{"id":{"repo_id":"buffalo","oai_identifier":"oai:ubir.buffalo.edu:10477/77925"},"canonical_url":"https://search.dev.ndltd.org/etd/buffalo/oai:ubir.buffalo.edu:10477/77925","repository":{"repo_id":"buffalo","name":"Buffalo","base_url":"https://ubir.buffalo.edu/oai/request"},"display":{"title":"Design of Metalloporphyrin Liposome for Biomedical Applications","abstract":"Ph.D.","abstract_html":"Ph.D.","abstract_has_math":false,"creators":["Shao, Shuai; 0000-0002-2682-1830"],"institution":"State University of New York at Buffalo","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":["Lovell, Jonathan","Biomedical Engineering"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2018,"date_issued":"2018-06-28T15:46:32Z","date_published":"2018-06-28T15:46:32Z","updated_at":"2026-07-27T19:05:05Z","subjects":["biomedical engineering"],"languages":["eng"],"rights":["Users of works found in University at Buffalo Institutional Repository (UBIR) are responsible for identifying and contacting the copyright owner for permission to reuse. University at Buffalo Libraries do not manage rights for copyright-protected works and cannot assist with permissions.","Copyright retained by author."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10477/77925","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Lovell, Jonathan","Biomedical Engineering"]},{"key":"dc:creator","label":"Author","values":["Shao, Shuai; 0000-0002-2682-1830"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2018-06-28T15:46:32Z","2018","2018-05-08 10:36:01"]},{"key":"dc:publisher","label":"Institution","values":["State University of New York at Buffalo"]},{"key":"dc:type","label":"Dc Type","values":["Text","Dissertation"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["biomedical engineering"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]},{"key":"dc:rights","label":"Dc Rights","values":["Users of works found in University at Buffalo Institutional Repository (UBIR) are responsible for identifying and contacting the copyright owner for permission to reuse. University at Buffalo Libraries do not manage rights for copyright-protected works and cannot assist with permissions.","Copyright retained by author."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/10477/77925"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Ph.D.","Compared with the porphyrin, metalloporphyrin compounds are more common in nature due to the quenching phototoxicity of porphyrin by the metal chelation. Meanwhile, the metal chelation confers diverse biomedical applications to the porphyrin molecules. Through conjugating metalloporphyrin with lyso-lipid, the obtained metallporphyrin-lipid can form the liposome bilayer structure, which is well-suited for theranostic applications. Motivated by the unique chemical property of metalloporphyrin, this thesis focuses on exploring the novel biomedical applications of metalloporphyrin liposome. Chapter 1 provides a comprehensive background on metalloporphyrin, especially reviewing existing metalloporphyrin nanoparticles for theranostic applications. Chapter 2 describes a novel and convenient method to stably attach His-tagged polypeptides to liposome based on the chelation between histidine and cobalt porphyrin lipid (CoPoP). The CoPoP immunogenic liposome is applied in the design of MPER vaccine against HIV disease. Chapter 3 demonstrates the capacity of CoPoP liposome as a multivalent antigens carrier and a potential universal vaccine against influenza is designed and evaluated. Chapter 4 introduces the synthesis of N-HPPH-lipid which can form a hydrated bilayer structure through the hydrogen bond between amine terminal and water molecules. When N-HPPH-liposome is chelated with Mn, an enhanced MR imaging can be observed. Chapter 5 presented a brief conclusion and some future directions. The metalloporphyrin nanoparticles represent a promising platform for developing theranostic functions. It is believed that number of versatile and useful metalloporphyrin nanoparticles will be designed and applied in the biomedical applications."]},{"key":"dc:format","label":"Dc Format","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Design of Metalloporphyrin Liposome for Biomedical Applications"]}]}],"canonical_facts":{"dc:contributor":["Lovell, Jonathan","Biomedical Engineering"],"dc:creator":["Shao, Shuai; 0000-0002-2682-1830"],"dc:date":["2018-06-28T15:46:32Z","2018","2018-05-08 10:36:01"],"dc:description":["Ph.D.","Compared with the porphyrin, metalloporphyrin compounds are more common in nature due to the quenching phototoxicity of porphyrin by the metal chelation. Meanwhile, the metal chelation confers diverse biomedical applications to the porphyrin molecules. Through conjugating metalloporphyrin with lyso-lipid, the obtained metallporphyrin-lipid can form the liposome bilayer structure, which is well-suited for theranostic applications. Motivated by the unique chemical property of metalloporphyrin, this thesis focuses on exploring the novel biomedical applications of metalloporphyrin liposome. Chapter 1 provides a comprehensive background on metalloporphyrin, especially reviewing existing metalloporphyrin nanoparticles for theranostic applications. Chapter 2 describes a novel and convenient method to stably attach His-tagged polypeptides to liposome based on the chelation between histidine and cobalt porphyrin lipid (CoPoP). The CoPoP immunogenic liposome is applied in the design of MPER vaccine against HIV disease. Chapter 3 demonstrates the capacity of CoPoP liposome as a multivalent antigens carrier and a potential universal vaccine against influenza is designed and evaluated. Chapter 4 introduces the synthesis of N-HPPH-lipid which can form a hydrated bilayer structure through the hydrogen bond between amine terminal and water molecules. When N-HPPH-liposome is chelated with Mn, an enhanced MR imaging can be observed. Chapter 5 presented a brief conclusion and some future directions. The metalloporphyrin nanoparticles represent a promising platform for developing theranostic functions. It is believed that number of versatile and useful metalloporphyrin nanoparticles will be designed and applied in the biomedical applications."],"dc:format":["application/pdf"],"dc:identifier":["http://hdl.handle.net/10477/77925"],"dc:language":["eng"],"dc:publisher":["State University of New York at Buffalo"],"dc:rights":["Users of works found in University at Buffalo Institutional Repository (UBIR) are responsible for identifying and contacting the copyright owner for permission to reuse. University at Buffalo Libraries do not manage rights for copyright-protected works and cannot assist with permissions.","Copyright retained by author."],"dc:subject":["biomedical engineering"],"dc:title":["Design of Metalloporphyrin Liposome for Biomedical Applications"],"dc:type":["Text","Dissertation"]},"updated_at":"2026-07-27T19:05:05Z"}