Chinese Journal of Tissue Engineering Research ›› 2014, Vol. 18 ›› Issue (43): 6990-6995.doi: 10.3969/j.issn.2095-4344.2014.43.017

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Preparation and characterization of poly D,L-lactide-co-glycolide CXCR4-miRNA nanoparticles

Gao Feng, Dong Qin, Cui Jie, Chen Pei, Wang Shao-liang   

  1. Department of Nephrology, Armed Police Hospital of Shanghai, Shanghai 201103, China
  • Received:2014-09-03 Online:2014-10-15 Published:2014-10-15
  • Contact: Dong Qin, Attending physician, Department of Nephrology, Armed Police Hospital of Shanghai, Shanghai 201103, China
  • About author:Gao Feng, Attending physician, Department of Nephrology, Armed Police Hospital of Shanghai, Shanghai 201103, China
  • Supported by:

    the Youth Fund of Shanghai Health Bureau, No. 2011Y126

Abstract:

BACKGROUND: Related studies have showed that poly D,L-lactide-co-glycolide can effectively package antisense oligonucleotides, small interfering RNA, microRNA. Poly D,L-lactide-co-glycolide can better protect them against the destruction of the enzymes in vivo and have slow the drug release. Therefore, the number of drug administration can be reduced to achieve a long-term and effective therapeutic effect.
OBJECTIVE: To prepare poly D,L-lactide -co-glycolide-CXCR4-miRNA-nano-particles and to research the characteristics of the prepared nanoparticles.
METHODS: Poly D,L-lactide-co-glycolide-CXCR4-miRNA nanoparticles were prepared by double emulsion-evaporation process. Ultraviolet spectrophotometry was utilized for measurement of encapsulation efficiency and drug-loading rate, observing the shape of nanoparticles by transmission electron microscope, and measuring the size and distribution of nanoparticles by laser particle size analyzer. Sustained-release characteristics of nanoparticle suspension were observed in phosphate buffer.
RESULTS AND CONCLUSION: The prepared nanoparticles were spherical-shaped, smooth, evently distributed and inadhesive. The particle size was mainly distributed within 143-502 nm, with an average diameter of 280 nm. 
The average drug loading was (0.515±0.023)%, the average encapsulation ratio was 50.2% and difference between batches was small. The nanoparticles could slowly release in vitro and the process initially experienced the fast-release stage, and then reached a basically stable platform stage at day 14. These finding indicate that the process to prepare poly D,L-lactide-co-glycolide CXCR4-miRNA-nanoparticles by double emulsion-evaporation is simple. The prepared nanoparticles are well targeted and exhibit sustained-release effects.


中国组织工程研究杂志出版内容重点:生物材料;骨生物材料; 口腔生物材料; 纳米材料; 缓释材料; 材料相容性;组织工程


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Key words: lactic acid, receptors, CXCR4, microRNAs, microspheres

CLC Number: