Citations
1 publicationsPublications from researchers using this productDescription
Amikacin is an aminoglycoside antibiotic[1]. Amikacin is used to treat a variety of infections caused by Gram-negative bacteria[2]. Amikacin can enter bacterial cells and bind to their ribosomes. By interfering with bacterial protein synthesis, it prevents normal bacterial growth and reproduction, thereby exerting its antibacterial effects [3]. Amikacin is widely used in the treatment of complex urinary tract infections, respiratory infections, and sepsis[4].
In vitro, Amikacin (0.003 - 25mg/mL) treatment of equine joint cells (including chondrocytes, synovial cells, adipose-derived and bone marrow-derived mesenchymal stem cells) induces rapid cell death within 1 hour in a dose-dependent manner. Moreover, the cytotoxicity of Amikacin is not mitigated by the presence of synovial fluid[5]. Amikacin (32mg/L) alone or in combination with 2mg/L Colistin can effectively kill bacteria within biofilms of mature Pseudomonas aeruginosa (PAO1 and CRPAO1) treatment for 24 hours[6].
In vivo, Amikacin (15mg/kg) combined with Imipenem (40mg/kg) administered intraperitoneally every 8 hours is used to treat mice infected with drug-resistant Escherichia coli. The combination of Amikacin and Imipenem significantly reduces the bacterial count in the blood of mice[7]. Amikacin (7.5mg/kg; every 12 hours) combined with Meropenem (200mg/kg; every 8 hours) administered intraperitoneally to mice infected with carbapenem-resistant Enterobacteriaceae (CRE). Compared to Meropenem monotherapy, the combination therapy significantly reduces bacterial density in the thigh muscles of mice and increases survival rates[8].
References:
[1] Ramirez MS, Tolmasky ME. Amikacin: Uses, Resistance, and Prospects for Inhibition. Molecules. 2017 Dec 19;22(12):2267.
[2] Meyer RD. Amikacin. Ann Intern Med. 1981 Sep;95(3):328-32.
[3] Jenkins A, Thomson AH, Brown NM, et al. Amikacin use and therapeutic drug monitoring in adults: do dose regimens and drug exposures affect either outcome or adverse events? A systematic review. J Antimicrob Chemother. 2016 Oct;71(10):2754-9.
[4] Kato H, Hamada Y. Amikacin Therapy in Japanese Pediatric Patients: Narrative Review. Int J Environ Res Public Health. 2022 Feb 10;19(4):1972.
[5] Pezzanite L, Chow L, Soontararak S, et al. Amikacin induces rapid dose-dependent apoptotic cell death in equine chondrocytes and synovial cells in vitro. Equine Vet J. 2020 Sep;52(5):715-724.
[6] Wang Y, Li C, Wang J, et al. The Efficacy of Colistin Combined with Amikacin or Levofloxacin against Pseudomonas aeruginosa Biofilm Infection. Microbiol Spectr. 2022 Oct 26;10(5):e0146822.
[7] Farhan SM, El-Baky RMA, Abdalla S, et al. In Vitro and In Vivo Effect of Amikacin and Imipenem Combinations against Multidrug-Resistant E. coli. Trop Med Infect Dis. 2022 Oct 2;7(10):281.
[8] Hagihara M, Kato H, Yamashita R, et al. In vivo study assessed meropenem and amikacin combination therapy against carbapenem-resistant and carbapenemase-producing Enterobacteriaceae strains. J Infect Chemother. 2020 Jan;26(1):1-7.
Protocol
| Cell experiment [1]: | |
Cell lines | Equine chondrocytes, synovial cells, bone marrow-derived mesenchymal stem cells (BMD-MSC), and adipose-derived mesenchymal stem cells (AD-MSC). |
Preparation Method | Cells were harvested from three donor horses and plated in triplicate wells for 48 hours prior to the addition of Amikacin(0.003 to 25mg/mL). Cells were maintained in complete DMEM media. |
Reaction Conditions | 0.003 to 25mg/mL; 12h |
Applications | Amikacin induced rapid, dose-dependent cytotoxic effects on all cell types, primarily through apoptosis. Amikacin exposure decreased cellular metabolism and mitochondrial mass, and suppressed cell proliferation. |
| Animal experiment [2]: | |
Animal models | Neutropenic ICR Swiss mice |
Preparation Method | Mice were intramuscularly inoculated with 10⁸cfu/mL of carbapenem-resistant Enterobacteriaceae (CRE) strains, followed by subcutaneous administration of Meropenem (200mg/kg every 8 hours) and Amikacin (7.5mg/kg every 12 hours) either alone or in combination. |
Dosage form | 7.5mg/kg; s.c. |
Applications | The combination therapy of Meropenem and Amikacin significantly reduced bacterial density in the thigh muscles and increased survival rates compared to Meropenem monotherapy. |
References: | |
Product Documents
Chemical Properties
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility
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