pH-controlled doxorubicin delivery from PDEAEMA-based nanogels

被引:19
|
作者
Pikabea, Aintzane [1 ]
Villar-Alvarez, Eva [2 ]
Forcada, Jacqueline [1 ]
Taboada, Pablo [2 ]
机构
[1] Univ Basque Country, UPV EHU, Fac Chem, Dept Appl Chem,Bionanoparticles Grp, Apdo 1072, Donostia San Sebastian 20080, Spain
[2] Univ Santiago de Compostela, Fac Phys, Particle Phys Dept, Colloids & Polymers Phys Grp, Campus Sur, Santiago De Compostela 15782, Spain
关键词
pH-responsive nanogels; PEGylation; Drug delivery systems; Doxorubicin; Cellular uptake; CONTROLLED DRUG-DELIVERY; IN-VIVO; POLYMER NANOPARTICLES; RESPONSIVE NANOGELS; PROTEIN ADSORPTION; GENE DELIVERY; STEM-CELLS; RELEASE; SERUM; MICROGELS;
D O I
10.1016/j.molliq.2018.06.068
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, the feasibility of some poly(2-(diethylamino)ethyl methacrylate) (PDEAEMA)-based pH-sensitive nanogels as drug nanocarriers is evaluated. The anticancer drug doxorubicin (DOXO) is successfully encapsulated into the nanogels, achieving high drug loading and encapsulation efficiency. It has been found that the in vitro delivery of DOXO from the nanogels was pH-dependent: DOXO release rate is accelerated by decreasing pH from 7.4 (healthy cells) to 5.2 (pH condition for endo/lysosomial compartments and unhealthy cells) due to the swelling of the nanogel particles. The uptake of DOXO-loaded nanogels into MDA-MB-231 tumoral cells and the progressive release of the drug from the nanogels to the cell nuclei are demonstrated by fluorescence microscopy measurements. These results suggest a great potential of these DOXO-loaded nanogels for antitumor drug delivery. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:321 / 329
页数:9
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