壳聚糖
化学
小干扰RNA
碳二亚胺
RNA干扰
抗体
共轭体系
基因沉默
凝聚
Zeta电位
纳米颗粒
分子生物学
细胞
基因传递
核糖核酸
生物物理学
转染
生物化学
纳米技术
基因
免疫学
生物
材料科学
聚合物
有机化学
作者
Jangwook Lee,Kyoung-Soo Yun,Chang Seon Choi,Seung-Hwa Shin,Hongseok Ban,Taiyoun Rhim,Sang Kyung Lee,Kuen Yong Lee
摘要
The intracellular delivery of small interfering RNA (siRNA) plays a key role in RNA interference (RNAi) and provides an emerging technique to treat various diseases, including infectious diseases. Chitosan has frequently been used in gene delivery applications, including siRNA delivery. However, studies regarding the modification of chitosan with antibodies specifically targeting T cells are lacking. We hypothesized that chitosan nanoparticles modified with T cell-specific antibodies would be useful for delivering siRNA to T cells. CD7-specific single-chain antibody (scFvCD7) was chemically conjugated to chitosan by carbodiimide chemistry, and nanoparticles were prepared by a complex coacervation method in the presence of siRNA. The mean diameter and zeta potential of the scFvCD7-chitosan/siRNA nanoparticles were approximately 320 nm and +17 mV, respectively, and were not significantly influenced by the coupling of antibody to chitosan. The cellular association of antibody-conjugated nanoparticles to CD4+ T cell lines as well as gene silencing efficiency in the cells was significantly improved compared to nonmodified chitosan nanoparticles. This approach to introducing T cell-specific antibody to chitosan nanoparticles may find useful applications for the treatment of various infectious diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI