SBIR-STTR Award

Assembled Porous Silica Membranes for Biomolecule Spe
Award last edited on: 5/15/2017

Sponsored Program
SBIR
Awarding Agency
NIH : NIGMS
Total Award Amount
$231,421
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Barry E Boyes

Company Information

Advanced Materials Technology Inc (AKA: AMT)

3521 Silverside Road Suite 1-K
Wilmington, DE 19810
Location: Single
Congr. District: 00
County: New Castle

Phase I

Contract Number: ----------
Start Date: ----    Completed: ----
Phase I year
2017
Phase I Amount
$231,421
Life sciences research and other critical bioanalytical applications would strongly benefit from faster and higher efficiency sample preparation processes. Sample preparation before high resolution analytical methods, such as HPLC or LC/MS, can require effort and cost nearly equivalent to the actual sample analysis and data reduction. Often, sample preparation for proteomic, glycoproteomic or glycomic analyses require one or more solid phase extraction (SPE) steps. The goals of the proposed work are to apply a new class of SPE materials to improve SPE performance for these challenging applications. Novel assembled porous silica membrane (APSM) materials have been discovered, which have features that could be well applied to SPE devices. The proposed research and development activities could yield designed materials that reduce time and effort for conducting SPE, and result in samples that are recovered at higher concentrations than the currently popular large diameter silica particle packed SPE devices. AMT has recently developed a low cost tape casting method to produce APSM materials with uniform and controlled porosity, using processes that are amenable to optimizing the materials for application to a variety of SPE sample types. In this proposal, one intention is to refine the tape casting and sintering processes to produce substantial quantities of monodisperse ASPM, to build on this technology to produce high specific surface area ASPM, and to apply these new materials in SPE devices to a variety of sample types for performance evaluation. The overall goal is to make available very high performance SPE products, superior to materials that are currently available, for application in analysis of complex biological samples, pharmaceutical and biopharmaceutical applications, in fact in any current application that uses SPE for biological molecule analyses. The separations technology described will directly lead to useful products for which there is a significant technical and market demand.

Public Health Relevance Statement:
Narrative Solid Phase Extraction (SPE) is a widely used sample preparation method in chemical analysis to separate mixtures of molecules from interferences, reaction mixture reagents, and the like. In terms of actual hands-on effort, sample preparation steps often dominate many analytical workflows. This method is broadly used in biomedical research, as well as in quality control and assurance for development and manufacture of therapeutic molecules. The current proposal is to use new knowledge in materials science and chemistry to enable faster and more efficient separations by SPE, potentially saving time and money, as well as enabling new uses of the method to understand the structure and function of biological molecules.

Project Terms:
abstracting; Address; analytical method; Area; ASPM gene; Biological; Biological Process; Biological Products; Biological Sciences; Biomedical Research; Caliber; Chemicals; Chemistry; comparative; Complex; cost; Cost Analysis; cost effective; data reduction; design; Development; Devices; Engineering; Evaluation; Exhibits; fitness; Formulation; glycoproteomics; Goals; High Pressure Liquid Chromatography; Hybrids; improved; Intention; Kinetics; Knowledge; Laboratories; Lead; liquid chromatography mass spectrometry; Marketing; materials science; meetings; Membrane; Methods; nanoparticle; new technology; novel; particle; Particle Size; Performance; Pharmacologic Substance; Phase; Polysaccharides; Porosity; Preparation; Process; product development; Production; Property; Proteins; Proteomics; prototype; quality assurance; Quality Control; Reaction; Reagent; Recovery; Research; research and development; Resolution; Sampling; Science; Silicon Dioxide; Solid; Speed; Structure; Surface; Technology; Testing; Therapeutic; Thick; Time; Work

Phase II

Contract Number: ----------
Start Date: ----    Completed: ----
Phase II year
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Phase II Amount
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