摘要
We report a facile method to synthesize hollow silica microtubes (SMTs) from electrospun cellulose acetate fiber precursors. Specific surface areas of up to 765 m 2 /g (Brunauer–Emmett–Teller) were measured for the SMTs, which had a typical wall thickness of ∼100 nm and submicron inner diameters. An average pore size of 4.6 nm and pore volume of 0.41 cm 3 /g were derived from Barrett–Joyner–Halenda fitting, whereas Horvath–Kawazoe pore size distribution analysis revealed microporous median pore size and maximum pore volume of 0.7 nm and 0.18 cm 3 /g, respectively. The as-prepared SMTs featuring micro- and mesoporous structures in the walls where amino-functionalized to facilitate a very high drug loading (15% by weight). Drug release profile revealed sustained release rates (79% of acetylsalicylic acid was released after 6 h). It is concluded that the high drug loading and sustained release resulted from the advantageous integration of SMTs' hollow structure and wall mesoporosity. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 42562.
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