Controlled Release of Hydrophilic Drug from Hollow Nanodots

被引:0
|
作者
Preedanorawut, Patitta [1 ]
Chatchawankanphanich, Orawan [2 ]
Yiamsawas, Doungporn [3 ]
Crespy, Daniel [1 ]
机构
[1] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Mol Sci & Engn, Dept Mat Sci & Engn, Rayong 21210, Thailand
[2] Natl Sci & Technol Dev Agcy NSTDA, Natl Ctr Genet Engn & Biotechnol BIOTEC, Pathum Thani 12120, Thailand
[3] Natl Sci & Technol Dev Agcy NSTDA, Natl Nanotechnol Ctr NANOTEC, Pathum Thani 12120, Thailand
关键词
colloidal delivery system; controlled release; hydrophilic molecules; hydrophobic ion pairing; prodrugs; MESOPOROUS SILICA NANOPARTICLES; SALICYLIC-ACID; DELIVERY-SYSTEM; ENHANCE; ENCAPSULATION; NANOCAPSULES; DOXORUBICIN; PLANT; GENE; RESISTANCE;
D O I
10.1002/smll.202409112
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Here the challenge of limited encapsulation efficiency of ionizable hydrophilic molecules in silica materials is addressed. Two effective strategies are showcased that allow high encapsulation efficiency of salicylic acid, while simultaneously maintaining the morphology and particle size of silica nanocapsules. These promising approaches involve the formation and encapsulation of a prodrug or the complexation of the hydrophilic payload with a hydrophobic moiety to form a complex that is dissociated in acidic conditions. Well-defined core-shell silica nanocapsules with a diameter of 6 nm are obtained and exhibited an encapsulation efficiency of over 90%. High amounts of salicylic acid are released in acidic conditions from silica nanocapsules entrapping the prodrug or the complex, leading to pH-responsive characteristics. This work demonstrates promising strategies for the encapsulation and the controlled release of hydrophilic fertilizers, pesticides or drugs.
引用
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页数:12
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