<?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>2026-09-20T19:02:22Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/36217" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/36217</identifier><datestamp>2022-01-13T07:54:33Z</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">Subra Suresh and Simona Socrate.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Prévost, Thibault Philippe</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. 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">2007-02-21T13:08:35Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2007-02-21T13:08:35Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2006</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2006</dim:field>
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   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">76906810</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2006.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (leaves 108-115).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The human fetal membrane, namely the chorioamnion, is the structural soft tissue retaining the amniotic fluid and the fetus during pregnancy. Its biomechanical integrity is crucial for maintaining a healthy gestation and a successful delivery. The premature rupture of the fetal membrane (PROM) can result in serious perinatal complications. Despite extensive research in this field, the mechanical and biochemical processes governing the membrane deformation and failure remain poorly understood. The aim of this study is to characterize the mechanical behavior of the chorioamnionic tissue along with its biochemical properties, through mechanical testing and biochemical analyses. In order to accomplish this goal, specific mechanical and biochemical testing protocols were developed. In vitro mechanical testing was performed on samples from seven patients under different uniaxial and biaxial loading conditions. Significant relaxation was noted under uniaxial loading while very limited creep was observed under biaxial loading. Biochemical measurements such as collagen and sulfated glycosaminoglycan contents were also obtained. In addition, a microstructurally based constitutive model for the fetal membrane is proposed.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">(cont.) The model allows for nonlinear hyperelastic response at large deformation. We also propose a framework to capture the time-dependent response of the tissue. The model was implemented in a finite element formulation to allow three-dimensional simulations of membrane deformation.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Thibault Philippe Prévost.</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">115 leaves</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>
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   <dim:field mdschema="dc" element="rights" qualifier="uri">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">Biomechanics of the human chorioamnion</dim:field>
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   	&lt;Title>Biomechanics of the human chorioamnion&lt;/Title>
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   	&lt;Abstract>The human fetal membrane, namely the chorioamnion, is the structural soft tissue retaining the amniotic fluid and the fetus during pregnancy. Its biomechanical integrity is crucial for maintaining a healthy gestation and a successful delivery. The premature rupture of the fetal membrane (PROM) can result in serious perinatal complications. Despite extensive research in this field, the mechanical and biochemical processes governing the membrane deformation and failure remain poorly understood. The aim of this study is to characterize the mechanical behavior of the chorioamnionic tissue along with its biochemical properties, through mechanical testing and biochemical analyses. In order to accomplish this goal, specific mechanical and biochemical testing protocols were developed. In vitro mechanical testing was performed on samples from seven patients under different uniaxial and biaxial loading conditions. Significant relaxation was noted under uniaxial loading while very limited creep was observed under biaxial loading. Biochemical measurements such as collagen and sulfated glycosaminoglycan contents were also obtained. In addition, a microstructurally based constitutive model for the fetal membrane is proposed.&lt;/Abstract>
   	&lt;Abstract>(cont.) The model allows for nonlinear hyperelastic response at large deformation. We also propose a framework to capture the time-dependent response of the tissue. The model was implemented in a finite element formulation to allow three-dimensional simulations of membrane deformation.&lt;/Abstract>
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