| Literature DB >> 30081302 |
Lingyu Zhang1, Manjie Zhang1, Li Zhou2, Qinghe Han3, Xiangjun Chen1, Shengnan Li1, Lu Li4, Zhongmin Su1, Chungang Wang5.
Abstract
Co-delivery of two drugs with diverse physicochemical properties and specific administration order for cancer theranostics are vitally important for drug resistance conquering and side effects reducing. Consequently, we explored a unique amphiphilic PCL-AuNC/Fe(OH)3-PAA Janus nanoparticle (JNP) to simultaneously preserve the hydrophilic drug (doxorubicin) and hydrophobic drug (docetaxel) in their distinct domains. Owing to their extraordinary heterostructure and independent pH and NIR sensitive properties, the optional sequential drug release by a single inorganic JNP was realized for the first time, and the results presented the synchronous release of two drugs had 5% better therapeutic effect. In addition, the excellent computed X-ray tomography/magnetic resonance (CT/MR) imaging capabilities from AuNC and Fe(OH)3 suggested our JNPs could effectively guide the cancer therapy. Furthermore, the mice treated with dual drug loaded PCL-AuNC/Fe(OH)3-PAA JNPs under near infrared (NIR) laser irradiation showed better tumor inhibition than solo drug, cocktail and dual drug treated groups, indicating the effectivity and significance of combined cancer therapy.Entities:
Keywords: Amphiphilic Janus nanoparticles; Bimodal imaging; Dual drug delivery; Optional sequential release; Synergistic therapy
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Year: 2018 PMID: 30081302 DOI: 10.1016/j.biomaterials.2018.07.060
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479