Controllable drug delivery by naþ/kþ atpase α1 targeting peptide conjugated dspe-peg nanocarriers for breast cancer

7Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Although Epirubicin (EPI) is a commonly used anthracycline for the treatment of breast cancer in clinic, the serious side effects limit its long-term administration including myelosuppression and cardiomyopathy. Nanomedicines have been widely utilized as drug delivery vehicles to achieve precise targeting of breast cancer cells. Herein, we prepared a DSPE-PEG nanocarrier conjugated a peptide, which targeted the breast cancer overexpression protein Naþ/Kþ ATPase a1 (NKA-a1). The nanocarrier encap-sulated the EPI and grafted with the NKA-a1 targeting peptide through the click reaction between maleimide and thiol groups. The EPI was slowly released from the nanocarrier after entering the breast cancer cells with the guidance of the targeting NKA-a1 peptide. The precise and controllable delivery and release of the EPI into the breast cancer cells dramatically inhibited the cells proliferation and migration in vitro and suppressed the tumor volume in vivo. These results demonstrate significant prospects for this nanocarrier as a promising platform for numerous chemotherapy drugs.

Cite

CITATION STYLE

APA

Yang, Y., Feng, Q., Ding, C., Kang, W., Xiao, X., Yu, Y., & Zhou, Q. (2021). Controllable drug delivery by naþ/kþ atpase α1 targeting peptide conjugated dspe-peg nanocarriers for breast cancer. Technology in Cancer Research and Treatment, 20(1), 1–8. https://doi.org/10.1177/15330338211027898

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free