CN106279497A - 一种pH敏感性葡萄糖印迹微凝胶的制备方法 - Google Patents

一种pH敏感性葡萄糖印迹微凝胶的制备方法 Download PDF

Info

Publication number
CN106279497A
CN106279497A CN201610655615.7A CN201610655615A CN106279497A CN 106279497 A CN106279497 A CN 106279497A CN 201610655615 A CN201610655615 A CN 201610655615A CN 106279497 A CN106279497 A CN 106279497A
Authority
CN
China
Prior art keywords
microgel
parts
glucose
preparation
imprinting
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201610655615.7A
Other languages
English (en)
Inventor
潘忠宁
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201610655615.7A priority Critical patent/CN106279497A/zh
Publication of CN106279497A publication Critical patent/CN106279497A/zh
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/04Acids; Metal salts or ammonium salts thereof
    • C08F220/06Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/14Methyl esters, e.g. methyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/26Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by elimination of a solid phase from a macromolecular composition or article, e.g. leaching out
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/26Esters containing oxygen in addition to the carboxy oxygen
    • C08F220/28Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
    • C08F220/281Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing only one oxygen, e.g. furfuryl (meth)acrylate or 2-methoxyethyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2201/00Foams characterised by the foaming process
    • C08J2201/04Foams characterised by the foaming process characterised by the elimination of a liquid or solid component, e.g. precipitation, leaching out, evaporation
    • C08J2201/042Elimination of an organic solid phase
    • C08J2201/0422Elimination of an organic solid phase containing oxygen atoms, e.g. saccharose
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/02Homopolymers or copolymers of acids; Metal or ammonium salts thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2333/06Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C08J2333/10Homopolymers or copolymers of methacrylic acid esters
    • C08J2333/12Homopolymers or copolymers of methyl methacrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2333/14Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing halogen, nitrogen, sulfur, or oxygen atoms in addition to the carboxy oxygen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Peptides Or Proteins (AREA)

Abstract

一种pH敏感性葡萄糖印迹微凝胶的制备方法,将1‑2份MAA、1份MMA、1份HEMA、0.6‑1份EGDMA和4份葡萄糖于烧杯中,静置混合30min,再加入0.5‑0.8份的SDS和200ml的水,将上述溶液转移至三口烧瓶中,40℃水浴搅拌溶解,通氮气30min,再加入0.8‑1.0份的APS,同时升温到75‑80℃,恒温搅拌反应5.5‑6h,生成微凝胶,将产品离心,过滤后,用洗脱液反复洗涤,再离心,过滤,然后冷冻干燥,即得。本发明的有益效果是:以甲基丙烯酸酯类单体构建分子印迹体系,以葡萄糖为模板分子,制备对葡萄糖具有识别性的pH敏感性分子印迹微凝胶。

Description

一种pH敏感性葡萄糖印迹微凝胶的制备方法
技术领域
本发明涉及材料合成方法,具体的是一种pH敏感性葡萄糖印迹微凝胶的制备方法。
背景技术
20世纪50年代, Hirshbergt等提出光致变色的概念,指出光成色与光漂白的循环可构成化学记忆模型,从而使光致变色材料用于光信息存储。光致变色反应材料是一个依靠光激发来改变吸收性质的材料,在激发撤除以后,诱导变色能力仍能保留。因此能在热作用条件下或在相应诱导吸收的光激发下返回原始状态。同时,光致变色材料具有可逆的行为,可以导致颜色的改变。 变色材料种类较多,结构也千差万别,有无机材料也有有机材料。有机光致变色化合物种类较多,如俘精酸酐类化合物、二芳基乙烯类化合物、席夫碱类化合物、吡喃类化合物以及螺吡喃和螺噁嗪类化合物等。有些有机光致材料已经开始了工业化。本研究以吲哚啉为母体设计合成了一种新型光致变色材料。
发明内容
本发明所要解决的技术问题在于提供一种pH敏感性葡萄糖印迹微凝胶的制备方法,提供一种新的合成方法。
本发明采用的合成方法,包括如下步骤:
将1-2份MAA、1份MMA、1份HEMA、0.6-1份EGDMA和4份葡萄糖于烧杯中,静置混合30min,再加入0.5-0.8份的SDS和200ml的水,将上述溶液转移至三口烧瓶中,40℃水浴搅拌溶解,通氮气30min,再加入0.8-1.0份的APS,同时升温到75-80℃,恒温搅拌反应5.5-6h,生成微凝胶,将产品离心,过滤后,用洗脱液反复洗涤,再离心,过滤,然后冷冻干燥,即得。
本发明的有益效果是:合成工艺简单,反应条件温和,生产成本较低,可重复性好究,以甲基丙烯酸酯类单体构建分子印迹体系,以葡萄糖为模板分子,制备对葡萄糖具有识别性的pH敏感性分子印迹微凝胶。
附图说明
图1是微凝胶的溶胀度。
具体实施方式
以下结合实例进一步说明本发明的内容,由技术常识可知,本发明也可通过其它的不脱离本发明技术特征的方案来描述,因此所有在本发明范围内或等同本发明范围内的改变均被本发明包含。
实施例1:将1份MAA、1份MMA、1份HEMA、0.6份EGDMA和4份葡萄糖于烧杯中,静置混合30min,再加入0.5份的SDS和200ml的水,将上述溶液转移至三口烧瓶中,40℃水浴搅拌溶解,通氮气30min,再加入0.8份的APS,同时升温到75℃,恒温搅拌反应5.5h,生成微凝胶,将产品离心,过滤后,用洗脱液反复洗涤,再离心,过滤,然后冷冻干燥,即得。
实施例2:将2份MAA、1份MMA、1份HEMA、1份EGDMA和4份葡萄糖于烧杯中,静置混合30min,再加入0.8份的SDS和200ml的水,将上述溶液转移至三口烧瓶中,40℃水浴搅拌溶解,通氮气30min,再加入1份的APS,同时升温到80℃,恒温搅拌反应6h,生成微凝胶,将产品离心,过滤后,用洗脱液反复洗涤,再离心,过滤,然后冷冻干燥,即得。
由图1可看出,微凝胶的溶胀度在pH为4~6间有一个阶跃性增大,显示出微凝胶具有明显的pH敏感性,
以与葡萄糖结构类似的果糖作为竞争底物,葡萄糖印迹微凝胶的选择吸附实验结果,印迹微凝胶对葡萄糖及果糖的吸附量差别较大,分离因子α为2.05。

Claims (1)

1.一种pH敏感性葡萄糖印迹微凝胶的制备方法,其特征在于:将1-2份MAA、1份MMA、1份HEMA、0.6-1份EGDMA和4份葡萄糖于烧杯中,静置混合30min,再加入0.5-0.8份的SDS和200ml的水,将上述溶液转移至三口烧瓶中,40℃水浴搅拌溶解,通氮气30min,再加入0.8-1.0份的APS,同时升温到75-80℃,恒温搅拌反应5.5-6h,生成微凝胶,将产品离心,过滤后,用洗脱液反复洗涤,再离心,过滤,然后冷冻干燥,即得。
CN201610655615.7A 2016-08-11 2016-08-11 一种pH敏感性葡萄糖印迹微凝胶的制备方法 Pending CN106279497A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610655615.7A CN106279497A (zh) 2016-08-11 2016-08-11 一种pH敏感性葡萄糖印迹微凝胶的制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610655615.7A CN106279497A (zh) 2016-08-11 2016-08-11 一种pH敏感性葡萄糖印迹微凝胶的制备方法

Publications (1)

Publication Number Publication Date
CN106279497A true CN106279497A (zh) 2017-01-04

Family

ID=57668415

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610655615.7A Pending CN106279497A (zh) 2016-08-11 2016-08-11 一种pH敏感性葡萄糖印迹微凝胶的制备方法

Country Status (1)

Country Link
CN (1) CN106279497A (zh)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104725556A (zh) * 2015-04-08 2015-06-24 福州大学 一种对pH敏感的葡萄糖选择吸附剂及其制备方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104725556A (zh) * 2015-04-08 2015-06-24 福州大学 一种对pH敏感的葡萄糖选择吸附剂及其制备方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
薛飞等: "葡萄糖检测用分子印迹光子晶体的研究", 《分析化学研究报告》 *

Similar Documents

Publication Publication Date Title
Zhang et al. Supramolecular chiroptical switches
Samanta et al. Reversible chromism of spiropyran in the cavity of a flexible coordination cage
Arabi et al. Molecular imprinting: green perspectives and strategies
Wu et al. Tetraphenylethene-induced free volumes for the isomerization of spiropyran toward multifunctional materials in the solid state
Pina et al. Chemistry and applications of flavylium compounds: a handful of colours
Renkecz et al. Molecularly imprinted polymer microspheres containing photoswitchable spiropyran-based binding sites
Wei et al. Review of the recent progress in photoresponsive molecularly imprinted polymers containing azobenzene chromophores
Zhu et al. Unimolecular photoconversion of multicolor luminescence on hierarchical self-assemblies
Teng et al. Advances and applications of chiral resolution in pharmaceutical field
Gaedke et al. Chiroptical inversion of a planar chiral redox-switchable rotaxane
Xiong et al. Enantioselective recognition for many different kinds of chiral guests by one chiral receptor based on tetraphenylethylene cyclohexylbisurea
Raeesi et al. Solid-state photochromism of spironaphthoxazine loaded microcapsules with photo-patterning and thermo-regulating features
CN107759803A (zh) 一种四巯基卟啉化合物及其制备方法和用途
CN109608414A (zh) 检测过氧亚硝酸根的荧光探针及其制备方法和应用
Jiang et al. Synthesis of molecularly imprinted organic–inorganic hybrid azobenzene materials by sol–gel for radiation induced selective recognition of 2, 4-dichlorophenoxyacetic acid
CN104549162B (zh) 一种用于分离手性物质的磁场流化床固定相的制备方法
Shi et al. Naphthalenediimide-based photochromic MOFs: Structure visualization upon radical formation, and applications in purple light detection, inkless printing and anti-counterfeiting
Stefanelli et al. Porphyrins Through the Looking Glass: Spectroscopic and mechanistic insights in supramolecular chirogenesis of new self-assembled porphyrin derivatives
CN106279497A (zh) 一种pH敏感性葡萄糖印迹微凝胶的制备方法
Kosheleva et al. New trends in molecular imprinting techniques
CN113185524B (zh) 含脲结构的六元螺环罗丹明光致变色荧光染料及其制备方法和应用
Steinke et al. Molecularly imprinted anisotropic polymer monoliths
Deng et al. Polymeric nanoparticles based on CDs with photoreversible dual-color fluorescence modulation
Kitayama et al. Interfacial photocrosslinking of polymer particles possessing nucleobase photoreactive groups for hollow/capsule polymer fabrication
CN111334070B (zh) 一类532nm激发的罗丹明类荧光染料及其制备方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20170104

WD01 Invention patent application deemed withdrawn after publication