Low-density lipoprotein-coupled micelles with reduction and pH dual sensitivity for intelligent co-delivery of paclitaxel and siRNA to breast tumor

Autor: Yang Liu, Ben-gang You, Wen-jing Zhu, Qiao-Ling Zhu, Chen-xi Qu, Zhi-qiang Yuan, Shu-di Yang, Fang Li, Xue-nong Zhang, Wei-liang Chen
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Small interfering RNA
Abcg2
Polymers
Pharmaceutical Science
02 engineering and technology
co-delivery
chemistry.chemical_compound
0302 clinical medicine
RNA interference
International Journal of Nanomedicine
Drug Discovery
Tissue Distribution
RNA
Small Interfering

Micelles
Original Research
Drug Carriers
biology
Chemistry
General Medicine
environmentally sensitive
Hydrogen-Ion Concentration
021001 nanoscience & nanotechnology
Drug Resistance
Multiple

Lipoproteins
LDL

Paclitaxel
030220 oncology & carcinogenesis
MCF-7 Cells
Female
RNA Interference
0210 nano-technology
Oxidation-Reduction
Biophysics
Mice
Nude

Bioengineering
Breast Neoplasms
Enhanced permeability and retention effect
Biomaterials
03 medical and health sciences
multidrug resistance
Cell Line
Tumor

micelle
Gene silencing
Animals
Humans
tumor targeting
Organic Chemistry
Multiple drug resistance
Drug Liberation
LDL receptor
Cancer research
biology.protein
Zdroj: International Journal of Nanomedicine
ISSN: 1178-2013
Popis: Wen-jing Zhu,1,* Shu-di Yang,1,* Chen-xi Qu,1 Qiao-ling Zhu,1,2 Wei-liang Chen,1 Fang Li,1 Zhi-qiang Yuan,1 Yang Liu,1 Ben-gang You,1 Xue-nong Zhang1 1Department of Pharmaceutics, College of Pharmaceutical Sciences, Soochow University, Suzhou, 2Department of Clinical Medicine, Nanjing Gulou Hospital, Nanjing, People’s Republic of China *These authors contributed equally to this work Abstract: Multidrug resistance (MDR) is a major obstacle for the clinical therapy of malignant human cancers. The discovery of RNA interference provides efficient gene silencing within tumor cells for reversing MDR. In this study, a new “binary polymer” low-density lipoprotein–N-succinyl chitosan–cystamine–urocanic acid (LDL–NSC–SS–UA) with dual pH/redox sensitivity and targeting effect was synthesized for the co-delivery of breast cancer resistance protein small interfering RNA (siRNA) and paclitaxel (PTX). In vivo, the co-delivering micelles can accumulate in tumor tissue via the enhanced permeability and retention effect and the specific recognition and combination of LDL and LDL receptor, which is overexpressed on the surface of tumor cell membranes. The siRNA–PTX-loaded micelles inhibited gene and drug release under physiological conditions while promoting fast release in an acid microenvironment or in the presence of glutathione. The micelles escaped from the lysosome through the proton sponge effect. Additionally, the micelles exhibited superior antitumor activity and downregulated the protein and mRNA expression levels of breast cancer resistance protein in MCF-7/Taxol cells. The biodistribution and antitumor studies proved that the siRNA–PTX-loaded micelles possessed prolonged circulation time with a remarkable tumor-targeting effect and effectively inhibited tumor growth. Therefore, the novel dual pH/redox-sensitive polymers co-delivering siRNA and PTX with excellent biocompatibility and effective reversal of MDR demonstrate a considerable potential in cancer therapy. Keywords: multidrug resistance, micelle, co-delivery, environmentally sensitive, tumor targeting 
Databáze: OpenAIRE