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DOI 10.1016/j.ijbiomac.2024.138565

Медицинская библиотека · International journal of biological macromolecules · 2024

American ginseng vesicles loaded hyaluronic acid hydrogel for ulcerative colitis.

Weng Ling, Zhao Min, Zhang Yumeng, Liu Xinyu, Wang Zheyong, Xu Ruixiang, Zhang Jiayi, Wang Yingjie, Wang Miao, Zhao Chunjie

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Аннотация

The present study introduces a novel therapeutic approach for ulcerative colitis (UC) utilizing American ginseng vesicles encapsulated within a hyaluronic acid (HA) hydrogel matrix. UC, a prevalent form of inflammatory bowel disease, is characterized by chronic inflammation of the colonic mucosa, leading to significant morbidity and compromised quality of life. Existing therapeutic modalities such as 5-Aminosalicylic acid (5-ASA) are associated with substantial side effects and a high recurrence rate. Thus, there is an unmet need for alternative treatments that offer enhanced efficacy with reduced adverse effects. Leveraging the anti-inflammatory properties of American ginseng vesicles HA -hydrogels of HA hydrogel (5-ASA + ANPs@HA), this study presents a targeted drug delivery system designed to provide localized therapy for UC. We synthesized the hydrogel matrix by HA and 1,4-butanediol diglycidyl ether (BDDE) at concentrations of 1 % NaOH and 0.8 %, v/v, respectively. The water content of the hydrogel was about 80 % to 90 %, and 82 % of Rb1 was released in 61 min. Our results demonstrate a significant reduction in disease symptoms, a substantial decrease in pro-inflammatory cytokines, and marked enhancement in mucosal healing following treatment with the 5-ASA + ANPs@HA. Collectively, these results suggest that the 5-ASA + ANPs@HA represents a promising therapeutic strategy for UC, warranting further investigation for clinical application.

Для цитирования: Weng Ling, Zhao Min, Zhang Yumeng, Liu Xinyu, Wang Zheyong, Xu Ruixiang, Zhang Jiayi, Wang Yingjie, Wang Miao, Zhao Chunjie. American ginseng vesicles loaded hyaluronic acid hydrogel for ulcerative colitis.. International journal of biological macromolecules. 2024. DOI: 10.1016/j.ijbiomac.2024.138565.

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