A bone-targeting delivery system carrying osteogenic phytomolecule icaritin prevents osteoporosis in mice

被引:78
作者
Huang, Le [1 ,2 ]
Wang, Xinluan [1 ,2 ,3 ]
Cao, Huijuan [3 ]
Li, Ling [3 ]
Chow, Dick Ho-Kiu [1 ,2 ]
Tian, Li [1 ,2 ]
Wu, Heng [1 ,2 ,4 ]
Zhang, Jiayong [5 ]
Wang, Nan [3 ]
Zheng, Lizhen [1 ,2 ]
Yao, Xinsheng [6 ]
Yang, Zhijun [5 ]
Qin, Ling [1 ,2 ,3 ]
机构
[1] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth, Dept Orthopaed & Traumatol, Musculoskeletal Res Lab, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth, Innovat Orthopaed Biomat & Drug Translat Res Lab, Hong Kong, Hong Kong, Peoples R China
[3] Chinese Acad Sci, Shenzhen Inst Adv Technol, Inst Biomed & Hlth Engn, Translat Med R&D Ctr, Shenzhen, Peoples R China
[4] Univ Minnesota, Dept Med, Box 736 UMHC, Minneapolis, MN 55455 USA
[5] Hong Kong Baptist Univ, Sch Chinese Med, Hong Kong, Hong Kong, Peoples R China
[6] Jinan Univ, Coll Pharm, Guangzhou 510632, Guangdong, Peoples R China
关键词
Bone targeting delivery system design; Icaritin; OVX; Estrogen-depletion; Osteoporosis; STEROID-ASSOCIATED OSTEONECROSIS; ADULT OVARIECTOMIZED RATS; POSTMENOPAUSAL WOMEN; REGIONAL-VARIATIONS; HERBA EPIMEDII; STROMAL CELLS; BETA-CATENIN; IN-VITRO; LIPOSOME; DOXORUBICIN;
D O I
10.1016/j.biomaterials.2018.07.046
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Targeting delivery system has been widely used in packaging drugs for medical therapies attributed to its high efficiency and efficacy. A Traditional Chinese Medicine (TCM) formula consisting of Herba Epimedii has previously been shown to effectively treat postmenopausal osteoporosis. We have subsequently found that icaritin, which was a flavonoid isolated from both Herba Epimedii and its serum metabolites after oral administration, inhibited the adipogenic capacity of bone mesenchymal stem cells (BMSCs) while promoted their osteogenesis. However, previous pharmacokinetic analyses have shown that icaritin had a short half-life in blood and only trace amounts of the molecule reach the bone tissue. To overcome this limitation, we developed a bone-targeting liposome containing an oligopeptide of eight aspartate residues (Asp8), which had previously been shown to specifically target the bone, encapsulating icaritin. In vivo, we found that the Asp8-icaritin-liposome enhanced bone formation in ovariectomized mice compared to an icaritin-liposome control lacking the Asp8 moiety. Through in vitro mechanistic studies we further found that icaritin inhibited adipogenesis through an Akt/GSK-beta/beta-catenin signaling pathway. Taken together, our study shows that Asp8-liposome as a bone-targeting delivery system is effective to carry an osteogenic phytomolecule for facilitating and enhancing its therapeutic effects on the prevention of estrogen depletion-induced osteoporosis. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:58 / 71
页数:14
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