| Literature DB >> 26071629 |
Jianbo Li1, Jinjie Zhang1, Yao Fu1, Xun Sun1, Tao Gong1, Jinghui Jiang1, Zhirong Zhang2.
Abstract
To inhibit both the local and systemic complications with acute pancreatitis, an effective therapy requires a drug delivery system that can efficiently overcome the blood-pancreas barrier while achieving lung-specific accumulation. Here, we report the first dual pancreas- and lung-targeting therapeutic strategy mediated by a phenolic propanediamine moiety for the treatment of acute pancreatitis. Using the proposed dual-targeting ligand, an anti-inflammatory compound Rhein has been tailored to preferentially accumulate in the pancreas and lungs with rapid distribution kinetics, excellent tissue-penetrating properties and minimum toxicity. Accordingly, the drug-ligand conjugate remarkably downregulated the proinflammatory cytokines in the target organs thus effectively inhibiting local pancreatic and systemic inflammation in rats. The dual-specific targeting therapeutic strategy may help pave the way for targeted drug delivery to treat complicated inflammatory diseases.Entities:
Keywords: 3-propane diamine; Acute pancreatitis; Dual specific-targeting; N,N,N′-trimethyl-N′-(4-hydroxy-3-methyl-benzyl)-1; Rhein; Systemic complication
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Year: 2015 PMID: 26071629 DOI: 10.1016/j.jconrel.2015.06.011
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776