<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jin BJ</submitter><funding>NIBIB NIH HHS</funding><funding>National Eye Institute</funding><funding>NEI NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIDDK NIH HHS</funding><funding>Emily&amp;apos;s Entourage</funding><funding>Cystic Fibrosis Foundation</funding><funding>National Institute of Biomedical Imaging and Bioengineering</funding><pagination>7675-7681</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6461040</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>90(12)</volume><pubmed_abstract>New high-throughput assay formats and innovative screening technologies are needed for miniaturized screens using small quantities of near-native, patient-derived cells. Here, we developed a hollow micropillar array method to screen compounds using epithelial cells cultured on a porous support, with the goal of screening thousands of compounds using a single 24 mm diameter transwell filter containing cultured cells. Test compounds (∼1 nL) in an alginate hydrogel were printed by microinjection in hollow cylindrical micropillars (height = 150 μm, inner diameter = 100 μm) spaced 300 μm apart in a square array configuration. Compounds were delivered by positioning the array near the surface of a cell layer, with 5-10 μm of distance between the micropillars and cell surface. Micropillar array g</pubmed_abstract><journal>Analytical chemistry</journal><pubmed_title>Hollow Micropillar Array Method for High-Capacity Drug Screening on Filter-Grown Epithelial Cells.</pubmed_title><pmcid>PMC6461040</pmcid><funding_grant_id>DK075302</funding_grant_id><funding_grant_id>R01 EB000415</funding_grant_id><funding_grant_id>R24 DK099803</funding_grant_id><funding_grant_id>EY13574</funding_grant_id><funding_grant_id>R01 DK075302</funding_grant_id><funding_grant_id>R01 DK101373</funding_grant_id><funding_grant_id>R01 EY013574</funding_grant_id><funding_grant_id>EB00415</funding_grant_id><funding_grant_id>R37 EB000415</funding_grant_id><funding_grant_id>DK101373</funding_grant_id><funding_grant_id>DK72517</funding_grant_id><funding_grant_id>P30 DK072517</funding_grant_id><funding_grant_id>DK099803</funding_grant_id><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Verkman AS</pubmed_authors><pubmed_authors>Jin BJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hollow Micropillar Array Method for High-Capacity Drug Screening on Filter-Grown Epithelial Cells.</name><description>New high-throughput assay formats and innovative screening technologies are needed for miniaturized screens using small quantities of near-native, patient-derived cells. Here, we developed a hollow micropillar array method to screen compounds using epithelial cells cultured on a porous support, with the goal of screening thousands of compounds using a single 24 mm diameter transwell filter containing cultured cells. Test compounds (∼1 nL) in an alginate hydrogel were printed by microinjection in hollow cylindrical micropillars (height = 150 μm, inner diameter = 100 μm) spaced 300 μm apart in a square array configuration. Compounds were delivered by positioning the array near the surface of a cell layer, with 5-10 μm of distance between the micropillars and cell surface. Micropillar array g</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2025-04-22T17:16:26.927Z</modification><creation>2019-06-06T21:10:27Z</creation></dates><accession>S-EPMC6461040</accession><cross_references><pubmed>29779372</pubmed><doi>10.1021/acs.analchem.8b01554</doi></cross_references></HashMap>