<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>51</viewCount><searchCount>0</searchCount></scores><additional><submitter>Gebeyehu A</submitter><funding>NSF-CREST center for Complex Material Design and also for Multidimensional Additive processing (CoManD) award</funding><funding>BLRD VA</funding><funding>The Research Centers in Minority Institutions (RCMI) program.</funding><funding>NIMHD NIH HHS</funding><funding>Department of Veterans Affairs Merit Review</funding><pagination>372</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7801509</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>A series of stable and ready-to-use bioinks have been developed based on the xeno-free and tunable hydrogel (VitroGel) system. Cell laden scaffold fabrication with optimized polysaccharide-based inks demonstrated that Ink H4 and RGD modified Ink H4-RGD had excellent rheological properties. Both bioinks were printable with 25-40 kPa extrusion pressure, showed 90% cell viability, shear-thinning and rapid shear recovery properties making them feasible for extrusion bioprinting without UV curing or temperature adjustment. Ink H4-RGD showed printability between 20 and 37 °C and the scaffolds remained stable for 15 days at temperature of 37 °C. 3D printed non-small-cell lung cancer (NSCLC) patient derived xenograft cells (PDCs) showed rapid spheroid growth of size around 500 µm in diameter and tumor microenvironment formation within 7 days. IC&lt;sub>50&lt;/sub> values demonstrated higher resistance of 3D spheroids to docetaxel (DTX), doxorubicin (DOX) and erlotinib compared to 2D monolayers of NSCLC-PDX, wild type triple negative breast cancer (MDA-MB-231 WT) and lung adenocarcinoma (HCC-827) cells. Results of flow property, shape fidelity, scaffold stability and biocompatibility of H4-RGD suggest that this hydrogel could be considered for 3D cell bioprinting and also for in-vitro tumor microenvironment development for high throughput screening of various anti-cancer drugs.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Polysaccharide hydrogel based 3D printed tumor models for chemotherapeutic drug screening.</pubmed_title><pmcid>PMC7801509</pmcid><funding_grant_id># 5U54MD0075007582-35</funding_grant_id><funding_grant_id># 1735968</funding_grant_id><funding_grant_id>I01 BX001164</funding_grant_id><funding_grant_id>BX00164</funding_grant_id><funding_grant_id>IK6 BX004015</funding_grant_id><funding_grant_id>G12 MD007582</funding_grant_id><funding_grant_id>U54 MD007582</funding_grant_id><pubmed_authors>Wang VZ</pubmed_authors><pubmed_authors>Haruna NF</pubmed_authors><pubmed_authors>Bagde A</pubmed_authors><pubmed_authors>Patel N</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Mondal A</pubmed_authors><pubmed_authors>Singh M</pubmed_authors><pubmed_authors>Arthur P</pubmed_authors><pubmed_authors>Rishi AK</pubmed_authors><pubmed_authors>Gebeyehu A</pubmed_authors><pubmed_authors>Surapaneni SK</pubmed_authors><pubmed_authors>Kutlehria S</pubmed_authors><view_count>51</view_count></additional><is_claimable>false</is_claimable><name>Polysaccharide hydrogel based 3D printed tumor models for chemotherapeutic drug screening.</name><description>A series of stable and ready-to-use bioinks have been developed based on the xeno-free and tunable hydrogel (VitroGel) system. Cell laden scaffold fabrication with optimized polysaccharide-based inks demonstrated that Ink H4 and RGD modified Ink H4-RGD had excellent rheological properties. Both bioinks were printable with 25-40 kPa extrusion pressure, showed 90% cell viability, shear-thinning and rapid shear recovery properties making them feasible for extrusion bioprinting without UV curing or temperature adjustment. Ink H4-RGD showed printability between 20 and 37 °C and the scaffolds remained stable for 15 days at temperature of 37 °C. 3D printed non-small-cell lung cancer (NSCLC) patient derived xenograft cells (PDCs) showed rapid spheroid growth of size around 500 µm in diameter and tumor microenvironment formation within 7 days. IC&lt;sub>50&lt;/sub> values demonstrated higher resistance of 3D spheroids to docetaxel (DTX), doxorubicin (DOX) and erlotinib compared to 2D monolayers of NSCLC-PDX, wild type triple negative breast cancer (MDA-MB-231 WT) and lung adenocarcinoma (HCC-827) cells. Results of flow property, shape fidelity, scaffold stability and biocompatibility of H4-RGD suggest that this hydrogel could be considered for 3D cell bioprinting and also for in-vitro tumor microenvironment development for high throughput screening of various anti-cancer drugs.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2024-11-07T13:11:34.961Z</modification><creation>2021-02-21T04:51:57Z</creation></dates><accession>S-EPMC7801509</accession><cross_references><pubmed>33431915</pubmed><doi>10.1038/s41598-020-79325-8</doi></cross_references></HashMap>