<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guha Thakurta S</submitter><funding>UNL Center for Biotechnology</funding><funding>Nebraska Research Initiative</funding><funding>NCRR NIH HHS</funding><funding>Department of Health and Human Services</funding><funding>Nebraska Department of Health and Human Services</funding><pagination>4798-4810</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4525705</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(11)</volume><pubmed_abstract>Chondrocyte-seeded scaffolds were cultured in an ultrasound (US)-assisted bioreactor, which supplied the cells with acoustic energy around resonance frequencies (~5.0 MHz). Polyurethane-polycarbonate (BM), chitosan (CS) and chitosan-n-butanol (CSB) based scaffolds with varying porosities were chosen and the following US regimen was employed: 15 kPa and 60 kPa, 5 min per application and 6 applications per day for 21 days. Non-stimulated scaffolds served as control. For BM scaffolds, US stimulation significantly impacted cell proliferation and depth-independent cell population density compared to controls. The highest COL2A1/COL1A1 ratios and ACAN mRNA were noted on US-treated BM scaffolds compared to controls. A similar trend was noted on US-treated cell-seeded CS and CSB scaffolds, though </pubmed_abstract><journal>Acta biomaterialia</journal><pubmed_title>Enhanced depth-independent chondrocyte proliferation and phenotype maintenance in an ultrasound bioreactor and an assessment of ultrasound dampening in the scaffold.</pubmed_title><pmcid>PMC4525705</pmcid><funding_grant_id>1R21RR024437-01A1</funding_grant_id><funding_grant_id>R21 RR024437</funding_grant_id><pubmed_authors>Kraft M</pubmed_authors><pubmed_authors>Viljoen HJ</pubmed_authors><pubmed_authors>Guha Thakurta S</pubmed_authors><pubmed_authors>Subramanian A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhanced depth-independent chondrocyte proliferation and phenotype maintenance in an ultrasound bioreactor and an assessment of ultrasound dampening in the scaffold.</name><description>Chondrocyte-seeded scaffolds were cultured in an ultrasound (US)-assisted bioreactor, which supplied the cells with acoustic energy around resonance frequencies (~5.0 MHz). Polyurethane-polycarbonate (BM), chitosan (CS) and chitosan-n-butanol (CSB) based scaffolds with varying porosities were chosen and the following US regimen was employed: 15 kPa and 60 kPa, 5 min per application and 6 applications per day for 21 days. Non-stimulated scaffolds served as control. For BM scaffolds, US stimulation significantly impacted cell proliferation and depth-independent cell population density compared to controls. The highest COL2A1/COL1A1 ratios and ACAN mRNA were noted on US-treated BM scaffolds compared to controls. A similar trend was noted on US-treated cell-seeded CS and CSB scaffolds, though </description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Nov</publication><modification>2025-05-31T23:33:49.379Z</modification><creation>2025-05-31T23:33:49.379Z</creation></dates><accession>S-EPMC4525705</accession><cross_references><pubmed>25065549</pubmed><doi>10.1016/j.actbio.2014.07.013</doi></cross_references></HashMap>