SBIR/STTR Research Award

Development of the NephroPlate: A high-throughput kidney-on-a-chip platform for identifying chronic kidney disease therapies

Award identifier 8ebfa9c1dae0f97dedd0cec46d085a9d5db75e43349e35f3a3288a3fa450ee97Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,993,146

Program and phase

SBIR · Phase II

Award year

2022

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
MIMETAS US, INC
Proposal award date
2022-08-16
Contract end date
2024-07-31
UEI
QGP7JLTGMAK9
Solicitation number
PA21-259
Topic code
400

Research abstract

Project Summary With chronic kidney disease on the rise, it is imperative that we identify better treatment strategies to avoid a healthcare crisis. Current therapeutic interventions address patient symptoms rather than the underly cause and thereby do not substantially slow disease advancement. Developing drugs to treat the underlying cause or disorder leading to CKD will address this need, however such advancements have been hampered by the lack of in vitro human kidney models used in the drug development pipeline. Thus, an in vitro model which accurately mimics individual human CKDs and can be screened for disease-relevant therapeutic interventions is urgently needed to identify targeted CKD interventions. This Phase II SBIR is a continuation of a successful Phase I and a collaborative effort between MIMETAS and the Children’s Hospital of Los Angeles (CHLA). Together we will focus on addressing the market need for a 3D kidney-on-a-chip platform, called the NephroPlate for use in drug discovery. The NephroPlate will enable the evaluation of kidney function in response to circulating and genetic factors of CKD-causing disorders. For this Phase II project, we will focus on glomerulopathies where we have previous experience, Alport syndrome and membranous nephropathy, and where there is a high demand from NephroPlate customers, diabetic nephropathy and APOL1 nephropathy. For each CKD, we will characterize phenotype (immunostaining, western blot, RNAseq) and glomerular filtration function by measuring the passage of fluorescent albumin and the trans-epithelial electrical resistance (TEER) within the microfluidic system. All systems will be validated to high-throughput drug screening standards. Filtrate from the glomerulus-on-a-chip cultures will be transferred to the proximal tubule-on-a-chip cultures to evaluate the impact of glomerular disease on proximal tubules. Finally, proteomics will be performed on the glomerular and proximal tubule filtrate to identify potential biomarkers specific to each CKD. Once executed these studies will establish the NephroPlate as a high-throughput drug screening platform for use by pharmaceutical companies and academic laboratories to investigate mechanisms of CKD diseases and ultimately identify disease-specific therapeutics.

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

5 SBIR/STTR records share this UEI (2016–2022). Reported award amounts total $4,752,885. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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