Mesoscopic simulation studies on the formation mechanism of drug loaded polymeric micelles

被引:22
|
作者
Wang, Yan [1 ,2 ]
Zhu, Dan Dan [2 ]
Zhou, Jian [1 ]
Wang, Qi Lei [2 ]
Zhang, Can Yang [3 ]
Liu, Yue Jin [1 ]
Wu, Zhi Min [1 ]
Guo, Xin Dong [2 ]
机构
[1] Xiangtan Univ, Sch Chem Engn, Xiangtan 411105, Peoples R China
[2] Beijing Univ Chem Technol, Coll Mat Sci & Engn, Beijing Lab Biomed Mat, Beijing 100029, Peoples R China
[3] Natl Ctr Nanosci & Technol China, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Dissipative particle dynamics; Micelle; Drug delivery; DISSIPATIVE PARTICLE DYNAMICS; TRIBLOCK COPOLYMERS; BLOCK-COPOLYMERS; SURFACTANT; BEHAVIOR; NANOPARTICLES; AGGREGATION; PARAMETERS; SOLVENTS; DELIVERY;
D O I
10.1016/j.colsurfb.2015.09.049
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, the formation of polymeric micelles as drug delivery vehicles in an aqueous environment is investigated by dissipative particle dynamics (DPD) simulations. Doxorubicin (DOX) is selected as the model drug, whereas docosahexaenoic acid (DHA) conjugated His10Lys10 (DHA-His(10)Lys(10)) as the drug carrier. It is shown from DPD simulation that drug molecules and DHA-His(10)Lys(10) molecules could aggregate and form micelles under a defined composition recipe; drug molecules are homogeneously distributed inside the carrier matrix, on whose surface the stabilizer lysine segments are absorbed. Under different compositions of drug and water, aggregate morphologies of polymeric micelles are observed as spherical, columnar, and lamellar structures. We finally proposed the formation mechanism of drug loaded polymeric micelles and apply it in practice by analyzing the simulated phenomena. All the results can effectively guide the experimental preparation of drug delivery system with desired properties or explore a novel polymeric micelle with high performance. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:536 / 544
页数:9
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