Tools for drug efficacy studies in perfused tissue models - Organ-on-a-chip tools that recapitulate human biology, physiology and pathology are urgently needed in
applied science research and drug testing to expedite discoveries while reducing research costs and animal
sacrifice. Unfortunately, most products incorporating circulation mimicking perfusion are too complicated for
researchers to use, incompatible with many protocols and reads, and low-throughput. Our goal is to change
this for ordinary lab personnel and for researchers across disciplines. We will make a researcher-centric
product that does not require special skills or training for use, a tool that is flexible enough to serve diverse
research objectives, and a tool that for pharmaceutical industry means a simple, low-cost solution for predictive
drug testing.
Lena Biosciences’ perfused, human, multi-organ platform will revolutionize preclinical testing of first line
therapy drugs that clear or metabolize slowly, saving pharmaceutical companies time and money while
reducing human safety hazards. The platform will be made in a standard, screening-accessible format known
to any user in life sciences, biotechnology and drug discovery for ease of use and user adoption. It will support
perfused, three-dimensional organ models for physiologically closer drug delivery and distribution by mimicking
drug distribution intra-tissue and intra-tissue resistance to drug transport. It will be especially well suited for in
vitro testing of high molecular weight, humanized therapeutics that are administered to patients intravenously
and retained in circulation for the period of weeks. Ultimately, the platform will also serve as a prognostic tool
by providing concentrated cell secretome, proteome and metabolome to prevent severe reactions in human
trials while facilitating identification of biomarkers, cellular and biochemical changes in response to drugs. The
utility of this human platform will be demonstrated using three-dimensional organ models of lung cancer, breast
cancer, brain and liver, and further validated by showing predictive in vitro efficacy and off-target toxicity testing
of approved drugs.