COMBINATION OF CIPROFLOXACIN AND SILVER NANOPARTICLES FOR TREATMENT OF MULTI-DRUG RESISTANT PSEUDOMONAS AERUGINOSA IN EGYPT

G. Mohamed
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Abstract

Pseudomonas aeruginosa was the most frightening pathogen that emergence in health facilities with increasing antibiotic resistance. Nanoparticles have reported as non-antibiotic therapeutic agents, that are highly effective in the treatment of P. aeruginosa infections. Combination therapy of nanoparticles and antibiotics considered an alternative therapeutic approach for restoring antibiotic activity. To achieve that goal, we used the synthetic silver nanoparticles in a combined form with ciprofloxacin against MDR P. aeruginosa. Fifty bacterial isolates that collected from different infection sites were confirmed as P. aeruginosa by detection of algD gene and Exotoxin A genes. Antibiotic sensitivity of P. aeruginosa strains was assessed by single diskdiffusion method. The most prevelant phenotype among P. aeruginosa were recorded. The synthetic nanoparticles AgNPs and ZnONPs were tested against all P. aeruginosa strains. minimum inhibitory conc (MIC) of ciprofloxacin and AgNPS was determined using microdilution method for 24 selected P. aeruginosa strains and in the range from 160-1280, 6-12mg/l, respectively. In vitro, the synergistic activity of ciprofloxacin and AgNPs was achieved in all combinations. Our finding approved that combination therapy depend on using nanoparticles considered a promising tool used to restore the activity of antibiotics.
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环丙沙星联合纳米银治疗埃及多重耐药铜绿假单胞菌
铜绿假单胞菌是卫生机构中出现的最可怕的病原体,抗生素耐药性日益增强。纳米颗粒作为非抗生素治疗剂,在铜绿假单胞菌感染的治疗中非常有效。纳米颗粒和抗生素的联合治疗被认为是恢复抗生素活性的替代治疗方法。为了实现这一目标,我们将合成银纳米颗粒与环丙沙星结合使用,以对抗耐多药铜绿假单胞菌。从不同感染部位分离的50株细菌,通过检测藻d基因和外毒素A基因,证实为铜绿假单胞菌。采用单片扩散法对铜绿假单胞菌进行药敏试验。记录了铜绿假单胞菌中最常见的表型。对合成的纳米AgNPs和ZnONPs进行了抗铜绿假单胞菌试验。采用微量稀释法测定了24株铜绿假单胞菌在160 ~ 1280、6 ~ 12mg/l范围内对环丙沙星和AgNPS的最小抑制浓度(MIC)。在体外,环丙沙星和AgNPs在所有组合下均具有协同作用。我们的研究结果证实,联合治疗依赖于使用纳米颗粒,这被认为是一种有前途的工具,用于恢复抗生素的活性。
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FORMULATION AND CHARACTERIZATIONS OF ROSUVASTATIN LOADED NANOSUSPENSION COMPARATIVE EVALUATION OF ANTICANCER AND ANTIBACTERIAL ACTIVITIES OF ENDOPHYTIC FUNGUS-DERIVED ZNO NANOPARTICLES AND CHEMICALLY SYNTHESIZED ZNO NANOPARTICLES PREPARATION AND EVALUATION OF SUSTAINED RELEASE MATRIX FORMULATIONS OF VORICONAZOLE PIM KINASES INHIBITORS AND PYRIMIDINE-BASED ANTICANCER AGENTS RECENT ADVANCES ON PYRIMIDINE DERIVATIVES AS ANTICANCER AGENTS.
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