RESUMO
A kind of core-shell hybrid nanoparticle comprised of a hollow mesoporous silica nanoparticles (HMS) core and a copolymer shell bearing N-(3,4-dihydroxyphenethyl) methacrylamide (DMA) and N-isopropylacrylamide (NIPAM) as responsive moieties was prepared. Moreover, the factors that could impact the surface morphology and hierarchical porous structure were discussed. In the presence of Fe3+, catechol-Fe3+ complexes were formed to achieve pH-responsive polymer shell, combining with thermal-sensitiveness of poly(N-isopropylacrylamide). Doxorubicin (DOX) was applied as a model drug and the behaviors of its loading/release behaviors were investigated to prove the idea. The results exhibited a significant drug loading capacity of 8.6% and embed efficiency of 94.6% under 1 mg ml-1 DOX/PBS solution. In fact, the loading capacity of drug can be easily improved to as high as 28.0% by increasing the DOX concentration. The vitro cytotoxicity assay also indicated that the as-prepared nanoparticles have no significant cytotoxicity on RAW 264.7 cells. The in vitro experiment showed that the cumulative release of DOX was obviously dependent on the temperature and pH values. This pH/temperature-sensitive hollow mesoporous silica nanosphere is expected to have potential applications in controlled drug release.
RESUMO
High-surface-area porous carbon nanosheets have been successfully prepared by direct carbonization of graphene oxide sandwiched poly(aniline-co-pyrrole). Benefiting from the distinct structure features of the poly(aniline-co-pyrrole) and its homogeneous deposition on the graphene oxide surface, the surface area of the porous carbon nanosheets is as high as 1606 m2 g-1.
RESUMO
Vinyl-SBA-15 mesoporous organosilica was synthesized and used as coating material of solid-phase microextraction (SPME) by two coating techniques (direct coating and sol-gel). The synthesized vinyl-SBA-15 organosilica had highly ordered mesoporous structure, good thermal stability and a specific surface area of 688 m² g⻹. The fibers prepared by two methods were evaluated by the extraction of non-polar compounds (BTEX, benzene, toluene, ethylbenzene, o-xylene) and polar compounds (phenols). The results showed that the vinyl-SBA-15 fibers prepared by two methods exhibited high thermal stability (310 °C for direct-coated and 350 °C for sol-gel) and excellent solvent durability in methanol and acetonitrile. The fibers also presented much better extraction performance for both polar compounds (phenols) and non-polar compounds (BTEX), compared to commercial polydimethylsiloxane (PDMS) fiber, as well as wide linear ranges, low detection limits (0.008-0.047 µg L⻹ for BTEX, sol-gel; 0.15-5.7 µg L⻹ for phenols, direct-coated), good repeatabilities (RSDs less than 5.4% for BTEX) and satisfying reproducibilities between fibers (RSDs less than 5.8% for BTEX). The self-made fibers were successfully used for the analysis of BTEX and phenols in three aqueous samples including tap water, mineral water and lake water, which demonstrated the applicability of the vinyl-SBA-15 fibers.