Kim Ki Su, Hyun Hoon, Yang Jeong-A, Lee Min Young, Kim Hyemin, Yun Seok-Hyun, Choi Hak Soo, Hahn Sei Kwang
Wellman Center for Photomedicine, Massachusetts General Hospital and Harvard Medical School , 65 Landsdowne Street, Cambridge, Massachusetts 02139, United States.
Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School , 330 Brookline Avenue, Boston, Massachusetts 02215, United States.
Biomacromolecules. 2015 Sep 14;16(9):3054-61. doi: 10.1021/acs.biomac.5b00933. Epub 2015 Aug 18.
We conducted real-time bioimaging of the hyaluronate-interferon α (HA-IFNα) conjugate using a biologically inert zwitterionic fluorophore of ZW800-1 for the treatment of hepatitis C virus (HCV) infection. ZW800-1 was labeled on the IFNα molecule of the HA-IFNα conjugate to investigate its biodistribution and clearance without altering its physicochemical and targeting characteristics. Confocal microscopy clearly visualized the effective in vitro cellular uptake of the HA-IFNα conjugate to HepG2 cells. After verifying the biological activity in Daudi cells, we conducted the pharmacokinetic analysis of the HA-IFNα conjugate, which confirmed its target-specific delivery to the liver with a prolonged residence time longer than that of PEGylated IFNα. In vivo and ex vivo bioimaging of the ZW800-1-labeled HA-IFNα conjugate directly showed real-time biodistribution and clearance of the conjugate that are consistent with the biological behaviors analyzed by an enzyme-linked immunosorbent assay. Furthermore, the elevated level of OAS1 mRNA in the liver confirmed in vivo antiviral activity of HA-IFNα conjugates. With the data taken together, we could confirm the feasibility of ZW800-1 as a biologically inert fluorophore and target-specific HA-IFNα conjugate for the treatment of HCV infection.
我们使用生物惰性的两性离子荧光团ZW800-1对透明质酸-干扰素α(HA-IFNα)偶联物进行实时生物成像,以治疗丙型肝炎病毒(HCV)感染。ZW800-1标记在HA-IFNα偶联物的IFNα分子上,以研究其生物分布和清除情况,同时不改变其物理化学和靶向特性。共聚焦显微镜清楚地观察到HA-IFNα偶联物对HepG2细胞有效的体外细胞摄取。在验证了对Daudi细胞的生物活性后,我们对HA-IFNα偶联物进行了药代动力学分析,结果证实其能靶向特异性地递送至肝脏,且停留时间延长,比聚乙二醇化干扰素α更长。对ZW800-1标记的HA-IFNα偶联物进行体内和体外生物成像,直接显示了该偶联物的实时生物分布和清除情况,这与通过酶联免疫吸附测定分析的生物学行为一致。此外,肝脏中OAS1 mRNA水平的升高证实了HA-IFNα偶联物的体内抗病毒活性。综合这些数据,我们可以确认ZW800-1作为生物惰性荧光团和靶向特异性HA-IFNα偶联物用于治疗HCV感染的可行性。