<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Filipowicz A</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Bioconjugates of a polyamidoamine (PAMAM) G3 dendrimer and an aldehyde were synthesized as carriers for vitamins A and B₆, and the bioavailability of these vitamins for skin nutrition was investigated.&lt;h4>Methods&lt;/h4>Nuclear magnetic resonance (NMR) and ultraviolet-visible methods were used to characterize the structure of the bioconjugates and for monitoring release of pyridoxal (Pyr) and pyridoxal phosphate (PLP) from these bioconjugates in vitro. A skin model permeation of bioconjugates was also studied in a Franz chamber.&lt;h4>Results&lt;/h4>A transdermal G3 PAMAM dendrimer was used to synthesize bioconjugates with trans-retinal (Ret), pyridoxal (Pyr), or PLP. These nanomolecules, containing up to four covalently linked Ret, Pyr, or PLP (G3(4Ret), G3(4Pyr), and G3(4PLP)),</pubmed_abstract><journal>International journal of nanomedicine</journal><pagination>4819-28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3439857</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Bioconjugates of PAMAM dendrimers with trans-retinal, pyridoxal, and pyridoxal phosphate.</pubmed_title><pmcid>PMC3439857</pmcid><pubmed_authors>Filipowicz A</pubmed_authors><pubmed_authors>Wolowiec S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bioconjugates of PAMAM dendrimers with trans-retinal, pyridoxal, and pyridoxal phosphate.</name><description>&lt;h4>Background&lt;/h4>Bioconjugates of a polyamidoamine (PAMAM) G3 dendrimer and an aldehyde were synthesized as carriers for vitamins A and B₆, and the bioavailability of these vitamins for skin nutrition was investigated.&lt;h4>Methods&lt;/h4>Nuclear magnetic resonance (NMR) and ultraviolet-visible methods were used to characterize the structure of the bioconjugates and for monitoring release of pyridoxal (Pyr) and pyridoxal phosphate (PLP) from these bioconjugates in vitro. A skin model permeation of bioconjugates was also studied in a Franz chamber.&lt;h4>Results&lt;/h4>A transdermal G3 PAMAM dendrimer was used to synthesize bioconjugates with trans-retinal (Ret), pyridoxal (Pyr), or PLP. These nanomolecules, containing up to four covalently linked Ret, Pyr, or PLP (G3(4Ret), G3(4Pyr), and G3(4PLP)),</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2025-04-19T15:53:18.802Z</modification><creation>2019-03-27T00:57:50Z</creation></dates><accession>S-EPMC3439857</accession><cross_references><pubmed>22973101</pubmed><doi>10.2147/IJN.S34175</doi></cross_references></HashMap>