Targeted Delivery of Anti-HER2 Affibody Conjugated Sterically Stabilized Cisplatin Liposome in HER2Receptor-Expressing Breast Cancer Models

Publish Year: 1394
نوع سند: مقاله کنفرانسی
زبان: English
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NASTARANCANSER01_163

تاریخ نمایه سازی: 26 شهریور 1395

Abstract:

HER2-targeted nanoparticle bioconjugates have shown to be capable of triggering receptormediatedendocytosis by combining the tumor-specificity of affibody molecules with drugdelivery features of a sophisticated macromolecular carrier. The purpose of this study was toinvestigate if the conjugation of Anti-HER2-affibody to cisplatin PEGylated liposomes canefficiently target cisplatin delivery to HER2+ breast tumor models and enhance thetherapeutic effectiveness of targeted liposomes. Affibody molecules were incubated with Mal-PEG2000-DSPE micelle to afford formation of a stable maleimide-mediated thioethercoupling to the COOH-terminal cysteine of the affibody. The covalent linkage was determinedby SDS-PAGE. Cisplatin loaded liposomes composed of HSPC/ cholesterol/ mPEG2000-DSPE (56.5:38.5:5 molar ratio) (150 mM) were prepared by ethanol injection and thephysicochemical properties of nanoparticles were characterized. Transfer of affibody intopreformed liposomes was carried out by post-insertion. The in vitro cytotoxicity and cellularuptake, and in vivo therapeutic activity of affibody-targeted (affisome) and non-targetedliposomes were tested in HER2+ SK-BR-3 and TUBO breast cancer models, respectively.Anti-HER2 affisome demonstrated a higher amount of platinum intracellularly, and affectedHER2+ SK-BR-3 cell death was at lower concentrations compared to its liposomecounterpart. Further, cisplatin-affisome showed greater therapeutic efficiency than nontargetedliposome in HER2+ TUBO models. Equally promising, the affisome-treated mice didextend the survival of animals by several days and even left one tumor-free survivor. Affibodytargetingendowed cisplatin liposome with significantly enhanced, albeit modest, therapeuticactivity in HER2-overexpressing tumor models, however, further values are yet to bedetermined to advance clinical translation of affibody-targeted liposome nanoparticles.

Authors

Seyedeh Hoda Alavizadeha

Biotechnology Research Center, Nanotechnology Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran

Mahmoud Reza jaafari

Biotechnology Research Center, Nanotechnology Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran