Self-assembled micelles based on gambogenic acid-phospholipid complex for sustained-release drug delivery

被引:11
|
作者
Wang, Beilei [1 ]
Cheng, Weiye [1 ]
Zhang, Caiyun [1 ]
Bao, Youmei [2 ]
Zha, Liqiong [1 ]
Qian, Jiajia [1 ]
Hong, Lufeng [1 ]
Chen, Weidong [1 ]
机构
[1] Anhui Univ Chinese Med, Coll Pharm, Hefei 230038, Anhui, Peoples R China
[2] Southern Med Univ, Sch Pharmaceut Sci, Guangzhou 510515, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
GNA; GNA-PLC; GNA-PLC micelles; self-assembly; in vitro release; pharmacokinetic; POLYPRENYLATED XANTHONES; INHIBITS PROLIFERATION; GARCINIA-HANBURYI; A549; CELLS; IN-VITRO; APOPTOSIS; MAPK; DISSOLUTION; STABILITY; SYSTEMS;
D O I
10.1080/02652048.2019.1656294
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Objective: To improve the water solubility and enhance the oral bioavailability of gambogenic acid (GNA). Methods: GNA-phospholipid complex (GNA-PLC) micelles were successfully prepared by anti-solvent method. Results: The encapsulation efficiency of GNA-PLC micelles can reach 99.33 % (w/w). The average particle size of the GNA-PLC micelles was 291.23 nm which was approximate agreed with the transmission electron microscopy (TEM). In vitro release profile showed the GNA-PLC and GNA-PLC micelles have significant sustained-release of GNA compared with crude GNA. Pharmacokinetic parameters indicated that the area under concentration-time curve (AUC(0 -> t)) of GNA in cases of GNA-PLC and GNA-PLC micelles are 2.04- and 3.92-fold higher than crude GNA, respectively. Conclusions: The better water solubility and higher bioavailability of GNA in GNA-PLC micelles with significant sustained-release of GNA endow the nanoparticle with great potential in GNA delivery system.
引用
收藏
页码:566 / 575
页数:10
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