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Biomaterial-engineered intra-articular drug delivery systems for osteoarthritis therapy
被引:89
|作者:
Kou, Longfa
[1
,2
]
Xiao, Shuyi
[1
,2
]
Sun, Rui
[1
,2
]
Bao, Shihui
[1
,2
]
Yao, Qing
[3
]
Chen, Ruijie
[1
,2
]
机构:
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Pharm, Wenzhou, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Peoples R China
[3] Wenzhou Med Univ, Sch Pharmaceut Sci, 109 Xueyuan West Rd, Wenzhou 325027, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Drug delivery system;
osteoarthritis;
nanomedicine;
retention time;
delayed release;
IN-VIVO EVALUATION;
POLY CAPROLACTONE MICROPARTICLES;
HYALURONIC-ACID HYDROGELS;
ARTICULAR-CARTILAGE;
PLGA MICROSPHERES;
THERMOSENSITIVE NANOPARTICLES;
KNEE OSTEOARTHRITIS;
GENE DELIVERY;
ANTIINFLAMMATORY PEPTIDES;
CHONDROITIN SULFATE;
D O I:
10.1080/10717544.2019.1660434
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Osteoarthritis (OA) is a progressive and degenerative disease, which is no longer confined to the elderly. So far, current treatments are limited to symptom relief, and no valid OA disease-modifying drugs are available. Additionally, OA relative joint is challenging for drug delivery, since the drugs experience rapid clearance in joint, showing a poor bioavailability. Existing therapeutic drugs, like non-steroidal anti-inflammatory drugs (NSAIDs) and corticosteroids, are not conducive for long-term use due to adverse effects. Though supplementations, including chondroitin sulfate and glucosamine, have shown beneficial effects on joint tissues in OA, their therapeutic use is still debatable. New emerging agents, like Kartogenin (KGN) and Interleukin-1 receptor antagonist (IL-1 ra), without a proper formulation, still will not work. Therefore, it is urgent to establish a suitable and efficient drug delivery system for OA therapy. In this review, we pay attention to various types of drug delivery systems and potential therapeutic drugs that may escalate OA treatments.
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页码:870 / 885
页数:16
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