<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Loh PS</submitter><funding>Ministry of Education</funding><funding>National University of Singapore</funding><funding>Agency for Science, Technology and Research</funding><pagination>370</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9962178</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(2)</volume><pubmed_abstract>Covalently closed dumbbell-shaped DNA delivery vectors comprising the double-stranded gene(s) of interest and single-stranded hairpin loops on both ends represent a safe, stable and efficacious alternative to viral and other non-viral DNA-based vector systems. As opposed to plasmids and DNA minicircles, dumbbells can be conjugated via the loops with helper functions for targeted delivery or imaging. Here, we investigated the non-covalent linkage of tri-antennary N-acetylgalactosamine (GalNAc3) or a homodimer of a CD137/4-1BB-binding aptamer (aptCD137-2) to extended dumbbell vector loops via complementary oligonucleotides for targeted delivery into hepatocytes or nasopharyngeal cancer cells. Enlarging the dumbbell loop size from 4 to 71 nucleotides for conjugation did not impair gene expres</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Non-Covalent Linkage of Helper Functions to Dumbbell-Shaped DNA Vectors for Targeted Delivery.</pubmed_title><pmcid>PMC9962178</pmcid><funding_grant_id>NUHSRO/2017/068/Bridging/06</funding_grant_id><funding_grant_id>H19H0G1006</funding_grant_id><funding_grant_id>T1-BSRG 2015-05</funding_grant_id><funding_grant_id>T1-2014Apr-02</funding_grant_id><pubmed_authors>Loh PS</pubmed_authors><pubmed_authors>Patzel V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Non-Covalent Linkage of Helper Functions to Dumbbell-Shaped DNA Vectors for Targeted Delivery.</name><description>Covalently closed dumbbell-shaped DNA delivery vectors comprising the double-stranded gene(s) of interest and single-stranded hairpin loops on both ends represent a safe, stable and efficacious alternative to viral and other non-viral DNA-based vector systems. As opposed to plasmids and DNA minicircles, dumbbells can be conjugated via the loops with helper functions for targeted delivery or imaging. Here, we investigated the non-covalent linkage of tri-antennary N-acetylgalactosamine (GalNAc3) or a homodimer of a CD137/4-1BB-binding aptamer (aptCD137-2) to extended dumbbell vector loops via complementary oligonucleotides for targeted delivery into hepatocytes or nasopharyngeal cancer cells. Enlarging the dumbbell loop size from 4 to 71 nucleotides for conjugation did not impair gene expres</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-25T23:05:11.696Z</modification><creation>2025-04-06T09:17:20.945Z</creation></dates><accession>S-EPMC9962178</accession><cross_references><pubmed>36839697</pubmed><doi>10.3390/pharmaceutics15020370</doi></cross_references></HashMap>