Oral delivery of a highly stable superoxide dismutase as a skin aging inhibitor

被引:6
作者
Dong, Liang [1 ,5 ]
Chen, Yongli [1 ,2 ]
Gu, Lihong [1 ]
Gan, Miao [1 ]
Carrier, Andrew [3 ]
Oakes, Ken [4 ]
Zhang, Xu [3 ]
Dong, Zhiyang [1 ]
机构
[1] Chinese Acad Sci, Inst Microbiol, State Key Lab Microbial Resources, POB 2714, Beijing 100080, Peoples R China
[2] Shenzhen Siyomicro Biotech CO Ltd, Shenzhen 518116, Peoples R China
[3] Cape Breton Univ, Dept Chem, 1250 Grand Lake Rd, Sydney, NS B1P 6L2, Canada
[4] Cape Breton Univ, Dept Biol, 1250 Grand Lake Rd, Sydney, NS B1P 6L2, Canada
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
加拿大自然科学与工程研究理事会;
关键词
Skin aging; Superoxide dismutase; Oral delivery; Antioxidant; Bioavailability; ANTIINFLAMMATORY PROPERTIES; TARGETED DELIVERY; D-GALACTOSE; ANTIOXIDANT; SUPPLEMENTATION; EXPRESSION; PROTECTS; MODEL; MICE;
D O I
10.1016/j.biopha.2023.114878
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
As an effective antioxidant enzyme, superoxide dismutase (SOD) has been widely used as a food supplement, cosmetic additive, and therapeutic agent. However, oral delivery of SOD is challenging due to its relative instability, limited bioavailability, and low absorption efficiency in the gastrointestinal (GI) tract. We addressed these issues using a highly stable superoxide dismutase (hsSOD) generated from a hot spring microbial sample. This SOD exhibited a specific activity of 5000 IU/mg while retaining its enzymatic activity under low pH en-vironments of an artificial GI system and in the presence of surfactants and various proteolytic enzymes. The inhibitory effects of hsSOD against skin-aging was evaluated under both in vitro and in vivo experiments using fibroblast cell and D-galactose induced aging-mouse models, respectively. Effective oral delivery of hsSOD promises wide applicability in pharmaceutical and food industries.
引用
收藏
页数:11
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