<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Liu Z</submitter><pubmed_abstract>The majority of current nanocarriers in cancer treatment fail to deliver encapsulated cargos to their final targets at therapeutic levels, which decreases the ultimate efficacy. In this work, a novel core-shell nanocarrier with a biodegradable property was synthesized for efficient drug release and subcellular organelle delivery. Initially, silver nanoparticles (AgNPs) were grafted with terminal double bonds originating from N, N'-bisacrylamide cystamine (BAC). Then, the outer coatings consisting of chitosan (CTS) and polyvinyl alcohol (PVA) were deposited on the surface of modified AgNPs using an emulsion method. To improve the stability, disulfide-containing BAC was simultaneously reintroduced to cross-link CTS. The as-prepared nanoparticles (CAB) possessed the desired colloidal stabilit</pubmed_abstract><journal>Frontiers in bioengineering and biotechnology</journal><pagination>882308</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9035699</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>pH/Redox/Lysozyme-Sensitive Hybrid Nanocarriers With Transformable Size for Multistage Drug Delivery.</pubmed_title><pmcid>PMC9035699</pmcid><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Liao L</pubmed_authors><pubmed_authors>Zhou D</pubmed_authors></additional><is_claimable>false</is_claimable><name>pH/Redox/Lysozyme-Sensitive Hybrid Nanocarriers With Transformable Size for Multistage Drug Delivery.</name><description>The majority of current nanocarriers in cancer treatment fail to deliver encapsulated cargos to their final targets at therapeutic levels, which decreases the ultimate efficacy. In this work, a novel core-shell nanocarrier with a biodegradable property was synthesized for efficient drug release and subcellular organelle delivery. Initially, silver nanoparticles (AgNPs) were grafted with terminal double bonds originating from N, N'-bisacrylamide cystamine (BAC). Then, the outer coatings consisting of chitosan (CTS) and polyvinyl alcohol (PVA) were deposited on the surface of modified AgNPs using an emulsion method. To improve the stability, disulfide-containing BAC was simultaneously reintroduced to cross-link CTS. The as-prepared nanoparticles (CAB) possessed the desired colloidal stabilit</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-19T13:00:13.853Z</modification><creation>2025-04-19T13:00:13.853Z</creation></dates><accession>S-EPMC9035699</accession><cross_references><pubmed>35480969</pubmed><doi>10.3389/fbioe.2022.882308</doi></cross_references></HashMap>