<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Campo H</submitter><funding>National Institute of Environmental Health Sciences</funding><funding>Bill &amp; Melinda Gates Foundation</funding><funding>NCCIH NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>Bill and Melinda Gates Foundation</funding><pagination>4821-4833</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11181516</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(22)</volume><pubmed_abstract>To accurately phenocopy human biology &lt;i>in vitro&lt;/i>, researchers have been reducing their dependence on standard, static two-dimensional (2D) cultures and instead are moving towards three-dimensional (3D) and/or multicellular culture techniques. While these culture innovations are becoming more commonplace, there is a growing body of research that illustrates the benefits and even necessity of recapitulating the dynamic flow of nutrients, gas, waste exchange and tissue interactions that occur &lt;i>in vivo&lt;/i>. However, cost and engineering complexity are two main factors that hinder the adoption of these technologies and incorporation into standard laboratory workflows. We developed LATTICE, a plug-and-play microfluidic platform able to house up to eight large tissue or organ models that c</pubmed_abstract><journal>Lab on a chip</journal><pubmed_title>A new tissue-agnostic microfluidic device to model physiology and disease: the lattice platform.</pubmed_title><pmcid>PMC11181516</pmcid><funding_grant_id>UH3ES029073</funding_grant_id><funding_grant_id>UG3 ES029073</funding_grant_id><funding_grant_id>UH3 ES029073</funding_grant_id><funding_grant_id>INV-003385</funding_grant_id><funding_grant_id>R01 AT008824</funding_grant_id><funding_grant_id>INV-007121</funding_grant_id><funding_grant_id>R01CA243249</funding_grant_id><funding_grant_id>R01 CA243249</funding_grant_id><pubmed_authors>Urbanek M</pubmed_authors><pubmed_authors>Lee HC</pubmed_authors><pubmed_authors>Zhang D</pubmed_authors><pubmed_authors>Boots CE</pubmed_authors><pubmed_authors>Kim JJ</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Dunne SF</pubmed_authors><pubmed_authors>Ingram A</pubmed_authors><pubmed_authors>Campo H</pubmed_authors><pubmed_authors>Woodruff TK</pubmed_authors><pubmed_authors>Pavone ME</pubmed_authors><pubmed_authors>Xiao S</pubmed_authors><pubmed_authors>Colina J</pubmed_authors><pubmed_authors>Murphy A</pubmed_authors><pubmed_authors>Yoon J</pubmed_authors><pubmed_authors>Wagner S</pubmed_authors><pubmed_authors>Zha D</pubmed_authors><pubmed_authors>Pattarawat P</pubmed_authors><pubmed_authors>Burdette JE</pubmed_authors><pubmed_authors>Rogers HB</pubmed_authors><pubmed_authors>Trotter K</pubmed_authors><pubmed_authors>Russo A</pubmed_authors></additional><is_claimable>false</is_claimable><name>A new tissue-agnostic microfluidic device to model physiology and disease: the lattice platform.</name><description>To accurately phenocopy human biology &lt;i>in vitro&lt;/i>, researchers have been reducing their dependence on standard, static two-dimensional (2D) cultures and instead are moving towards three-dimensional (3D) and/or multicellular culture techniques. While these culture innovations are becoming more commonplace, there is a growing body of research that illustrates the benefits and even necessity of recapitulating the dynamic flow of nutrients, gas, waste exchange and tissue interactions that occur &lt;i>in vivo&lt;/i>. However, cost and engineering complexity are two main factors that hinder the adoption of these technologies and incorporation into standard laboratory workflows. We developed LATTICE, a plug-and-play microfluidic platform able to house up to eight large tissue or organ models that c</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-04T18:54:33.849Z</modification><creation>2025-04-04T18:54:33.849Z</creation></dates><accession>S-EPMC11181516</accession><cross_references><pubmed>37846545</pubmed><doi>10.1039/d3lc00378g</doi></cross_references></HashMap>