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        <datestamp>2026-03-24</datestamp>
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          <dc:description>Submission published under a 24 month embargo labeled 'Closed Access', the embargo will last until 2027-12-01</dc:description>
          <dc:description>The student, Akshit Mahajan, accepted the attached license on 2025-12-12 at 12:14.</dc:description>
          <dc:description>The student, Akshit Mahajan, submitted this Thesis for approval on 2025-12-12 at 12:25.</dc:description>
          <dc:description>This Thesis was approved for publication on 2025-12-12 at 13:19.</dc:description>
          <dc:description>DSpace SAF Submission Ingestion Package generated from Vireo submission #23098 on 2026-02-19 at 20:10:06</dc:description>
          <dc:title>Long silicon microfluidic needles for VTA and in-vivo differential neurochemical measurement</dc:title>
          <dc:creator>Mahajan, Akshit</dc:creator>
          <dc:date>2025-12-12</dc:date>
          <dc:contributor>Vlasov, Yurii</dc:contributor>
          <dc:subject>Neural Probe</dc:subject>
          <dc:subject>Process Development</dc:subject>
          <dc:subject>Aluminum oxide</dc:subject>
          <dc:subject>Silicon Nitride</dc:subject>
          <dc:subject>VTA</dc:subject>
          <dc:language>eng</dc:language>
          <dc:description>This thesis presents the design, fabrication, and preliminary in vivo evaluation of long silicon microfluidic neural probes intended for high-resolution neurochemical sampling from deep brain nuclei such as the ventral tegmental area in mice. The work first analyzes stress-induced bending in thinfilm cantilever structures on silicon-on-insulator substrates and develops a multilayer stress-balancing strategy using plasma-enhanced chemical vapor deposited silicon nitride to compensate compressive stress from the buried oxide, enabling fabrication of 8–10 mm needles with sub-100 µm tip deviation in the best cases. Further on, I explore aluminum oxide hard mask integration processes, and its etch characterization to provide high etch selectivity over silicon nitride and silicon oxide and to improve channel yield by mitigating photoresist-induced clogging in buried microfluidic networks. Finally, I propose and test out several probe architectures for differential in-vivo nanodialysis measurements. Collectively, these advances in stress engineering, hard mask integration, and probe-level fluidic design establish a robust platform for future long-term, multi-state neurochemical recordings and for combining localized drug delivery with mass-spectrometry-based analysis in deep brain regions.</dc:description>
          <dc:date>2025-12</dc:date>
          <dc:type>Thesis</dc:type>
          <dc:identifier>https://hdl.handle.net/2142/132805</dc:identifier>
          <dc:rights>Copyright 2025 Akshit Mahajan</dc:rights>
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            <department>Electrical &amp; Computer Eng</department>
            <discipline>Electrical &amp; Computer Engr</discipline>
            <grantor>University of Illinois Urbana-Champaign</grantor>
            <name>M.S.</name>
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