Preparation and physicochemical characterization of topical quercetin loaded liposome

被引:2
作者
Bavarsad, Neda [1 ,2 ]
Hemmati, Golnaz [3 ]
Ataee, Shirin [3 ]
Karampour, Neda Sistani [4 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Nanotechnol Res Ctr, Ahvaz, Iran
[2] Ahvaz Jundishapur Univ Med Sci, Dept Pharmaceut, Sch Pharm, Ahvaz, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Student Res Comm, Sch Pharm, Ahvaz, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Dept Pharmacol, Sch Pharm, Ahvaz, Iran
关键词
Quercetin; Liposome; Fusion; Topical; IN-VITRO; DRUG-DELIVERY; VIVO; ABSORPTION; GEMCITABINE; FLAVONOIDS; EFFICACY; CARRIERS;
D O I
10.30827/ars.v60i1.8201
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The use of herbal extracts in recent years has been of great interest to researchers around the world. Quercetin antoxidant properties play an important role in various fields of health. Objective: Due to the low skin permeability and poor solubility in aqua media, quercetin liposome formulation has been used to obtain topical use of this substance. Methods: In this study, liposomal quercetin was prepared by fusion method and the physicochemical characteristics of the formulation, including particle size, incorporation efficiency and in vitro drug release were evaluated. Results: The particle size of formulations were between 7.68 to 58.1 nm. The incorporation efficiency of formulations were in range of 80.55 to 96.80 percent. In vitro drug release of formulations were about 60 to 70 percent. Conclusion: According to the results obtained, it can be said that the use of this substance as a liposomal formulation can improve physicochemical properties of the drug in the laboratory conditions and provide it as a suitable candidate for further in vivo and clinical studies.
引用
收藏
页码:41 / 46
页数:6
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