A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound

A Master of Science thesis in Chemical Engineering by Saniha Aysha Ajith entitled, “A Novel Cancer Treatment Platform Utilizing Her2- Immunoliposomes And Ultrasound”, submitted in May 2020. Thesis advisor is Dr. Ghaleb Husseini. Soft copy is available (Thesis, Approval Signatures, Completion Certifi...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلف الرئيسي: Ajith, Saniha Aysha (author)
التنسيق: doctoralThesis
منشور في: 2020
الموضوعات:
الوصول للمادة أونلاين:http://hdl.handle.net/11073/16717
الوسوم: إضافة وسم
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author Ajith, Saniha Aysha
author_facet Ajith, Saniha Aysha
author_role author
dc.contributor.none.fl_str_mv Husseini, Ghaleb
dc.creator.none.fl_str_mv Ajith, Saniha Aysha
dc.date.none.fl_str_mv 2020-06-21T07:38:27Z
2020-06-21T07:38:27Z
2020-05
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.identifier.none.fl_str_mv 35.232-2020.09
http://hdl.handle.net/11073/16717
dc.language.none.fl_str_mv en_US
dc.subject.none.fl_str_mv Drug delivery
Liposomes
Ultrasound
Trastuzumab
Chemotherapy
Herceptin
dc.title.none.fl_str_mv A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
dc.type.none.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/doctoralThesis
description A Master of Science thesis in Chemical Engineering by Saniha Aysha Ajith entitled, “A Novel Cancer Treatment Platform Utilizing Her2- Immunoliposomes And Ultrasound”, submitted in May 2020. Thesis advisor is Dr. Ghaleb Husseini. Soft copy is available (Thesis, Approval Signatures, Completion Certificate, and AUS Archives Consent Form).
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network_acronym_str aus
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oai_identifier_str oai:repository.aus.edu:11073/16717
publishDate 2020
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spelling A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and UltrasoundAjith, Saniha AyshaDrug deliveryLiposomesUltrasoundTrastuzumabChemotherapyHerceptinA Master of Science thesis in Chemical Engineering by Saniha Aysha Ajith entitled, “A Novel Cancer Treatment Platform Utilizing Her2- Immunoliposomes And Ultrasound”, submitted in May 2020. Thesis advisor is Dr. Ghaleb Husseini. Soft copy is available (Thesis, Approval Signatures, Completion Certificate, and AUS Archives Consent Form).Cancer is defined as the uncontrolled growth of cells in the body. It is one of the leading causes of death worldwide. One of the most common approaches to destroy cancer cells is via chemotherapy treatment, in which anti-cancer therapeutics are administered to the body. However, chemotherapy causes various adverse effects, including cardiotoxicity, nausea, anemia, and many more. To counteract these undesired effects, different smart drug delivery systems have been researched, in which nanocarriers can be used to exploit the enhanced permeability and retention (EPR) effect of cancerous tumors. Once the nanocarrier reaches the desired tumor site, external triggers can be applied to control the release of anti-neoplastic agents in that specific area. This study focuses on the use of liposomes conjugated with the monoclonal antibody, Trastuzumab, which is loaded with the chemotherapeutic drug, Doxorubicin, to target the overexpressed HER2 receptors on the surface of many breast cancer cells. Dynamic light scattering (DLS) was used to determine the liposome size, which was found to be 94.9 ± 1.29 nm for the immunoliposomes and 91.2 ± 1.47 nm for the NH2-terminated control liposomes. The concentration of lipids in the liposomes was determined using the Stewart Assay and the protein content using the BCA Assay. The external trigger used for the controlled release of the drug was low-frequency ultrasound. The release profiles of the control liposomes and immunoliposomes were studied at three different power densities, namely 7.46, 9.85, and 17.31 mW/cm2. Results showed that the immunoliposomes were slightly more sensitive to ultrasound and released a higher amount of drug in comparison to the control liposomes. Finally, drug release was modeled using nine kinetic models, namely: Zero-order, First-order, Higuchi, Hixon-Crowell, Korsmeyer-Peppas, Baker-Lonsdale, Weibull, Hopfenberg, and Gompertz. After linearizing the release data, the Baker-Lonsdale model provided the best fit. The future scope of this thesis involves using high-frequency ultrasound (HFUS) to release the drug, as well as in vitro and in vivo studies to determine the feasibility of using this drug delivery platform in hospitals and clinics around the globe.College of EngineeringDepartment of Chemical EngineeringMaster of Science in Chemical Engineering (MSChE)Husseini, Ghaleb2020-06-21T07:38:27Z2020-06-21T07:38:27Z2020-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfapplication/pdf35.232-2020.09http://hdl.handle.net/11073/16717en_USoai:repository.aus.edu:11073/167172025-06-26T12:22:05Z
spellingShingle A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
Ajith, Saniha Aysha
Drug delivery
Liposomes
Ultrasound
Trastuzumab
Chemotherapy
Herceptin
status_str publishedVersion
title A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
title_full A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
title_fullStr A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
title_full_unstemmed A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
title_short A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
title_sort A Novel Cancer Treatment Platform Utilizing HER2-Immunoliposomes and Ultrasound
topic Drug delivery
Liposomes
Ultrasound
Trastuzumab
Chemotherapy
Herceptin
url http://hdl.handle.net/11073/16717