Decoy Oligodeoxynucleotides, Polysaccharides, and Targeted Peptide-Functionalized Gold Nanorods for the Combined Treatment of Rheumatoid Arthritis.
Nan ZhangShasha ZhangChunyu XuLingling FuTuanbing LiuYongxing ZhaoPublished in: Advanced healthcare materials (2018)
Autoimmune diseases like rheumatoid arthritis (RA) possess complicated pathogenesis. Therefore, RA is hard to treat by monotherapies in clinical setting. All-in-one treatments that target inflamed joints and act efficiently are highly needed. Gold compounds are old anti-RA therapies and are fabricated into gold nanorods (GNRs) that serve as anti-RA therapeutics as well as nanocarriers for anti-inflammatory nucleic acid drug-NF-κB-decoy oligodeoxynucleotides (dODNs). A targeted peptide to vascular cell adhesion molecule-1 (VCAM-1) (PVCAM-1 ) is modified onto the GNRs to facilitate enhanced accumulation of GNRs in inflamed tissues and enhanced cellular uptake of GNRs by inflamed cells. dODNs loaded and PVCAM-1 modified GNRs (GNRs-dODN-PVCAM-1 ) are covered by polysialic acid (PSA) to protect GNRs-dODN-PVCAM-1 in vivo. Simultaneous GNRs, dODN, and thermotherapy show synergic effect on the reduction of TNF-α and IL-6 in inflamed macrophages and blood vessel cells. The simultaneous triple therapy (GNRs-dODN-PSA-PVCAM-1 +laser) demonstrates excellent anti-inflammatory efficacy in vitro and in vivo.
Keyphrases
- rheumatoid arthritis
- disease activity
- anti inflammatory
- induced apoptosis
- prostate cancer
- cancer therapy
- cell adhesion
- ankylosing spondylitis
- interstitial lung disease
- drug delivery
- nucleic acid
- signaling pathway
- emergency department
- endoplasmic reticulum stress
- inflammatory response
- systemic sclerosis
- quantum dots
- mass spectrometry
- stem cells
- high resolution
- idiopathic pulmonary fibrosis
- reduced graphene oxide
- radical prostatectomy
- cell death
- cell therapy
- drug release