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Colon-targeted delivery of liver hydrolysates: Efficacy in reversing carbon tetrachloride-induced liver damage

机译:结肠靶向肝水解产物的输送:逆转四氯化碳诱导的肝损伤的功效

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摘要

Liver hydrolysates contain various active polypeptides with multiple physiological functions. Oral colon-targeted drug delivery is a potential delivery approach for proteins and therapeutic polypeptides. The aim of this study was to assess the enhancement of the protective effect of liver hydrolysates on liver injury by using a colon-targeted delivery system. Rats were orally administered with a colon-targeted capsule with or without swine liver hydrolysates (22.5 or 5.625 mg/kg) or given the same daily doses of liver hydrolysates via the regular gavage route for 30 days, followed by induction of liver injury with carbon tetrachloride (CCl4). Pathological analysis showed that liver hydrolysates delivered via the colon-targeted capsules had a significant improving protective effect on CCl4-induced damage to the rats' liver when compared to liver hydrolysates administered intragastrically by gavage. This study supports the feasibility of oral colon-targeted drug delivery for proteins, therapeutic polypeptides, and functional food.
机译:肝水解产物包含具有多种生理功能的各种活性多肽。口服结肠靶向药物递送是蛋白质和治疗性多肽的潜在递送方法。这项研究的目的是通过使用结肠靶向递送系统评估肝水解产物对肝损伤的保护作用的增强。给大鼠口服结肠靶向胶囊,有或没有猪肝水解液(22.5或5.625 mg / kg),或通过常规管饲途径每天给予相同剂量的肝水解液,持续30天,然后用碳诱导肝损伤四氯化物(CCl4)。病理分析表明,与通过管饲法在胃内给予的肝水解物相比,通过结肠靶向胶囊递送的肝水解物对CCl4诱导的大鼠肝脏损伤具有明显改善的保护作用。这项研究支持口服结肠靶向药物递送蛋白质,治疗性多肽和功能性食品的可行性。

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