Publications by authors named "Pelin L Candarlıoglu"

Increasing the use of microphysiological systems (MPS) in Three Rs and regulatory applications is a nuanced but important goal, which would also help increase their scientific impact. There are three distinct and important stakeholder groups that each play a unique role in expediting the use of MPS for regulatory purpose - namely, commercial MPS developers, end-users and regulators. Additionally, non-profit organisations, such as the 3Rs Collaborative (3RsC), can help coordinate these efforts.

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Here, we present a bioengineering approach to emulate the human bone marrow in vitro. Our developmentally inspired method uses self-organization of human hematopoietic stem and progenitor cells and vascular endothelial cells cultured in a three-dimensional microphysiological system to create vascularized, perfusable tissue constructs that resemble the hematopoietic vascular niche of the human marrow. The microengineered niche is capable of multilineage hematopoiesis and can generate functionally mature human myeloid cells that can intravasate into perfused blood vessels, providing a means to model the mobilization of innate immune cells from the marrow.

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Microphysiological systems (MPS) are gaining broader application in the pharmaceutical industry but have primarily been leveraged in early discovery toxicology and pharmacology studies with small molecules. The adoption of MPS offers a promising avenue to reduce animal use, improve in-vitro-to-in-vivo translation of pharmacokinetics/pharmacodynamics and toxicity correlation, and provide mechanistic understanding of model species suitability. While MPS have demonstrated utility in these areas with small molecules and biologics, MPS models in cell therapy development have not been fully explored, let alone validated.

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Article Synopsis
  • * The workshop aimed to identify opportunities for standardizing MPS and finding pathways for their use in regulatory decision-making, involving representatives from the FDA and 26 global regulatory organizations.
  • * Participants agreed that while developing specific standards for every context may be challenging, creating broadly applicable standards could be a more feasible approach to enhance the acceptance of CIVM/MPS in regulatory frameworks.
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  • Organ on Chip (OoC) technology has gained significant attention in the last decade from both basic and applied science sectors, focusing on improving human health research.
  • The Biochemical Society aims to review the state of OoC technology, identify bottlenecks, and explore future directions to enhance its application in science and society.
  • A recent conference gathered various stakeholders, including academics, regulators, and technology developers, to discuss the challenges and requirements to make OoC more effective in the pharmaceutical industry and reduce reliance on animal testing.
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Article Synopsis
  • - Organ-on-chip (OoC) systems are advanced microfluidic models that replicate the structure and function of real organs better than traditional 2D models.
  • - These systems hold promise for improving studies on drug efficacy and toxicity, leading to more relevant results for human health and disease mechanisms.
  • - The article discusses current applications of OoCs and explores future possibilities for their use in drug discovery.
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Here we report a new technique, Correlative Light-Ion Microscopy (CLIM), to correlate SEM-like micrographs with fluorescence images. This technique presents significant advantages over conventional methods in enabling topographical and biochemical information to be correlated with nanoscale resolution without destroying the fluorescence signal. We demonstrate the utility of CLIM for a variety of investigations of cell substrate interactions validating its potential to become a routine procedure in biomedical research.

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