Porous-wall hollow glass microspheres as novel potential nanocarriers for biomedical applications

Abstract Porous-wall hollow glass microspheres (PW-HGMs) are a novel form of glass material consisting of a 10- to 100-μm-diameter hollow central cavity surrounded by a 1-μm-thick silica shell. A tortuous network of nanometer-scale channels completely penetrates the shell. We show here that these ch...

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Veröffentlicht in:Nanomedicine 2010-02, Vol.6 (1), p.127-136
Hauptverfasser: Li, Shuyi, MD, PhD, Nguyen, Lynsa, BS, Xiong, Hairong, MD, Wang, Meiyao, PhD, Hu, Tom C.-C., PhD, She, Jin-Xiong, PhD, Serkiz, Steven M., PhD, Wicks, George G., PhD, Dynan, William S., PhD
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Sprache:eng
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Zusammenfassung:Abstract Porous-wall hollow glass microspheres (PW-HGMs) are a novel form of glass material consisting of a 10- to 100-μm-diameter hollow central cavity surrounded by a 1-μm-thick silica shell. A tortuous network of nanometer-scale channels completely penetrates the shell. We show here that these channels promote size-dependent uptake and controlled release of biological molecules in the 3- to 8-nm range, including antibodies and a modified single-chain antibody variable fragment. In addition, a 6-nm (70-kDa) dextran can be used to gate the porous walls, facilitating controlled release of an internalized short interfering RNA. PW-HGMs remained in place after mouse intratumoral injection, suggesting a possible application for the delivery of anticancer drugs. The combination of a hollow central cavity that can carry soluble therapeutic agents with mesoporous walls for controlled release is a unique characteristic that distinguishes PW-HGMs from other glass materials for biomedical applications. From the Clinical Editor Porous-wall hollow glass microspheres (PW-HGMs) are a novel form of glass microparticles with a tortuous network of nanometer-scale channels. These channels allow size-dependent uptake and controlled release of biological molecules including antibodies and single-chain antibody fragments. PW-HGMs remained in place after mouse intratumoral injection, suggesting a possible application for the delivery of anti-cancer drugs.
ISSN:1549-9634
1549-9642
DOI:10.1016/j.nano.2009.06.004