Enhancement of therapeutic efficacy of betanin for diabetes treatment by liposomal nanocarriers

被引:62
作者
Amjadi, Sajed [1 ,2 ]
Abbasi, Mehran Mesgari [3 ]
Shokouhi, Behrooz [4 ]
Ghorbani, Marjan [5 ]
Hamishehkar, Hamed [3 ]
机构
[1] Urmia Univ, Dept Food Sci & Technol, Fac Agr, Orumiyeh, Iran
[2] Tabriz Univ Med Sci, Biotechnol Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Dept Pathol, Tabriz, Iran
[5] Tabriz Univ Med Sci, Stem Cell Res Ctr, Tabriz, Iran
关键词
Betanin; Nanoliposomes; Sustained release; Digestion stability; Diabetes; OXIDATIVE STRESS; IN-VIVO; STABILITY; DELIVERY; BIOAVAILABILITY; STREPTOZOTOCIN; NANOPARTICLES; NANOLIPOSOMES; ENCAPSULATION; IMPROVEMENT;
D O I
10.1016/j.jff.2019.05.015
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Betanin is a bioactive compound with a high antioxidant activity and therapeutic potential. However, incomplete oral absorption and low stability of betanin limit its application. To surmount these limitations, betanin was encapsulated with nanoliposomes, nanoparticles exhibiting suitable physicochemical properties. Additionally, betanin-loaded nanoliposomes revealed a relatively good sustained release profile in the simulated gastric and intestinal fluids. In vitro digestion stability of betanin and its antioxidant activity were significantly improved by liposomal encapsulation. These nanocarriers were assessed in vivo for their therapeutic potency in streptozotocin induced rats. The results showed that the administration of betanin-loaded nanoliposomes was significantly more effective than free betanin in positively regulate hyperglycemia, hyperlipidemia and oxidative stress. Moreover, the histopathological analysis showed that the tissue damage in kidney, liver and pancreas was reduced in the betanin-loaded nanoliposomes treated diabetic rats. In conclusion nanoliposomes are suitable nanocarriers for improving the stability and therapeutic potential of betanin.
引用
收藏
页码:119 / 128
页数:10
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