首页|自组装脂质体纳米载体对骨肉瘤细胞Saos-2靶向递送及凋亡的影响

自组装脂质体纳米载体对骨肉瘤细胞Saos-2靶向递送及凋亡的影响

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目的 以天然脂肪酸月桂酸和硬脂酸为骨架,利用它们在二甲基甲酰胺(dimethylformamide,DMF)中的自组装构建了一种脂质体纳米载体并负载阿霉素,对其靶向人骨肉瘤细胞Saos-2及凋亡情况进行考察。方法 采用自组装制备了负载阿霉素的脂质体纳米载体,采用激光共聚焦考察了其靶向人骨肉瘤细胞Saos-2能力,采用Annexin V-FITC染色技术考察了脂质体纳米载体对人骨肉瘤细胞Saos-2凋亡的影响。结果 自组装脂质体纳米载体与人骨肉瘤细胞Saos-2孵育48h时,荧光强度最高,绿色荧光的 自组装脂质体纳米载体会围绕在骨肉瘤细胞Saos-2周围,相对于同剂量DMF的对照组,自组装脂质体纳米载体组的细胞无论是早期凋亡还是晚期凋亡的比例均有所增加。结论 负载阿霉素的脂质体纳米载体能准确地靶向人骨肉瘤细胞Saos-2,并加速人骨肉瘤细胞Saos-2的凋亡。
Study on targeted delivery and apoptosis effects of self-assembled liposome nano-carriers on osteosarcoma cells Saos-2
Objective Using natural fatty acids lauric acid and stearic acid as the backbone,a liposome nanocarrier was constructed through their self-assembly in dimethylformamide(DMF)and loaded with doxorubicin.Its targeting ability to hu-man osteosarcoma cells Saos-2 and apoptosis were investigated.Methods Doxorubicin-loaded liposome nanocarriers were pre-pared by self-assembly.The targeting ability of the nanocarriers to human osteosarcoma cells Saos-2 was examined using confo-cal laser scanning microscopy.The effect of liposome nanocarriers on the apoptosis of human osteosarcoma cells Saos-2 was in-vestigated using Annexin V-FITC staining technique.Results When the self-assembled liposome nanocarriers were incubated with human osteosarcoma cells Saos-2 for 48 hours,the fluorescence intensity was the highest.The green fluorescent self-as-sembled liposome nanocarriers surrounded the osteosarcoma cells Saos-2.Compared to the control group with the same dose of DMF,both early and late apoptotic cell proportions increased in the self-assembled liposome nanocarrier group.Conclusion Doxorubicin-loaded liposome nanocarriers can accurately target human osteosarcoma cells Saos-2 and accelerate their apoptosis.

liposome nanocarriersdoxorubicinosteosarcoma cells saos-2cell targetingapoptosis

陈康尧

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福建省福州市第二总医院骨科,福州 350007

脂质体纳米载体 阿霉素 骨肉瘤细胞Saos-2 细胞靶向 细胞凋亡

福州市科技计划项目福建省创伤骨科急救与康复临床医学研究中心项目

2021-S-1662020Y2014

2024

福建医药杂志
中华医学会福建分会

福建医药杂志

影响因子:0.525
ISSN:1002-2600
年,卷(期):2024.46(3)
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