<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Benasutti H</submitter><funding>NIBIB NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institute of Biomedical Imaging and Bioengineering</funding><pagination>2747-2755</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6231230</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(11)</volume><pubmed_abstract>Opsonization (coating) of nanoparticles with complement C3 component is an important mechanism that triggers immune clearance and downstream anaphylactic and proinflammatory responses. The variability of complement C3 binding to nanoparticles in the general population has not been studied. We examined complement C3 binding to dextran superparamagnetic iron oxide nanoparticles (superparamagnetic iron oxide nanoworms, SPIO NWs, 58 and 110 nm) and clinically approved nanoparticles (carboxymethyl dextran iron oxide ferumoxytol (Feraheme, 28 nm), highly PEGylated liposomal doxorubicin (LipoDox, 88 nm), and minimally PEGylated liposomal irinotecan (Onivyde, 120 nm)) in sera from healthy human individuals. SPIO NWs had the highest variation in C3 binding (n = 47) between subjects, with a 15-30 fo</pubmed_abstract><journal>Bioconjugate chemistry</journal><pubmed_title>Variability of Complement Response toward Preclinical and Clinical Nanocarriers in the General Population.</pubmed_title><pmcid>PMC6231230</pmcid><funding_grant_id>R01 CA194058</funding_grant_id><funding_grant_id>R01 EB022040</funding_grant_id><funding_grant_id>EB022040</funding_grant_id><funding_grant_id>CA194058</funding_grant_id><funding_grant_id>UL1 TR001082</funding_grant_id><pubmed_authors>Simberg D</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Vu VP</pubmed_authors><pubmed_authors>Groman E</pubmed_authors><pubmed_authors>Scheinman R</pubmed_authors><pubmed_authors>Benasutti H</pubmed_authors><pubmed_authors>Saba L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Variability of Complement Response toward Preclinical and Clinical Nanocarriers in the General Population.</name><description>Opsonization (coating) of nanoparticles with complement C3 component is an important mechanism that triggers immune clearance and downstream anaphylactic and proinflammatory responses. The variability of complement C3 binding to nanoparticles in the general population has not been studied. We examined complement C3 binding to dextran superparamagnetic iron oxide nanoparticles (superparamagnetic iron oxide nanoworms, SPIO NWs, 58 and 110 nm) and clinically approved nanoparticles (carboxymethyl dextran iron oxide ferumoxytol (Feraheme, 28 nm), highly PEGylated liposomal doxorubicin (LipoDox, 88 nm), and minimally PEGylated liposomal irinotecan (Onivyde, 120 nm)) in sera from healthy human individuals. SPIO NWs had the highest variation in C3 binding (n = 47) between subjects, with a 15-30 fo</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Nov</publication><modification>2026-05-06T06:21:48.969Z</modification><creation>2019-03-27T00:07:24Z</creation></dates><accession>S-EPMC6231230</accession><cross_references><pubmed>29090582</pubmed><doi>10.1021/acs.bioconjchem.7b00496</doi></cross_references></HashMap>