International Journal of Nanomedicine · 2023 · 17 citations · 36 references
PharmacyOncologyPharmacologyDrug DeliveryNanoparticle Drug DeliveryTargeted Drug DeliveryCancer Drug DeliveryCancer NanomedicineNanocarriers For TherapeuticsNanomaterials For Drug DeliveryNanomedicineReactive Oxygen Species-responsive Drug DeliveryCancer Cell ApoptosisChemotherapy DeliveryNanocarrier BiodistributionNanoparticle Cellular UptakeNanoparticle CytotoxicityNanoparticle DeliveryNanoparticle-based ChemotherapyReactive Oxygen Species-responsive Nanoparticles
Background: Triple negative breast cancer (TNBC) is one of the most aggressive tumors with high metastasis and mortality, which constitutes 15~20% of all breast cancers. Chemotherapy remains main therapeutic option in the treatment of patients with TNBC. Methods: We developed reactive oxygen species (ROS)-responsive galactosylated nanoparticles (DOX@NPs) as an efficiently targeted carrier for doxorubicin (DOX) delivery to inhibit the growth of TNBC in vitro and in vivo. DOX@NPs were composed of polyacrylate galactose and phenylboronic derivatives conjugation. The in vitro cytotoxicity, cellular uptake, cell apoptosis and cycle distribution of tumor cells treated with different formulations were investigated. Meanwhile in vivo biodistribution and antitumor effects were investigated in a 4T1 tumor-bearing mouse model. Results: . Furthermore, our data suggested that DOX@NPs could effectively trigger tumor cells apoptosis and cycle arrest, efficiently accumulate into tumor sites, and suppress tumor growth without adverse side effects. Conclusion: Our results suggested DOX@NP with potent potential as a promising nanocarrier for TNBC therapy, which deserved further investigation for other cancer treatment.
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Stimuli-responsive polymer-doxorubicin conjugate: Antitumor mechanism and potential as nano-prodrug
Kai Chen, Hao Cai, Hu Zhang et al. · Acta Biomaterialia · 2018 · 130 citations
Alba Llop‐Guevara, Sibylle Loibl, Guillermo Villacampa et al. · Annals of Oncology · 2021 · 101 citations · Full text
Life Sciences, Genetics, Oncology +10