Transferrin-Conjugated Polymeric Nanoparticle for Receptor-Mediated Delivery of Doxorubicin in Doxorubicin-Resistant Breast Cancer Cells

• Main Authors: Zar Chi Soe (Author), Jun Bum Kwon (Author), Raj Kumar Thapa (Author), Wenquan Ou (Author), Hanh Thuy Nguyen (Author), Milan Gautam (Author), Kyung Taek Oh (Author), Han-Gon Choi (Author), Sae Kwang Ku (Author), Chul Soon Yong (Author), Jong Oh Kim (Author)
• Format: Book
• Published: MDPI AG, 2019-02-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Summary

In this study, a transferrin (T_f)-conjugated polymeric nanoparticle was developed for the targeted delivery of the chemotherapeutic agent doxorubicin (Dox) in order to overcome multi-drug resistance in cancer treatment. Our objective was to improve Dox delivery for producing significant antitumor efficacy in Dox-resistant (R) breast cancer cell lines with minimum toxicity to healthy cells. The results of our experiments revealed that Dox was successfully loaded inside a transferrin (T_f)-conjugated polymeric nanoparticle composed of poloxamer 407 (F127) and 123 (P123) (Dox/F127<i>&</i>P123-T_f), which produced nanosized particles (~90 nm) with a low polydispersity index (~0.23). The accelerated and controlled release profiles of Dox from the nanoparticles were characterized in acidic and physiological pH and Dox/F127<i>&</i>P123-T_f enhanced Dox cytotoxicity in OVCAR-3, MDA-MB-231, and MDA-MB-231(R) cell lines through induction of cellular apoptosis. Moreover, Dox/F127<i>&</i>P123-T_f inhibited cell migration and altered the cell cycle patterns of different cancer cells. In vivo study in MDA-MB-231(R) tumor-bearing mice demonstrated enhanced delivery of nanoparticles to the tumor site when coated in a targeting moiety. Therefore, Dox/F127<i>&</i>P123-T_f has been tailored, using the principles of nanotherapeutics, to overcome drug-resistant chemotherapy.

Item Description

1999-4923
10.3390/pharmaceutics11020063