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        <datestamp>2026-10-01T16:20:05Z</datestamp>
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          <dc:title>Formulation strategies for modifying drug release from preformed solid implants</dc:title>
          <dc:creator>Elizabeth Magill (13159279)</dc:creator>
          <dc:subject>PUREID: 657740024</dc:subject>
          <dc:subject>Implantable device</dc:subject>
          <dc:subject>medical device</dc:subject>
          <dc:subject>drug delivery</dc:subject>
          <dc:subject>pharmaceutical technology</dc:subject>
          <dc:subject>pharmacy</dc:subject>
          <dc:subject>3D printing</dc:subject>
          <dc:subject>formulation</dc:subject>
          <dc:subject>controlled release</dc:subject>
          <dc:description>Long-acting implantable drug delivery devices offer a means to overcoming current challenges within pharmacy such as pill fatigue, poor adherence to medication, low oral bioavailability, and dose-limiting side effects. Controlling drug release from such devices, however, remains a central challenge to their clinical translation. Accordingly, this thesis presents strategies to modulate and predict drug release from biodegradable solid implants. &lt;br&gt;&lt;br&gt;Three model compounds were used throughout this thesis, carvedilol (CAR), amitriptyline hydrochloride (AMT), and risperidone (RIS). An analytical method was developed and validated for each compound according to the International Council for Harmonisation (ICH) guideline Q2 R2. &lt;br&gt;&lt;br&gt;Subsequently, three experimental chapters were developed outlining various methods of drug release modifications to solid-formed implantable devices.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis is embargoed until 31 December 2030.&lt;/i&gt;</dc:description>
          <dc:date>2026-10-01T16:20:05Z</dc:date>
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          <dc:identifier>10.17034/32641875.v1</dc:identifier>
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          <dc:rights>Open Access after 2030-12-31</dc:rights>
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