<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang L</submitter><funding>Science and Technology Project of Guangxi</funding><funding>Innovation Project of Guangxi Graduate Education</funding><funding>Guilin University of Technology</funding><pagination>509</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10216006</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(5)</volume><pubmed_abstract>The efficacies and toxicities of chiral drug enantiomers are often dissimilar, necessitating chiral recognition methods. Herein, a polylysine-phenylalanine complex framework was used to prepare molecularly imprinted polymers (MIPs) as sensors with enhanced specific recognition capabilities for levo-lansoprazole. The properties of the MIP sensor were investigated using Fourier-transform infrared spectroscopy and electrochemical methods. The optimal sensor performance was achieved by applying self-assembly times of 30.0 and 25.0 min for the complex framework and levo-lansoprazole, respectively, eight electropolymerization cycles with &lt;i>o&lt;/i>-phenylenediamine as the functional monomer, an elution time of 5.0 min using an ethanol/acetic acid/H&lt;sub>2&lt;/sub>O mixture (2/3/8, &lt;i>V&lt;/i>/&lt;i>V&lt;/i>/&lt;i</pubmed_abstract><journal>Biosensors</journal><pubmed_title>Development of Levo-Lansoprazole Chiral Molecularly Imprinted Polymer Sensor Based on the Polylysine-Phenylalanine Complex Framework Conformational Separation.</pubmed_title><pmcid>PMC10216006</pmcid><funding_grant_id>Guike AD19110059</funding_grant_id><funding_grant_id>GUTQDJJ2016024</funding_grant_id><funding_grant_id>YCSW2022332</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Ouyang H</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of Levo-Lansoprazole Chiral Molecularly Imprinted Polymer Sensor Based on the Polylysine-Phenylalanine Complex Framework Conformational Separation.</name><description>The efficacies and toxicities of chiral drug enantiomers are often dissimilar, necessitating chiral recognition methods. Herein, a polylysine-phenylalanine complex framework was used to prepare molecularly imprinted polymers (MIPs) as sensors with enhanced specific recognition capabilities for levo-lansoprazole. The properties of the MIP sensor were investigated using Fourier-transform infrared spectroscopy and electrochemical methods. The optimal sensor performance was achieved by applying self-assembly times of 30.0 and 25.0 min for the complex framework and levo-lansoprazole, respectively, eight electropolymerization cycles with &lt;i>o&lt;/i>-phenylenediamine as the functional monomer, an elution time of 5.0 min using an ethanol/acetic acid/H&lt;sub>2&lt;/sub>O mixture (2/3/8, &lt;i>V&lt;/i>/&lt;i>V&lt;/i>/&lt;i</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-04T20:56:25.495Z</modification><creation>2025-04-04T20:56:25.495Z</creation></dates><accession>S-EPMC10216006</accession><cross_references><pubmed>37232870</pubmed><doi>10.3390/bios13050509</doi></cross_references></HashMap>