References
- Zokaeifar, H.; Balcázar, J. L.; Kamarudin, M. S.; Sijam, K.; Arshad, A.; Saad, C. R. Selection and Identification of Non-Pathogenic Bacteria Isolated from Fermented Pickles with Antagonistic Properties against Two Shrimp Pathogens. J. Antibiot. 2012, 65, 289–294. DOI: https://doi.org/10.1038/ja.2012.17.
- Schaumburg, F.; Carrell, C. S.; Henry, C. S. Rapid Bacteria Detection at Low Concentrations Using Sequential Immunomagnetic Separation and Paper-Based Isotachophoresis. Anal. Chem. 2019, 91, 9623–9630. DOI: https://doi.org/10.1021/acs.analchem.9b01002.
- Havelaar, A. H.; Kirk, M. D.; Torgerson, P. R.; Gibb, H. J.; Hald, T.; Lake, R. J.; Praet, N.; Bellinger, D. C.; de Silva, N. R.; Gargouri, N.; et al. World Health Organization Global Estimates and Regional Comparisons of the Burden of Foodborne Disease in 2010. PLoS Med. 2015, 12, e1001923. DOI: https://doi.org/10.1371/journal.pmed.1001923.
- Váradi, L.; Luo, J. L.; Hibbs, D. E.; Perry, J. D.; Anderson, R. J.; Orenga, S.; Groundwater, P. W. Methods for the Detection and Identification of Pathogenic Bacteria: Past, Present, and Future. Chem. Soc. Rev. 2017, 46, 4818–4832. DOI: https://doi.org/10.1039/C6CS00693K.
- Lindahl, J. H.; Grace, D. The Consequences of Human Actions on Riskes of Infectious Diseases: A Review. Infect. Ecol. Epidemiol. 2015, 5, 30048. DOI: https://doi.org/10.3402/iee.v5.30048.
- Lim, S. H.; Mix, S.; Anikst, V.; Budvytiene, I.; Eiden, M.; Churi, Y.; Queralto, N.; Berliner, A.; Martino, R. A.; Rhodes, P. A.; Banaei, N. Bacterial Culture Detection and Identification in Blood Agar Plates with an Optoelectronic Nose. Analyst 2016, 141, 918–925. DOI: https://doi.org/10.1039/C5AN01990G.
- Huang, X. X.; Urosevic, N.; Inglis, T. J. J. Accelerated Bacterial Detection in Blood Culture by Enhanced Acoustic Flow Cytometry (AFC) following Peptide Nucleic Acid Fluorescence in Situ Hybridization (PNA-FISH). PLoS ONE 2019, 14, e0201332. DOI: https://doi.org/10.1371/journal.pone.0201332.
- Higgins, J. A.; Azad, A. F. Use of Polymerase Chain Reaction to Detect Bacteria in Arthropods: A Review. J. Med. Entomol. 1995, 32, 213–222. DOI: https://doi.org/10.1093/jmedent/32.3.213.
- Zhang, H.; Morrison, S.; Tang, Y.-W. Multiplex Plymerase Chain Reaction Tests for Detection of Pathogens Associated with Gastroenteritis. Clin. Lab. Med. 2015, 35, 461–486. DOI: https://doi.org/10.1016/j.cll.2015.02.006.
- Wan, Y.; Qi, P.; Zhang, D.; Wu, J.; Wang, Y. Manganese Oxide Nanowire-Mediated Enzyme-Linked Immunosorbent Assay. Biosens. Bioelectron. 2012, 33, 69–74. DOI: https://doi.org/10.1016/j.bios.2011.12.033.
- Li, X.; Li, X.; Guo, Y.; Liu, Y.; Mei, S.; Song, X.; Li, J.; Grugbaye, A. G.; Li, J.; Xu, K. Development and Assessment of a Paper-Based Enzyme-Linked Immunosorbent Assay for the Colorimetric Diagnosis of Human Brucellosis. Anal. Lett. 2019, 52, 1614–1628. DOI: https://doi.org/10.1080/00032719.2018.1563939.
- Jeong, W.-J.; Choi, S.-H.; Lee, H.-S.; Lim, Y.-B. A Fluorescent Supramolecular Biosensor for Bacterial Detection via Binding-Induced Changes in Coiled-Coil Molecular Assembly. Sens. Actuat. B 2019, 290, 93–99. DOI: https://doi.org/10.1016/j.snb.2019.03.112.
- Muniandy, S.; Teh, S. J.; Thong, K. L.; Thiha, A.; Dinshaw, I. J.; Lai, C. W.; Ibrahim, F.; Leo, B. F. Carbon Nanomaterial-Based Electrochemical Biosensors for Foodborne Bacterial Detection. Crit. Rev. Anal. Chem. 2019, 49, 510–533. DOI: https://doi.org/10.1080/10408347.2018.1561243.
- Sun, J.; Huang, J.; Li, Y.; Lv, J.; Ding, X. A Simple and Rapid Colorimetric Bacteria Detection Method Based on Bacterial Inhibition of Glucose Oxidase-Catalyzed Reaction. Talanta 2019, 197, 304–309. DOI: https://doi.org/10.1016/j.talanta.2019.01.039.
- Zaidi, S. A. Molecular Imprinting Polymers and Their Composites: A Promising Material for Diverse Applications. Biomater. Sci. 2017, 5, 388–402. DOI: https://doi.org/10.1039/C6BM00765A.
- Carrasco, S.; Benito-Peña, E.; Navarro-Villoslada, F.; Langer, J.; Sanz-Ortiz, M. N.; Reguera, J.; Liz-Marzán, L. M.; Moreno-Bondi, M. C. Multibranched Gold–Mesoporous Silica Nanoparticles Coated with a Molecularly Imprinted Polymer for Label-Free Antibiotic Surface-Enhanced Raman Scattering Analysis. Chem. Mater. 2016, 28, 7947–7954. DOI: https://doi.org/10.1021/acs.chemmater.6b03613.
- Garcia Lopez, J.; Piletska, E. V.; Whitcombe, M. J.; Czulak, J.; Piletsky, S. A. Application of Molecularly Imprinted Polymer Nanoparticles for Degradation of the Bacterial Autoinducer N-Hexanoyl Homoserine Lactone. Chem. Commun. 2019, 55, 2664–2667. DOI: https://doi.org/10.1039/C8CC07685E.
- Tamahkar, E.; Bakhshpour, M.; Denizli, A. Molecularly Imprinted Composite Bacterial Cellulose Nanofibers for Antibiotic Release. J. Biomater. Sci., Polym. Ed. 2019, 30, 450–461. DOI: https://doi.org/10.1080/09205063.2019.1580665.
- Juric, D.; Rohner, N. A.; Von Recum, H. A. Molecular Imprinting of Cyclodextrin Supramolecular Hydrogels Improves Drug Loading and Delivery. Macromol. Biosci. 2019, 19, 1800246. DOI: https://doi.org/10.1002/mabi.201800246.
- Mokhtari, P.; Ghaedi, M. Water Compatible Molecularly Imprinted Polymer for Controlled Release of Riboflavin as Drug Delivery System. European Poly. J. 2019, 118, 614–618. DOI: https://doi.org/10.1016/j.eurpolymj.2019.06.038.
- Zaidi, S. A. Molecular Imprinted Polymer as Drug Delivery Vehicles. Drug Deliv. 2014, 161, 1–10. DOI: https://doi.org/10.3109/10717544.2014.970297.
- Turiel, E.; Martín-Esteban, A. Molecularly Imprinted Polymers-Based Microextraction Techniques. Trends Anal. Chem. 2019, 118, 574–586. DOI: https://doi.org/10.1016/j.trac.2019.06.016.
- Zaidi, S. A.; Lee, S. M.; Cheong, W. J. Open Tubular Capillary Columns with Basic Templates Made by the Generalized Preparation Protocol in Capillary Electrochromatography Chiral Separation and Template Structural Effects on Chiral Separation Capability. J. Chromatogr. A. 2011, 1218, 1291–1299. DOI: https://doi.org/10.1016/j.chroma.2010.12.117.
- Essousi, H.; Barhoumi, H. Electroanalytical Application of Molecular Imprinted Polyaniline Matrix for Dapsone Determination in Real Pharmaceutical Samples. J. Electroanal. Chem. 2018, 818, 131–139. DOI: https://doi.org/10.1016/j.jelechem.2018.04.039.
- Hussain, S.; Zaidi, S. A.; Vikraman, D.; Kim, H.-S.; Jung, J. Facile Preparation of Molybdenum Carbide (Mo2C) Nanoparticles and Its Effective Utilization in Electrochemical Sensing of Folic Acid via Imprinting. Biosens. Bioelectron. 2019, 140, 111330. DOI: https://doi.org/10.1016/j.bios.2019.111330.
- Zaidi, S. A. Effective Imprinting of an Anticancer Drug, 6-Thioguanine, via Mussel Inspired Self-Polymerization of Dopamine over Reduced Graphene Oxide. Analyst 2019, 144, 2345–2352. DOI: https://doi.org/10.1039/C8AN02348D.
- Zaidi, S. A. Utilization of an Environmentally-Friendly Monomer for an Efficient and Sustainable Adrenaline Imprinted Electrochemical Sensor Using Graphene. Electrochim. Acta 2018, 274, 370–377. DOI: https://doi.org/10.1016/j.electacta.2018.04.119.
- Li, S.; Cao, S.; Whitcombe, M. J.; Piletsky, S. A. Size Matters: Challenges in Imprinting Macromolecules. Progress Polym. Sci. 2014, 39, 145–163. DOI: https://doi.org/10.1016/j.progpolymsci.2013.10.002.
- Boysen, R. I. Advances in the Development of Molecularly Imprinted Polymers for the Separation and Analysis of Proteins with Liquid Chromatography. J. Sep. Sci. 2019, 42, 51–71. DOI: https://doi.org/10.1002/jssc.201800945.
- Nagaoka, T.; Shiigi, H.; Tokonami, S.; Saimatsu, K. Entrapment of Whole Cell Bacteria into Conducting Polymers. J. Flow Inj. Anal. 2012, 29, 7–10.
- Templier, V.; Roux, A.; Roupioz, Y.; Livache, T. Ligands for Label-Free Detection of Whole Bacteria on Biosensors: A Review. Trends Anal. Chem. 2016, 79, 71–79. DOI: https://doi.org/10.1016/j.trac.2015.10.015.
- Tokonami, S.; Iida, T. Review: Novel Sensing Strategies for Bacterial Detection Based on Active and Passive Methods Driven by External Field. Anal. Chim. Acta 2017, 988, 1–16. DOI: https://doi.org/10.1016/j.aca.2017.07.034.
- Idil, N.; Mattiasson, B. Imprinting of Microorganisms for Biosensor Applications. Sensors 2017, 17, 708. DOI: https://doi.org/10.3390/s17040708.
- Aherne, A.; Alexander, C.; Payne, M. J.; Perez, N.; Vulfson, E. N. Bacteria-Mediated Lithography of Polymer Surfaces. J. Am. Chem. Soc. 1996, 118, 8771–8772. DOI: https://doi.org/10.1021/ja960123c.
- Shen, X.; Bonde, J. S.; Kamra, T.; Low, L. B.; Leo, J. C.; Linke, D.; Ye, L. Bacterial Imprinting at Pickering Emulsion Interfaces. Angew. Chem. Int. Ed. 2014, 53, 10687–10690. DOI: https://doi.org/10.1002/anie.201406049.
- Schirhagl, R.; Hall, E. W.; Fuereder, I.; Zare, R. N. Separation of Bacteria with Imprinted Polymeric Films. Analyst 2012, 137, 1495. DOI: https://doi.org/10.1039/c2an15927a.
- Cohen, T.; Starosvetsky, J.; Cheruti, U.; Armon, R. Whole Cell Imprinting in Sol-Gel Thin Films for Bacterial Recognition in Liquids: Macromolecular Fingerprinting. IJMS. 2010, 11, 1236–1252. DOI: https://doi.org/10.3390/ijms11041236.
- Starosvetsky, J.; Cohen, T.; Cheruti, U.; Dragoljub, D.; Armon, R. Effects of Physical Parameters on Bacterial Cell Adsorption onto Pre-Imprinted Sol-Gel Films. Jbnb. 2012, 03, 499–507. DOI: https://doi.org/10.4236/jbnb.2012.324051.
- Jafari, H.; Amiri, M.; Abdi, E.; Navid, S. L.; Bouckaert, J.; Jijie, R.; Boukherroub, R.; Szunerits, S. Entrapment of Uropathogenic E. coli Cells into Ultra-Thin Sol-Gel Matrices on Gold Thin Films: A Low Cost Alternative for Impedimetric Bacteria Sensing. Biosens. Bioelectron. 2019, 124-125, 161–166. DOI: https://doi.org/10.1016/j.bios.2018.10.029.
- Chowdhury, A. D.; De, A.; Chaudhuri, C. R.; Bandyopadhyay, K.; Sen, P. Label Free Polyaniline Based Impedimetric Biosensor for Detection of E. coli O157:H7 Bacteria. Sens. Actuator B 2012, 171-172, 916–923. DOI: https://doi.org/10.1016/j.snb.2012.06.004.
- Escamilla-Gómez, V.; Campuzano, S.; Pedrero, M.; Pingarrón, J. M. Gold Screenprinted-Based Impedimetric Immunobiosensors for Direct and Sensitive Escherichia coli Quantisation. Biosens. Bioelectron 2009, 24, 3365–3371. DOI: https://doi.org/10.1016/j.bios.2009.04.047.
- Maalouf, R.; Fournier-Wirth, C.; Coste, J.; Chebib, H.; Saïkali, Y.; Vittori, O.; Errachid, A.; Cloarec, J.-P.; Martelet, C.; Jaffrezic-Renault, N. Label-Free Detection of Bacteria by Dlectrochemical Impedance Spectroscopy:comparison to Surface Plasmon Resonance. Anal. Chem. 2007, 79, 4879–4886. DOI: https://doi.org/10.1021/ac070085n.
- Tokonami, S.; Nakadoi, Y.; Takahashi, M.; Ikemizu, M.; Kadoma, T.; Saimatsu, K.; Dung, L. Q.; Shiigi, H.; Nagaoka, T. Label-Free and Selective Bacteria Detection Using a Film with Transferred Bacterial Configuration. Anal. Chem. 2013, 85, 4925–4929. − DOI: https://doi.org/10.1021/ac3034618.
- Tokonami, S.; Nakadoi, Y.; Nakata, H.; Takami, S.; Kadoma, T.; Shiigi, H.; Nagaoka, T. Recognition of Gram-Negative and Gram-Positive Bacteria with a Functionalized Conducting Polymer Film. Res. Chem. Intermed. 2014, 40, 2327–2335. DOI: https://doi.org/10.1007/s11164-014-1609-6.
- Shan, X.; Yamauchi, T.; Yamamoto, Y.; Shiigi, H.; Nagaoka, T. A Rapid and Specific Bacterial Detection Method Based on Cell-Imprinted Microplates. Analyst 2018, 143, 1568–1574. DOI: https://doi.org/10.1039/C7AN02057K.
- Bers, K.; Eersels, K.; van Grinsven, B.; Daemen, M.; Bogie, J. F. J.; Hendriks, J. J. A.; Bouwmans, E. E.; Püttmann, C.; Stein, C.; Barth, S.; et al. Heat-Transfer Resistance Measurement Method (HTM) Based Cell Detection at Trace Levels Using a Progressive Enrichment Approach with Highly Selective Cell-Binding Surface Imprints. Langmuir 2014, 30, 3631–3639., − DOI: https://doi.org/10.1021/la5001232.
- Redeker, E. S.; Eersels, K.; Akkermans, O.; Royakkers, J.; Dyson, S.; Nurekeyeva, K.; Ferrando, B.; Cornelis, P.; Peeters, M.; Wagner, P.; et al. Biomimetic Bacterial Identification Platform Based on Thermal Wave Transport Analysis (TWTA) through Surface-Imprinted Polymers. ACS Infect. Dis. 2017, 3, 388–397., − DOI: https://doi.org/10.1021/acsinfecdis.7b00037.
- Grinsven, B. v.; Eersels, K.; Erkens-Hulshof, S.; Diliën, H.; Nurekeyeva, K.; Cornelis, P.; Klein, D.; Crijns, F.; Tuijthof, G.; Wagner, P.; et al. SIP-Based Thermal Detection Platform for the Direct Detection of Bacteria Obtained from a Contaminated Surface. Phys. Status Solidi A 2018, 215, 1700777., DOI: https://doi.org/10.1002/pssa.201700777.
- Qi, P.; Wan, Y.; Zhang, D. Impedimetric Biosensor Based on Cell-Mediated Bioimprinted Films for Bacterial Detection. Biosens. Bioelectron. 2013, 39, 282–288. DOI: https://doi.org/10.1016/j.bios.2012.07.078.
- Golabi, M.; Kuralay, F.; Jager, E. W. H.; Beni, V.; Turner, A. P. F. Electrochemical Bacterial Detection Using Poly(3-Aminophenylboronic Acid)-Based Imprinted Polymer. Biosens. Bioelectron. 2017, 93, 87–93. DOI: https://doi.org/10.1016/j.bios.2016.09.088.
- Gur, S. D.; Bakhshpour, M.; Denizli, A. Selective Detection of Escherichia coli Caused UTIs with Surface Imprinted Plasmonic Nanoscale Sensor. Mater. Sci. Eng. C 2019, 104, 109869. DOI: https://doi.org/10.1016/j.msec.2019.109869.
- Rachkov, A.; Minoura, N. Recognition of Oxytocin and Oxytocin‐Related Peptides in Aqueous Media Using a Molecularly Imprinted Polymer Synthesized by the Epitope Approach. J. Chromatogr. A. 2000, 889, 111–118. ‐DOI: https://doi.org/10.1016/S0021-9673(00)00568-9.
- Singh, M.; Gupta, N.; Raghuwanshi, R. Epitope Imprinting Approach to Monitor Diseases. J. Mol. Genet. Med. 2017, 11, 1000270.
- Kushwaha, A.; Srivastava, J.; Singh, A. K.; Anand, R.; Raghuwanshi, R.; Rai, T.; Singh, M. Epitope Imprinting of Mycobacterium leprae Bacteria via Molecularly Imprinted Nanoparticles Using Multiple Monomers Approach. Biosens. Bioelectron. 2019, 145, 111698. DOI: https://doi.org/10.1016/j.bios.2019.111698.
- Poller, A.-M.; Spieker, E.; Lieberzeit, P. A.; Preininger, C. Surface Imprints: Advantageous Application of Ready2use Materials for Bacterial Quartz-Crystal Microbalance Sensors. ACS Appl. Mater. Interfaces 2017, 9, 1129–1135. DOI: https://doi.org/10.1021/acsami.6b13888.
- Mankar, J. S.; Sharma, M. D.; Rayalu, S. S.; Krupadam, R. J. Molecularly Imprinted Microparticles (microMIPs) Embedded with Reduced Graphene Oxide for Capture and Destruction of E. coli in Drinking Water. Mater. Sci. Eng, C. 2020, 110, 110672. DOI: https://doi.org/10.1016/j.msec.2020.110672.
- Bao, H.; Yang, B.; Zhang, X.; Lei, L.; Li, Z. Bacteria-Templated Fabrication of a Charge Heterogeneous Polymeric Interface for Highly Specific Bacterial Recognition. Chem. Commun. 2017, 53, 2319–2322. DOI: https://doi.org/10.1039/C6CC09242J.
- Tokonami, S.; Shimizu, E.; Tamura, M.; Iida, T. Mechanism in External Field Mediated Trapping of Bacteria Sensitive to Nanoscale Surface Chemical Structure. Sci. Rep. 2017, 7, 16651. DOI: https://doi.org/10.1038/s41598-017-15086-1.
- Khan, M. A. R.; Moreira, F. T. C.; Riu, J.; Sales, M. G. F. Plastic Antibody for the Electrochemical Detection of Bacterial Surface Proteins. Sens. Actuators B 2016, 233, 697–704. DOI: https://doi.org/10.1016/j.snb.2016.04.075.
- Gupta, N.; Singh, R. S.; Shah, K.; Prasad, R.; Singh, M. Epitope Imprinting of Iron Binding Protein of Neisseria meningitidis Bacteria through Multiple Monomers Imprinting Approach. J. Mol. Recognit. 2018, 31, e2709. DOI: https://doi.org/10.1002/jmr.2709.
- Erturk, G.; Hedstrom, M.; Mattiasson, B.; Ruzgas, T.; Lood, R. Highly Sensitive Detection and Quantification of the Secreted Bacterial Benevolence Factor RoxP Using a Capacitive Biosensor: A Possible Early Detection System for Oxidative Skin Diseases. PLoS ONE 2018, 13, e0193754. DOI: https://doi.org/10.1371/journal.pone.0193754.
- Khan, M. A. R.; Aires Cardoso, A. R.; F. Sales, M. G.; Merino, S.; Tomás, J. M.; Rius, F. X.; Riu, J. Artificial Receptors for the Electrochemical Detection of Bacterialflagellar Filaments from Proteus mirabilis. Sens. Actuators B 2017, 244, 732–741. DOI: https://doi.org/10.1016/j.snb.2017.01.018.
- Patel, M. K.; Solanki, P. R.; Kumar, A.; Khare, S.; Gupta, S.; Malhotra, B. D. Electrochemical DNA Sensor for Neisseria meningitidis Detection. Biosens. Bioelectron. 2010, 25, 2586–2591. DOI: https://doi.org/10.1016/j.bios.2010.04.025.
- Shi, X.; Kadiyala, U.; VanEpps, J. S.; Ya, S.-T. Culture-Free Bacterial Detection and Identification from Blood with Rapid, Phenotypic, Antibiotic Susceptibility Testing. Sci. Rep. 2018, 8, 3416.
- Faridi, M. A.; Ramachandraiah, H.; Banerjee, I.; Ardabili, S.; Zelenin, S.; Russom, A. Elasto-Inertial Microfluidics for Bacteria Separation from Whole Blood for Sepsis Diagnostics. J. Nanobiotechnol. 2017, 15, 3.
- Jiang, H.; Jiang, D.; Shao, J.; Sun, X. Magnetic Molecularly Imprinted Polymer Nanoparticles Based Electrochemical Sensor for the Measurement of Gram-Negative Bacterial Quorum Signaling Molecules (N-Acyl-Homoserine-Lactones). Biosens. Bioelectron. 2016, 75, 411–419. DOI: https://doi.org/10.1016/j.bios.2015.07.045.
- Luyao Ma, L.; Shaolong Feng, S.; de la Fuente-Nunez, C.; Hancock, R. E. W.; Lu, X. Development of Molecularly Imprinted Polymers to Block Quorum Sensing and Inhibit Bacterial Biofilm Formation. ACS Appl. Mater. Interfaces 2018, 10, 18450–18457. DOI: https://doi.org/10.1021/acsami.8b01584.
- Cai, W.; Li, H.-H.; Lu, Z. X.; Collinson, M. M. Bacteria Assisted Protein Imprinting in Sol–Gel Derived Films. Analyst 2018, 143, 555–563. DOI: https://doi.org/10.1039/C7AN01509G.
- Lee, M.-H.; Thomas, J. L.; Chen, W.-J.; Li, M. H.; Shih, C.-P.; Lin, H.-Y. Fabrication of Bacteria-Imprinted Polymer Coated Electrodes for Microbial Fuel Cells. ACS Sustain. Chem. Eng. 2015, 3, 1190–1196. − DOI: https://doi.org/10.1021/acssuschemeng.5b00138.