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In vitro evaluation and cellular biocompatibility of Scutellarein-loaded PLGA nanoparticle
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DOI   10.11656/j.issn.1673-9043.2014.01.10
Key Words   controlled release;PLGA nanoparticles;Scutellarein;biocompatibility
Author NameAffiliationE-mail
LI Nan Tianjin State Key Laboratory of Modern Chinese Medicine, Engineering Research Center of Modern Chinese Medicine Discovery and Preparation Technique, Tianjin Univesity of TCM, Tianjin 300193, China  
LIU Zhi-dong Tianjin State Key Laboratory of Modern Chinese Medicine, Engineering Research Center of Modern Chinese Medicine Discovery and Preparation Technique, Tianjin Univesity of TCM, Tianjin 300193, China  
FAN Li-li Tianjin State Key Laboratory of Modern Chinese Medicine, Engineering Research Center of Modern Chinese Medicine Discovery and Preparation Technique, Tianjin Univesity of TCM, Tianjin 300193, China  
LI Lin Tianjin State Key Laboratory of Modern Chinese Medicine, Engineering Research Center of Modern Chinese Medicine Discovery and Preparation Technique, Tianjin Univesity of TCM, Tianjin 300193, China  
WANG Ai-chao Tianjin State Key Laboratory of Modern Chinese Medicine, Engineering Research Center of Modern Chinese Medicine Discovery and Preparation Technique, Tianjin Univesity of TCM, Tianjin 300193, China  
GUO Li-li Tianjin State Key Laboratory of Modern Chinese Medicine, Engineering Research Center of Modern Chinese Medicine Discovery and Preparation Technique, Tianjin Univesity of TCM, Tianjin 300193, China  
PAN Wei-san Shenyang Phanmaceatieal University, Shenyang 110016, China ppwwss@163.com 
Abstract
    [Objective] To prepare Scutellarein loaded PLGA nanoparticles and characterize the physicochemical properties, in vitro release behavior and biocompatibility of HCEpic cells. [Methods] The PLGA nanoparticles were prepared by emulsion solvent diffusion method. The characterization and release effect of PLGA NPs in vitro were evaluated. The main outcome measures included size, Zeta potential, Encapsulation efficiency, the drug content of the final nanoparticles etc. The in vitro release curve was drawn. The cytotoxicity of PLGA NPs were evaluated by cell proliferation assay. [Results] The particle sizes, Zeta potential, Encapsulation efficiency and the drug content of the final nanoparticles were 128.4 nm, -21.1 mV, (92.5±2.35)% and (23.12±1.45)%, respectively. The release of Scutellarein from PLGA nanoparticles were markedly reduced compared with Scutellarein solution. Cell proliferation assay revealed the PLGA-NPs did not damage the cell growth in vitro, indicating a good compatibility. [Conclusion] The PLGA-NPs prepared by emulsion solvent diffusion method have a good release effect and good biocompatibility in vitro.

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