Development of gelatin-coated nanoliposomes loaded with β-cyclodextrin/ vitamin D3 inclusion complex for nutritional therapy

被引:21
作者
Ebrahimi, Alireza [1 ,2 ,3 ]
Hamishehkar, Hamed [3 ]
Amjadi, Sajed [4 ]
机构
[1] Tabriz Univ Med Sci, Fac Nutr & Food Sci, Student Res Comm, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Nutr & Food Sci, Biotechnol Res Ctr, Dept Food Sci & Technol, Tabriz, Iran
[3] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[4] Urmia Univ, Fac Agr, Dept Food Sci & Technol, POB 57561-51818, Orumiyeh, Iran
关键词
Surface coating; Drug-in-cyclodextrin-in-liposomes; Electrostatic interaction; In vitro release; C NANOLIPOSOMES; IN-LIPOSOMES; STABILITY; SOLUBILITY;
D O I
10.1016/j.foodchem.2023.136346
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aim of this study was to synthesize of beta-cyclodextrin/Vitamin D3 (beta CD/VitD3) inclusion complex and encapsulation of this complex with gelatin-coated nanoliposomes (NLPs). Fourier transform infrared spectros-copy confirmed the formation of beta CD/VitD3 inclusion complex. In the next step, different gelatin concentrations (1, 2, and 4 mg/mL) were used to surface coat the blank NLPs. The concentration of 2 mg/mL of gelatin was chosen as the optimal concentration for coating the complex-loaded NLPs by considering particle size, morphology, and zeta potential. The particle size and zeta potential of the coated complex-loaded NLPs were 117 +/- 2.55 nm and 19.8 +/- 1.25 mV, respectively. The images taken by transmission electron microscopy confirmed the formation of a biopolymer layer of gelatin around the NLPs' vesicles. The complex encapsulation efficiency inside the NLPs was 81.09%. The beta CD/VitD3 complex loaded NLPs and its coated form exhibited a controlled release profile in simulated gastrointestinal condition.
引用
收藏
页数:10
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