SBIR/STTR Research Award

Silk-based biospecimen stabilization for exposure assessment diagnostics

Award identifier 2f12e5e39b6569af26abf1a119b35886dd4281a5e1064350585f113425d3e56eAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$225,000

Program and phase

SBIR · Phase I

Award year

2015

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
VAXESS TECHNOLOGIES INC
Proposal award date
2015-06-01
Contract end date
2016-05-31
UEI
HNLJN8YZPVJ3
Solicitation number
ES14-005
Topic code
NIEHS

Research abstract

DESCRIPTION provided by applicant There is a critical need for a stabilization platform that can preserve biospecimen integrity completely free of cold storage requirements Such a technology would allow researchers clinicians and government personnel to conduct biomonitoring in field conditions i e without requiring visits to the outpatient lab Our long trm goal is to develop a platform technology that maximizes the stability of a wide range of biospecimens in a novel silk protein matrix and that seamlessly integrates with downstream analytics The objective is to evaluate the ability of a silk matrix to stabilize a number of bioanalytes demonstrate integration of the silk system with several standard and emerging analytical techniques and to prove the enhanced performance of silk based protection to commercially available solid stabilizers in accelerated aging studies Our central hypothesis is that silk will comply with minimally or non invasive biospecimen collection routes and provide comparable analyte retention to continuous frozen storage while improving recovery as compared to commercially available dried blood spot techniques Our hypothesis has been formulated based on our preliminary data using silk to stabilize antibodies plasma proteins and nucleic acids from complex fluids such as whole blood plasma serum and saliva Therefore in the first aim we will develop analytical methods to quantitate hazardous compound levels in plasma laden silk matrices This will be accomplished by incorporating techniques previously validated for use in analyzing dried blood spots Modifications of silk molecular weight by proteolytic degradation can provide a route to remedy any potential negative impacts of the silk protein on downstream chromatographic techniques As a second aim we seek to enhance the recovery of hazardous compounds from silk matrices For this aim we will incorporate soluble additives to the silk protein reconstitution solutions to disable charge or hydrophobic mediated interactions that may retain the analyte prior to chromatographic separation The expected outcomes would be a broader fundamental basis behind silk stabilization and new methods to translate these findings towards biospecimen recovery and storage as they pertain to biomonitoring The rationale for the proposed research is that once recovery and stability of these biomarkers is proven to be augmented by a silk encapsulate diagnostic kits can be outfitted with various silk formats which can then be used as a platform system for full validatio in follow on studies in Phase II Success with the planned approach can positively impact many areas of need in the field of diagnostics and epidemiology These needs include alternative approaches at solid biospecimen stabilization and translation validation of analytical techniques important for hazard exposures Furthermore by offering methods to interface with finger prick volumes i e less invasive quantities of whole blood a silk based stabilization system could significantly reduce financial burdens associated with the outpatient clinic and in turn increase accessibility PUBLIC HEALTH RELEVANCE The proposed research is relevant to public health because it will enable transformative approaches at dried biospecimen transport to laboratory facilities improving testing accuracy and obviating the need for patient travel With more widespread adoption the entire healthcare system and epidemiological biomonitoring programs will see reduced costs and improved accuracy of testing due to improved sample integrity

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

11 SBIR/STTR records share this UEI (2015–2024). Reported award amounts total $9,792,329. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, National Science Foundation

Agency intelligence

Department of Health and Human Services

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