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        <identifier>oai:figshare.com:article/32805464</identifier>
        <datestamp>2026-10-01T16:15:55Z</datestamp>
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          <dc:title>Development and evaluation of microneedle systems for sustained transdermal delivery of entecavir</dc:title>
          <dc:creator>Yidan Luo (7064915)</dc:creator>
          <dc:subject>PUREID: 674794732</dc:subject>
          <dc:subject>transdermal drug delivery</dc:subject>
          <dc:subject>microneedles</dc:subject>
          <dc:subject>prodrug strategy</dc:subject>
          <dc:subject>long-acting delivery</dc:subject>
          <dc:subject>entecavir</dc:subject>
          <dc:subject>hepatitis B</dc:subject>
          <dc:subject>nanoparticles</dc:subject>
          <dc:subject>pharmacokinetics</dc:subject>
          <dc:description>Hepatitis B virus (HBV) infection is a major global health issue, requiring long-term antiviral therapy. While entecavir (ETV) is a potent first-line agent for Hepatitis B treatment, its clinical effectiveness is often compromised by strict fasting requirements and the burden of daily adherence. Thus, there is a clear clinical need for alternative delivery strategies that offer sustained release and reduce dosing frequency. This study explored microneedle (MN)-based transdermal systems as alternative platforms for sustained ETV delivery. Both dissolving microneedles (DMNs) incorporating the lipidic prodrug entecavir-3-palmitate (EV-P) and hydrogel-forming microneedles (HFMNs) loaded with ETV were evaluated. EV-P-loaded DMNs achieved sustained systemic exposure for up to 28 days following a single administration in vivo. The HFMN-reservoir system enabled sustained delivery over 48 hours with enhanced systemic exposure relative to oral dosing. The findings support the feasibility of MN-mediated sustained delivery of ETV and provide insight into the design of long-acting transdermal systems for chronic antiviral therapy.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis is embargoed until 31 July 2031.&lt;/i&gt;</dc:description>
          <dc:date>2026-10-01T16:15:55Z</dc:date>
          <dc:type>Text</dc:type>
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          <dc:identifier>10.17034/32805464.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2031-07-31</dc:rights>
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