Synthesis of castasterone selective polymers prepared by molecular imprinting

Kugimiya, Akimitsu; Matsui, Jun; Abé, Hiroshi; Aburatani, Masakazu; Takeuchi, Toshio

doi:10.1016/s0003-2670(98)00095-6

Cited by 31 publications

(7 citation statements)

References 18 publications

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“…[352][353][354][355][356][357][358][359][360][361] A comparative study of covalent (boronic acid) and non-covalent (MAA-based) approaches to the imprinting of castasterone has been reported but no concrete conclusions have been drawn as to which approach is the best. 362 Non-covalent approach. In non-covalent imprinting [363][364][365][366][367][368][369] the interactions between functional monomer and template during polymerization are the same as those between polymer and template in the rebinding step.…”

Section: 329mentioning

confidence: 99%

Molecular imprinting science and technology: a survey of the literature for the years up to and including 2003

Andersson²,

et al. 2006

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Over 1450 references to original papers, reviews and monographs have herein been collected to document the development of molecular imprinting science and technology from the serendipitous discovery of Polyakov in 1931 to recent attempts to implement and understand the principles underlying the technique and its use in a range of application areas. In the presentation of the assembled references, a section presenting reviews and monographs covering the area is followed by papers dealing with fundamental aspects of molecular imprinting and the development of novel polymer formats. Thereafter, literature describing attempts to apply these polymeric materials to a range of application areas is presented.

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Section: 329mentioning

confidence: 99%

Molecular imprinting science and technology: a survey of the literature for the years up to and including 2003

Andersson²,

et al. 2006

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“…[3][4][5][6] In general, MIPs are synthesized by bulk or solution polymerization in organic media, followed by grinding and sieving. [7,8] The grinding and sieving process is timeconsuming and detrimental to some of the binding sites. The ground MIP particles are also irregularly shaped, which results in low efficient column packing for chromatography.…”

Section: Introductionmentioning

confidence: 99%

Preparation and Properties of Salicylic Acid‐Imprinted Polymers from Emulsions

Qiu

Zhang

2008

Macromolecular Symposia

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Summary: Molecularly imprinted polymers with specific recognition to salicylic acid (SA-MIPs) were prepared by oil-in-water emulsion polymerization using salicylic acid as template, acrylamide as functional monomer, and ethylene glycol dimethacrylate as crosslinker. The morphology and size distribution of the SA-MIPs were detected by SEM and photon cross correlation spectrometry. Equilibrium binding experiments and Scatchard analyses were carried out to investigate the selectivity of the SA-MIPs. The results show that the SA-MIPs exhibit a higher affinity and selectivity to salicylic acid than to m-hydroxybenzoic acid and sulfosalicylic acid. Two classes of binding sites were produced in the SA-MIPs and the equilibrium dissociation constants were estimated to be 2.03 and 9.97 mmol/L, respectively.

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“…For the preparation of molecularly imprinted polymers against sugars [12±14] and plant steroid hormone [15] bearing cis-diol groups, p-vinylbenzeneboronic acid was used as the functional monomer. In this study, two types of sialic acid imprinted polymer-coated QCMs were prepared.…”

Section: Resultsmentioning

confidence: 99%