R8修饰具有壳核结构的磷脂纳米粒的制备及其体外摄取研究
Study on the preparation and properties of R8 conjugated PLGA-lecithin-PEG core-shell nanoparticles in vitro
作者:周劲;张倩玉;陈雯霏;傅灵;刘亚圆;何勤;
Author:
收稿日期: 年卷(期)页码:2013,28(05):-441-443
期刊名称:华西药学杂志
Journal Name:WEST CHINA JOURNAL OF PHARMACEUTICAL SCIENCES
关键字:R8;壳核;磷脂纳米粒;细胞摄取
Key words:
基金项目:国家自然科学基金资助项目(批准号:81072599)
中文摘要
目的采用磷脂和聚乳酸羟基乙酸共聚物(PLGA)制备细胞穿膜肽R8介导的具有壳核结构的磷脂纳米粒,筛选处方并考察其理化性质和体外细胞摄取效率。方法采用一步沉淀法制备具有壳核结构的磷脂纳米粒,考察其形态、粒径及电位,并通过HepG2细胞与PLGA纳米粒比较摄取效率。结果所制备的R8修饰磷脂纳米粒在电镜下观察其外观为球形,平均粒径为96.8±5.5 nm,Zeta电位为-13.50±2.23 mV。体外细胞摄取实验表明:HepG2细胞对经R8修饰的磷脂纳米粒的摄取效率分别是无R8修饰的磷脂纳米粒和PLGA纳米粒的2.1倍和3.2倍。结论该磷脂纳米粒制备方法简单,与无R8修饰磷脂纳米粒和PLGA纳米粒相比,经R8和磷脂修饰的纳米粒可显著提高细胞摄取效率。
英文摘要
[1]Langer R.Drug delivery and targeting[J].Nature,1998,392:5-10.
[2]Ferrari M.Cancer nanotechnology:Opportunities and challenges[J].Nat Rev Cancer,2005,5:161-171.
[3]Gupta H,Pharm B,Pharm M,et al.Sparfloxacin-loaded PLGAnanoparticles for sustained ocular drug delivery[J].Nanomedi-cine,2010,6(2):324-333.
[4]Zhang L,Chan JM,Gu FX,et al.Self-assembled lipid-polymerhybrid nanoparticles:A robust drug delivery platform[J].ACSNano,2008,2(4):1696-1702.
[5]Kale A,Torchilin V.Enhanced transfection of tumor cells in vivousing“Smart”pH-sensitive TAT-modified pegylated lipo-somes[J].J Drug Targeting,2007,15(3):538-545.
[6]Noriyuki M,Yoshito T,Miki T,et al.Anti-neovasculartherapy byuse of tumor neovasculature-targeted long-circulating liposome[J].JCR,2004,100(3):41-52.
[7]Beata C,Allan ED,Bradford AM,et al.Substantiating in vivomagnetic brain tumor targeting of cationic iron oxidenanocarriers-via adsorptive surface masking[J].Biomaterials,2009,3(4):1-8.
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