<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bajgiran KR</submitter><funding>Louisiana Board of Regents</funding><pagination>1211</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8540845</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(10)</volume><pubmed_abstract>Droplet microfluidics offers a wide range of applications, including high-throughput drug screening and single-cell DNA amplification. However, these platforms are often limited to single-input conditions that prevent them from analyzing multiple input parameters (e.g., combined cellular treatments) in a single experiment. Droplet multiplexing will result in higher overall throughput, lowering cost of fabrication, and cutting down the hands-on time in number of applications such as single-cell analysis. Additionally, while lab-on-a-chip fabrication costs have decreased in recent years, the syringe pumps required for generating droplets of uniform shape and size remain cost-prohibitive for researchers interested in utilizing droplet microfluidics. This work investigates the potential of sim</pubmed_abstract><journal>Micromachines</journal><pubmed_title>Simultaneous Droplet Generation with In-Series Droplet T-Junctions Induced by Gravity-Induced Flow.</pubmed_title><pmcid>PMC8540845</pmcid><funding_grant_id>LEQSF(2019-20)-RD-D-05</funding_grant_id><pubmed_authors>Cordova AS</pubmed_authors><pubmed_authors>Elkhanoufi R</pubmed_authors><pubmed_authors>Dorman JA</pubmed_authors><pubmed_authors>Bajgiran KR</pubmed_authors><pubmed_authors>Melvin AT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Simultaneous Droplet Generation with In-Series Droplet T-Junctions Induced by Gravity-Induced Flow.</name><description>Droplet microfluidics offers a wide range of applications, including high-throughput drug screening and single-cell DNA amplification. However, these platforms are often limited to single-input conditions that prevent them from analyzing multiple input parameters (e.g., combined cellular treatments) in a single experiment. Droplet multiplexing will result in higher overall throughput, lowering cost of fabrication, and cutting down the hands-on time in number of applications such as single-cell analysis. Additionally, while lab-on-a-chip fabrication costs have decreased in recent years, the syringe pumps required for generating droplets of uniform shape and size remain cost-prohibitive for researchers interested in utilizing droplet microfluidics. This work investigates the potential of sim</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-04T10:21:34.771Z</modification><creation>2025-04-04T10:21:34.771Z</creation></dates><accession>S-EPMC8540845</accession><cross_references><pubmed>34683262</pubmed><doi>10.3390/mi12101211</doi></cross_references></HashMap>