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国家重点基础研究发展计划(2013CB932502)

作品数:6 被引量:34H指数:2
相关作者:黄容琴朱建华更多>>
相关机构:复旦大学更多>>
发文基金:国家重点基础研究发展计划国家自然科学基金更多>>
相关领域:医药卫生化学工程农业科学矿业工程更多>>

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Improved method for synthesis of low molecular weight protamine–siRNA conjugate被引量:1
2018年
RNAi technology has aroused wide public interest due to its high efficiency and specificity to treat multiple types of diseases. However, the effective delivery of siRNA remains a challenge due to its large molecular weight and strong anionic charge. Considering their remarkable functions in vivo and features that are often desired in drug delivery carriers, biomimetic systems for siRNA delivery become an effective and promising strategy. Based on this, covalent attachment of synthetic cell penetrating peptides(CPP) to siRNA has become of great interest. We developed a monomeric covalent conjugate of low molecular weight protamine(LMWP, a well-established CPP) and siRNA via a cytosol-cleavable disulfide linkage using PEG as a crosslinker. Results showed that the conjugates didn't generate coagulation, and exhibited much better RNAi potency and intracellular delivery compared with the conventional charge-complexed CPP/siRNA aggregates. Three different synthetic and purification methods were compared in order to optimize synthesis efficiency and product yield. The methodology using hetero-bifunctional NHS–PEG–OPSS as a crosslinker to synthesize LMWP–siRNA simplified the synthesis and purification process and produced the highest yield. These results pave the way towards siRNA biomimetic delivery and future clinical translation.
Zhili YuJunxiao YeXing PeiLu SunErgang LiuJianxin WangYongzhuo HuangSeung Jin LeeHuining He
关键词:SIRNACONJUGATECROSSLINKER
大胞饮介导载小干扰RNA的脂蛋白仿生纳米结构靶向治疗Ras激活脑胶质瘤
研究发现,Ras信号传导通路的过度激活与人类众多肿瘤的发生和发展过程密切相关。然而,针对该通路,研究者至今仍没有找到一个安全有效的治疗药物。作为细胞内吞的一种形式,大胞饮在Ras激活的肿瘤细胞摄取胞外蛋白营养过程中发挥着...
黄佳琳
关键词:靶向治疗脑胶质瘤小干扰RNA
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[^(18)F]FPTZFA的合成及显像研究
2015年
为研究正电子核素18F标记的叶酸衍生物([18F]FPTZFA)的合成及其在小鼠体内的生物学分布,以叶酸为起始原料,通过叶酸上羧基与2-叠氮基乙胺上氨基的成酯反应,将叠氮基团标记至叶酸,得到γ-叶酸-2-叠氮基乙酰胺(FA-N3);同时以硝基羟基吡啶为原料,经过三步取代反应,将炔基、F连接至吡啶环上得到2-氟-3-(戊-4-炔基氧)吡啶(19F-PyKYNE)。19F-PyKYNE在K18F/K222作用下生成18F-PyKYNE。18F-PyKYNE的炔基与FA-N3的叠氮基团,在硫酸铜、抗坏血酸钠催化下发生点击化学反应,得到最终产物[18F]FPTZFA。整个放射性标记过程仅需40min,[18F]FPTZFA放化纯度达51%,放化产率达37%。[18F]FPTZFA经放射性半制备高效液相色谱(High Performance Liquid Chromatography,HPLC)分离纯化后,观察其在不同时间段荷瘤小鼠体内的组织分布。荷瘤小鼠脏器及组织切片后的放射自显影显示[18F]FPTZFA的摄取集中在肝、肾和肿瘤组织。其中30min肿瘤组织、肌肉的单位质量组织的放射性占注射剂量放射性的百分比(%ID/g)比值为3.6,肿瘤、血液的%ID/g比值为3.2。初步断定[18F]FPTZFA有较好的肿瘤靶向性。
周达鸣朱建华
关键词:^18F叶酸
Biomimetic nanoparticles for inflammation targeting被引量:27
2018年
There have been many recent exciting developments in biomimetic nanoparticles for biomedical applications. Inflammation, a protective response involving immune cells, blood vessels,and molecular mediators directed against harmful stimuli, is closely associated with many human diseases.As a result, biomimetic nanoparticles mimicking immune cells can help achieve molecular imaging and precise drug delivery to these inflammatory sites. This review is focused on inflammation-targeting biomimetic nanoparticles and will provide an in-depth look at the design of these nanoparticles to maximize their benefits for disease diagnosis and treatment.
Kai JinZimiao LuoBo ZhangZhiqing Pang
生物可降解无机介孔纳米材料研究进展被引量:1
2017年
近年来,无机介孔纳米材料由于比表面积大、孔结构有序可控、比孔容大等优秀性质而受到化学、材料、物理、医药等领域科研人员重点关注。但在生物临床诊疗应用中,无机介孔纳米材料在机体内的相对难降解、排泄也是亟待解决的问题。本文将围绕科研领域最受关注的几种无机介孔材料,综述目前最为可行的无机介孔纳米材料的生物可降解性质改造策略。
李诚意黄容琴
关键词:纳米材料生物可降解性
Overcoming oral insulin delivery barriers: application of cell penetrating peptide and silica-based nanoporous composites被引量:3
2013年
Huining HEJunxiao YEJianyong SHENGJianxin WANGYongzhuo HUANGGuanyi CHENJingkang WANGVictor C YANG
关键词:胰岛素分泌口服给药细胞摄取纳米孔
Ultrasound-mediated targeted microbubbles: a new vehicle for cancer therapy被引量:2
2013年
Junxiao YEHuining HEJunbo GONGWeibing DONGYongzhuo HUANGJianxin WANGGuanyi CHENVictor C YANG
关键词:微泡癌症治疗肿瘤细胞凋亡化疗药物
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