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Related Concept Videos

Combined Effects of Drugs: Synergism01:27

Combined Effects of Drugs: Synergism

Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
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Antibiotic Selection

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Pharmacokinetic–Pharmacodynamic Relationship: Influence of Elimination Half-Life on Effect Duration01:23

Pharmacokinetic–Pharmacodynamic Relationship: Influence of Elimination Half-Life on Effect Duration

Drug elimination from the body primarily occurs through metabolic and excretion pathways. Hepatic metabolism transforms lipophilic drugs into hydrophilic forms for excretion, typically via enzymatic processes classified as phase I (modification) and phase II (conjugation). Renal excretion eliminates drugs and metabolites through filtration and secretion in the kidneys. Impairment in liver or kidney function can hinder these processes, delaying drug clearance and extending the drug’s half-life.
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Inhibitors of Bacterial Protein Synthesis

Aminoglycosides constitute a highly potent class of bactericidal antibiotics that exert their antimicrobial effects by targeting the bacterial ribosome, specifically disrupting protein synthesis. These polycationic molecules consist of amino-modified sugars linked via glycosidic bonds to an aminocyclitol core such as 2-deoxystreptamine or streptamine. Their strong positive charges facilitate tight binding to the negatively charged phosphate backbone of ribosomal RNA (rRNA), primarily at the 16S...
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Penicillin, one of the earliest and most widely used antibiotics, is produced industrially by the filamentous fungus Penicillium chrysogenum. Large stirred-tank bioreactors ranging from tens to hundreds of thousands of liters maintain tightly controlled temperature, pH, and dissolved oxygen conditions to support fungal metabolism and maximize antibiotic yield. Penicillin is a secondary metabolite, synthesized primarily during the stationary growth phase, which requires a carefully managed...
Microbiota Modulation by Antibiotics01:21

Microbiota Modulation by Antibiotics

Antibiotics have revolutionized modern medicine by saving countless lives from bacterial infections. However, their widespread use has inadvertently harmed the delicate balance of the human gut microbiota. The gut microbiota, a complex community of bacteria, archaea, viruses, and fungi, plays a vital role in regulating metabolism, immune responses, and maintaining intestinal health. Antibiotics, especially broad-spectrum types, disrupt this ecosystem by eradicating both harmful and beneficial...

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Related Experiment Video

Updated: Jul 1, 2026

Quadruple-Checkerboard: A Modification of the Three-Dimensional Checkerboard for Studying Drug Combinations
11:15

Quadruple-Checkerboard: A Modification of the Three-Dimensional Checkerboard for Studying Drug Combinations

Published on: July 24, 2021

[Optimization of antibiotics in combination].

Li-Hua Zhang1, Ling-Feng Wang, Zhao-Yan Meng

  • 1Department of Pharmacy, Third Affiliated Hospital of Inner Mongolia Medical College, Baotou 014010, PR China.

Zhonghua Shao Shang Za Zhi = Zhonghua Shaoshang Zazhi = Chinese Journal of Burns
|September 13, 2008
PubMed
Summary

Combining antibiotics like amikacin and ceftazidime enhances antibacterial activity against Pseudomonas aeruginosa. Pharmacokinetic/pharmacodynamic analysis helps optimize treatment regimens for improved clinical efficacy.

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High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method
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Antimicrobial Synergy Testing by the Inkjet Printer-assisted Automated Checkerboard Array and the Manual Time-kill Method

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Last Updated: Jul 1, 2026

Quadruple-Checkerboard: A Modification of the Three-Dimensional Checkerboard for Studying Drug Combinations
11:15

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Published on: July 24, 2021

High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method
07:51

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Antimicrobial Synergy Testing by the Inkjet Printer-assisted Automated Checkerboard Array and the Manual Time-kill Method
12:03

Antimicrobial Synergy Testing by the Inkjet Printer-assisted Automated Checkerboard Array and the Manual Time-kill Method

Published on: April 18, 2019

Area of Science:

  • Microbiology
  • Pharmacology
  • Infectious Diseases

Background:

  • Pseudomonas aeruginosa is a significant opportunistic pathogen.
  • Antibiotic resistance necessitates novel treatment strategies.
  • Combination therapy is a key approach to combat resistant bacteria.

Purpose of the Study:

  • To evaluate in vitro antibacterial activity of Ciprofloxacin and Amikacin combined with beta-lactams against Pseudomonas aeruginosa.
  • To optimize antibiotic treatment regimens using pharmacokinetic/pharmacodynamic (PK/PD) principles and drug sensitivity testing.

Main Methods:

  • Checkerboard titration and broth dilution methods were used to determine minimal inhibitory concentrations (MICs).
  • Fractional inhibitory concentration (FIC) index was calculated to assess synergistic effects.
  • Pharmacokinetic/pharmacodynamic (PK/PD) parameters (Cmax/MIC and T>MIC) were evaluated.

Main Results:

  • Amikacin and Ceftazidime combination demonstrated synergistic effects in 57.6% of strains.
  • Ciprofloxacin combined with Ceftazidime, Cefepime, Imipenem/Cilastatin, or Meropenem showed synergistic or additive effects.
  • PK/PD evaluation identified Cmax/MIC for aminoglycosides/fluoroquinolones and T>MIC for beta-lactams as key parameters.

Conclusions:

  • Antibiotic combinations significantly reduce MICs and enhance antibacterial activity.
  • Combinations primarily result in synergistic or additive effects, with no observed antagonistic effects.
  • PK/PD analysis is crucial for planning optimal combination regimens and improving clinical outcomes.