Chinese Journal of Tissue Engineering Research ›› 2011, Vol. 15 ›› Issue (25): 4615-4618.doi: 10.3969/j.issn.1673-8225.2011.25.014

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Delayed release of compound chitosan nano-microspheres PLGA/nHA control-releasing carrier systems

An Shi-chang, Sun Jian, Li Ya-li, Xu Yao-xiang, Wang Ke, Chen Li-qiang, Xiao Wen-lin   

  1. Departocent of Oral and Maxillofacial Surgery, Affiliated Hospital of Qingdao University Medical School, Qingdao  266021, Shandong Province, China
  • Received:2010-11-18 Revised:2010-12-18 Online:2011-06-18 Published:2014-01-10
  • Contact: Sun Jian, Doctor, Professor, Chief physician, Master’s supervisor, Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Qingdao University Medical School, Qingdao 266021, Shandong Province, China sunjianqy@126.com
  • About author:An Shi-chang★, Studying for master’s degree, Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Qingdao University Medical School, Qingdao 266021, Shandong Province, China anshichang510@163.com

Abstract:

BACKGROUND: Polylactic acid-glycolic acid (PLGA) is a kind of biodegradable polymer with excellent biocompatibility, plasticity and certain strength and toughness. But its degradation products are acidic, which can affect local pH and inhibit tissue growth.
OBJECTIVE: To prepare composite scaffolds with excellent characteristics of delayed release of proteins.
METHODS: Using bovine serum album (BSA) as model protein, chitosan microspheres (CMs) were prepared by ionotropic gelation. Ice particulates were used as porogen. Composite scaffolds were prepared with CMs/nHA/PLGA by freeze-drying. Scanning electron microscope, transmission electron microscope, mercury porosimeter and universal testing machine ware used to observe the characteristic and morphology of the composite scaffolds.
RESULTS AND CONCLUSION: The CMs were spherical in shape with a regular surface. The diameters of the CMs were in the range of 220-770 nm, mainly ranging 380-650 nm. The encapsulation efficiency of the CMs was 68.3%, and the loading capacity was 39.2%. The both were related with the initial concentration of BSA. The pore diameter of the composite scaffolds was about 125-355 m, the porosity was 83.4%, and the compressive strength was about 1.4-2.1 MPa. The cumulative degradation was 28.6% at 10 weeks. The cumulative release of BSA from PLGA/nHA scaffolds was 85% in 2 days, which from CMs and CMs/nHA/PLGA scaffolds was 48.9% and 35.7% in 9 days. The CMs microspheres and CMs/nHA/PLGA scaffolds have a desirable release rates for BSA and strength, are expected to use as carrier for growth factor and bone tissue engineering scaffolds.

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