共 180 条
Drug Delivery and Therapy Strategies for Osteoporosis Intervention
被引:6
作者:

Ma, Mingyang
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China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China

Zeng, Huiling
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China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China

Yang, Pei
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China Pharmaceut Univ, Sch Sci, Nanjing 211198, Peoples R China China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China

Xu, Jiabing
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机构:
Taizhou Inst Drug Control, Taizhou 225316, Peoples R China China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China

Zhang, Xingwang
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机构:
Jinan Univ, Sch Pharm, Dept Pharmaceut, Guangzhou 510632, Peoples R China China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China

He, Wei
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机构:
Tongji Univ, Shanghai Skin Dis Hosp, Sch Med, Shanghai 200443, Peoples R China China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China
机构:
[1] China Pharmaceut Univ, Sch Pharm, Nanjing 211198, Peoples R China
[2] China Pharmaceut Univ, Sch Sci, Nanjing 211198, Peoples R China
[3] Taizhou Inst Drug Control, Taizhou 225316, Peoples R China
[4] Jinan Univ, Sch Pharm, Dept Pharmaceut, Guangzhou 510632, Peoples R China
[5] Tongji Univ, Shanghai Skin Dis Hosp, Sch Med, Shanghai 200443, Peoples R China
来源:
MOLECULES
|
2023年
/
28卷
/
18期
基金:
中国国家自然科学基金;
关键词:
osteoporosis;
drug delivery;
targeted drug delivery;
bone tissue engineering;
microneedles;
TRANSDERMAL DELIVERY;
MICRONEEDLE ARRAY;
SALMON-CALCITONIN;
ORAL DELIVERY;
IN-VITRO;
BONE;
HYDROXYAPATITE;
NANOPARTICLE;
SYSTEMS;
UPDATE;
D O I:
10.3390/molecules28186652
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
With the advent of the aging society, osteoporosis (OP) risk increases yearly. Currently, the clinical usage of anti-OP drugs is challenged by recurrent side effects and poor patient compliance, regardless of oral, intravenous, or subcutaneous administration. Properly using a drug delivery system or formulation strategy can achieve targeted drug delivery to the bone, diminish side effects, improve bioavailability, and prolong the in vivo residence time, thus effectively curing osteoporosis. This review expounds on the pathogenesis of OP and the clinical medicaments used for OP intervention, proposes the design approach for anti-OP drug delivery, emphatically discusses emerging novel anti-OP drug delivery systems, and enumerates anti-OP preparations under clinical investigation. Our findings may contribute to engineering anti-OP drug delivery and OP-targeting therapy.
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