Preparation, characterization, and evaluation of antibacterial and cytotoxic activity of chitosan-polyethylene glycol nanoparticles loaded with amoxicillin as a novel drug delivery system

被引:5
作者
Guncum, Enes [1 ]
Isiklan, Nuran [2 ]
Anlas, Ceren [3 ]
Bulut, Elif [4 ]
Bakirel, Tulay [3 ]
机构
[1] Kirikkale Univ, Fac Vet Med, Dept Pharmacol & Toxicol, Yahsihan, Turkiye
[2] Kirikkale Univ, Fac Sci & Arts, Dept Chem, Yahsihan, Turkiye
[3] Istanbul Univ Cerrahpasa, Fac Vet Med, Dept Pharmacol & Toxicol, Istanbul, Turkiye
[4] Republ Turkey Minist Hlth, Dept Zoonot & Vector Borne Dis, Ankara, Turkiye
关键词
Amoxicillin; nanoparticles; chitosan; polyethylene glycol; antibacterial activity; cytotoxicity; IN-VITRO RELEASE; PEG NANOPARTICLES; TARGETED DELIVERY; ANTITUMOR-ACTIVITY; PARTICLE-SIZE; PROTEIN; ACID); BIOCOMPATIBILITY; 5-FLUOROURACIL; CLARITHROMYCIN;
D O I
10.1080/09205063.2023.2179269
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study, nanoparticles of amoxicillin (AMX) were prepared using chitosan (CHI) and polyethylene glycol (PEG). The physicochemical properties of the particles were investigated by FT-IR, DSC, SEM, and zeta potential analyses. The nanoparticles showed a spherical shape, and the average size of formulations was within the range of 696.20 +/- 24.86 - 359.53 +/- 7.41 nm. Zeta potential data demonstrated that the formulations had positive surface charges with a zeta potential range of 21.38 +/- 2.28 - 7.73 +/- 1.66 mV. FTIR analysis showed that the drug was successfully entrapped in the nanoparticles. DSC results suggested that the drug was present in amorphous form in the polymer matrix. In vitro release studies demonstrated that the release pattern consisted of two phases, with an initial burst release followed by a controlled and sustained release. The MTT assay results on mouse fibroblast cell line indicated that the prepared formulations did not affect the viability of the cells. In the in vitro antibacterial activity test, it was found that the drug-loaded nanoparticles have AMX-equivalent antibacterial activity against E. coli, and S. aureus. These findings revealed that the obtained nanoparticles might be a promising and safe nanocarrier system for efficient delivery of AMX.
引用
收藏
页码:1660 / 1682
页数:23
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