| Literature DB >> 22835645 |
Ping Gong1, Bihua Shi, Mingbin Zheng, Bi Wang, Pengfei Zhang, Dehong Hu, Duyang Gao, Zonghai Sheng, Cuifang Zheng, Yifan Ma, Lintao Cai.
Abstract
Aptamers have emerged as promising molecular probes for cancer diagnosis. However, their application for in vivo cancer imaging remains limitation due to the poor stability in blood and the degradation by nucleases. In the present study, we generated PEI/aptamer molecular complexes for cancer imaging in vivo by using deoxyribonuclease (DNase)-activatable fluorescence probes (DFProbes) to monitor DNA degradation. The results showed that the complexes with PEI at the N/P ratio from 3.8 to 15 effectively prevented the degradation of DFProbes both in vitro and in vivo. Moreover, PEI successfully protected TD05 aptamers from DNase degradation without affecting its specific recognition of Ramos cells. In tumor bearing mice, PEI/aptamer molecular complexes further demonstrated superior passive tumor targeting and extended circulation time as compared with free aptamer. Hence, the well-defined PEI/aptamer probe is a novel strategy to deliver targeted aptamer for tumor diagnosis and imaging in vivo.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22835645 DOI: 10.1016/j.biomaterials.2012.07.011
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479