foundation of Heilongjiang Province, No. LBH-10283

Abstract:

BACKGROUND: Epirubicin hydrochloride is a kind of broad-spectrum antibiotics, and the disadvantages in the clinical application are faster drug release and low drug concentrations of target tissue. Epirubicin hydrochloride can widely distribute in various organs after intravenous administration with obvious side effects.
OBJECTIVE: To prepare the epirubicin hydrochloride nano-targeted delivery according to the shortages of epirubicin hydrochloride in the clinical application.
METHODS: The epirubicin hydrochloride nano-targeted delivery was prepared with the carrier of folate-conjugated epirubicin hydrochloride albumin nanoparticles by the method of emulsification-high pressure homogenization. Particles size, distribution and Zeta potential were detected by laser particle size analyzer. The morphology of epirubicin hydrochloride nanoparticles was observed by scanning electron microscope.In addition, encapsulation capability, loading content and drug release of the folate-conjugated epirubicin hydrochloride albumin nanoparticles were analyzed by high-performance liquid chromatography.
RESULTS AND CONCLUSION: The results showed that the nanoparticles were spherical and well distributed. The mean particle size was (157.73±0.4) nm, and mean Zeta potential was (-30.85±0.43) mV. The encapsulation efficiency was 96.24% and the loading content was 22.78%. The results of simulate drug releasing results showed that the drug release curve could be divided into two phases, microspheres release in the burst release phase could reach 42.6% at 24 hours, nanoparticles release could be lasted for a long time in the sustained-release stage, and the drug release could reach to 84.1% at 112 hours. The drug release rate of the drug-loaded nanoparticles remained stable. The epirubicin hydrochloride nano-targeted delivery prepared with emulsification-high pressure homogenization has uniform particle size, narrow size distribution, high encapsulation efficiency and loading content, and has certain release effect.

Key words: biomaterials, nanobiomaterials, epirubicin hydrochloride, bovine serum album, floate, target delivery, nanoparticles, emulsification-high pressure homogenization technique, releasing in vitro, other grants-supported paper

CLC Number: