头孢唑林
Zeta电位
壳聚糖
肺炎克雷伯菌
抗菌剂
化学
细菌生长
纳米颗粒
微生物学
抗生素
大肠杆菌
纳米技术
材料科学
细菌
生物
生物化学
有机化学
基因
遗传学
作者
Bushra Jamil,Huma Habib,Shahid Ahmad Abbasi,Habib Nasir,Abdur Rahman,Asma Rehman,Habib Bokhari,Muhammad Imran
标识
DOI:10.1016/j.carbpol.2015.09.078
摘要
Antibiotic resistance against Gram-negative microbes is considered as an alarming phenomenon that needs to be addressed urgently to develop better therapeutic solutions. The aim of the present research work was to investigate and develop cefazolin loaded chitosan nanoparticles (CSNPs) as a potential tool against multidrug resistant pathogens. Empty and drug loaded CSNPs were prepared by ionic gelation method. It was observed by Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) based studies that CSNPs were less than 100 nm in size and displayed homogeneity both in shape and size. Encapsulation of cefazolin has not increased the size of nano systems. Zeta sizer results revealed that both systems have positive zeta potential of more or less +50 mV, thus contributing towards a stable formulation. Encapsulation efficiency was directly proportional to the increase in the concentration of antibiotic (28-62%). Furthermore, growth kinetics study had demonstrated excellent antimicrobial potential of cefazolin loaded CSNPs against multi drug resistant Klebsiella pneumoniae, Pseudomonas aeroginosa and Extended Spectrum Beta Lactamase (ESBL) positive Escherichia coli.
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