"Thunderstruck": Plasma-Polymer-Coated Porous Silicon Microparticles As a Controlled Drug Delivery System

被引:26
作者
McInnes, Steven J. P. [1 ]
Michl, Thomas D. [2 ]
Delalat, Bahman [1 ]
Al-Bataineh, Sameer A. [2 ]
Coad, Bryan R. [2 ]
Vasilev, Krasimir [2 ]
Griesser, Hans J. [2 ]
Voelcker, Nicolas H. [1 ]
机构
[1] Univ S Australia, Future Ind Inst, ARC Ctr Excellence Convergent Bionano Sci & Techn, Adelaide, SA 5001, Australia
[2] Univ S Australia, Future Ind Inst, Mawson Lakes, SA 5095, Australia
关键词
plasma polymerization; fluorinated coating; particle coating; porous silicon; controlled drug release; SURFACE MODIFICATION; TRIGGERED RELEASE; NANOPARTICLES; PARTICLES; PH;
D O I
10.1021/acsami.5b12433
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Controlling the release kinetics from a drug carrier is crucial to maintain a drug's therapeutic window. We report the use of biodegradable porous silicon microparticles (pSi MPs) loaded with the anticancer drug camphothecin, followed by a plasma polymer overcoating using a loudspeaker plasma reactor. Homogenous "Teflon-like" coatings were achieved by tumbling the particles by playing AC/DC's song "Thunderstruck". The overcoating resulted in a markedly slower release of the cytotoxic drug, and this effect correlated positively with the plasma polymer coating times, ranging from 2-fold up to more than 100-fold. Ultimately, upon characterizing and verifying pSi MP production, loading, and coating with analytical methods such as time-of flight secondary ion mass spectrometry, scanning electron microscopy, thermal gravimetry, water contact angle measurements, and fluorescence microscopy, human neuroblastoma cells were challenged with pSi MPs in an in-vitro assay, revealing a significant time delay in cell death onset.
引用
收藏
页码:4467 / 4476
页数:10
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