<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zheng A</submitter><funding>NCATS NIH HHS</funding><funding>NEI NIH HHS</funding><funding>NIDCD NIH HHS</funding><pagination>452-460</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11964604</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>40(2)</volume><pubmed_abstract>We have developed sustained Dex (dexamethasone) capsule implants for sustained local delivery for inflammatory disease treatment. Four different biodegradable polymers were used as capsule materials: polycaprolactone (PCL), poly(lactic acid) (PLA), 90 : 10 poly(lactic-co-glycolide) (PLGA), and 50 : 50 PLGA. The drug release profiles from the four types of capsule were compared and the profiles were fit to a cylindrical reservoir first-order kinetics model. As a result, 50 : 50 PLGA showed the fastest release with the largest permeability and partition coefficient at 0.4909 nm/s and 1.9519, respectively. On the other hand, PCL showed the slowest release with the smallest permeability and partition coefficient at 0.1915 nm/s and 0.8872, respectively. The results indicate that the drug releas</pubmed_abstract><journal>The Korean journal of chemical engineering</journal><pubmed_title>Biodegradable dexamethasone polymer capsule for long-term release.</pubmed_title><pmcid>PMC11964604</pmcid><funding_grant_id>R21 DC021038</funding_grant_id><funding_grant_id>R15 EY031500</funding_grant_id><funding_grant_id>R03 TR004429</funding_grant_id><pubmed_authors>Debele T</pubmed_authors><pubmed_authors>Park Y</pubmed_authors><pubmed_authors>Zheng A</pubmed_authors><pubmed_authors>Dion G</pubmed_authors><pubmed_authors>Waterkotte T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biodegradable dexamethasone polymer capsule for long-term release.</name><description>We have developed sustained Dex (dexamethasone) capsule implants for sustained local delivery for inflammatory disease treatment. Four different biodegradable polymers were used as capsule materials: polycaprolactone (PCL), poly(lactic acid) (PLA), 90 : 10 poly(lactic-co-glycolide) (PLGA), and 50 : 50 PLGA. The drug release profiles from the four types of capsule were compared and the profiles were fit to a cylindrical reservoir first-order kinetics model. As a result, 50 : 50 PLGA showed the fastest release with the largest permeability and partition coefficient at 0.4909 nm/s and 1.9519, respectively. On the other hand, PCL showed the slowest release with the smallest permeability and partition coefficient at 0.1915 nm/s and 0.8872, respectively. The results indicate that the drug releas</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-07-14T03:02:33.843Z</modification><creation>2025-07-14T03:02:33.843Z</creation></dates><accession>S-EPMC11964604</accession><cross_references><pubmed>40177070</pubmed><doi>10.1007/s11814-022-1358-y</doi></cross_references></HashMap>