Binding and recognition ability of molecularly imprinted polymer toward p-nitrophenol

2012 ◽  
Vol 125 (4) ◽  
pp. 2549-2555 ◽  
Author(s):  
Fu Qiang An ◽  
Bao Jiao Gao ◽  
Xiao Qin Feng
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Recognition Ability

Molecularly imprinted polymer based on CdTe@SiO2 quantum dots as a fluorescent sensor for the recognition of norepinephrine

The Analyst ◽  
2014 ◽  
Vol 139 (22) ◽  
pp. 5785-5792 ◽  
Author(s):  
Fangdi Wei ◽  
Yanzi Wu ◽  
Guanhong Xu ◽  
Yankun Gao ◽  
Jing Yang ◽  
...  
Keyword(s):  
Quantum Dots ◽  
Molecularly Imprinted Polymer ◽  
Fluorescent Sensor ◽  
Rat Plasma ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Recognition Ability

A fluorescent sensor with recognition ability for norepinephrine was simply prepared and actually used to determine norepinephrine in rat plasma.

A simple method for creating molecularly imprinted polymer-coated bacterial cellulose nanofibers

2014 ◽  
Vol 68 (6) ◽  
Author(s):  
Theeraphon Piacham ◽  
Chartchalerm Isarankura-Na-Ayudhya ◽  
Virapong Prachayasittikul
Keyword(s):  
Bacterial Cellulose ◽  
Molecularly Imprinted Polymer ◽  
Binding Capacity ◽  
Cellulose Nanofibers ◽  
Polymerization Process ◽  
Imprinted Polymer ◽  
Simple Method ◽  
Molecularly Imprinted ◽  
Industrial Sectors ◽  
Recognition Ability

AbstractMolecularly imprinted polymer-coated bacterial cellulose nanofibers have been prepared by immersing solvent treated-bacterial cellulose into a dilute pre-polymerization mixture solution prior to the polymerization process. The quercetin-imprinted polymer coating bacterial cellulose (QIP-BC) nanofibers show discrete nanoparticles encapsulated along the BC nanofibers. The binding capacity of dried QIP-BC was approximately 3 mg per gram of the polymer. The obtained results indicated that QIP-BC nanofibers provided a three fold higher recognition ability for quercetin than quercetin-imprinted nanospheres. This technique can be easily used to combine two fascinating materials like BC nanofibers and molecularly imprinted polymers (MIPs) to afford promising polymer composites that are useful in various innovative applications in biomedical, pharmaceutical, and industrial sectors.

A novel molecularly imprinted polymer thin film at surface of ZnO nanorods for selective fluorescence detection of para-nitrophenol

RSC Advances ◽  
2015 ◽  
Vol 5 (55) ◽  
pp. 44088-44095 ◽  
Author(s):  
Xiao Wei ◽  
Zhiping Zhou ◽  
Tongfan Hao ◽  
Hongji Li ◽  
Yanzhuo Zhu ◽  
...  
Keyword(s):  
Thin Film ◽  
Molecular Recognition ◽  
Fluorescence Detection ◽  
Molecularly Imprinted Polymer ◽  
Zno Nanorods ◽  
Surface Imprinting ◽  
Imprinted Polymer ◽  
Polymer Thin Film ◽  
Molecularly Imprinted ◽  
Recognition Ability

A novel MIPs-based ZnO nanorods with molecular recognition ability for para-nitrophenol was successfully synthesized via a surface imprinting-directing polymerization.

Molecularly imprinted polymer nanospheres based on Mn-doped ZnS QDs via precipitation polymerization for room-temperature phosphorescence probing of 2,6-dichlorophenol

RSC Advances ◽  
2015 ◽  
Vol 5 (26) ◽  
pp. 19799-19806 ◽  
Author(s):  
Xiao Wei ◽  
Zhiping Zhou ◽  
Tongfan Hao ◽  
Hongji Li ◽  
Yongsheng Yan
Keyword(s):  
Molecular Recognition ◽  
Molecularly Imprinted Polymer ◽  
Room Temperature ◽  
Precipitation Polymerization ◽  
Imprinted Polymer ◽  
Room Temperature Phosphorescence ◽  
Molecularly Imprinted ◽  
Recognition Ability ◽  
Polymer Nanospheres ◽  
Mn Doped

A novel MIPs-based RTP QDs with molecular recognition ability for 2,6-dichlorophenol was successfully synthesized via precipitation polymerization.

Efficient synthesis of narrowly dispersed hydrophilic and magnetic molecularly imprinted polymer microspheres with excellent molecular recognition ability in a real biological sample

2014 ◽  
Vol 50 (17) ◽  
pp. 2208-2210 ◽  
Author(s):  
Man Zhao ◽  
Cong Zhang ◽  
Ying Zhang ◽  
Xianzhi Guo ◽  
Husheng Yan ◽  
...  
Keyword(s):  
Molecular Recognition ◽  
Molecularly Imprinted Polymer ◽  
Biological Sample ◽  
Polymer Microspheres ◽  
Efficient Synthesis ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Magnetic Molecularly Imprinted Polymer ◽  
Efficient Approach ◽  
Recognition Ability

A facile and highly efficient approach to obtain uniform hydrophilic and magnetic molecularly imprinted polymer microspheres with excellent molecular recognition ability in a real biological sample is described.

Recognition ability of temperature responsive molecularly imprinted polymer hydrogels

Soft Matter ◽  
2011 ◽  
Vol 7 (5) ◽  
pp. 1986 ◽  
Author(s):  
Xueyong Liu ◽  
Tao Zhou ◽  
Ziwei Du ◽  
Zhong Wei ◽  
Junhua Zhang
Keyword(s):  
Molecularly Imprinted Polymer ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Polymer Hydrogels ◽  
Temperature Responsive ◽  
Recognition Ability

Chiral Separation of Amlodipine and its Enantiomer on a Molecularly Imprinted Polymer-Based Stationary Phase

2013 ◽  
Vol 706-708 ◽  
pp. 36-39 ◽  
Author(s):  
Zhi Wei Li ◽  
Xing Jia ◽  
Chun Mei Xu ◽  
Lei Liu ◽  
De Cai Fu
Keyword(s):  
Stationary Phase ◽  
Flow Rate ◽  
Molecularly Imprinted Polymer ◽  
Mobile Phase ◽  
Chiral Stationary Phase ◽  
Thermal Polymerization ◽  
Imprinted Polymer ◽  
Molecularly Imprinted ◽  
Recognition Ability ◽  
Polymerization Method

A new chiral stationary phase for amlodipine (3-ethyl 5-methyl-2 -[(-2-(aminoethoxymethyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate) based on a molecularly imprinted polymer has been prepared by radiation polymerization method and used for chromatographic separation of the chiral enantiomers. The effects on the separation of mobile phase and flow rate were investigated, and the optimum conditions for HPLC were shown to be: mobile phase, chloroform; flow rate, 0.3 ml min-1; at room temperature. The results has shown that the amlodipine-imprinted polymer was capable of recognizing the enantiomeric difference between the template and its R-enantiomer, whereas the non-imprinted and thermal polymerization polymer have no chiral recognition ability for the enantiomers.

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