Glutathione-sensitive hollow mesoporous silica nanoparticles for controlled drug delivery

JOURNAL OF CONTROLLED RELEASE

卷:282

Article; Proceedings Paper

Moghaddam, Seyyed Pouya Hadipour^1,2  Yazdimamaghani, Mostafa^1,2  Ghandehari, Hamidreza^1,2,3 

[1] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA

[2] Univ Utah, Nano Inst Utah, Utah Ctr Nanomed, Salt Lake City, UT 84112 USA

[3] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA

关键词: Tunable;    Structural difference;    Hollow mesoporous silica nanoparticles;    GSH-sensitive;    Degradable;    High loading capacity;   

DOI  :  10.1016/j.jconrel.2018.04.032

来源: Elsevier

【 摘 要 】

Tunable glutathione (GSH)-sensitive hollow mesoporous silica nanoparticles (HMSiO2 NPs) were developed using a structural difference-based selective etching strategy. These organosilica hollow nanoparticles contained disulfide linkages (S-S) in the outer shell which were degraded by GSH. The particles were compared with their nonGSH-sensitive tetraethyl orthosilicate (TEOS) HMSiO2 counterparts in terms of their synthesis method, characterization, doxorubicin (DOX) release profile, and in vitro cytotoxicity in MCF-7 breast cancer cells. Transmission electron microscopy (TEM) of the particles indicated that the fabricated HMSiO2 NPs had an average diameter of 130 +/- 5 nm. Thermogravimetric analysis (TGA) revealed that GSH-sensitive particles had approximately 5.3% more weight loss than TEOS HMSiO2 NPs. Zeta potential of these redox-responsive particles was -23 +/- 1 mV at pH 6 in deionized (DI) water. Nitrogen adsorption-desorption isotherm revealed that the surface area of the hollow mesoporous nanoreservoirs was roughly 446 +/- 6 m(2) g(-1) and the average diameter of the pores was 2.3 +/- 0.5 nm. TEM images suggest that the nanoparticles started to lose mass integrity from Day 1. The particles showed a high loading capacity for DOX (8.9 +/- 0.5%) as a model drug, due to the large voids existing in the hollow structures. Approximately 58% of the incorporated DOX released within 14 days in phosphate buffered saline (PBS) at pH 6 and in the presence of 10mM of GSH, mimicking intracellular tumor microenvironment while release from TEOS HMSiO2 NPs was only c.a. 18%. The uptake of these hollow nanospheres by MCF-7 cells and RAW 264.7 macrophages was evaluated using TEM and confocal microscopy. The nanospheres were shown to accumulate in the endolysosomal compartments after incubation for 24 h with the maximum uptake of c.a. 2.1 +/- 0.3% and 5.2 +/- 0.4%, respectively. Cytotoxicity of the nanospheres was investigated using CCK-8 assay. Results indicate that intact hollow particles (both GSH-sensitive and TEOS HMSiO2 NPs) were nontoxic to MCF-7 cells after incubation for 24 h within the concentration range of 0-1000 mu g ml(-1). DOX-loaded GSH-sensitive nanospheres containing 6 mu g ml(-1) of DOX killed c.a. 51% of MCF-7 cells after 24 h while TEOS HMSiO2 NPs killed c. a. 20% with the difference being statistically significant. Finally, cytotoxicity data in RAW 264.7 macrophages and NIH 3T3 fibroblasts shows that intact GSH-sensitive HMSiO2 NPs did not show any toxic effects on these cells with the concentrations equal or < 125 mu g ml(-1).

【 授权许可】

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