Development of ROS-sensitive capofungin hydrogel by crosslinking chitosan with four-arm polyethylene glycol derivative for treatment of vulvovaginal candidiasis

被引:0
作者
Pan, Hui [1 ]
Xu, Junjing [1 ]
Wang, Ruizhe [1 ]
Cheng, Min [2 ]
Wang, Yuzhen [3 ]
Song, Bo [1 ]
机构
[1] Shandong Second Med Univ, Sch Pharm, Weifang 261053, Peoples R China
[2] Shandong Second Med Univ, Basic Med Sch, Weifang 261053, Peoples R China
[3] Shandong Second Med Univ, Med Imaging Specialty, Weifang 261053, Peoples R China
关键词
Chitosan hydrogel; Polyethylene glycol; Crosslinker; Reactive oxygen species; Candida albicans; Vulvovaginal candidiasis; ALBICANS;
D O I
10.1016/j.ijbiomac.2024.135157
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both exogenous and endogenous reactive oxygen species (ROS) in vulvovaginal candidiasis (VVC) play pivotal roles in promoting the hyphal formation of Candida albicans (CA), which suggests that clearing ROS could inhibit CA hyphae formation. A ROS-sensitive hydrogel (CAS@4Arm-PB/CS) was formulated by using a novel four-arm polyethylene glycol (4Arm-PEG) derivative (4Arm-PB) as a crosslinking agent, chitosan (CS) as the hydrogel matrix, and caspofungin (CAS) as the antifungal drug against CA. The ROS-sensitivity, disintegration mechanism, crosslinking action, swelling degree, microstructure, modulus, and rheological properties of 4Arm-PB were characterized. According to the results, 5.0 % 4Arm-PB could quickly and efficiently cross-link 0.5 mg/mL of CS. The ROS-sensitivity of 4Arm-PB was 10-50 mu M, indicating a strong ROS sensitivity. The in vitro and in vivo anti-CA results indicated that CAS@4Arm-PB/CS not only cleared endogenous and exogenous ROS and inhibited the formation of CA hyphae and biofilm but also contributed beneficially to the treatment of VVC mice caused by CA infection, implying a certain safety aspect and an in vivo applicability. This research introduces a novel functional crosslinking agent for CS hydrogel formulation, presenting a new avenue for hydrogel-based drug delivery systems and therapeutic strategies for VVC treatment.
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页数:14
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