2004
DOI: 10.1073/pnas.0404806101
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A rapid bioassay for single bacterial cell quantitation using bioconjugated nanoparticles

Abstract: The rapid and sensitive determination of pathogenic bacteria is extremely important in biotechnology, medical diagnosis, and the current fight against bioterrorism. Current methods either lack ultrasensitivity or take a long time for analysis. Here, we report a bioconjugated nanoparticle-based bioassay for in situ pathogen quantification down to single bacterium within 20 min. The bioconjugated nanoparticle provides an extremely high fluorescent signal for bioanalysis and can be easily incorporated with biorec… Show more

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Cited by 528 publications
(362 citation statements)
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References 24 publications
(25 reference statements)
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“…3 The sizes of NPs are typically about 2 orders of magnitude smaller than a bacterium, which allows the attachment of multiple NPs onto a bacterial cell rendering easy magnet-mediated separation. 3,4 Moreover, the small NPs have faster kinetics in solution as compared to their micrometer-sized counterparts, which can result in fast detection.Our journey commenced with functionalization of silica-coated magnetite NP (NP 1) with D-mannose (Man) through either a triazole linker (MGNP 2) formed by the [2+3] Huisgen reaction 5 or an amide linkage (MGNP 3) (Schemes 1 and S1). With our covalent approach, 6 all carbohydrates are uniformly oriented on the NP surface, which is crucial for high performances in cell-capturing studies.…”
mentioning
confidence: 99%
“…3 The sizes of NPs are typically about 2 orders of magnitude smaller than a bacterium, which allows the attachment of multiple NPs onto a bacterial cell rendering easy magnet-mediated separation. 3,4 Moreover, the small NPs have faster kinetics in solution as compared to their micrometer-sized counterparts, which can result in fast detection.Our journey commenced with functionalization of silica-coated magnetite NP (NP 1) with D-mannose (Man) through either a triazole linker (MGNP 2) formed by the [2+3] Huisgen reaction 5 or an amide linkage (MGNP 3) (Schemes 1 and S1). With our covalent approach, 6 all carbohydrates are uniformly oriented on the NP surface, which is crucial for high performances in cell-capturing studies.…”
mentioning
confidence: 99%
“…tissues, blood and single cells). [1][2][3][4][5][6][7][8][9][10][11] In microarray and microspot techniques, spatial resolution of individual reactive sites on a chip is extremely important. At the same time, improved labeling and detection technologies are required to analyze smaller sample volumes and to measure samples on a limited solid-phase area.…”
Section: Introductionmentioning
confidence: 99%
“…After silanization, amino-silanized beads were rinsed thoroughly with ethanol and then washed by DMF. Amino-silanized beads were suspended in DMF and reacted with 10% succinic anhydride in DMF solution under N 2 gas for 6 h with continuous shaking [23]. Amino beads were reacted with 10% succinic anhydride with addition of a catalytic amount of 4-(dimethylamino)pyridine (DMAP) in DMF solution under N 2 gas for 4 h with continuous shaking.…”
Section: Preparation Of Succinic Anhydride and Succinic Acid Modifiedmentioning
confidence: 99%