<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18</volume><submitter>Dong H</submitter><pubmed_abstract>A personalized medication regimen provides precise treatment for an individual and can be guided by pre-clinical drug screening. The economical and high-efficiency simulation of the liver tumor microenvironment (TME) in a drug-screening model has high value yet challenging to accomplish. Herein, we propose a simulation of the liver TME with suspended alginate-gelatin hydrogel capsules encapsulating patient-derived liver tumor multicellular clusters, and the culture of patient-derived tumor organoids(PDTOs) for personalized pre-clinical drug screening. The hydrogel capsule offers a 3D matrix environment with mechanical and biological properties similar to those of the liver &lt;i>in vivo&lt;/i>. As a result, 18 of the 28 patient-derived multicellular clusters were successfully cultured as PDTOs. </pubmed_abstract><journal>Bioactive materials</journal><pagination>164-177</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8961426</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Culture of patient-derived multicellular clusters in suspended hydrogel capsules for pre-clinical personalized drug screening.</pubmed_title><pmcid>PMC8961426</pmcid><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Bian S</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Song P</pubmed_authors><pubmed_authors>Dong H</pubmed_authors><pubmed_authors>Xie H</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Zheng S</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Song G</pubmed_authors><pubmed_authors>Song W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Culture of patient-derived multicellular clusters in suspended hydrogel capsules for pre-clinical personalized drug screening.</name><description>A personalized medication regimen provides precise treatment for an individual and can be guided by pre-clinical drug screening. The economical and high-efficiency simulation of the liver tumor microenvironment (TME) in a drug-screening model has high value yet challenging to accomplish. Herein, we propose a simulation of the liver TME with suspended alginate-gelatin hydrogel capsules encapsulating patient-derived liver tumor multicellular clusters, and the culture of patient-derived tumor organoids(PDTOs) for personalized pre-clinical drug screening. The hydrogel capsule offers a 3D matrix environment with mechanical and biological properties similar to those of the liver &lt;i>in vivo&lt;/i>. As a result, 18 of the 28 patient-derived multicellular clusters were successfully cultured as PDTOs. </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T23:16:36.877Z</modification><creation>2025-04-04T23:16:36.877Z</creation></dates><accession>S-EPMC8961426</accession><cross_references><pubmed>35387168</pubmed><doi>10.1016/j.bioactmat.2022.03.020</doi></cross_references></HashMap>