Optimization of amine-rich multilayer thin films for the capture and quantification of prostate-specific antigen

It is demonstrated that poly(allylamine hydrochloride)/poly(styrenesulfonate) (PAH/SPS) multilayer films can be successfully tailored for the capture and detection of small biomolecules in dilute concentrations. Based on in vitro results, these films could be potentially applied for rapid and high-t...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 31(2015), 19 vom: 19. Mai, Seite 5479-88
1. Verfasser: Polak, Roberta (VerfasserIn)
Weitere Verfasser: Bradwell, Grinia M, Gilbert, Jonathan B, Danielsen, Scott, Beppu, Marisa M, Cohen, Robert E, Rubner, Michael F
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2015
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Biomarkers, Tumor Polyamines Polystyrenes polyallylamine 30551-89-4 polystyrene sulfonic acid 70KO0R01RY mehr... Prostate-Specific Antigen EC 3.4.21.77
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520 |a It is demonstrated that poly(allylamine hydrochloride)/poly(styrenesulfonate) (PAH/SPS) multilayer films can be successfully tailored for the capture and detection of small biomolecules in dilute concentrations. Based on in vitro results, these films could be potentially applied for rapid and high-throughput diagnosis of dilute biomarkers in serum or tissue. PAH presents functional amino groups that can be further reacted with desired chemistries in order to create customizable and specific surfaces for biomolecule capture. A variety of film assembly characteristics were tested (pH, molecular weight of PAH, and ionic strength) to tune the biotinylation and swelling behavior of these films to maximize detection capabilities. The resultant optimized biotinylated PAH/SPS 9.3/9.3 system was utilized in conjunction with quantum dots (Qdots) to capture and detect a dilute biomarker for prostate cancer, prostate-specific antigen (PSA). Compared to previous work, our system presents a good sensitivity for PSA detection within the clinically relevant range of 0.4-100 ng/mL 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a Research Support, U.S. Gov't, Non-P.H.S. 
650 7 |a Biomarkers, Tumor  |2 NLM 
650 7 |a Polyamines  |2 NLM 
650 7 |a Polystyrenes  |2 NLM 
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650 7 |a 30551-89-4  |2 NLM 
650 7 |a polystyrene sulfonic acid  |2 NLM 
650 7 |a 70KO0R01RY  |2 NLM 
650 7 |a Prostate-Specific Antigen  |2 NLM 
650 7 |a EC 3.4.21.77  |2 NLM 
700 1 |a Bradwell, Grinia M  |e verfasserin  |4 aut 
700 1 |a Gilbert, Jonathan B  |e verfasserin  |4 aut 
700 1 |a Danielsen, Scott  |e verfasserin  |4 aut 
700 1 |a Beppu, Marisa M  |e verfasserin  |4 aut 
700 1 |a Cohen, Robert E  |e verfasserin  |4 aut 
700 1 |a Rubner, Michael F  |e verfasserin  |4 aut 
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773 1 8 |g volume:31  |g year:2015  |g number:19  |g day:19  |g month:05  |g pages:5479-88 
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