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作 者:卢光照 侯成[1] 张翮[1] 孙治国[1] 鲁莹[1] 钟延强[1] 邹豪[1]
出 处:《药学学报》2017年第12期1942-1950,共9页Acta Pharmaceutica Sinica
基 金:国家自然科学基金资助项目(30801441;81773278);军队后勤科研重大项目(AWS14J011)
摘 要:本文制备光敏感型活性氧自由基(reactive oxygen species,ROS)响应脂质体,研究其体外抗肿瘤活性。采用硫酸铵梯度法制备共输送光敏剂八丁氧基酞菁钯[1,4,8,11,15,18,22,25-octabutoxypalladium phthalocyanine,Pd PC(OBu)_8]与盐酸多柔比星(doxorubicin hydrochloride,DOX)的脂质体[liposome loaded with Pd PC(OBu)_8and DOX,LPD],考察LPD的粒径、zeta电位、透射电镜照片、光敏感型ROS响应药物的光响应释放及在血清中稳定性,进一步考察LPD在MCF-7细胞中的细胞毒性、细胞摄取及细胞内单线态氧(singlet oxygen,~1O_2)水平。结果显示,LPD的粒径为(169.3±1.2)nm,PDI为0.198±0.003,粒径均匀,zeta电位为(-39.8±0.8)m V。LPD具有良好的光响应释放特性,在730 nm激光以300 m W·cm^(-2)光照强度下,5 min内DOX释放率达到95.5%。LPD能显著促进DOX的细胞摄取,而且光照时细胞内能产生大量~1O_2。与游离DOX相比,LPD未光照时IC_(50)下降67.9%,光照时IC_(50)下降85.7%。因此,光敏ROS响应脂质体是具有前景的给药系统。Photo-sensitive reactive oxygen species(ROS)responsive liposomes loaded with 1,4,8,11,15,18,22,25-octabutoxypalladium phthalocyanine[Pd PC(OBu)8]and doxorubicin hydrochloride(DOX)(LPD)were prepared by(NH4)2SO4-gradient method.LPD was characterized with transmission electron microscopy(TEM),dynamic light scattering particle size,zeta potentials,photo-sensitive ROS-responsive DOX release behaviors and the serum stability in vitro.LPD cytotoxicity,DOX uptake and singlet oxygen production in MCF-7 cells were evaluated.The results showed that the particle size of LPD was(169.3±1.2)nm,PDI of LPD was 0.198±0.003 and zeta potentials of LPD was(-39.8±0.8)m V.The accumulated release of DOX reached 95.5%in 5 min under 730 nm laser irradiation(300 m W·cm^(-2)).The DOX uptake of liposome was increased and ~1O2 was generated.The half inhibition concentration(IC(50))of DOX in LPD with irradiation group was decreased by 85.7%and no irradiation group was decreased by 67.9%compared with free DOX group in MCF-7 cells.Therefore,photo-sensitive ROS-responsive liposomes would be a promising drug delivery system for tumor therapy.
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