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姚鑫

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供职机构:北京大学更多>>
发文基金:国家教育部博士点基金国家自然科学基金国家重点基础研究发展计划更多>>
相关领域:医药卫生更多>>

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邻硝基苯丙酸紫杉醇偶联物的自组装载药系统及其制备方法和应用
本发明涉及一种邻硝基苯丙酸紫杉醇偶联物的自组装载药系统,其特征在于,所述的载药系统包含邻硝基苯丙酸紫杉醇偶联物,液体溶剂,以及任选包含表面活性剂或增溶材料。该无载体或含少量载体的自组装纳米系统具有纳米给药系统的优势,同时...
张烜姚鑫
邻硝基苯丙酸紫杉醇偶联物的自组装载药系统及其制备方法和应用
本发明涉及一种邻硝基苯丙酸紫杉醇偶联物的自组装载药系统,其特征在于,所述的载药系统包含邻硝基苯丙酸紫杉醇偶联物,液体溶剂,以及任选包含表面活性剂或增溶材料。该无载体或含少量载体的自组装纳米系统具有纳米给药系统的优势,同时...
张烜姚鑫
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The targeting effect of H_7K(R_2)_2-modified pH-sensitive liposomes on U87-MG cells
2015年
The present study aimed to investigate the targeting effect of H7K(R2)2-modified pH -sensitive liposomes on U87-MG cells. Using coumarin-6 as a fluorescence probe, we prepared H7K(R2)2-modified p H-sensitive liposomes(designated as coumarin-6-PSL-H7K(R2)2). The flow cytometry assay was used to evaluate the effect of H7K(R2)2 proportions on the cellular uptake and endocytosis pathways of coumarin--6--PSL--H7K(R2)2 on U87-MG cells. The circular dichroism(CD) spectroscopy assay was used to investigate the secondary structures of H7K(R2)2 peptide at pH 7.4 and H 6.8, respectively. Our results indicated that the 2.5% proportion of H7K(R2)2 in the coumarin-6--PSL-H7K(R2)2 was superior to those of 1% and 3.5% of H7K(R2)2. The uptake of coumarin--6-PSL--H7K(R2)2 on U87--MG cells was not inhibited by filipin, M-β--CD or chlorpromazine. The secondary structure of H7K(R2)2 at pH 6.8 was mostly presented as β--turn. In conclusion, we suggested that the appropriate proportion of H7K(R2)2 in the H7K(R2)2--modified pH--sensitive liposomes could be set at 2.5%. The cellular uptake pathway for H7K(R2)2-modified pH--sensitive liposomes was via the cell penetrating capacity of H7K(R2)2 which responded to acidic condition. The secondary structure of H7K(R2)2 at pH 6.8, which was presented as the shape of hairpin, might be mainly responsible for its targeting and cell penetrating effect.
赵阳任伟钟婷王超张卫强黄丹张爽郭阳姚鑫张烜张强
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