微泡
纳米技术
纳米颗粒
催化作用
材料科学
药物输送
化学
计算机科学
生物化学
小RNA
基因
作者
Víctor Sebastián,María Sancho‐Albero,Manuel Arruebo,Ana M. Pérez‐López,Belén Rubio‐Ruíz,Pilar Martín‐Duque,Asier Unciti‐Broceta,Jesús Santamarı́a
出处
期刊:Nature Protocols
[Springer Nature]
日期:2020-11-27
卷期号:16 (1): 131-163
被引量:23
标识
DOI:10.1038/s41596-020-00406-z
摘要
The use of exosomes as selective delivery vehicles of therapeutic agents, such as drugs or hyperthermia-capable nanoparticles, is being intensely investigated on account of their preferential tropism toward their parental cells. However, the methods used to introduce a therapeutic load inside exosomes often involve disruption of their membrane, which may jeopardize their targeting capabilities, attributed to their surface integrins. On the other hand, in recent years bio-orthogonal catalysis has emerged as a new tool with a myriad of potential applications in medicine. These bio-orthogonal processes, often based on Pd-catalyzed chemistry, would benefit from systems capable of delivering the catalyst to target cells. It is therefore highly attractive to combine the targeting capabilities of exosomes and the bio-orthogonal potential of Pd nanoparticles to create new therapeutic vectors. In this protocol, we provide detailed information on an efficient procedure to achieve a high load of catalytically active Pd nanosheets inside exosomes, without disrupting their membranes. The protocol involves a multistage process in which exosomes are first harvested, subjected to impregnation with a Pd salt precursor followed by a mild reduction process using gas-phase CO, which acts as both a reducing and growth-directing agent to produce the desired nanosheets. The technology is scalable, and the protocol can be conducted by any researcher having basic biology and chemistry skills in ~3 d.
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