赵应征, 罗渝昆, 唐杰, 张彦, 林倩, 梅兴国. 脂质体和脂质微泡对细胞膜的声孔作用比较J. 药学学报, 2006, 41(12): 1176-1179.
引用本文: 赵应征, 罗渝昆, 唐杰, 张彦, 林倩, 梅兴国. 脂质体和脂质微泡对细胞膜的声孔作用比较J. 药学学报, 2006, 41(12): 1176-1179.
ZHAO Ying-zheng, LUO Yu-kun, TANG Jie, ZHANG Yan, LIN Qian, MEI Xing-guo. Comparison of sonoporation effect of liposomes and phospholipids-based microbubbles on cultured cell membraneJ. Acta Pharmaceutica Sinica, 2006, 41(12): 1176-1179.
Citation: ZHAO Ying-zheng, LUO Yu-kun, TANG Jie, ZHANG Yan, LIN Qian, MEI Xing-guo. Comparison of sonoporation effect of liposomes and phospholipids-based microbubbles on cultured cell membraneJ. Acta Pharmaceutica Sinica, 2006, 41(12): 1176-1179.

脂质体和脂质微泡对细胞膜的声孔作用比较

Comparison of sonoporation effect of liposomes and phospholipids-based microbubbles on cultured cell membrane

  • 摘要: 目的研究两种脂质载体——脂质体和脂质微泡对细胞膜的声孔作用。方法应用体外培养的乳腺癌细胞SK-BR-3,考察脂质体和脂质微泡在低频超声条件下,对SK-BR-3细胞膜的声孔作用,应用原子力显微镜观察超声后即刻和24 h的SK-BR-3细胞表面变化。结果超声可使细胞丧失贴壁性能,形态变圆,脂质微泡的加入明显增强这种作用。原子力显微镜观察表明,对照组(正常细胞单纯超声照射)细胞膜表面孔道暂时增大,部分细胞膜表面孔道直径大于1 μm。2%和5%脂质体+超声照射组和对照组无明显差别。脂质微泡+超声照射组对细胞膜结构有明显影响,2%脂质微泡+超声照射组产生的细胞膜表面孔道直径在1~3 μm,24 h内可以恢复。5%脂质微泡+超声照射组产生的细胞膜孔道直径2~4 μm,24 h内不能完全恢复。结论2%脂质微泡可以产生较强的声孔作用,使细胞膜上出现可逆性孔道,有利于药物或基因递送到细胞内。

     

    Abstract: AimTo compare sonoporation effect of two phospholipids-based vectors-liposomes and microbubbles on cultured cell membrane. MethodsA breast cancer cell line SK-BR-3 was exposed to ultrasound alone, 2% or 5% liposome + ultrasound and 2% or 5% microbubble + ultrasound, separately. Immediately after the experiment and 24 h after ultrasound exposure, atomic-force microscopy (AFM) scanning was used to observe the membrane change of SK-BR-3 cells. ResultsAfter ultrasound exposure, normal SK-BR-3 cells more or less lost their natural shape, showing elliptic outline with obtuse curved boundary. In groups added with phospholipids-based microbubbles, more obtuse curved boundary of cells was observed. The membrane pores of SK-BR-3 cells had apparent changes after ultrasound exposure. With AFM technique, membrane pores under ultrasound alone or ultrasound with liposomes conditions were enlarged, the diameter of some pores exceeding 1 μm. But all the membrane pores in these conditions returned to normal appearance after 24 hours. In ultrasound with 2% microbubble condition, most membrane pores were about 1-3 μm in size and returned to normal appearance after 24 h. In ultrasound with 5% microbubble condition, however, pores of most cell membrane porosity was about 2-4 μm and did not totally return to normal appearance after 24 h. ConclusionAt 2%concentration, phospholipids-based microbubble could enhance ultrasonic sonoporation effect and produce reparable membrane pores on SK-BR-3 cells, which appeared to be a promising vehicle for drug and gene delivery.

     

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