http://jcps.bjmu.edu.cn

Journal of Chinese Pharmaceutical Sciences ›› 2018, Vol. 27 ›› Issue (8): 517-529.DOI: 10.5246/jcps.2018.08.053

• Original articles •     Next Articles

Treatment of cervical cancer by siRNA-loaded chitosan-coated calcium phosphate nanoparticles

Piaopiao Li1, Yi Yan1, Haitao Zhang1,2, Ru Wang1, Huhu Han1, Jiancheng Wang1*   

  1. 1. Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
    2. School of Pharmaceutical Sciences, Central South University, Changsha, Hunan 410013, China
  • Received:2018-05-13 Revised:2018-06-19 Online:2018-09-04 Published:2018-06-30
  • Contact: Tel.: +86-010-82805932, E-mail: wang-jc@bjmu.edu.cn
  • Supported by:

    National Natural Science Foundation of China (Grant No. 81473158, 81690264 and 81773650), the New Drug R&D program of China (Grant No. 2018ZX09721003-004) and the Opening Project of Key Laboratory of Drug Targeting and Drug Delivery System, Ministry of Education (Sichuan University).

Abstract:

In the present study, a chitosan-coated calcium phosphate nanoparticle (CS/CaP/siRNA NP) was developed to deliver siRNA for treatment of cervical cancer. The CS/CaP/siRNA NPs were prepared by the nano-precipitation method. The resulted NPs had a uniform spherical morphology with a size of ~194 nm and a zeta potential of ~+27 mV. In vitro experiments demonstrated that these NPs could efficiently deliver siEGFR into Hela cells and significantly down-regulate the EGFR expression level, which was probably associated with enhanced cell adhesion of chitosan, leading to extended residence time of cell internalization. Then the internalized CS/CaP/siRNA NPs exhibited pH-responsive disassembly of NPs, resulting in the enhanced release of siRNA and rapid lysosomal escape into cytoplasm. Moreover, in vivo anticancer results showed that the CS/CaP/siRNA NPs had significant inhibitory effects on tumor growth after intratumoral injection in Hela tumor xenografted nude mice, accompanying with no obvious changes of body weight during the whole experimental period. All these results indicated that the CS/CaP/siRNA NPs would have great potential to deliver siRNA for the treatment of cervical cancer via mucosal administration.

Key words: siRNA delivery, Chitosan, Calcium phosphate, pH-sensitive, Cervical cancer

CLC Number: 

Supporting: