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Dismantling the Necroptotic Engine: An Oral Theranostic Nanosponge for Ulcerative Colitis
Yao Xiao1,2,3,4, Xu Chen1,2,3,4, Jingnan Liao5
1Department of Geriatric Surgery, Xiangya Hospital, Central South University, Changsha, China.
Abstract:
Ulcerative Colitis (UC) treatments often lack target specificity and have significant side effects. A key pathological driver is the excessive necroptosis of intestinal epithelial cells (IECs), which disrupts the gut barrier. To address this, we designed an intelligent oral theranostic nanoplatform, CurN@I, to dismantle the necroptosis-inflammation axis. CurN@I consists of a barium sulfate (BaSO4) core for computed tomography (CT) imaging, encapsulated within a pH-responsive silk protein nanosponge. This scaffold is co-loaded with a necroptosis inhibitor (Necrostatin-1s, Nec-1s) and an antioxidant (demethoxycurcumin, DMC). The nanostructure is condensed in the acidic stomach but swells at the neutral pH of the inflamed intestine for localized drug release. Its negative surface charge facilitates durable electrostatic adhesion to the inflamed mucosa. In murine UC models, oral CurN@I significantly outperformed first-line clinical drugs. Mechanistic analysis showed it inhibits IEC necroptosis, alleviates oxidative stress, promotes barrier regeneration, and reshapes the gut microbiome. This work presents a non-invasive, targeted oral strategy that integrates diagnosis with multi-faceted therapy to restore intestinal homeostasis, demonstrating strong potential for clinical translation.
Insights
This study introduces CurN@I, an oral nanoplatform for Ulcerative Colitis (UC). It targets intestinal inflammation and cell death, offering a new diagnostic and therapeutic approach for gut health.
Area of Science:
- Gastroenterology and Nanomedicine
- Biomaterials and Drug Delivery
Background:
- Ulcerative Colitis (UC) treatments face challenges with specificity and side effects.
- Excessive intestinal epithelial cell (IEC) necroptosis drives UC pathology and gut barrier dysfunction.
Purpose of the Study:
- To develop an intelligent oral theranostic nanoplatform, CurN@I, for Ulcerative Colitis.
- To target and dismantle the necroptosis-inflammation axis in the gut.
Main Methods:
- Designed CurN@I with a barium sulfate core for CT imaging, a pH-responsive silk nanosponge, and co-loaded necroptosis inhibitor (Necrostatin-1s) and antioxidant (demethoxycurcumin).
- Utilized pH-responsive swelling and negative surface charge for localized drug release and mucosal adhesion.
- Evaluated efficacy in murine UC models.
Main Results:
- Oral CurN@I demonstrated superior performance compared to first-line clinical drugs in murine UC models.
- The nanoplatform inhibited IEC necroptosis, reduced oxidative stress, and promoted gut barrier regeneration.
- CurN@I treatment reshaped the gut microbiome and restored intestinal homeostasis.
Conclusions:
- CurN@I presents a non-invasive, targeted oral theranostic strategy for Ulcerative Colitis.
- The integrated diagnostic and multi-faceted therapeutic approach shows significant potential for clinical translation.
- This nanoplatform effectively addresses UC by targeting key pathological mechanisms.
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