Hydrophobic spray emitters for ultrahigh sensitivity microLC-MS for clinical biomarker analysis

Information

  • Research Project
  • 9776732
  • ApplicationId
    9776732
  • Core Project Number
    R43GM133343
  • Full Project Number
    1R43GM133343-01
  • Serial Number
    133343
  • FOA Number
    PA-18-574
  • Sub Project Id
  • Project Start Date
    3/1/2019 - 5 years ago
  • Project End Date
    8/31/2019 - 5 years ago
  • Program Officer Name
    KREPKIY, DMITRIY
  • Budget Start Date
    3/1/2019 - 5 years ago
  • Budget End Date
    8/31/2019 - 5 years ago
  • Fiscal Year
    2019
  • Support Year
    01
  • Suffix
  • Award Notice Date
    2/28/2019 - 5 years ago
Organizations

Hydrophobic spray emitters for ultrahigh sensitivity microLC-MS for clinical biomarker analysis

Abstract The intense efforts for proteomics and biomarker discovery carried out by major research consortia such as EDRN (Early Detection Research Network) have generated many biomarkers, including those that are FDA-approved. However the transfer of biomarker detection and screening from research to clinical has been unsuccessful. The nanoLC-MS technique used in proteomic biomarker discovery is wrought with the inherent fragility and variability of the components of the experimental set-up. The weakest link in this transfer process is the fused silica spray emitter and columns which are easily clogged and damaged, and dead-volume must be painstaking eliminated because of the low flow-rate of sub- microliter/min to minimize peak broadening. Phoenix S&T has discovered patent-pending and patented metallic and plastic spray emitters with reduced surface interactions with the aqueous component of the buffer such that the cone-jet mode spray with high ion production efficiency are consistently and robustly produced at flow-rates from sub-microliter/min up to >100 uL/min. No fragile equipment is needed for use with these emitters. At flow-rates of a few microliters/min, the dead-volume elimination requirement is relaxed. The sensitivity obtained with these emitters at flow-rates less than 10 uL/min has been shown to be comparable to or exceeding that obtained with nanoLC-MS. These attributes offered by the new spray emitters make the transfer of the methods for biomarker screening into the clinics for medical decision making much more feasible. The proposed research aims to characterize these emitters to optimize the performance and durability of the emitters and enable reproducible manufacturing, and also to create plastic spray emitters with the potential of having the additional benefits of a ?softer? ionization that reduces in-source fragmentation and being disposable when used with dirty clinical samples. The learning? from the proposed research on these emitters may also open up possibility of 2D electrospray-MS devices for high throughput analyses of cellular functions in the future.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    149857
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:149857\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    PHOENIX S AND T, INC.
  • Organization Department
  • Organization DUNS
    128600546
  • Organization City
    Chadds Ford
  • Organization State
    PA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    19317
  • Organization District
    UNITED STATES