<?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>2026-09-19T19:48:09Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/67612" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/67612</identifier><datestamp>2022-01-13T07:54:36Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131023</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">Evelyn N. Wang.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Cho, Han-Jae Jeremy</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Mechanical Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Mechanical Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2011-12-09T21:32:28Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2011-12-09T21:32:28Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/67612</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">765450856</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2011.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (p. 78-79).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Electroporation of lipid bilayers is widely used in DNA transfection, gene therapy, and targeted drug delivery and has potential applications in water desalination and filtration. A better, more thorough molecular understanding is needed, however, before such devices can be effectively used and developed. From aqueous pore formation theory, electroporation behavior is known to be largely dictated by surface energy. We hypothesize that this surface energy can be described by separate head and tail components of the lipid molecules, which can be obtained experimentally. In this thesis, we demonstrated a basic ability to electroporate lipid bilayers as well as verify its electrical behavior. We formed lipid monolayer and bilayer films and studied their wetting properties using water, formamide, and diiodomethane. We determined that the strong interaction between polar liquids (water and formamide) and hydrophilic substrates (mica and glass) can affect the wetting behavior and quality of films. In addition, we verified that the resulting surface energy of lipid tails is mostly nonpolar. The insights of this work offer a first step towards characterizing the surface energies of different lipids and how they relate to the electroporation behavior.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Han-Jae Jeremy Cho.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.M.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">79 p.</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">M.I.T. theses are protected by 
copyright. They may be viewed from this source for any purpose, but 
reproduction or distribution in any format is prohibited without written 
permission. See provided URL for inquiries about 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">Mechanical Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Surface tension and electroporation of lipid bilayers</dim:field>
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   	&lt;Title>Surface tension and electroporation of lipid bilayers&lt;/Title>
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   	&lt;PublicationDate>2011&lt;/PublicationDate>
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        	&lt;DisplayName>Cho, Han-Jae Jeremy&lt;/DisplayName>
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            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
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    &lt;Keyword>Mechanical Engineering.&lt;/Keyword>
   	&lt;Abstract>Electroporation of lipid bilayers is widely used in DNA transfection, gene therapy, and targeted drug delivery and has potential applications in water desalination and filtration. A better, more thorough molecular understanding is needed, however, before such devices can be effectively used and developed. From aqueous pore formation theory, electroporation behavior is known to be largely dictated by surface energy. We hypothesize that this surface energy can be described by separate head and tail components of the lipid molecules, which can be obtained experimentally. In this thesis, we demonstrated a basic ability to electroporate lipid bilayers as well as verify its electrical behavior. We formed lipid monolayer and bilayer films and studied their wetting properties using water, formamide, and diiodomethane. We determined that the strong interaction between polar liquids (water and formamide) and hydrophilic substrates (mica and glass) can affect the wetting behavior and quality of films. In addition, we verified that the resulting surface energy of lipid tails is mostly nonpolar. The insights of this work offer a first step towards characterizing the surface energies of different lipids and how they relate to the electroporation behavior.&lt;/Abstract>
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