Gastroretentive Raft Forming System for Enhancing Therapeutic Effect of Drug‐Loaded Hollow Mesoporous Silica on Gastric Ulcers

Author:

Chen Huayuan12,Pan Li3,Zhang Chengyu4,Liu Lin12,Tu Bin5,Liu Ergang2,Huang Yongzhuo12456ORCID

Affiliation:

1. School of Pharmaceutical Sciences Southern Medical University Guangzhou 510515 China

2. Zhongshan Institute for Drug Discovery Shanghai Institute of Materia Medica Chinese Academy of Sciences Zhongshan 528400 China

3. School of Pharmacy Zunyi Medical University Zunyi 563003 China

4. Artemisinin Research Center Guangzhou University of Chinese Medicine 12 Jichang Road Guangzhou 510450 China

5. State Key Laboratory of Drug Research Shanghai Institute of Materia Medica Chinese Academy of Sciences Shanghai 201203 China

6. NMPA Key Laboratory for Quality Research and Evaluation of Pharmaceutical Excipients Shanghai 201203 China

Abstract

AbstractGastric ulcers are characterized by damage to the stomach lining and are often triggered by substances such as ethanol and non‐steroidal anti‐inflammatory drugs. Patchouli alcohol (PA) has demonstrated effectiveness in treating gastric ulcers through antioxidative and anti‐inflammatory effects. However, the water insolubility of PA and rapid gastric emptying cause low drug concentration and poor absorption in the stomach, resulting in limited treatment efficacy of PA. This study develops an oral gastroretentive raft forming system (GRFDDS) containing the aminated hollow mesoporous silica nanoparticles (NH2‐HMSN) for PA delivery. The application of NH2‐HMSN can enhance PA‐loading capacity and water dispersibility, promoting bio‐adhesion to the gastric mucosa and sustained drug release. The incorporation of PA‐loaded NH2‐HMSN (NH2‐HMSN‐PA) into GRFDDS can facilitate gastric drug retention and achieve long action, thereby improving therapeutic effects. The results reveal that NH2‐HMSN‐PA protects the gastric mucosa damage by inhibiting NLRP3‐mediated pyroptosis. The GRFDDS, optimized through orthogonal design, demonstrates the gastric retention capacity and sustained drug release, exhibiting significant therapy efficacy in an ethanol‐induced acute gastric ulcers model and an aspirin‐induced chronic gastric ulcers model through antioxidation, anti‐pyroptosis, and anti‐inflammation. This study provides a potential strategy for enhancing druggability of insoluble natural compounds and therapeutic management of gastric ulcers.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

National Outstanding Youth Science Fund Project of National Natural Science Foundation of China

Publisher

Wiley

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