Preparation and in vitro evaluation of novel cross-linked chondroitin sulphate nanoparticles by aluminium ions for encapsulation of green tea flavonoids

被引:3
作者
Varshosaz, Jaleh [1 ,2 ]
Asefi, Hajar [3 ]
Hashemi-Beni, Batool [4 ]
Ghaffari, Solmaz [3 ]
Davoudi, Ali [5 ]
机构
[1] Isfahan Univ Med Sci, Sch Pharm, Dept Pharmaceut, Esfahan, Iran
[2] Isfahan Univ Med Sci, Novel Drug Delivery Syst Res Ctr, Esfahan, Iran
[3] Islamic Azad Univ IAUPS, Pharmaceut Sci Branch, Dept Med Nanotechnol, Tehran, Iran
[4] Isfahan Univ Med Sci, Sch Med, Dept Anat Sci, Esfahan, Iran
[5] Shiraz Univ Med Sci, Dept Med Nanotechnol, Shiraz, Iran
关键词
nanoparticles; encapsulation; biomedical materials; particle size; nanofabrication; nanomedicine; electrokinetic effects; cellular biophysics; polymer blends; molecular biophysics; molecular configurations; biochemistry; curing; surface morphology; scanning electron microscopy; differential scanning calorimetry; dyes; precipitation; in vitro evaluation; cross-linked chondroitin sulphate nanoparticles; aluminium ions; green tea flavonoids; sulphated glycosaminoglycan biopolymer; sugars; catechin; ionic gelation method; cross-linking agent concentration; curing time; size; 176; nm; time; 24; h; calcium precipitation; 3-fold proliferation effect; antioxidant activity; chatechin loaded chondroitin sulphate NPs; Alizarin red staining; osteoblasts; calcification; 3-[4; 5-dimethylthiazol-2-yl]-2; 5-diphenyl tetrazolium bromide assay; mesenchymal stem cells; cell viability; chelating activity; thermal behaviour; release efficiency; loading efficiency; zeta potential; stirring speed; MESENCHYMAL STEM-CELLS; OSTEOGENIC DIFFERENTIATION; CHITOSAN NANOPARTICLES; BONE-MARROW; EGCG; DELIVERY; CYTOTOXICITY; CATECHINS; THERAPY;
D O I
10.1049/iet-nbt.2017.0298
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chondroitin sulphate is a sulphated glycosaminoglycan biopolymer composed over 100 individual sugars. Chondroitin sulphate nanoparticles (NPs) loaded with catechin were prepared by an ionic gelation method using AlCl3 and optimised for polymer and cross-linking agent concentration, curing time and stirring speed. Zeta potential, particle size, loading efficiency, and release efficiency over 24h (RE24%) were evaluated. The surface morphology of NPs was investigated by scanning electron microscopy and their thermal behaviour by differential scanning calorimetric. Antioxidant effect of NPs was determined by chelating activity of iron ions. The cell viability of mesenchymal stem cells was determined by 3-[4, 5-dimethylthiazol-2-yl]-2, 5-diphenyl tetrazolium bromide assay and the calcification of osteoblasts was studied by Alizarin red staining. The optimised NPs showed particle size of 176nm, zeta potential of -20.8mV, loading efficiency of 93.3% and RE24% of 80.6%. The chatechin loaded chondroitin sulphate NPs showed 70-fold more antioxidant activity, 3-fold proliferation effect and higher calcium precipitation in osteoblasts than free catechin.
引用
收藏
页码:757 / 763
页数:7
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