4.6 Article

On the Move-Sensitive Fluorescent Aptassay on Board Catalytic Micromotors for the Determination of Interleukin-6 in Ultra-Low Serum Volumes for Neonatal Sepsis Diagnostics

期刊

ACS SENSORS
卷 7, 期 10, 页码 3144-3152

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssensors.2c01635

关键词

micromotors; on-the-move aptassay; graphene; fluorescence microscopy; interleukin-6; neonate sepsis

资金

  1. TRANSNANOAVANSES program [S2018/NMT-4349]
  2. Community of Madrid
  3. MCIN/AEI [PID2020-118154GB-I00]
  4. DISCOVER-UAH-CM Project [REACT UE-CM2021-01]
  5. Community of Madrid (CAM)
  6. European Union (UE), through the European Regional Development Fund (ERDF)
  7. EU

向作者/读者索取更多资源

We propose a graphene oxide/nickel/platinum nanoparticle micromotor-based fluorescent aptassay for the determination of interleukin-6 (IL-6) in serum samples from low-birth-weight infants with sepsis suspicion. The method offers high sensitivity and specificity, and allows for analysis in low sample volumes, simplifying the testing process.
A graphene oxide/nickel/platinum nanoparticle micromotor (MM)-based fluorescent aptassay is proposed to determine interleukin-6 (IL-6) in serum samples from low-birth-weight infants (gestational age of less than 32 weeks and birthweight below 1000 g) with sepsis suspicion. In this kind of patients, IL-6 has demonstrated good sensitivity and specificity for the diagnosis of sepsis, both for early and late onset sepsis. The approach was based on the adsorption of the aptamer for IL-6 tagged with 6-FAM as a fluorescent label (AptIL-6, lambda em = 520 nm) on the graphene oxide external layer (MMGO-AptIL-6) inducing fluorescence quenching (OFF state) and a subsequent on-the-move affinity recognition of IL-6 from AptIL-6 (IL-6-AptIL-6 complex) recovering the fluorescence (ON state). An aptamer against IL-6 was selected and developed by the systematic evolution of ligands by exponential enrichment technology. This approach displayed a suitable linear range of 0.07-1000 pg mL-1 (r = 0.995) covering the cut-offand clinical practice levels, allowing direct determination without any dilution and simplifying the analysis as well as exhibiting an excellent sensitivity (LOD = 0.02 pg mL-1) in ultralow volumes of diagnostic clinical samples (2 mu L). A high agreement between IL-6 levels obtained from our MM-based approach and the method used by the Hospital was obtained (relative error < 3%). The MM-based aptassay is competitive in comparison with that of the Hospital, in terms of a significant reduction of the sample volume (15 times less) and enhanced sensitivity, employing similar analysis times. These results position MM technology with enough potential to achieve high sensitivities in low sample volumes, opening new avenues in diagnosis based on low sample volumes.

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