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Development of Magnetic Assays for Quantification of Serum Proteins and Enzymatic Activity
Development of Magnetic Assays for Quantification of Serum Proteins and Enzymatic Activity
Development of Magnetic Assays for Quantification of Serum Proteins and Enzymatic Activity

상세정보

자료유형  
 학위논문 서양
최종처리일시  
20250211150912
ISBN  
9798383168189
DDC  
610
저자명  
Sveiven, Michael.
서명/저자  
Development of Magnetic Assays for Quantification of Serum Proteins and Enzymatic Activity
발행사항  
[Sl] : University of California, San Diego, 2024
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2024
형태사항  
102 p
주기사항  
Source: Dissertations Abstracts International, Volume: 85-12, Section: B.
주기사항  
Advisor: O'Donoghue, Anthony;Hall, Drew;Fraley, Stephanie.
학위논문주기  
Thesis (Ph.D.)--University of California, San Diego, 2024.
초록/해제  
요약This research focused on using giant magnetoresistive (GMR) biosensors for point-of-care testing to improve disease diagnosis and monitoring, thereby aiding healthcare decision-making. With their ability to detect subtle changes in local magnetic fields, GMR sensors offer a multiplexed and highly sensitive solution for various biomedical applications. By optimizing the surface chemistry for stable and reproducible conjugation of various biomolecules, the versatile platform enabled specific protein binding, including antibodies for Insulin-like Growth Factor Binding Protein-4 (IBP4) and Sex Hormone Binding Globulin (SHBG), as well as double-stranded DNA substrates for nuclease activity quantitation and protease substrates for quantitation of proteases such as papain and human neutrophil elastase. This work resulted in proof-of-concept of a sensitive, multiplexed, and point-of-care assay for predicting spontaneous preterm birth in pregnant mothers, critical as the complications posed by preterm birth (delivery before 37 weeks of pregnancy) are a leading cause of newborn morbidity and mortality. The assays were validated against mass spectrometry, showing high agreement. These assays have the potential to revolutionize prenatal care by providing timely and precise information to healthcare providers, ultimately improving outcomes for both mothers and infants. We expanded the capabilities of GMR sensors to multiplexed hydrolase quantification, including proteases and nucleases in biological samples. This development is vital for diseases marked by recurrent bacterial lung infections, such as chronic obstructive pulmonary disease and cystic fibrosis. This work highlights the transformative potential of GMR sensors in offering rapid and comprehensive insights into patients' health to enhance healthcare decision-making and improve patient outcomes.
일반주제명  
Bioengineering
일반주제명  
Biomedical engineering
일반주제명  
Biochemistry
키워드  
Biosensors
키워드  
Diagnostics
키워드  
Disease monitoring
키워드  
Giant magnetoresistance
키워드  
Point-of-care testing
기타저자  
University of California, San Diego Bioengineering
기본자료저록  
Dissertations Abstracts International. 85-12B.
전자적 위치 및 접속  
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■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a610
■1001  ▼aSveiven,  Michael.
■24510▼aDevelopment  of  Magnetic  Assays  for  Quantification  of  Serum  Proteins  and  Enzymatic  Activity
■260    ▼a[Sl]▼bUniversity  of  California,  San  Diego▼c2024
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2024
■300    ▼a102  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  85-12,  Section:  B.
■500    ▼aAdvisor:  O'Donoghue,  Anthony;Hall,  Drew;Fraley,  Stephanie.
■5021  ▼aThesis  (Ph.D.)--University  of  California,  San  Diego,  2024.
■520    ▼aThis  research  focused  on  using  giant  magnetoresistive  (GMR)  biosensors  for  point-of-care  testing  to  improve  disease  diagnosis  and  monitoring,  thereby  aiding  healthcare  decision-making.  With  their  ability  to  detect  subtle  changes  in  local  magnetic  fields,  GMR  sensors  offer  a  multiplexed  and  highly  sensitive  solution  for  various  biomedical  applications.  By  optimizing  the surface  chemistry  for  stable  and  reproducible  conjugation  of  various  biomolecules,  the  versatile  platform  enabled  specific  protein  binding,  including  antibodies  for  Insulin-like  Growth  Factor  Binding  Protein-4  (IBP4)  and  Sex  Hormone  Binding  Globulin  (SHBG),  as  well  as  double-stranded  DNA  substrates  for  nuclease  activity  quantitation  and  protease  substrates  for  quantitation  of  proteases  such  as  papain  and  human  neutrophil  elastase.  This  work  resulted  in  proof-of-concept  of  a  sensitive,  multiplexed,  and  point-of-care  assay  for  predicting  spontaneous  preterm  birth  in  pregnant  mothers,  critical  as  the  complications  posed  by  preterm  birth  (delivery  before  37  weeks  of  pregnancy)  are  a  leading  cause  of  newborn  morbidity  and  mortality.  The  assays  were  validated  against  mass  spectrometry,  showing  high  agreement.  These  assays  have  the  potential  to  revolutionize  prenatal  care  by  providing  timely  and  precise  information  to  healthcare  providers,  ultimately  improving  outcomes  for  both  mothers  and  infants.  We  expanded  the  capabilities  of  GMR  sensors  to  multiplexed  hydrolase  quantification,  including  proteases  and  nucleases  in  biological  samples.  This  development  is  vital  for  diseases  marked  by  recurrent  bacterial  lung  infections,  such  as  chronic  obstructive  pulmonary  disease  and  cystic  fibrosis.  This  work  highlights  the  transformative  potential  of  GMR  sensors  in  offering  rapid  and  comprehensive  insights  into  patients'  health  to  enhance  healthcare  decision-making  and  improve  patient  outcomes.
■590    ▼aSchool  code:  0033.
■650  4▼aBioengineering
■650  4▼aBiomedical  engineering
■650  4▼aBiochemistry
■653    ▼aBiosensors
■653    ▼aDiagnostics
■653    ▼aDisease  monitoring
■653    ▼aGiant  magnetoresistance
■653    ▼aPoint-of-care  testing
■690    ▼a0202
■690    ▼a0541
■690    ▼a0487
■690    ▼a0769
■71020▼aUniversity  of  California,  San  Diego▼bBioengineering.
■7730  ▼tDissertations  Abstracts  International▼g85-12B.
■790    ▼a0033
■791    ▼aPh.D.
■792    ▼a2024
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17160119▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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