| Literature DB >> 35006949 |
Jin Cao1, Qiwen Pan1, Shifang Bei1,2, Mingxue Zheng1, Zhenyan Sun1, Xueyong Qi1, Song Shen1.
Abstract
Combined chemotherapy and sonodynamic therapy (chemo-SDT) based on the nanoplatform/nanocarrier is a potential antitumor strategy that has shown higher therapeutic efficacy than any monotherapy. Therefore, a safe and effective multifunctional system with a concise design and simple preparation process is urgently needed. In this work, by using a one-step cross-linking method, a multifunctional nanosystem, which employs phycocyanin nanoparticles (PCNPs) as a nanocarrier to deliver the chemotherapy drug docetaxel (DTX) and a nanosonosensitizer to generate reactive oxygen species (ROS), was prepared and evaluated (PCNP-DTX). Under low-intensity ultrasound irradiation, PCNP-DTX retained the ROS generation ability of phycocyanin and caused the destruction of mitochondrial potential. PCNP was also revealed to be an acidic and ultrasound-sensitive carrier with good biocompatibility. In addition to its cumulation behavior in tumors, PCNP can achieve tumor-targeted delivery and release of DTX. PCNP-DTX has also been proven to have a significant chemo-SDT synergy effect when low-intensity ultrasound was applied, showing enhanced antitumor activity both in vitro and in vivo. This study provides a concise yet promising nanoplatform based on the natural protein phycocyanin for achieving an effective, targeted, and synergetic chemo-SDT for antitumor therapy.Entities:
Keywords: chemo-sonodynamic therapy; docetaxel; drug delivery; phycocyanin; protein nanoparticle
Mesh:
Substances:
Year: 2021 PMID: 35006949 DOI: 10.1021/acsabm.1c00745
Source DB: PubMed Journal: ACS Appl Bio Mater ISSN: 2576-6422