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Hyaluronic acid based nanocrystals hydrogels for enhanced topical delivery of drug: A case study
被引:29
|作者:
Wei, Shaofeng
[1
]
Xie, Jin
[1
]
Luo, Yijing
[1
]
Ma, Yueqin
[2
]
Tang, Shunxi
[1
]
Yue, Pengfei
[1
]
Yang, Ming
[1
]
机构:
[1] Jiangxi Univ Tradit Chinese Med, 1688 MEILING Ave, Nanchang 330004, Jiangxi, Peoples R China
[2] 94th Hosp Peoples Liberat Army, Dept Pharmaceut, Nanchang, Jiangxi, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Hyaluronic acid;
Nanocrystals;
Nanogels;
Network structure;
Transdermal permeation;
SKIN INFLAMMATION;
NANOSUSPENSIONS;
BAICALIN;
BIOAVAILABILITY;
MICROEMULSION;
RUTAECARPINE;
RESVERATROL;
EVODIAMINE;
VESICLES;
GEL;
D O I:
10.1016/j.carbpol.2018.08.112
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
The objective of this study is to use a carbohydrate polymer hyaluronic acid (HLA) as matrix to design novel transdermal nanogel loading poorly soluble drug nanocrystals. Baicalin nanocrystals (BCA-NC) were prepared by coupling homogenization technology and spray-drying technology. The morphology, the rheological behavior and transdermal permeation studies of HLA based BCA-NC-gel were evaluated. The results demonstrated that the BCA-NC could be successfully prepared in terms of trehalose after spray-drying. The trehalose could prevent the aggregation of BCA-NC during spray-drying. It was discovered that, the BCA-NC-gel with 1% HLA possessed the favorable gelatin capacity and thinning shear rheological property. In vitro transdermal permeation studies of BCA-NC-gel/HLA studies indicated a marked increase in the skin permeation of BCA. And the transdermal flux of BCA-NC-gel with 1% HLA were 20.65-fold higher (p < 0.01) than that of coarse BCA-gel, which could be attributed to particles size reduction of BCA-NC and bioadhesive property of HLA. And the morphology characterization of BCA-NC-gel/HLA demonstrated that BCA-NC could be imprisoned into the gel network of HLA, which might prevent it from aggregation in gel. In conclusion, HLA based nanogel system is a promising carrier for effectively transdermal delivery of poorly soluble drug.
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页码:64 / 71
页数:8
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