Title : Orally Delivered Antisense Oligodeoxyribonucleotides of TNF-α via Polysaccharide-Based Nanocomposites Targeting Intestinal Inflammation.

Pub. Date : 2019 Mar

PMID : 30714345






3 Functional Relationships(s)
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1 Herein, a promising strategy for effective delivery of phosphorothioated antisense oligodeoxyribonucleotide of TNF-alpha (PS-ATNF-alpha), targeting the intestinal inflammation based on the interaction of the single chain of triple helical beta-glucan (s-LNT) with poly-deoxyadenylic acid [poly(dA)], and the colon-specific degradation of chitosan-alginate (CA) hydrogel, is reported. poly(dA) tumor necrosis factor Homo sapiens
2 Herein, a promising strategy for effective delivery of phosphorothioated antisense oligodeoxyribonucleotide of TNF-alpha (PS-ATNF-alpha), targeting the intestinal inflammation based on the interaction of the single chain of triple helical beta-glucan (s-LNT) with poly-deoxyadenylic acid [poly(dA)], and the colon-specific degradation of chitosan-alginate (CA) hydrogel, is reported. poly(dA) tumor necrosis factor Homo sapiens
3 The target gene of PS-ATNF-alpha, with a poly(dA) tail through a disulfide bond (-SS-), interacts with s-LNT to form a rod-like nanocomposite of s-LNT/poly(dA)-SS-PS-ATNF-alpha, which significantly inhibits lipopolysaccharide (LPS)-induced TNF-alpha at the protein level by 38.2% and mRNA level by 48.9% in RAW264.7 macrophages. poly(dA) tumor necrosis factor Homo sapiens