Ding Zhongpeng, Ying Qianyi, Lei Jing, Zhang Ningchen, Xia Yu, Du Yilin, Xu Beihua, Shi Senlin
College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Pharmacy Department, Lishui Second People's Hospital, Lishui, China.
Front Pharmacol. 2025 Feb 24;16:1544302. doi: 10.3389/fphar.2025.1544302. eCollection 2025.
To investigate the therapeutic effects of the PRAC on acute liver injury and its potential as an ingredient in drugs and nutraceuticals.
Microwave-assisted extraction technology combined with Box-Behnken model combined with the three kinds of artificial neural networks was used to optimize PRAC extraction process. Characterize the structure and composition of PRAC. In order to prevent PRAC from being degraded by the gastrointestinal environment, PRAC-loaded liposomes were fabricated. The efficacy of PRAC-loaded liposomes was evaluated by three acute liver injury animal models prepared according to different mechanisms.
The best yield of PRAC was 4.49%, and the purity reached up to 86.53% by optimizing the microwave parameters using Box-Behnken model combined with the three kinds of artificial neural networks. PRAC was characterized as a galactan having a backbone consisting predominately of →4)-D-Gal-(1→ and →4)-D-Glc-(1→ with a molecular weight of 12.713 kDa. The PRAC-loaded liposome obtained had a size about 340 nm with a polydispersity index 0.234. The entrapment efficiency was 70.12% and the drug loading was 1.24%. Liposomes can be fully released in the gastrointestinal environment within 12 h and have long-term stability at 4°C. The therapeutic effect of PRAC liposomes on acute liver injury was confirmed by three animal models of acute liver injury.
PRAC is a potential drug for the treatment of acute liver injury.
研究PRAC对急性肝损伤的治疗作用及其作为药物和营养保健品成分的潜力。
采用微波辅助萃取技术结合Box-Behnken模型与三种人工神经网络来优化PRAC的提取工艺。对PRAC的结构和组成进行表征。为防止PRAC被胃肠道环境降解,制备了载PRAC脂质体。通过根据不同机制制备的三种急性肝损伤动物模型评估载PRAC脂质体的疗效。
通过结合Box-Behnken模型与三种人工神经网络优化微波参数,PRAC的最佳产率为4.49%,纯度高达86.53%。PRAC被表征为一种半乳聚糖,其主链主要由→4)-D-半乳糖-(1→和→4)-D-葡萄糖-(1→组成,分子量为12.713 kDa。所得载PRAC脂质体的粒径约为340 nm,多分散指数为0.234。包封率为70.12%,载药量为1.24%。脂质体可在12小时内在胃肠道环境中完全释放,并在4℃下具有长期稳定性。三种急性肝损伤动物模型证实了PRAC脂质体对急性肝损伤的治疗作用。
PRAC是一种治疗急性肝损伤的潜在药物。