摘要:
The invention relates to a super-paramagnetic composite particle with core/shell structure, preparation method and use thereof. The composite particle is consisted of a core portion and a shell portion coated on the surface of the core portion, wherein said core portion is 10–70% by weight and said shell portion is 30–90% by weight based on the total weight of the composite particle, and said core portion is consisted of magnetic particles of Fe3O4, γ-Fe2O3 or other ferric oxides, or magnetic particles of ferrites of tervalent ferrum and bivalent manganese, nickel, zinc or copper, and the said shell portion is consisted of elementary gold or silver. The particle has an average diameter of 0.05–50 μm. The preparation method comprises preparing the core portion magnetic particle by chemical co-precipitation and depositing gold or silver to coat the magnetic particle by chemical reduction. The composite particle can label biological materials or nonbiological materials selected from the group consisted of nucleic acid, antigen, antibody, enzyme, polypeptide, polysaccharide, avidin, streptavidin or cell and the like, and be used in biological test and nonbiological test.
摘要翻译:本发明涉及具有核/壳结构的超顺磁复合颗粒,其制备方法和用途。 复合颗粒由核心部分和涂覆在芯部分表面上的壳部分组成,其中所述芯部分为10-70重量%,所述壳部分为基于总重量的30-90重量% 复合颗粒和所述芯部分由Fe 3 O 4 O 3,γ-Fe 2 O 3 3的磁性颗粒组成, 或其它三价铁氧化物,或铁酸盐和二价锰,镍,锌或铜的铁氧体的磁性颗粒,并且所述壳部分由基本金或银组成。 颗粒的平均直径为0.05-50μm。 制备方法包括通过化学共沉淀制备核心部分磁性颗粒,并通过化学还原沉积金或银来涂覆磁性颗粒。 复合颗粒可以标记选自核酸,抗原,抗体,酶,多肽,多糖,抗生物素蛋白,链霉抗生物素蛋白或细胞等的生物材料或非生物材料,并用于生物试验和非生物试验。
摘要:
The invention relates to Polysaccharide-coated GoldMag particles (DPGPs) and the method of its synthesis, which characterized GoldMag particles as a core and natural or synthetic biodegradable polysaccharide such as dextran, cyclodextrin and derivatives as shell. DPGPs are synthesized by mixing Polysaccharide-coated GoldMag particles (DPGPs) with drug through physical bond. The preparation of the drug-loaded composite particles include: preparing the polysaccharide-coated GoldMag particles and then loading the drug on the polysaccharide-coated GoldMag particles. The drug-loading process is carried out through directly mixing the polysaccharide-coated GoldMag particles with the drug solution by the shaker. That means the polysaccharide-coated GoldMag particles load the drug through affinity adsorption.