2015
DOI: 10.1016/j.jcis.2014.12.054
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Azide-functionalized hollow silica nanospheres for removal of antibiotics

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Cited by 33 publications
(22 citation statements)
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“…Another passive functional group, poly(ethylene oxide), can be used to tune the surface charge of silica nanocapsules which, in turn, reduced the damaging interactions of the nanocapsules with red blood cells and platelets [107]. Reactive organic functional groups can also be incorporated onto silica shells to provide facile linker chemistry (e.g., thiol [98][99][100], azide [101], alkyl [102,105], epoxide [32], amine [103,104,106], or alkoxy [107]). The linker is especially important for conjugating various functional molecules or biomolecules onto the surfaces of silica nanocapsules, including stimuli-responsive materials (e.g., chitosan [32] and α-cyclodextrine [20,108]), targeting molecules (e.g., antibody [16] and folic acid [20]), fluorescence imaging agents (e.g., near-IR dye [16], coumarin blue dye [57], fluorescein isothiocyanate [31,58,64], and rhodamine B…”
Section: Biomoleculesmentioning
confidence: 99%
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“…Another passive functional group, poly(ethylene oxide), can be used to tune the surface charge of silica nanocapsules which, in turn, reduced the damaging interactions of the nanocapsules with red blood cells and platelets [107]. Reactive organic functional groups can also be incorporated onto silica shells to provide facile linker chemistry (e.g., thiol [98][99][100], azide [101], alkyl [102,105], epoxide [32], amine [103,104,106], or alkoxy [107]). The linker is especially important for conjugating various functional molecules or biomolecules onto the surfaces of silica nanocapsules, including stimuli-responsive materials (e.g., chitosan [32] and α-cyclodextrine [20,108]), targeting molecules (e.g., antibody [16] and folic acid [20]), fluorescence imaging agents (e.g., near-IR dye [16], coumarin blue dye [57], fluorescein isothiocyanate [31,58,64], and rhodamine B…”
Section: Biomoleculesmentioning
confidence: 99%
“…The silanol groups enable conjugation of organic functional groups either through covalent siloxane bonds or electrostatic interactions.There are two approaches that are commonly used for incorporating functional organic moieties onto silica shells through formation of covalent bonds, i.e., co-condensation and postsynthetic grafting. Using co-condensation methods, an organoalkoxysilane compound is added together with a silica precursor such as TEOS during the synthesis of silica nanocapsules (onepot)[98][99][100][101][102]. In contrast, a post-synthetic grafting process facilitates conjugation of organic functional groups to the exposed silica surfaces after the silica nanocapsules are formed[32,[103][104][105][106][107].…”
mentioning
confidence: 99%
“…For surface Huisgen click reaction, reflection infrared techniques , Raman and X‐ray photoelectron spectroscopy (XPS) have been employed with success. Particularly XPS brought strong supporting evidence for tracking the change in the surface chemical composition of materials after attachment of azido‐functionalized compounds to the surface followed by surface‐confined click reactions resulting in the attachment of polymers , biomacromolecules or metallic nanoparticles .…”
Section: Introductionmentioning
confidence: 99%
“…Although, these processes showed good efficiencies the technical complexity, the use of chemicals associated with relatively high costs have hindered their use. On the other hand, adsorption has been considered one of the most effective method for antibiotic removal and different materials such as polystyrene resins [11], silica nanospheres [12], zeolite [13], birnessite [14], graphene [15,16] have been investigated. Specifically for the adsorption of ␤-lactam antibiotics several materials such as carbon nanotubes [17], activated carbon [18] and bentonite [19] have been investigated.…”
Section: Introductionmentioning
confidence: 99%