In this study, we prepared PLLA/bpV（pic） microspheres, a bpV（pic） controlled release system and examined their ability to protect nerve cells and promote axonal growth. PLLA microspheres were prepared by employing...In this study, we prepared PLLA/bpV（pic） microspheres, a bpV（pic） controlled release system and examined their ability to protect nerve cells and promote axonal growth. PLLA microspheres were prepared by employing the o/w single emulsification-evaporation technique. Neural stem cells and dorsal root ganglia were divided into 3 groups in terms of the treatment they received： a routine medium group（cultured in DMEM）, a PLLA microsphere group（DMEM containing PLLA microspheres alone） and a PLLA/bpV（pic） group [DMEM containing PLLA/bpV（pic） microspheres]. The effects of PLLA/bpV（pic） microspheres were evaluated by the live-dead test and measurement of axonal length. Our results showed that PLLA/bpV（pic） granulation rate was（88.2±5.6）%; particle size was（16.8±3.1）%, drug loading was（4.05±0.3）%; encapsulation efficiency was（48.5±1.8）%. The release time lasted for 30 days. In PLLA/bpV（pic） microsphere group, the cell survival rate was（95.2 ±4.77）%, and the length of dorsal root ganglion（DRG） was 718±95 μm, which were all significantly greater than those in ordinary routine medium group and PLLA microsphere group. This preliminary test results showed the PLLA/bpV（pic） microspheres were successfully prepared and they could promote the survival and growth of neural cells in DRG.展开更多
基金supported by Science and Technology Plan-ning Project of Guangdong Province,China(No.2011B031800205)
文摘In this study, we prepared PLLA/bpV（pic） microspheres, a bpV（pic） controlled release system and examined their ability to protect nerve cells and promote axonal growth. PLLA microspheres were prepared by employing the o/w single emulsification-evaporation technique. Neural stem cells and dorsal root ganglia were divided into 3 groups in terms of the treatment they received： a routine medium group（cultured in DMEM）, a PLLA microsphere group（DMEM containing PLLA microspheres alone） and a PLLA/bpV（pic） group [DMEM containing PLLA/bpV（pic） microspheres]. The effects of PLLA/bpV（pic） microspheres were evaluated by the live-dead test and measurement of axonal length. Our results showed that PLLA/bpV（pic） granulation rate was（88.2±5.6）%; particle size was（16.8±3.1）%, drug loading was（4.05±0.3）%; encapsulation efficiency was（48.5±1.8）%. The release time lasted for 30 days. In PLLA/bpV（pic） microsphere group, the cell survival rate was（95.2 ±4.77）%, and the length of dorsal root ganglion（DRG） was 718±95 μm, which were all significantly greater than those in ordinary routine medium group and PLLA microsphere group. This preliminary test results showed the PLLA/bpV（pic） microspheres were successfully prepared and they could promote the survival and growth of neural cells in DRG.
