<?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>2026-09-20T05:12:49Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/158314" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/158314</identifier><datestamp>2025-04-08T04:22:30Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131024</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">Tarkanian, Michael J.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Chyr, Gloria Un</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">2025-03-05T15:26:51Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2025-03-05T15:26:51Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2020-05</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="submitted">2025-03-04T15:57:34.820Z</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1721.1/158314</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">Electrospinning is a cheap and quick method of creating non-woven scaffolds for tissue regeneration and growth with the proper fiber diameter for cell adhesion. However, electrospun scaffolds lack large pores between fibers and result in a densely packed mesh in which cells can adhere only to the surface of the material. Control of scaffold fiber size and porosity is critical to ensure scaffolds have a fiber diameter appropriate for cell adhesion and a high-enough porosity to allow for cell migration through the material. This thesis aims to demonstrate the tunability and control of electrospun gelatin scaffolds to make them viable for use in tissue regeneration by altering grounded collector geometry and thus the electric field that nanofiber deposition follows. Previous electrospinning experiments show that processing parameters such as flow rate and voltage can affect fiber diameter and porosity, but are still insufficient in achieving dimensions viable for cell migration. Scaffold porosity is substantially more affected by the grounded collector geometry. By modifying collector geometry, pore size can be controlled without affecting fiber morphology and the deposition of gelatin nanofibers can be aligned or patterned to mimic natural tissue scaffolds. Introduction of a non-conductive, woven mesh in between the collector and source may allow further control of deposition patterns and thus scaffold construction. The path of electrospun fibers and the deposition patterns can be predicted by modeling the electric field.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree">S.B.</dim:field>
   <dim:field mdschema="dc" element="publisher">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights">In Copyright - Educational Use Permitted</dim:field>
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   <dim:field mdschema="dc" element="title">Tunability of Electrospun Scaffolds for Tissue Engineering</dim:field>
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   	&lt;Title>Tunability of Electrospun Scaffolds for Tissue Engineering&lt;/Title>
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   	&lt;PublicationDate>2020-05&lt;/PublicationDate>
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        	&lt;DisplayName>Chyr, Gloria Un&lt;/DisplayName>
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            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
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   	&lt;Abstract>Electrospinning is a cheap and quick method of creating non-woven scaffolds for tissue regeneration and growth with the proper fiber diameter for cell adhesion. However, electrospun scaffolds lack large pores between fibers and result in a densely packed mesh in which cells can adhere only to the surface of the material. Control of scaffold fiber size and porosity is critical to ensure scaffolds have a fiber diameter appropriate for cell adhesion and a high-enough porosity to allow for cell migration through the material. This thesis aims to demonstrate the tunability and control of electrospun gelatin scaffolds to make them viable for use in tissue regeneration by altering grounded collector geometry and thus the electric field that nanofiber deposition follows. Previous electrospinning experiments show that processing parameters such as flow rate and voltage can affect fiber diameter and porosity, but are still insufficient in achieving dimensions viable for cell migration. Scaffold porosity is substantially more affected by the grounded collector geometry. By modifying collector geometry, pore size can be controlled without affecting fiber morphology and the deposition of gelatin nanofibers can be aligned or patterned to mimic natural tissue scaffolds. Introduction of a non-conductive, woven mesh in between the collector and source may allow further control of deposition patterns and thus scaffold construction. The path of electrospun fibers and the deposition patterns can be predicted by modeling the electric field.&lt;/Abstract>
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