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https://doi.org/10.5599/admet.4.2.286

Dose optimization of ceftriaxone-vancomycin combination using fractional inhibitory concentration kinetics in resistant bacteria

Vishnu D Sharma   ORCID icon orcid.org/0000-0003-0517-4336 ; Venus Medicine Research Centre, Hill Top Estate, Bhatoli Kalan, H.P., India
Aman Singla ; Venus Medicine Research Centre, Hill Top Estate, Bhatoli Kalan, H.P., India
Manu Chaudhary ; Venus Medicine Research Centre, Hill Top Estate, Bhatoli Kalan, H.P., India
Mukesh Kumar ; Venus Medicine Research Centre, Hill Top Estate, Bhatoli Kalan, H.P., India
Anuj Bhatnagar ; Venus Medicine Research Centre, Hill Top Estate, Bhatoli Kalan, H.P., India
Shailesh Kumar ; Venus Medicine Research Centre, Hill Top Estate, Bhatoli Kalan, H.P., India
Manish Taneja ; Venus Medicine Research Centre, Hill Top Estate, Bhatoli Kalan, H.P., India

Puni tekst: engleski, pdf (959 KB) str. 241-260 preuzimanja: 1.638* citiraj
APA 6th Edition
Sharma, V.D., Singla, A., Chaudhary, M., Kumar, M., Bhatnagar, A., Kumar, S. i Taneja, M. (2016). Dose optimization of ceftriaxone-vancomycin combination using fractional inhibitory concentration kinetics in resistant bacteria. ADMET and DMPK, 4 (3), 241-260. https://doi.org/10.5599/admet.4.2.286
MLA 8th Edition
Sharma, Vishnu D, et al. "Dose optimization of ceftriaxone-vancomycin combination using fractional inhibitory concentration kinetics in resistant bacteria." ADMET and DMPK, vol. 4, br. 3, 2016, str. 241-260. https://doi.org/10.5599/admet.4.2.286. Citirano 16.10.2021.
Chicago 17th Edition
Sharma, Vishnu D, Aman Singla, Manu Chaudhary, Mukesh Kumar, Anuj Bhatnagar, Shailesh Kumar i Manish Taneja. "Dose optimization of ceftriaxone-vancomycin combination using fractional inhibitory concentration kinetics in resistant bacteria." ADMET and DMPK 4, br. 3 (2016): 241-260. https://doi.org/10.5599/admet.4.2.286
Harvard
Sharma, V.D., et al. (2016). 'Dose optimization of ceftriaxone-vancomycin combination using fractional inhibitory concentration kinetics in resistant bacteria', ADMET and DMPK, 4(3), str. 241-260. https://doi.org/10.5599/admet.4.2.286
Vancouver
Sharma VD, Singla A, Chaudhary M, Kumar M, Bhatnagar A, Kumar S i sur. Dose optimization of ceftriaxone-vancomycin combination using fractional inhibitory concentration kinetics in resistant bacteria. ADMET and DMPK [Internet]. 2016 [pristupljeno 16.10.2021.];4(3):241-260. https://doi.org/10.5599/admet.4.2.286
IEEE
V.D. Sharma, et al., "Dose optimization of ceftriaxone-vancomycin combination using fractional inhibitory concentration kinetics in resistant bacteria", ADMET and DMPK, vol.4, br. 3, str. 241-260, 2016. [Online]. https://doi.org/10.5599/admet.4.2.286

Sažetak
The notorious Staphylococcus aureus resistant strains with ever changing resistance patterns have limited treatment options and have led to substantial number of deaths. Almost dried antibiotic pipeline has led us to look into combinations of already approved antibiotics for tackling rising incidence of antibacterial resistance. Recommended use of vancomycin and ceftriaxone together for treating severe infections involving resistant S. aureus is limited by dose adjustments and different dose frequencies. We have developed a pharmacodynamically synergistic fixed dose combination (FDC) of ceftriaxone and vancomycin (2:1), for eliminating individual component dose adjustments and frequencies. For identification of optimum exposure-response of FDC, one compartment in vitro system was used for dose escalation, fractionation and dose-response studies. The in-silico pharmacokinetic/pharmacodynamic (PK/PD) modeling, simulations and validations were done. The results suggested % T>MICcomb (percentage of time fractional inhibitory concentrations of the drugs combined remained above the MICcomb [minimum inhibitory concentration for FDC]) followed by AUCcomb/MICcomb (ratio of area under fractional inhibitory curves to MICcomb) can predict the exposure (dose of FDC)-response (reduction in bacterial load) relationships effectively (r2 >0.9). Total exposure of 6 g in two divided doses (3 g each) was identified to be optimum. Monte Carlo simulations were performed to evaluate the effect of increasing doses against different MICs. Clinical breakpoint of the FDC was identified to be 4 µg/mL, which was 2 fold higher than that of vancomycin suggesting better antibacterial coverage.

Ključne riječi
PK/PD modelling; Fixed dose combination; Monte Carlo simulations; Antibacterial resistance

Hrčak ID: 167045

URI
https://hrcak.srce.hr/167045

Posjeta: 1.886 *