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作 者:黄际薇[1] 姜彩云[1] 罗宇燕[1] 郭喆霏[1] 张永明[1] HUANG Jiwei;JIANG Caiyun;LUO Yuyan;GUO Zhefei;ZHANG Yongming(Department of Pharmacy,the Third Affiliated Hospital of Sun Yat-sen University,Guangzhou 510630,China)
机构地区:[1]中山大学附属第三医院药剂科
出 处:《中山大学学报(自然科学版)》2019年第5期114-118,共5页Acta Scientiarum Naturalium Universitatis Sunyatseni
基 金:广东省自然科学基金(2017A030313897);广东省临床用药研究基金(2019XQ12);广州市科技计划项目(2012J4300071)
摘 要:结合纳米粒优良的载药特性和细胞膜作为外壳来包载合成的纳米粒内核,使其伪装成内源性物质,减少网状内皮系统的摄取和免疫识别,构建一个新型的药物递送系统——红细胞膜仿生纳米粒递药体系。采用反溶剂法制得纳米粒(nanoparticles,NP),采用离心法提取红细胞膜(red blood cell membranes,RBCM),红细胞膜与纳米粒不同比例共挤压不同次数来制备红细胞膜仿生纳米粒(red blood cell membranes biomimetic nanoparticles,RBCM-NP)。通过透射电镜、马尔文粒度仪来表征NP和RBCM-NP,利用生物素化纳米粒(biotinylated nanoparticle,BTNP),与链霉亲和素(streptavidin,ST)孵育会发生聚集反应来研究红细胞膜的覆盖程度。NP和RBCM-NP粒径均一,优化处方红细胞膜能够完全包裹住纳米粒,重现性良好。The study reported a novel drug delivery system,red blood cell membranes biomimetic nanoparticles(RBCM-NP)drug delivery system.The system was constructed by combining the excellent drug-carrying properties of nanoparticles and cell membranes as shells to encapsulate the synthesized nanoparticle which makes it disguise as an endogenous substance to reduce uptake of reticuloendothelial system and immune recognition.Nanoparticles(NP)were prepared by reverse solvent method,while red blood cell membranes(RBCM)were extracted by centrifugal extraction.Different ratios of RBCM and NP were co-extruded for different times to prepare RBCM-NP.RBCM-NP were characterized by transmission electron microscopy and Malvern particle size meter.The aggregation reaction of biotinylated nanoparticle(BTNP)and streptavidin(ST)were used to study the coverage of red blood cell membranes.The particle sizes of NP and RBCM-NP were uniformed.In optimized formulation,RBCM could completely encapsulate NP with good reproducibility.
分 类 号:R945[医药卫生—微生物与生化药学]
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