2022
DOI: 10.1039/d2lc00233g
|View full text |Cite
|
Sign up to set email alerts
|

From saliva to SNP: non-invasive, point-of-care genotyping for precision medicine applications using recombinase polymerase amplification and giant magnetoresistive nanosensors

Abstract: Genetic testing is considered a cornerstone of the precision medicine paradigm. Genotyping of single nucleotide polymorphisms (SNPs) has been shown to provide insights into several important issues, including therapy selection...

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
12
0

Year Published

2022
2022
2025
2025

Publication Types

Select...
6
1

Relationship

2
5

Authors

Journals

citations
Cited by 21 publications
(12 citation statements)
references
References 56 publications
0
12
0
Order By: Relevance
“…We also consider further reduction of assay times to be feasible given past work on similar tests that saw turnaround times of ~15 minutes [37] . Finally, we believe that this assay is a prime candidate for deployment as a point-of-care tool, as has been done with other GMR assays [23] , [37] , [38] . In the future, this neutralizing antibody test could be conducted in a self-contained, single-use cartridge on which all sample and fluid handling would be automated.…”
Section: Discussionmentioning
confidence: 86%
“…We also consider further reduction of assay times to be feasible given past work on similar tests that saw turnaround times of ~15 minutes [37] . Finally, we believe that this assay is a prime candidate for deployment as a point-of-care tool, as has been done with other GMR assays [23] , [37] , [38] . In the future, this neutralizing antibody test could be conducted in a self-contained, single-use cartridge on which all sample and fluid handling would be automated.…”
Section: Discussionmentioning
confidence: 86%
“…The GMR biosensor chips used in this work comprised an array of 80 multilayer spin-valve nanosensors and were fabricated, as previously described. , Each chip was wire-bonded to a custom-designed printed circuit board (PCB) (Figure S2) that was designed to interface with complementary signal acquisition and conditioning circuitry. , Individual sensors were functionalized with amino-modified single-stranded DNA (ssDNA) capture probes (Table S1) via a surface silanization method described previously. , Briefly, the chip was rinsed sequentially by acetone, methanol, and isopropanol. Then, to ensure that the probes could more effectively bind to the sensor surface, the chip was treated in a bath of 15% hydrogen peroxide (Certified ACS, Sigma-Aldrich) in distilled water for 15 min, then 10% (3-aminopropyl)­triethoxysilane (Sigma-Aldrich) in acetone for 30 min, and then 5% glutaraldehyde (Fisher Scientific) in distilled water for 30 min.…”
Section: Methodsmentioning
confidence: 99%
“…36,37 Each chip was wire-bonded to a custom-designed printed circuit board (PCB) (Figure S2) that was designed to interface with complementary signal acquisition and conditioning circuitry. 39,43 Individual sensors were functionalized with amino-modified single-stranded DNA (ssDNA) capture probes (Table S1) via a surface silanization method described previously. 48,49 Briefly, the chip was rinsed sequentially by acetone, methanol, and isopropanol.…”
Section: ■ Experimental Sectionmentioning
confidence: 99%
See 2 more Smart Citations