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Preparation of iron oxide silica particles for Zika viral RNA extraction

机译:用于Zika病毒RNA提取的氧化铁二氧化硅颗粒的制备。

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摘要

In this work, a robust synthetic pathway for magnetic core preparation and silica surface coating of magnetic microparticles is presented. Silica-coated magnetic particles are widely used to extract DNA and RNA from various biological samples. We present a novel route for the synthesis of iron oxide silica particles (Fe3O4@Silica) and demonstrate their performance for extracting ZIKA viral RNA from serum. The iron (II, III) oxide (Fe3O4), magnetite core is first prepared by ammonia neutralization of ferrous and ferric chloride aqueous solution under argon, followed by the addition of citrate salt to stabilize the surface of the resultant magnetic nanospheres. After this one-pot, two-step synthesis, the magnetic nanospheres are consumed during silica coating by hydrolysis of tetraethoxysilane (TEOS) under alkaline condition. The final product is a sphere-like magnetic aggregate with a size range of 1–2 micron. By simply suspending the magnetic aggregates in guanidinium chloride solution, the silica surface can be prepared for RNA binding. The RNA extraction efficiency was evaluated by extracting ZIKA viral RNA from serum followed by a PCR-based assay. The data indicate excellent recovery of target RNA and removal of PCR inhibitors. This manufacturing procedure for the silica coated microparticles provides a low-cost, effective and ready for scale-up method whose performance is equivalent to commercial alternatives such as magnetic silica surface particles for DNA and RNA sample preparations. The cost of the clinical assays could be largely decreased due to the 100 fold reduction in cost by replacing the commercially available magnetic particles with the developed material for RNA extraction.
机译:在这项工作中,提出了用于磁芯制备和磁性微粒二氧化硅表面涂层的稳健合成途径。二氧化硅涂层的磁性颗粒被广泛用于从各种生物样品中提取DNA和RNA。我们提出了一种合成氧化铁二氧化硅颗粒(Fe3O4 @ Silica)的新颖途径,并证明了它们从血清中提取ZIKA病毒RNA的性能。首先通过在氩气下氨中和亚铁和氯化铁水溶液,然后添加柠檬酸盐以稳定所得磁性纳米球的表面,来制备氧化铁(II,III)(Fe3O4)磁芯。在这一一锅,两步合成之后,在碱性条件下通过四乙氧基硅烷(TEOS)的水解在二氧化硅涂覆过程中消耗了磁性纳米球。最终产品是球形的磁性聚集体,大小范围为1-2微米。通过简单地将磁性聚集体悬浮在氯化胍溶液中,可以制备二氧化硅表面用于RNA结合。通过从血清中提取ZIKA病毒RNA,然后进行基于PCR的分析来评估RNA提取效率。数据表明靶RNA的极好的回收率和PCR抑制剂的去除。这种用于二氧化硅涂覆的微粒的制造程序提供了一种低成本,有效且易于放大的方法,其性能与商业替代产品相当,例如用于DNA和RNA样品制备的磁性二氧化硅表面颗粒。由于用开发的用于RNA提取的材料替代了商用磁性颗粒,可将成本降低100倍,因此可大大降低临床测定的成本。

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