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        <identifier>oai:figshare.com:article/33861986</identifier>
        <datestamp>2026-09-16T16:31:01Z</datestamp>
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        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Combination of
Polymeric Microneedles with Specific
Peptide for TNF‑α Sensing Via Noninvasive Detection in
Interstitial Fluid</dc:title>
          <dc:creator>Anna Palma (24996476)</dc:creator>
          <dc:creator>Concetta Di Natale (4394620)</dc:creator>
          <dc:creator>Daniele Tammaro (5155268)</dc:creator>
          <dc:creator>Elena Lagreca (10888542)</dc:creator>
          <dc:creator>Alessia Cugudda (23719881)</dc:creator>
          <dc:creator>Sara La Manna (8631078)</dc:creator>
          <dc:creator>Vincenzo Ferraro (5155280)</dc:creator>
          <dc:creator>Veronica Vespini (1794763)</dc:creator>
          <dc:creator>Simonetta Grilli (1551520)</dc:creator>
          <dc:creator>Pier Luca Maffettone (5155271)</dc:creator>
          <dc:creator>Sara Coppola (1794769)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>tumor necrosis factor</dc:subject>
          <dc:subject>results reported show</dc:subject>
          <dc:subject>limitations commonly associated</dc:subject>
          <dc:subject>equilibrium dissociation constant</dc:subject>
          <dc:subject>cost diagnostic systems</dc:subject>
          <dc:subject>clinically relevant biomarkers</dc:subject>
          <dc:subject>&gt;- glycolic acid</dc:subject>
          <dc:subject>remote biomedicine solution</dc:subject>
          <dc:subject>reach higher concentrations</dc:subject>
          <dc:subject>fabricated via micro</dc:subject>
          <dc:subject>dimensional fluorescence assay</dc:subject>
          <dc:subject>labeled p52 variant</dc:subject>
          <dc:subject>interstitial fluid microneedle</dc:subject>
          <dc:subject>assured peptide stability</dc:subject>
          <dc:subject>translating monoclonal antibody</dc:subject>
          <dc:subject>mechanical testing confirmed</dc:subject>
          <dc:subject>low production costs</dc:subject>
          <dc:subject>generation minimally invasive</dc:subject>
          <dc:subject>fluid particularly sensitive</dc:subject>
          <dc:subject>p52 peptide directly</dc:subject>
          <dc:subject>α monitoring directly</dc:subject>
          <dc:subject>interstitial fluid</dc:subject>
          <dc:subject>minimally invasive</dc:subject>
          <dc:subject>time monitoring</dc:subject>
          <dc:subject>scalable solution</dc:subject>
          <dc:subject>fluorescence microscopy</dc:subject>
          <dc:subject>achieved via</dc:subject>
          <dc:subject>p52 peptide</dc:subject>
          <dc:subject>α concentrations</dc:subject>
          <dc:subject>specific peptide</dc:subject>
          <dc:subject>peptide immobilization</dc:subject>
          <dc:subject>p11 peptide</dc:subject>
          <dc:subject>affinity peptide</dc:subject>
          <dc:subject>∼ 0</dc:subject>
          <dc:subject>synthetic high</dc:subject>
          <dc:subject>subsequently functionalized</dc:subject>
          <dc:subject>stable immobilization</dc:subject>
          <dc:subject>simple surface</dc:subject>
          <dc:subject>scalable three</dc:subject>
          <dc:subject>reliable conjugation</dc:subject>
          <dc:subject>polymeric microneedles</dc:subject>
          <dc:subject>platform lies</dc:subject>
          <dc:subject>platform exhibited</dc:subject>
          <dc:subject>picomolar range</dc:subject>
          <dc:subject>overcome using</dc:subject>
          <dc:subject>negative control</dc:subject>
          <dc:subject>ml ).</dc:subject>
          <dc:subject>linear response</dc:subject>
          <dc:subject>lactic -&lt;</dc:subject>
          <dc:subject>inflammatory cytokines</dc:subject>
          <dc:description>Microneedle (MN)-based biosensors offer a minimally invasive
and
blood-free approach for real-time monitoring of clinically relevant
biomarkers in interstitial fluid (ISF). Pro-inflammatory cytokines
such as Tumor Necrosis Factor-α (TNF-α) can reach higher
concentrations in ISF than in serum, which makes this fluid particularly
sensitive for detecting early local inflammatory responses. Here,
we introduce an antibody-free MN biosensor employing a synthetic high-affinity
peptide (P52) for TNF-α recognition in ISF. The novelty of the
platform lies in the stable immobilization of the P52 peptide directly
on mechanically robust polymeric MNs for a scalable three-dimensional
fluorescence assay. The results reported show how the limitations
commonly associated with translating monoclonal antibody-based molecular
recognition could be overcome using a functionalized polymeric microneedle
platform. Poly(lactic-&lt;i&gt;co&lt;/i&gt;-glycolic acid) MNs were
fabricated via micro-molding and subsequently functionalized with
the P52 peptide. A simple surface-conjugation protocol was employed,
which assured peptide stability, low production costs, and reliable
conjugation. Comprehensive morphological, mechanical, and chemical
characterizations were performed through SEM and fluorescence microscopy.
Quantitative detection was achieved via a sandwich-type fluorescence
assay using an FITC-labeled P52 variant, enabling evaluation of capture
efficiency in simulated ISF across graded TNF-α concentrations.
The platform exhibited a linear response with a limit of detection
of ∼0.2 pM (∼3 pg/mL). Peptide immobilization on MNs
enhanced binding affinity, shifting the equilibrium dissociation constant
from the nanomolar to the picomolar range. The P11 peptide was used
as a negative control for sequence-dependent TNF-α recognition.
Mechanical testing confirmed the robustness of the functionalized
MNs without structural failure. Overall, this peptide-functionalized
MN platform represents a robust, sensitive, and scalable solution
for point-of-care TNF-α monitoring directly in ISF, paving the
way for next-generation minimally invasive and low-cost diagnostic
systems that will revolutionize the remote biomedicine solution.</dc:description>
          <dc:date>2026-09-16T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Media</dc:type>
          <dc:identifier>10.1021/acsomega.6c07406.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/media/Combination_of_Polymeric_Microneedles_with_Specific_Peptide_for_TNF_Sensing_Via_Noninvasive_Detection_in_Interstitial_Fluid/33861986</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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