抗溃疡药
药物输送
克拉霉素
幽门螺杆菌
药品
甲硝唑
药理学
质子抑制剂泵
抗生素
铋
医学
生物医学工程
纳米技术
材料科学
化学
内科学
生物化学
冶金
作者
Qi Wang,Yu Xu,Rui Xue,Jingmin Fan,Hang Yu,Jiawei Guan,Hongzheng Wang,Min Li,Yu Wei,Zhi Xie,Rong Qi,Xin Jia,Bo Han
出处
期刊:Small
[Wiley]
日期:2022-02-08
卷期号:18 (9)
被引量:17
标识
DOI:10.1002/smll.202104660
摘要
Abstract Bismuth‐containing therapies are suggested as first‐line and rescue alternatives for gastric ulcer (GU) treatment and Helicobacter pylori eradication. The current treatment strategy is called quadruple therapy and includes proton pump inhibitors, bismuth, and two broad‐band antibiotics. This fact may affect medication compliance, leading to a resistance rate of more than 25% to clarithromycin or metronidazole. To counter this, from the perspective of natural products, an intragastric‐targeting all‐in‐one theranostic platform is established: a drug carrier microcapsule composed of multiple synergistic antiulcer drugs, including bismuth, gallotannin, and antibiotics is obtained (BiG@MCs), and the therapeutic effects of BiG@MCs in rodent models are further evaluated. The results show that the BiG@MCs are spherical with homogeneous particle size (3 ± 0.5 µm) and can be response‐released to the acidic environment of the stomach (pH 2.0–3.0), preventing the premature release of the BiG@MCs in physiological conditions. It is worth noting that the bismuth component can be easily identified by computed tomography and other detection instruments, which provide the possibility for drug tracing. In summary, these results indicate that BiG@MCs provide a versatile intragastric‐targeting drug delivery platform for GU therapeutics.
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