Preparation and characterization of (betamethasone sodium phosphate intercalated layered double hydroxide)@liposome nanocomposites

被引:18
|
作者
Zhang, Yaping [1 ]
Wu, Xiaowen [2 ]
Li, Haiping [3 ]
Du, Na [1 ]
Song, Shue [1 ]
Hou, Wanguo [1 ,3 ]
机构
[1] Shandong Univ, Minist Educ, Key Lab Colloid & Interface Chem, Jinan 250100, Shandong, Peoples R China
[2] Xinjiang Normal Univ, Inst Chem & Chem Engn, Urumqi 830000, Peoples R China
[3] Shandong Univ, Natl Engn Technol Res Ctr Colloidal Mat, Jinan 250100, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Layered double hydroxide; Liposome; Betamethasone sodium phosphate; Nanocomposite; Assembly; Control release; DOUBLE HYDROXIDE NANOPARTICLES; PEGYLATED PHOSPHOLIPID MEMBRANE; CONTROLLED-RELEASE PROPERTIES; METAL HYDROXIDE; DRUG-DELIVERY; NANOHYBRIDS; DEXAMETHASONE; COMPOSITE; VESICLES; CAMPTOTHECIN;
D O I
10.1016/j.colsurfa.2017.06.063
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
Herein, we report a nanocomposite of betamethasone sodium phosphate (BMP), a glucocorticoid drug, intercalated layered double hydroxide (LDH) nanohybrids encapsulated in liposomes, denoted as BLN@LSs. The BMP-LDH nanohybrids (BLNs) were firstsynthesized via a coassembly route between BMP anions and LDH single-layer nanosheets (SLNSs), and then coated with liposomes consisting of lecithin and cholesterol. The re-dispersity, stability, and drug release behavior of the so-obtained nanocomposites were investigated. Compared with BLNs, the BLN@LSs exhibit excellent water re-dispersity and stability as well as enhanced drug sustained-release performance. The drug release processes can be described using the pseudo-second-order kinetic model, and intraparticle diffusion is the release rate-limiting step. Our work demonstrates that liposome-coating for drug-LDH nanohybrids is an effective strategy to enhance their water dispersity and sustained-release performances, and that (drug-LDH)@LS nanocomposites are a potential drug delivery system.
引用
收藏
页码:824 / 831
页数:8
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