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          <dc:title>Nanofibrous
Poly(amino acid ester) Dressing for Promoting
Diabetic Wound Healing via Spatiotemporal Coordination of Immunomodulation
and Tissue Regeneration</dc:title>
          <dc:creator>Li Ma (46633)</dc:creator>
          <dc:creator>Ying Feng (151159)</dc:creator>
          <dc:creator>Kaijun Li (634814)</dc:creator>
          <dc:creator>Yangrui Du (14801251)</dc:creator>
          <dc:creator>Hexin Zhou (24035742)</dc:creator>
          <dc:creator>Ying Ji (285782)</dc:creator>
          <dc:creator>Kaikai Ma (3116910)</dc:creator>
          <dc:creator>Tao Shuai (25114836)</dc:creator>
          <dc:creator>Gongyan Liu (6170081)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>timely proinflammatory response</dc:subject>
          <dc:subject>spontaneous shift toward</dc:subject>
          <dc:subject>held electrospinning using</dc:subject>
          <dc:subject>amino acid ester</dc:subject>
          <dc:subject>allowing sustained release</dc:subject>
          <dc:subject>accelerated wound closure</dc:subject>
          <dc:subject>spatiotemporal metabolic modulation</dc:subject>
          <dc:subject>diabetic wound microenvironment</dc:subject>
          <dc:subject>rationally designed arginine</dc:subject>
          <dc:subject>breathable nanofibrous dressing</dc:subject>
          <dc:subject>wound epidermis</dc:subject>
          <dc:subject>spatiotemporal coordination</dc:subject>
          <dc:subject>nanofibrous poly</dc:subject>
          <dc:subject>diabetic wounds</dc:subject>
          <dc:subject>work offers</dc:subject>
          <dc:subject>tissue regeneration</dc:subject>
          <dc:subject>thereby restoring</dc:subject>
          <dc:subject>spatially promoting</dc:subject>
          <dc:subject>situ &lt;/</dc:subject>
          <dc:subject>responsive degradation</dc:subject>
          <dc:subject>reparative state</dc:subject>
          <dc:subject>promising strategy</dc:subject>
          <dc:subject>progressive deterioration</dc:subject>
          <dc:subject>often overlooked</dc:subject>
          <dc:subject>mimicking dressing</dc:subject>
          <dc:subject>initially promoting</dc:subject>
          <dc:subject>extracellular matrix</dc:subject>
          <dc:subject>even led</dc:subject>
          <dc:subject>epidermal keratinocytes</dc:subject>
          <dc:subject>conventional treatments</dc:subject>
          <dc:subject>containing degradants</dc:subject>
          <dc:subject>commercial dressings</dc:subject>
          <dc:subject>based poly</dc:subject>
          <dc:subject>21 days</dc:subject>
          <dc:subject>14 days</dc:subject>
          <dc:description>Effective
healing of diabetic wounds requires spatiotemporal coordination
of immunoregulation and tissue regeneration, which is often overlooked
in conventional treatments. Here, we developed an extracellular matrix-mimicking
dressing, termed ANM, that modulates arginine utilization within the
diabetic wound microenvironment to re-establish the spatiotemporal
coordination of healing. ANM was &lt;i&gt;in situ&lt;/i&gt; fabricated
by hand-held electrospinning using a rationally designed arginine-
and norvaline-based poly(ester amide), yielding a conformable and
breathable nanofibrous dressing. Its porous and hydrolyzable structure
enabled moisture- and enzyme-responsive degradation, allowing sustained
release of arginine- and norvaline-containing degradants. These bioactive
degradants cooperatively modulated macrophage phenotypic transitions,
initially promoting a timely proinflammatory response, followed by
a spontaneous shift toward a pro-reparative state, thereby restoring
the temporally sequenced inflammatory program in diabetic wounds.
Meanwhile, ANM locally upregulated inducible nitric oxide synthase
(iNOS) and arginase-1 in the peri-wound epidermis, spatially promoting
the proliferation and differentiation of epidermal keratinocytes and
accelerating re-epithelialization. In contrast to commercial dressings
that failed to support healing and even led to progressive deterioration
over 21 days, ANM significantly promoted collagen deposition and angiogenesis
and accelerated wound closure in db/db mice by 14 days. This work
offers a promising strategy for treating chronic nonhealing wounds
through spatiotemporal metabolic modulation.</dc:description>
          <dc:date>2026-09-26T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Media</dc:type>
          <dc:identifier>10.1021/acsnano.6c07848.s002</dc:identifier>
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          <dc:rights>CC BY-NC 4.0</dc:rights>
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