2010
DOI: 10.1016/j.aca.2009.11.008
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Molecularly imprinted layer-coated silica nanoparticles for selective solid-phase extraction of bisphenol A from chemical cleansing and cosmetics samples

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Cited by 137 publications
(66 citation statements)
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“…It has been demonstrated that the untargeted compounds can be selectively washed off from the multi-template MIP surface due to their weaker non-specific interactions with the polymer [31]. Contrarily, some researchers have indicated that the use of a dummy template during polymerization increased the selectivity of the final MIPs that target more that target one compound [39,40].…”
Section: Multi-templatingmentioning
confidence: 99%
“…It has been demonstrated that the untargeted compounds can be selectively washed off from the multi-template MIP surface due to their weaker non-specific interactions with the polymer [31]. Contrarily, some researchers have indicated that the use of a dummy template during polymerization increased the selectivity of the final MIPs that target more that target one compound [39,40].…”
Section: Multi-templatingmentioning
confidence: 99%
“…Polymers which obtained these techniques, demonstrated much better access to binding cavities. These type of MIP were synthetized for selective recognition of BPA and tetrabromobisphenol A [41,43]. In situ polymerization techniques, whereas, found that the application for preparation of block co-polymer of 4-VP and EGDMA for BPA as a target molecule.…”
Section: Molecularly Imprinted Polymers (Mips)mentioning
confidence: 99%
“…BPA, BPF, tetrabromobisphenol A, nonylophenols and their derivatives) from various environmental samples (river water, wastewaters, sewage sludge, sediments, soils), food, biological samples (serum, urine) and cosmetics [35,36,[40][41][42][43].…”
Section: Molecularly Imprinted Polymers (Mips)mentioning
confidence: 99%
“…So, PTMS as functional monomer was employed for the imprinting and recognition process, possibly owing to the hydrophobic interaction and p-p interaction. The weakly polar acetonitrile was chosen as porogen because strongly polar solvents could counteract the formation of affinity bonds for templates, and acetic acid was chosen as the activator during the synthesis of molecularly imprinted sol-gel [35]. Thus, the imprinting process of PAHs regularly encoded the PAH shape of -SiO-SiO-SiO-conjoined to a functional phenyl group, and the specific cavity was formed after the imprinted molecule was eluted.…”
Section: Preparation and Characterization Of Mips For Pahsmentioning
confidence: 99%