<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T04:38:54Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/111334" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/111334</identifier><datestamp>2026-06-16T18:52:44Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Robert S. Langer and Daniel S. Kohane.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Rwei, Alina Yu-Hsin</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department of Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2017-09-15T15:29:36Z</dim:field>
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   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2017</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/111334</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1003290774</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2017.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">"June 2017." Cataloged from PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Pain management would be greatly enhanced by a formulation that would provide local anesthesia at the time desired by patients, with the desired intensity and duration. Current treatment for many pain states - including localized pain - often involves systemic medications such as opioids that have significant side effects. Externally triggerable drug delivery systems provide a strategy for the delivery of therapeutic agents preferentially to the target site at the desired timing, dosage, and duration, presenting the ability to enhance therapeutic efficacy while reducing side effects. Here we have developed light- and ultrasound- triggerable liposomes that provide on-demand nerve block at the desired timing, intensity and duration. The responsiveness of the liposomes towards the external triggering was studied in vitro, where the light triggerable system showed 5.6% drug release upon irradiation with 730 nm light and the ultrasound triggerable system showed 5.4% drug release upon insonation 1 MHz, 3W/cm² ultrasound. Sciatic nerve blockades for up to a duration of 2h was successfully achieved with safe dosage of light (730 nm, 75 mW/cm², 15 min) or ultrasound (1 MHz, 3W/cm², 10 min). Sciatic nerve block could be triggered repeatedly with light or ultrasound for more than 5 times upon a single injection. The duration of nerve block showed a linear relationship with the energy density of the triggering event, which was controlled by duration and intensity of the external energy source. Tissue reaction was benign. Such on-demand nerve block systems have promising potential to provide personalized and effective local anesthesia that will enhance pain management.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Alina Yu-Hsin Rwei.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">104 pages</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Repeatable and adjustable on-demand local anesthesia using externally-triggerable liposomes</dim:field>
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   	&lt;Title>Repeatable and adjustable on-demand local anesthesia using externally-triggerable liposomes&lt;/Title>
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   	&lt;PublicationDate>2017&lt;/PublicationDate>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>Pain management would be greatly enhanced by a formulation that would provide local anesthesia at the time desired by patients, with the desired intensity and duration. Current treatment for many pain states - including localized pain - often involves systemic medications such as opioids that have significant side effects. Externally triggerable drug delivery systems provide a strategy for the delivery of therapeutic agents preferentially to the target site at the desired timing, dosage, and duration, presenting the ability to enhance therapeutic efficacy while reducing side effects. Here we have developed light- and ultrasound- triggerable liposomes that provide on-demand nerve block at the desired timing, intensity and duration. The responsiveness of the liposomes towards the external triggering was studied in vitro, where the light triggerable system showed 5.6% drug release upon irradiation with 730 nm light and the ultrasound triggerable system showed 5.4% drug release upon insonation 1 MHz, 3W/cm² ultrasound. Sciatic nerve blockades for up to a duration of 2h was successfully achieved with safe dosage of light (730 nm, 75 mW/cm², 15 min) or ultrasound (1 MHz, 3W/cm², 10 min). Sciatic nerve block could be triggered repeatedly with light or ultrasound for more than 5 times upon a single injection. The duration of nerve block showed a linear relationship with the energy density of the triggering event, which was controlled by duration and intensity of the external energy source. Tissue reaction was benign. Such on-demand nerve block systems have promising potential to provide personalized and effective local anesthesia that will enhance pain management.&lt;/Abstract>
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