色谱
色譜
색보
Chinese Journal of Chromatography
2015年
9期
957-965
,共9页
郑鹏磊%罗智敏%畅瑞苗%葛燕辉%杜玮%常春%傅强
鄭鵬磊%囉智敏%暢瑞苗%葛燕輝%杜瑋%常春%傅彊
정붕뢰%라지민%창서묘%갈연휘%두위%상춘%부강
表面分子印迹聚合物%青霉噻唑酸%分子识别%吸附性能
錶麵分子印跡聚閤物%青黴噻唑痠%分子識彆%吸附性能
표면분자인적취합물%청매새서산%분자식별%흡부성능
surface molecularly imprinted polymer%penicilloic acid ( PEOA)%molecular rec-ognition%adsorption properties
针对青霉素药物及乳制品中致敏杂质青霉噻唑酸( PEOA)的特异性分离分析,采用表面印迹聚合法,以青霉噻唑酸为模板分子,制备青霉噻唑酸分子印迹聚合物( PEOA?MIPs)。通过静态吸附、吸附动力学及选择性实验考察其吸附性能,结果显示PEOA?MIPs对青霉噻唑酸有特异的识别能力和快速的传质速率,饱和吸附量为122?78 mg/g,静态吸附和吸附速率分别符合Langmuir模型和准二级动力学方程,表明MIPs的吸附是以化学吸附为主的单分子层吸附。利用扫描电镜( SEM)、红外光谱( FT?IR)和热重分析( TGA)对聚合物进行表征,结果显示聚合物成功接枝在硅胶表面,并具有良好的热稳定性。 PEOA?MIPs对PEOA具有特异的识别能力,可用作萃取介质,为建立快速分离分析致敏杂质青霉噻唑酸的方法提供基础。
針對青黴素藥物及乳製品中緻敏雜質青黴噻唑痠( PEOA)的特異性分離分析,採用錶麵印跡聚閤法,以青黴噻唑痠為模闆分子,製備青黴噻唑痠分子印跡聚閤物( PEOA?MIPs)。通過靜態吸附、吸附動力學及選擇性實驗攷察其吸附性能,結果顯示PEOA?MIPs對青黴噻唑痠有特異的識彆能力和快速的傳質速率,飽和吸附量為122?78 mg/g,靜態吸附和吸附速率分彆符閤Langmuir模型和準二級動力學方程,錶明MIPs的吸附是以化學吸附為主的單分子層吸附。利用掃描電鏡( SEM)、紅外光譜( FT?IR)和熱重分析( TGA)對聚閤物進行錶徵,結果顯示聚閤物成功接枝在硅膠錶麵,併具有良好的熱穩定性。 PEOA?MIPs對PEOA具有特異的識彆能力,可用作萃取介質,為建立快速分離分析緻敏雜質青黴噻唑痠的方法提供基礎。
침대청매소약물급유제품중치민잡질청매새서산( PEOA)적특이성분리분석,채용표면인적취합법,이청매새서산위모판분자,제비청매새서산분자인적취합물( PEOA?MIPs)。통과정태흡부、흡부동역학급선택성실험고찰기흡부성능,결과현시PEOA?MIPs대청매새서산유특이적식별능력화쾌속적전질속솔,포화흡부량위122?78 mg/g,정태흡부화흡부속솔분별부합Langmuir모형화준이급동역학방정,표명MIPs적흡부시이화학흡부위주적단분자층흡부。이용소묘전경( SEM)、홍외광보( FT?IR)화열중분석( TGA)대취합물진행표정,결과현시취합물성공접지재규효표면,병구유량호적열은정성。 PEOA?MIPs대PEOA구유특이적식별능력,가용작췌취개질,위건립쾌속분리분석치민잡질청매새서산적방법제공기출。
On account of the specificity and reproducibility for the determination of penicilloic acid in penicillin, this study aims to prepare penicilloic acid imprinted polymers ( PEOA?MIPs) by surface polymerization method at the surface of modified silica particles by using penicilloic acid ( PEOA) as the template molecule, methacrylic acid ( MAA) as the functional monomer, ethylene glycol dimethacrylate ( EGDMA) as the cross linker, and methanol/acetonitrile as the solvents. The synthesis conditions were optimized, and PEOA?MIPs had the best adsorption capacity when the molar ratio of template molecule/functional monomer was 1∶4, cross linking degree was 85% and the solvent ratio of methanol/acetonitrile was 1∶1 ( v/v) . The adsorption properties were evaluated by adsorption experiments, including the adsorption isotherms, kinetics and selectivity. The adsorption process between PEOA?MIPs and PEOA fitted the Lang?muir adsorption isotherm with the maximum adsorption capacity of 122?78 mg/g and the pseu?do?second?order reaction kinetics with fast adsorption kinetics ( the equilibrium time of 45 min) . The as?synthesized PEOA?MIPs were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy ( FT?IR), and thermal gravimetric analysis ( TGA) . The results indicated that the MIPs layer has been successfully grafted on the surface of SiO2 microparticles and the PEOA?MIPs had the excellent thermal stability. The PEOA?MIPs showed the highest selective recognition for PEOA. The PEOA?MIPs possess a high adsorption capacity, rapid mass?transfer rate and high selectivity to PEOA when compared with non?imprinted polymers ( PEOA?NIPs) . The PEOA?MIPs was expected to be used as the solid phase extraction medium and this study provides the potential applications for fast recognition and analysis of the penicilloic acid in penicillin.