Through layer-by-layer method, the authors have constructed three Au nanoplexes: AuPEI/RNA/PEI, AuPEI/RNA/PEI-mPEG, and AuPEI/NA/PEI-PEG-FA. All the nanoplexes are characterized by UV-vis spectrometry, DLS, and zeta potential. The surface density of the first layer PEI and second layer RNA were also determined. Moreover, the Au nanoplexes can protect siRNA from RNase degradation and are stable in cell culture medium.
siGLuc-ppp, ssRNA80, and siF17 were delivered by the assembled Au nanoplexes, and the results were analyzed by GLuc assay, TB assay, and Luciferase assay. In terms of RNA delivery, the Au nanoplexes AuPEI/RNA/PEI exhibited excellent gene silencing efficiency (or causing severe cell death) in the absence of the serum during the transfection. In terms of targeted delivery, PEGylation greatly reduces the nonspecific delivery of siRNA caused by AuPEI/siRNA/PEI. However, no apparent difference is found between AuPEI/RNA/PEI-mPEG and AuPEI/RNA/PEI-PEG-FA.
Fast fabrication, versatility, and ability for siRNA protection are the major characters of our new developed Au nanoplex system. The high gene silencing efficiency in the absence of serum makes it an excellent delivery agent for negative-charged macromolecules in vitro. However, the application of the system in targeted delivery needs more exploration.
","abstract_html":"<p>Through layer-by-layer method, the authors have constructed three Au nanoplexes: AuPEI/RNA/PEI, AuPEI/RNA/PEI-mPEG, and AuPEI/NA/PEI-PEG-FA. All the nanoplexes are characterized by UV-vis spectrometry, DLS, and zeta potential. The surface density of the first layer PEI and second layer RNA were also determined. Moreover, the Au nanoplexes can protect siRNA from RNase degradation and are stable in cell culture medium.</p> <p>siGLuc-ppp, ssRNA<sub>80</sub>, and siF17 were delivered by the assembled Au nanoplexes, and the results were analyzed by GLuc assay, TB assay, and Luciferase assay. In terms of RNA delivery, the Au nanoplexes AuPEI/RNA/PEI exhibited excellent gene silencing efficiency (or causing severe cell death) in the absence of the serum during the transfection. In terms of targeted delivery, PEGylation greatly reduces the nonspecific delivery of siRNA caused by AuPEI/siRNA/PEI. However, no apparent difference is found between AuPEI/RNA/PEI-mPEG and AuPEI/RNA/PEI-PEG-FA.</p> <p>Fast fabrication, versatility, and ability for siRNA protection are the major characters of our new developed Au nanoplex system. The high gene silencing efficiency in the absence of serum makes it an excellent delivery agent for negative-charged macromolecules in vitro. However, the application of the system in targeted delivery needs more exploration.</p>","abstract_has_math":false,"creators":["Shi, Yongliang"],"institution":null,"degree_name":"Master of Science (MS)","degree_level":"Masters Thesis","degree_discipline":"Chemistry and Biochemistry","degree_department":null,"school":null,"contributors":["Faqing Huang","Douglas Masterson","Yanlin Guo"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2014,"date_issued":"2014-08-01T07:00:00Z","date_published":"2014-08-01T07:00:00Z","updated_at":"2026-07-24T05:44:27Z","subjects":["gold nanoparticles","siRNA delivery","cancer-targeted delivery","Biotechnology","Medical Biochemistry","Nanomedicine"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://aquila.usm.edu/masters_theses/37","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Faqing Huang","Douglas Masterson","Yanlin Guo"]},{"key":"dc:creator","label":"Author","values":["Shi, Yongliang"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.available","label":"Dc Date Available","values":["2014-08-01T07:00:00Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry and Biochemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Masters Thesis"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Master of Science (MS)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["gold nanoparticles","siRNA delivery","cancer-targeted delivery","Biotechnology","Medical Biochemistry","Nanomedicine"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://aquila.usm.edu/masters_theses/37"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Through layer-by-layer method, the authors have constructed three Au nanoplexes: AuPEI/RNA/PEI, AuPEI/RNA/PEI-mPEG, and AuPEI/NA/PEI-PEG-FA. All the nanoplexes are characterized by UV-vis spectrometry, DLS, and zeta potential. The surface density of the first layer PEI and second layer RNA were also determined. Moreover, the Au nanoplexes can protect siRNA from RNase degradation and are stable in cell culture medium.
siGLuc-ppp, ssRNA80, and siF17 were delivered by the assembled Au nanoplexes, and the results were analyzed by GLuc assay, TB assay, and Luciferase assay. In terms of RNA delivery, the Au nanoplexes AuPEI/RNA/PEI exhibited excellent gene silencing efficiency (or causing severe cell death) in the absence of the serum during the transfection. In terms of targeted delivery, PEGylation greatly reduces the nonspecific delivery of siRNA caused by AuPEI/siRNA/PEI. However, no apparent difference is found between AuPEI/RNA/PEI-mPEG and AuPEI/RNA/PEI-PEG-FA.
Fast fabrication, versatility, and ability for siRNA protection are the major characters of our new developed Au nanoplex system. The high gene silencing efficiency in the absence of serum makes it an excellent delivery agent for negative-charged macromolecules in vitro. However, the application of the system in targeted delivery needs more exploration.
"]},{"key":"dc:title","label":"Title","values":["Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery"]}]}],"canonical_facts":{"dc:contributor":["Faqing Huang","Douglas Masterson","Yanlin Guo"],"dc:creator":["Shi, Yongliang"],"dc:date.available":["2014-08-01T07:00:00Z"],"dc:description.abstract":["Through layer-by-layer method, the authors have constructed three Au nanoplexes: AuPEI/RNA/PEI, AuPEI/RNA/PEI-mPEG, and AuPEI/NA/PEI-PEG-FA. All the nanoplexes are characterized by UV-vis spectrometry, DLS, and zeta potential. The surface density of the first layer PEI and second layer RNA were also determined. Moreover, the Au nanoplexes can protect siRNA from RNase degradation and are stable in cell culture medium.
siGLuc-ppp, ssRNA80, and siF17 were delivered by the assembled Au nanoplexes, and the results were analyzed by GLuc assay, TB assay, and Luciferase assay. In terms of RNA delivery, the Au nanoplexes AuPEI/RNA/PEI exhibited excellent gene silencing efficiency (or causing severe cell death) in the absence of the serum during the transfection. In terms of targeted delivery, PEGylation greatly reduces the nonspecific delivery of siRNA caused by AuPEI/siRNA/PEI. However, no apparent difference is found between AuPEI/RNA/PEI-mPEG and AuPEI/RNA/PEI-PEG-FA.
Fast fabrication, versatility, and ability for siRNA protection are the major characters of our new developed Au nanoplex system. The high gene silencing efficiency in the absence of serum makes it an excellent delivery agent for negative-charged macromolecules in vitro. However, the application of the system in targeted delivery needs more exploration.
"],"dc:identifier":["https://aquila.usm.edu/masters_theses/37"],"dc:subject":["gold nanoparticles","siRNA delivery","cancer-targeted delivery","Biotechnology","Medical Biochemistry","Nanomedicine"],"dc:title":["Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery"],"thesis:degree_discipline":["Chemistry and Biochemistry"],"thesis:degree_level":["Masters Thesis"],"thesis:degree_name":["Master of Science (MS)"]},"updated_at":"2026-07-24T05:44:27Z"}