Poly(amino acid)s;
Nanoparticles;
Drug release;
Liquid crystal;
Self-assembly;
AMPHIPHILIC TRIBLOCK COPOLYMERS;
DRUG-RELEASE;
MAGNETIC HYPERTHERMIA;
PH;
NANOCOMPOSITE;
MICELLES;
HYDROGEL;
D O I:
10.1016/j.molliq.2022.120891
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:
Drug-loaded nanoparticles can lower the adverse effects of antitumor drugs and have good biosafety. Herein, a series of amphiphilic poly (amino acid)s materials were designed to prepare drug-loaded nanoparticles by physical encapsulation and chemical bonding. The introduction of cholesterol makes the material show the properties of liquid crystal, and facilitates the regular arrangement of macro-molecules so that it can be well self-assembled. The morphologies with different shapes in different envi-ronments such as spheres or rod were observed. CCK-8 experiment proved the synthesized material was low-toxic to normal cells, and had significant targeting and proliferation inhibition of cancer cells. Nanoparticles entered cells slowly through endocytosis and interact with lysosomes to release drugs. Drug release in vitro shows that the nanoparticles have temperature/pH dual responsiveness.(c) 2022 Elsevier B.V. All rights reserved.
机构:
Univ Santiago de Compostela, Fac Fis, Dept Fis Mat Condensada, Santiago De Compostela, SpainUniv Sonora, Posgrad Nanotecnol, Dept Fis, Rosales & Transversal, Hermosillo 83000, Sonora, Mexico
Barbosa, Silvia
Taboada, Pablo
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机构:
Univ Santiago de Compostela, Fac Fis, Dept Fis Mat Condensada, Santiago De Compostela, SpainUniv Sonora, Posgrad Nanotecnol, Dept Fis, Rosales & Transversal, Hermosillo 83000, Sonora, Mexico