pH-controlled release feature of chitosan assembled silica nanoparticles containing nano-formulated curcumin over in vitro gastric and physiological condition

被引:9
作者
Saputra, Ozi Adi [1 ,2 ,3 ]
Safitriono, Wahyu Nur [4 ]
Maharani, Dyah Ellyawati Kusumaningtyas [4 ]
Febiana, Amalia [5 ]
Wibowo, Fajar Rakhman [5 ]
机构
[1] Acad Sinica, Taiwan Int Grad Program, Sustainable Chem Sci & Technol, Taipei 11529, Taiwan
[2] Acad Sinica, Inst Chem, Taipei 11529, Taiwan
[3] Natl Taiwan Univ, Coll Engn, Dept Chem Engn, Taipei 10617, Taiwan
[4] Univ Sebelas Maret, Master Program Chem, Surakarta 57126, Indonesia
[5] Univ Sebelas Maret, Fac Math & Nat Sci, Dept Chem, Surakarta 57126, Indonesia
关键词
Antioxidant; Biomaterials; Drug delivery; Mesoporous materials; Nanoparticles; WATER EMULSIONS; DELIVERY; NANOEMULSION; CYTOTOXICITY; ANTIOXIDANT; STABILITY; LECITHIN; SYSTEM;
D O I
10.1016/j.fbio.2023.102793
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Low water solubility leading to poor bioavailability has an impact on the decreasing of curcumin uptake in the body, resulting in a deficiency of its medicinal benefits. This study aims to overcome the limitations of curcumin by formulating a nano-emulsion called curcumin emulsion (CE). Furthermore, in order to improve the physi-cochemical properties and drug release features, the CE was encapsulated within chitosan-assembled mesoporous silica nanoparticles (Chi@SiO2@CE). This material was prepared using a one-pot method and was characterized by Attenuated-total reflectance (ATR-FTIR), Particle Size Analyzer (PSA), Thermogravimetric analysis (TGA), N2 adsorption-desorption, Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM). Additionally, antioxidant activity and in vitro drug release were also conducted. The study demonstrated that CE has strong antioxidant activity (IC50 = 14.14 & mu;M) compared to curcumin alone. Additionally, the Chi@SiO2@CE exhibited pH-controlled release behavior, with less than 20% release of curcumin under an artificial gastric environment and 50% release under pH 7.4 conditions within 24 h. Therefore, this research suggest that Chi@SiO2@CE material has potential as a pH-responsive drug delivery material.
引用
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页数:12
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