{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,18]],"date-time":"2026-01-18T09:41:54Z","timestamp":1768729314880,"version":"3.49.0"},"reference-count":123,"publisher":"MDPI AG","issue":"8","license":[{"start":{"date-parts":[[2014,8,18]],"date-time":"2014-08-18T00:00:00Z","timestamp":1408320000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Molecules"],"abstract":"<jats:p>The selection of natural and chemical compounds for potential applications in new pharmaceutical formulations constitutes a time-consuming procedure in drug screening. To overcome this issue, new devices called biosensors, have already demonstrated their versatility and capacity for routine clinical diagnosis. Designed to perform analytical analysis for the detection of a particular analyte, biosensors based on the coupling of proteins to amperometric and optical devices have shown the appropriate selectivity, sensibility and accuracy. During the last years, the exponential demand for pharmacokinetic studies in the early phases of drug development, along with the need of lower molecular weight detection, have led to new biosensor structure materials with innovative immobilization strategies. The result has been the development of smaller, more reproducible biosensors with lower detection limits, and with a drastic reduction in the required sample volumes. Therefore in order to describe the main achievements in biosensor fields, the present review has the main aim of summarizing the essential strategies used to generate these specific devices, that can provide, under physiological conditions, a credible molecule profile and assess specific pharmacokinetic parameters.<\/jats:p>","DOI":"10.3390\/molecules190812461","type":"journal-article","created":{"date-parts":[[2014,8,18]],"date-time":"2014-08-18T11:17:36Z","timestamp":1408360656000},"page":"12461-12485","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":31,"title":["Trends in Protein-Based Biosensor Assemblies for Drug Screening and Pharmaceutical Kinetic Studies"],"prefix":"10.3390","volume":"19","author":[{"given":"Ana","family":"Gon\u00e7alves","sequence":"first","affiliation":[{"name":"CICS-UBI Centro de Investiga\u00e7\u00e3o em Ci\u00eancias da Sa\u00fade, Universidade da Beira Interior,  6201-506 Covilh\u00e3, Portugal"}]},{"given":"Augusto","family":"Pedro","sequence":"additional","affiliation":[{"name":"CICS-UBI Centro de Investiga\u00e7\u00e3o em Ci\u00eancias da Sa\u00fade, Universidade da Beira Interior,  6201-506 Covilh\u00e3, Portugal"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4041-1504","authenticated-orcid":false,"given":"F\u00e1tima","family":"Santos","sequence":"additional","affiliation":[{"name":"CICS-UBI Centro de Investiga\u00e7\u00e3o em Ci\u00eancias da Sa\u00fade, Universidade da Beira Interior,  6201-506 Covilh\u00e3, Portugal"}]},{"given":"Lu\u00eds","family":"Martins","sequence":"additional","affiliation":[{"name":"CICS-UBI Centro de Investiga\u00e7\u00e3o em Ci\u00eancias da Sa\u00fade, Universidade da Beira Interior,  6201-506 Covilh\u00e3, Portugal"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5658-5445","authenticated-orcid":false,"given":"Cl\u00e1udio","family":"Maia","sequence":"additional","affiliation":[{"name":"CICS-UBI Centro de Investiga\u00e7\u00e3o em Ci\u00eancias da Sa\u00fade, Universidade da Beira Interior,  6201-506 Covilh\u00e3, Portugal"}]},{"given":"Jo\u00e3o","family":"Queiroz","sequence":"additional","affiliation":[{"name":"CICS-UBI Centro de Investiga\u00e7\u00e3o em Ci\u00eancias da Sa\u00fade, Universidade da Beira Interior,  6201-506 Covilh\u00e3, Portugal"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6910-7576","authenticated-orcid":false,"given":"Lu\u00eds","family":"Passarinha","sequence":"additional","affiliation":[{"name":"CICS-UBI Centro de Investiga\u00e7\u00e3o em Ci\u00eancias da Sa\u00fade, Universidade da Beira Interior,  6201-506 Covilh\u00e3, Portugal"}]}],"member":"1968","published-online":{"date-parts":[[2014,8,18]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"1030","DOI":"10.1016\/j.drudis.2013.04.006","article-title":"Global analytical strategy to measure drug\u2013plasma protein interactions: From high-throughput to in-depth analysis","volume":"18","author":"Vuignier","year":"2013","journal-title":"Drug Discov. 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