<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Sette A</submitter><pubmed_abstract>Titanium dioxide (TiO&lt;sub>2&lt;/sub>) has been widely used in many nanotechnology areas including nanomedicine, where it could be proposed for the photodynamic and sonodynamic cancer therapies. However, TiO&lt;sub>2&lt;/sub> nanoformulations have been shown to be toxic for living cells. In this article, we report the development of a new delivery system, based on nontoxic TiO&lt;sub>2&lt;/sub> nanoparticles, further conjugated with a monoclonal antibody against a novel and easily accessible tumor marker, e.g., the Kv 11.1 potassium channel. We synthesized, by simple solvothermal method, dicarboxylic acid-terminated PEG TiO&lt;sub>2&lt;/sub> nanocrystals (PEG-TiO&lt;sub>2&lt;/sub> NPs). Anti-Kv 11.1 monoclonal antibodies (Kv 11.1-Mab) were further linked to the terminal carboxylic acid groups. Proper conjugation was </pubmed_abstract><journal>Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology</journal><pagination>2111</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3857862</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development of novel anti-Kv 11.1 antibody-conjugated PEG-TiO&lt;sub>2&lt;/sub> nanoparticles for targeting pancreatic ductal adenocarcinoma cells.</pubmed_title><pmcid>PMC3857862</pmcid><pubmed_authors>Crociani O</pubmed_authors><pubmed_authors>Sette A</pubmed_authors><pubmed_authors>Spadavecchia J</pubmed_authors><pubmed_authors>Landoulsi J</pubmed_authors><pubmed_authors>Casale S</pubmed_authors><pubmed_authors>Arcangeli A</pubmed_authors><pubmed_authors>Haye B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of novel anti-Kv 11.1 antibody-conjugated PEG-TiO&lt;sub>2&lt;/sub> nanoparticles for targeting pancreatic ductal adenocarcinoma cells.</name><description>Titanium dioxide (TiO&lt;sub>2&lt;/sub>) has been widely used in many nanotechnology areas including nanomedicine, where it could be proposed for the photodynamic and sonodynamic cancer therapies. However, TiO&lt;sub>2&lt;/sub> nanoformulations have been shown to be toxic for living cells. In this article, we report the development of a new delivery system, based on nontoxic TiO&lt;sub>2&lt;/sub> nanoparticles, further conjugated with a monoclonal antibody against a novel and easily accessible tumor marker, e.g., the Kv 11.1 potassium channel. We synthesized, by simple solvothermal method, dicarboxylic acid-terminated PEG TiO&lt;sub>2&lt;/sub> nanocrystals (PEG-TiO&lt;sub>2&lt;/sub> NPs). Anti-Kv 11.1 monoclonal antibodies (Kv 11.1-Mab) were further linked to the terminal carboxylic acid groups. Proper conjugation was </description><dates><release>2013-01-01T00:00:00Z</release><publication>2013</publication><modification>2025-04-04T07:25:24.694Z</modification><creation>2019-03-27T01:18:16Z</creation></dates><accession>S-EPMC3857862</accession><cross_references><pubmed>24348091</pubmed><doi>10.1007/s11051-013-2111-6</doi></cross_references></HashMap>