<HashMap><database>biostudies-literature</database><scores/><additional><submitter>de Hoyos-Vega JM</submitter><funding>NIDDK NIH HHS</funding><funding>Mayo Clinic</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>115896</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10916504</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>248</volume><pubmed_abstract>A common challenge in microfluidic cell cultures has to do with analysis of cell function without replacing a significant fraction of the culture volume and disturbing local concentration gradients of signals. To address this challenge, we developed a microfluidic cell culture device with an integrated bioanalysis unit to enable on-chip analysis of picoliter volumes of cell-conditioned media. The culture module consisted of an array of 140 microwells with a diameter of 300 m which were made low-binding to promote organization of cells into 3D spheroids. The bioanalysis module contained a droplet generator unit, 15 micromechanical valves and reservoirs loaded with reagents. Each 0.8 nL droplet contained an aliquot of conditioned media mixed with assay reagents. The use of microvalves allowe</pubmed_abstract><journal>Biosensors &amp; bioelectronics</journal><pubmed_title>Microfluidic 3D hepatic cultures integrated with a droplet-based bioanalysis unit.</pubmed_title><pmcid>PMC10916504</pmcid><funding_grant_id>DK134661</funding_grant_id><funding_grant_id>R21 CA236612</funding_grant_id><funding_grant_id>DK084567</funding_grant_id><funding_grant_id>R01 DK111378</funding_grant_id><funding_grant_id>P30 DK084567</funding_grant_id><funding_grant_id>R21 CA126716</funding_grant_id><funding_grant_id>R01 DK107255</funding_grant_id><funding_grant_id>CA236612</funding_grant_id><funding_grant_id>R01 DK134661</funding_grant_id><funding_grant_id>DK107255</funding_grant_id><pubmed_authors>Garcia-Cordero JL</pubmed_authors><pubmed_authors>Stybayeva G</pubmed_authors><pubmed_authors>Matveyenko A</pubmed_authors><pubmed_authors>de Hoyos-Vega JM</pubmed_authors><pubmed_authors>Gonzalez-Suarez AM</pubmed_authors><pubmed_authors>Revzin A</pubmed_authors><pubmed_authors>Malhi H</pubmed_authors><pubmed_authors>Cedillo-Alcantar DF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microfluidic 3D hepatic cultures integrated with a droplet-based bioanalysis unit.</name><description>A common challenge in microfluidic cell cultures has to do with analysis of cell function without replacing a significant fraction of the culture volume and disturbing local concentration gradients of signals. To address this challenge, we developed a microfluidic cell culture device with an integrated bioanalysis unit to enable on-chip analysis of picoliter volumes of cell-conditioned media. The culture module consisted of an array of 140 microwells with a diameter of 300 m which were made low-binding to promote organization of cells into 3D spheroids. The bioanalysis module contained a droplet generator unit, 15 micromechanical valves and reservoirs loaded with reagents. Each 0.8 nL droplet contained an aliquot of conditioned media mixed with assay reagents. The use of microvalves allowe</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T09:07:37.596Z</modification><creation>2025-04-04T09:07:37.596Z</creation></dates><accession>S-EPMC10916504</accession><cross_references><pubmed>38176252</pubmed><doi>10.1016/j.bios.2023.115896</doi></cross_references></HashMap>