TY - JOUR
A1 - Ozcelikay, Goksu
A1 - Kurbanoglu, Sevinc
A1 - Zhang, Xiaorong
A1 - Söz, Çağla Kosak
A1 - Wollenberger, Ulla
A1 - Ozkan, Sibel A.
A1 - Yarman, Aysu
A1 - Scheller, Frieder W.
T1 - Electrochemical MIP Sensor for Butyrylcholinesterase
JF - Polymers
N2 - Molecularly imprinted polymers (MIPs) mimic the binding sites of antibodies by substituting the amino acid-scaffold of proteins by synthetic polymers. In this work, the first MIP for the recognition of the diagnostically relevant enzyme butyrylcholinesterase (BuChE) is presented. The MIP was prepared using electropolymerization of the functional monomer o-phenylenediamine and was deposited as a thin film on a glassy carbon electrode by oxidative potentiodynamic polymerization. Rebinding and removal of the template were detected by cyclic voltammetry using ferricyanide as a redox marker. Furthermore, the enzymatic activity of BuChE rebound to the MIP was measured via the anodic oxidation of thiocholine, the reaction product of butyrylthiocholine. The response was linear between 50 pM and 2 nM concentrations of BuChE with a detection limit of 14.7 pM. In addition to the high sensitivity for BuChE, the sensor responded towards pseudo-irreversible inhibitors in the lower mM range.
KW - molecularly imprinted polymers
KW - biomimetic sensors
KW - butyrylcholinesterase
KW - o-phenylenediamine
KW - rivastigmine
Y1 - 2019
U6 - https://doi.org/10.3390/polym11121970
SN - 2073-4360
VL - 11
IS - 12
PB - MDPI
CY - Basel
ER -
TY - JOUR
A1 - Ozcelikay, Goksu
A1 - Kurbanoglu, Sevinc
A1 - Yarman, Aysu
A1 - Scheller, Frieder W.
A1 - Ozkan, Sibel A.
T1 - Au-Pt nanoparticles based molecularly imprinted nanosensor for electrochemical detection of the lipopeptide antibiotic drug Daptomycin
JF - Sensors and actuators : B, Chemical
N2 - In this work, a novel electrochemical molecularly imprinted polymer (MIP) sensor for the detection of the lipopeptide antibiotic Daptomycin (DAP) is presented which integrates gold decorated platinum nanoparticles (Au-Pt NPs) into the nanocomposite film. The sensor was prepared by electropolymerization of o-phenylenediamine (o-PD) in the presence of DAP using cyclic voltammetry. Cyclic voltammetry and differential pulse voltammetry were applied to follow the changes in the MIP-layer related to rebinding and removal of the target DAP by using the redox marker [Fe(CN)(6)](3-/4-). Under optimized operational conditions, the MIP/Au-Pt NPs/ GCE nanosensor exhibits a linear response in the range of 1-20 pM towards DAP. The limit of detection and limit of quantification were determined to be 0.161pM +/- 0.012 and 0.489pM +/- 0.012, respectively. The sensitivity towards the antibiotics Vancomycin and Erythromycin and the amino acids glycine and tryptophan was below 7 percent as compared with DAP. Moreover, the nanosensor was also successfully used for the detection of DAP in deproteinated human serum samples.
KW - molecularly imprinted polymer
KW - Daptomycin
KW - platinum nanoparticles
KW - gold
KW - nanoparticles
KW - modified electrodes
Y1 - 2020
U6 - https://doi.org/10.1016/j.snb.2020.128285
SN - 0925-4005
VL - 320
PB - Elsevier Science
CY - Amsterdam
ER -
TY - JOUR
A1 - Yarman, Aysu
A1 - Kurbanoglu, Sevinc
A1 - Jetzschmann, Katharina J.
A1 - Ozkan, Sibel A.
A1 - Wollenberger, Ulla
A1 - Scheller, Frieder W.
T1 - Electrochemical MIP-Sensors for Drugs
JF - Current Medicinal Chemistry
N2 - In order to replace bio-macromolecules by stable synthetic materials in separation techniques and bioanalysis biomimetic receptors and catalysts have been developed: Functional monomers are polymerized together with the target analyte and after template removal cavities are formed in the "molecularly imprinted polymer" (MIP) which resemble the active sites of antibodies and enzymes. Starting almost 80 years ago, around 1,100 papers on MIPs were published in 2016. Electropolymerization allows to deposit MIPs directly on voltammetric electrodes or chips for quartz crystal microbalance (QCM) and surface plasmon resonance (SPR). For the readout of MIPs for drugs amperometry, differential pulse voltammetry (DPV) and impedance spectroscopy (EIS) offer higher sensitivity as compared with QCM or SPR. Application of simple electrochemical devices allows both the reproducible preparation of MIP sensors, but also the sensitive signal generation. Electrochemical MIP-sensors for the whole arsenal of drugs, e.g. the most frequently used analgesics, antibiotics and anticancer drugs have been presented in literature and tested under laboratory conditions. These biomimetic sensors typically have measuring ranges covering the lower nano-up to millimolar concentration range and they are stable under extreme pH and in organic solvents like nonaqueous extracts.
KW - Biomimetic sensors
KW - molecularly imprinted polymers
KW - drug sensors
KW - drug imprinting
KW - electropolymerization
KW - electrochemical sensors
Y1 - 2018
U6 - https://doi.org/10.2174/0929867324666171005103712
SN - 0929-8673
SN - 1875-533X
VL - 25
IS - 33
SP - 4007
EP - 4019
PB - Bentham Science Publishers LTD
CY - Sharjah
ER -
TY - JOUR
A1 - Kurbanoglu, Sevinc
A1 - Yarman, Aysu
T1 - Simultaneous determination of hydrochlorothiazide and irbesartan from pharmaceutical dosage forms with RP-HPLC
T1 - Farmasötik Dozaj Formlarında TF-YPSK ile Hidroklorotiyazid ve
İrbesartanın Eş Zamanlı Tayini
JF - Turkish journal of pharmaceutical sciences
N2 - Objectives: In this work, a simple and rapid liquid chromatographic method for the simultaneous determination of irbesartan (IRBE) and hydrochlorothiazide (HCT) was developed and validated by reverse phase high performance liquid chromatography (RP-HPLC).
Materials and Methods: Experimental conditions such as different buffer solutions, various pH values, temperature, composition of the mobile phase, and the effect of flow rate were optimized.
Results: The developed RP-HPLC method for these antihypertensive agents was wholly validated and IRBE was detected in the linear range of 0.1-25 mu g mL(-1) and HCT was detected in the linear range of 0.25-25 mu g mL(-1). Moreover, the suggested chromatographic technique was successfully applied for the determination of the drugs in human serum and pharmaceutical dosage forms with limit of detection values of 0.008 mu g mL(-1) for IRBE and 0.012 mu g mL(-1) for HCT.
Conclusion: The proposed rapid analysis method of these antihypertensive drugs can be easily used and applied by pharmaceutical companies for which the analysis time is important.
N2 - Amaç: Bu çalışmada, irbesartan (IRBE) ve hidroklorotiyazidin (HCT) eşzamanlı tayini için basit ve hızlı bir ters fazlı yüksek performanslı sıvı
kromatografisi (TF-YPSK) yöntemi geliştirilmiş ve validasyon çalışmaları yapılmıştır.
Gereç ve Yöntemler: Deneysel koşullar; farklı tampon çözeltileri, çeşitli pH değerleri, sıcaklık, mobil fazın bileşimi, akış hızının etkisi gibi
parametrelerin üzerinden optimize edildi.
Bulgular: Bu antihipertansif ajanlar için geliştirilen TF-YPSK yönteminin tüm validasyon parametrelerine ilişkin çalışmalar yapılmış, ve IRBE 0,1-25
μg mL-1 doğrusal aralığında ve HCT 0,25-25 μg mL-1 doğrusal aralığında tespit edilmiştir. Ayrıca önerilen TF-YPSK yöntemi ile IRBE için 0,008 μg
mL-1 ve HCT için 0,012 μg mL-1 tayin alt sınır değerleri bulunmuştur. Geliştirilen yöntem, insan serumunda ve farmasötik dozaj formlarında bulunan
IRBE ve HCT’nin belirlenmesi için başarıyla uygulanmıştır.
Sonuç: Bu antihipertansif ilaçların miktar tayininde önerilen YPSK analiz yönteminin, analiz süresinin önemli olduğu ilaç firmalarında rahatlıkla
kullanılabileceği ve uygulanabileceği düşünülmektedir.
KW - HPLC
KW - irbesartan
KW - hydrochlorothiazide
KW - pharmaceutical dosage forms
Y1 - 2020
U6 - https://doi.org/10.4274/tjps.galenos.2019.76094
SN - 1304-530X
VL - 17
IS - 5
SP - 523
EP - 527
PB - Turkish Pharmacists Association
CY - Çankaya-Ankara
ER -
TY - GEN
A1 - Ozcelikay, Goksu
A1 - Kurbanoglu, Sevinc
A1 - Zhang, Xiaorong
A1 - Söz, Çağla Kosak
A1 - Wollenberger, Ulla
A1 - Ozkan, Sibel A.
A1 - Yarman, Aysu
A1 - Scheller, Frieder W.
T1 - Electrochemical MIP Sensor for Butyrylcholinesterase
T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
N2 - Molecularly imprinted polymers (MIPs) mimic the binding sites of antibodies by substituting the amino acid-scaffold of proteins by synthetic polymers. In this work, the first MIP for the recognition of the diagnostically relevant enzyme butyrylcholinesterase (BuChE) is presented. The MIP was prepared using electropolymerization of the functional monomer o-phenylenediamine and was deposited as a thin film on a glassy carbon electrode by oxidative potentiodynamic polymerization. Rebinding and removal of the template were detected by cyclic voltammetry using ferricyanide as a redox marker. Furthermore, the enzymatic activity of BuChE rebound to the MIP was measured via the anodic oxidation of thiocholine, the reaction product of butyrylthiocholine. The response was linear between 50 pM and 2 nM concentrations of BuChE with a detection limit of 14.7 pM. In addition to the high sensitivity for BuChE, the sensor responded towards pseudo-irreversible inhibitors in the lower mM range.
T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1138
KW - molecularly imprinted polymers
KW - biomimetic sensors
KW - butyrylcholinesterase
KW - o-phenylenediamine
KW - rivastigmine
Y1 - 2021
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-501854
SN - 1866-8372
IS - 1138
ER -
TY - JOUR
A1 - Yarman, Aysu
A1 - Kurbanoğlu, Sevinç
A1 - Zebger, Ingo
A1 - Scheller, Frieder W.
T1 - Simple and robust
BT - the claims of protein sensing by molecularly imprinted polymers
JF - Sensors and actuators : B, Chemical : an international journal devoted to research and development of chemical transducers
N2 - A spectrum of 7562 publications on Molecularly Imprinted Polymers (MIPs) has been presented in literature within the last ten years (Scopus, September 7, 2020). Around 10 % of the papers published on MIPs describe the recognition of proteins. The straightforward synthesis of MIPs is a significant advantage as compared with the preparation of enzymes or antibodies. MIPs have been synthesized from only one up to six functional monomers while proteins are made up of 20 natural amino acids. Furthermore, they can be synthesized against structures of low immunogenicity and allow multi-analyte measurements via multi-target synthesis. Electrochemical methods allow simple polymer synthesis, removal of the template and readout. Among the different sensor configurations electrochemical MIP-sensors provide the broadest spectrum of protein analytes. The sensitivity of MIP-sensors is sufficiently high for biomarkers in the sub-nanomolar region, nevertheless the cross-reactivity of highly abundant proteins in human serum is still a challenge. MIPs for proteins offer innovative tools not only for clinical and environmental analysis, but also for bioimaging, therapy and protein engineering.
KW - Molecularly imprinted polymer
KW - Plastibodies
KW - Functional scaffolds
KW - Biomimetic sensors
KW - Proteins
Y1 - 2021
U6 - https://doi.org/10.1016/j.snb.2020.129369
SN - 0925-4005
SN - 1873-3077
VL - 330
PB - Elsevier Science
CY - Amsterdam [u.a.]
ER -
TY - JOUR
A1 - Yarman, Aysu
A1 - Kurbanoglu, Sevinc
T1 - Molecularly imprinted polymer-based sensors for SARS-CoV-2
BT - where are we now?
JF - Biomimetics
N2 - Since the first reported case of COVID-19 in 2019 in China and the official declaration from the World Health Organization in March 2021 as a pandemic, fast and accurate diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has played a major role worldwide. For this reason, various methods have been developed, comprising reverse transcriptase-polymerase chain reaction (RT-PCR), immunoassays, clustered regularly interspaced short palindromic repeats (CRISPR), reverse transcription loop-mediated isothermal amplification (RT-LAMP), and bio(mimetic)sensors. Among the developed methods, RT-PCR is so far the gold standard. Herein, we give an overview of the MIP-based sensors utilized since the beginning of the pandemic.
KW - molecularly imprinted polymers
KW - biomimetic sensors
KW - SARS-CoV-2
Y1 - 2022
U6 - https://doi.org/10.3390/biomimetics7020058
SN - 2313-7673
VL - 7
IS - 2
PB - MDPI
CY - Basel
ER -