4.7 Article

Smart Responsive Quercetin-Conjugated Glycol Chitosan Prodrug Micelles for Treatment of Inflammatory Bowel Diseases

Journal

MOLECULAR PHARMACEUTICS
Volume 18, Issue 3, Pages 1419-1430

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.0c01245

Keywords

glycol chitosan; quercetin; nanomicelles; dual responsive; drug delivery; IBD

Funding

  1. National Natural Science Foundation of China [21977012, 21672021, 21572018, 81973764, 31370974]
  2. Joint Project of BRCBC (Biomedical Translational Engineering Research Center of BUCT-CJFH) [XK2020-06]
  3. Beijing Municipal Science and Technology Project [Z181100001718218]

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The GC-B-Que micelles exhibit pH/ROS dual-responsive properties and sustained release behavior, showing better therapeutic efficacy than free drugs in treating colitis. These micelles have the potential for oral delivery and provide an alternative strategy for designing smart responsive nanocarriers for catechol-based drugs.
The incidence and progression of inflammatory bowel disease are closely related to oxidative stress caused by excessive production of reactive oxygen species (ROS). To develop an efficacious and safe nanotherapy against inflammatory bowel diseases (IBD), we designed a novel pH/ROS dual-responsive prodrug micelle GC-B-Que as an inflammatory-targeted drug, which was comprised by active quercetin (Que) covalently linked to biocompatible glycol chitosan (GC) by aryl boronic ester as a responsive linker. The optimized micelles exhibited well-controlled physiochemical properties and stability in a physiological environment. Time-dependent NMR spectra traced the changes in the polymer structure in the presence of H2O2, confirming the release of the drug. The in vitro drug release studies indicated a low release rate (<20 wt %) in physiological conditions, but nearly complete release (>95 wt % after 72 h incubation) in a pH 5.8 medium containing 10 mu M H2O2, exhibiting a pH/ROS dualresponsive property and sustained release behavior. Importantly, the negligible drug release in a simulated gastric environment in 1 h allowed us to perform intragastric administration, which has potential to achieve the oral delivery by mature enteric-coating modification in future. Further in vivo activities and biodistribution experiments found that the GC-B-Que micelles tended to accumulate in intestinal inflammation sites and showed better therapeutic efficacy than the free drugs (quercetin and mesalazine) in a colitis mice model. Typical inflammatory cytokines including TNF-alpha, IL-6, and iNOS were significantly suppressed by GC-B-Que micelle treatment. Our work promoted inflammatory-targeted delivery and intestinal drug accumulation for active single drug quercetin and improved the therapeutic effect of IBD. The current study also provided an alternative strategy for designing a smart responsive nanocarrier for a catechol-based drug to better achieve the target drug delivery.

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