Hierarchical hydroxyapatite/polyelectrolyte microcapsules capped with AuNRs for remotely triggered drug delivery

被引:22
作者
Zhu, Xiaoyi [1 ]
Shi, Jun [1 ]
Ma, He [1 ]
Chen, Ruixia [1 ]
Li, Jingguo [2 ]
Cao, Shaokui [1 ]
机构
[1] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Peoples Hosp, Zhengzhou 450003, Henan, Peoples R China
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2019年 / 99卷
基金
中国国家自然科学基金;
关键词
Hydroxyapatite; Natural polyelectrolyte; Au nanorods; Microcapsules; Self-assembly; NIR-/pH-responsiveness; HOLLOW MESOPOROUS HYDROXYAPATITE; COATED GOLD NANORODS; HYBRID MICROPARTICLES; INTRACELLULAR DRUG; RELEASE; MICROSPHERES; THERAPY; PH; FUNCTIONALIZATION; DEGRADABILITY;
D O I
10.1016/j.msec.2019.02.078
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In the present paper, a smart drug delivery platform combining the hollow hierarchical hydroxyapatite (HAP), chitosan/hyaluronic acid polyelectrolyte multilayers and Au nanorods (AuNRs) had been prepared via a layer-by-layer (LbL) technique. AuNRs capped on the surface of HAP/polyelectrolyte hybrid microcapsules acted as the "gate-keeper" to obstruct the leakage of loaded drug and endow the hybrid microcapsules with excellent near-infrared (NIR)-triggered drug release property. In vitro drug release results indicated that the hybrid microcapsules exhibited distinguished pH- and NIR-responsive drug release properties. More interestingly, relatively high DOX release could be observed at pH 4.5 upon NIR laser irradiation owing to the hybrid matrix disintegration in acidic media and the noteworthy photothermal transition effect of AuNRs. The cell viability results demonstrated that the hybrid microcapsules possessed excellent biocompatibility. The present paper provides a facile and green route to fabricate hierarchical multi-responsive drug carriers with high drug loading capacity and outstanding biocompatibility, which are highly attractive for remotely controllable drug delivery.
引用
收藏
页码:1236 / 1245
页数:10
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