• Gentamicin sulfate, USP packaged and labeled.

click on thumbnail to zoom
SKU: G006

Size  
Quantity:
  Click 'Bulk Order' for 10 or more
Price: make selection(s)
Description

Gentamicin Sulfate, USP is an aminoglycoside antibiotic complex discovered in 1963 derived from fermentation of  Micromonospora purpurea or M. echinospora.  Gentamicin is composed of different components including Gentamicin C complex  (gentamicin C1gentamicin C1a, and gentamicin C2) which makes  up 80% of the compound and has the highest antibacterial activity, along with Gentamicin A, B, X, and a few others which make up the remaining 20% of Gentamicin and have lower antibiotic activity.  Gentamicin Sulfate is suitable for use in cell culture to prevent and control bacterial contamination and the compound is soluble in water (50 mg/ml).

Gentamicin Sulfate, USP conforms to United States Pharmacopoeia specifications. 

For more Gentamicin products, click here.

    CAS Number

    1405-41-0

    Mechanism of Action

    Aminoglycosides are a widespread and versatile group of bioactive natural products. They target the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from acceptor to donor. This results in an inability to read mRNA ultimately producing a faulty or nonexistent protein.

    Storage Conditions

    2-8°C

    Tariff Code

    2941.90.1010

    Spectrum

    Gentamicin Sulfate is a broad-spectrum antibiotic targeting Gram-positive and Gram-negative bacteria. It is effective against several strains of Mycoplasma. It also combats certain β-lactam sensitive VRE or vancomycin resistant Enterococcus; a "superbug."

Applications

    Cancer Applications

    Ovarian melanoma tumor cells was studied in 3D culture and Gentamicin Sulfate was used to prevent contamination when studying ovarian cell lines (OVCAR3, SKOV3, 222, EG, and A2780-PAR ) and normal ovarian surface epithelial cell lines (HIO 1120 and HIO 180). Tumor cells formed matrix-rich tubular networks containing channels surrounding spheroids of tumor cells, and this network may represent either a primitive microcirculatory-like network, or a remodeled vascularized portion of a tumor (Sood et al, 2001).

    Eukaryotic Cell Culture Applications

    Gentamicin was found to inhibit Glucose-6-phosphate dehydrogenase (G6PD) enzyme activity in rat erythrocytes (Temel et al, 2018).

    A bovine macrophage (Bomac) cell line was used but proved to be contaminated with BVDV (bovine viral diarrhea virus).  Both infected and cured cells were tested for uptake of Mycoplasma bovis in an in vitro model to dissect the molecular and cellular details of bovine mycoplasmosis using Gentamicin from TOKU-E in a gentamicin protection assay (Burgi et al, 2018).

    Gentamicin is an effective in vitro bacterial inhibitor that is nontoxic in tissue culture. It was non-toxic to RMK (Rhesus monkey kidney), HeLa, amnion, GMK, and WI-38 cell lines. It can also be used in virus tissue culture as it does not inhibit virus replication. (Rudin et al, 1970).

    Porcine intestinal epithelial cell line IPEC-J2 cell monolayers were used to study the toxicity of Gentamicin in cell culture.  Authors found it did not affect IPEC-J2 cell monolayer integrity via the disruption of cell membranes and did not increase the incidence of toxic effects related to membrane permeation (Gyetvai et al, 2015).


    When primary cultures of embryonic rat fibroblasts are exposed to Gentamicin, they develop typical lysosomal phospholipidosis characterized by decreased sphingomyelinase activity, increase in lipid phosphorus, and appearance of 'myeloid bodies' in lysosomes. However, when inhibitors of cysteine proteinases were used (leupeptin, E-64), authors observed a protective effect which could be due to increased sphingomyelinase activity (Montenez et al, 1984).

    Microbiology Applications

    Gentamicin sulfate is commonly used as a selective agent to select for cells containing the gentamicin resistance gene, aacj-AaphD or aacC1. Gentamicin sulfate is generall used at a concentration of 10 - 50 µg/mL for eukaryotic cell culture and 15 ug/ml for prokaryotic cells.

     

    Media Supplements

    Gentamicin can be used as a selective agent in several types of isolation media:

    Columbia Blood Agar - Gardnerella vaginalis Selective Supplement

    VRE Medium - VRE Selective Supplement

    Burkholderia cepacia Agar Base - Burkholderia cepacia Selective Supplement

    Plant Biology Applications

    Gentamicin sulfate inhibited differentiation of tracheary elements in pith parenchyma cells in cultures of romaine lettuce (Lactuca sativa L. var. Romana) at concentrations of 50-100 µg/ml. Similar results were obtained with cultured explants of Jerusalem artichoke tuber (Helianthus tuberosus L.). Callus formation was suppressed with increasing levels of Gentamicin Sulfate in both tissue systems. When studying cell division or xylem differentiation in culture, it is best to use ≤ 10 µg/ml.

Specifications

    Form

    Powder

    Appearance

    White or almost white powder

    Source

    Micromonospora spp.

    Impurity Profile

    Gentamicin C1: 25.0 -50.0%
    Gentamicin C1a: 10.0 - 35.0%
    Gentamicin C2a + C2: 25.0 - 55.0%

    Water Content (Karl Fischer)

    Loss on drying: <18.0%

    pH

    3.5 - 5.5

    Optical Rotation

    +107° - +121°

    Assay

    (on the dry basis): >590 µg/mL

    Loss on Drying

    Not more than 18.0%

    Residue On Ignition

    Not more than 1.0%

    Residual Solvents

    Methanol: Not more than 1.0%

    Endotoxin

    Not more than 0.71 EU/mg

References

    References

    Bürgi N, Josi C, Bürki S and Schweizer, Pilo P (2018) Mycoplasma bovis co-infection with bovine viral diarrhea virus in bovine macrophages. Vet. Res. 49(1):2. PMID 29316971 

    Gyetvai B et al (2015)  Gentamicin sulphate permeation through porcine intestinal epithelial cell monolayer. Act. Vet. Hung. 63(1): 60-68  PMID 25655415

    Kadurugamuwa JL, Clarke AJ and Beveridge TJ (1993) Surface action of gentamicin on Pseudomonas aeruginosa. J. Bacteriol 175(18):5798-5805 PMID 8376327

    Martin NL and Bevridge TJ (1986) Gentamicin interaction with Pseudomonas aeruginosa. Antimicrob. Agents Chemother. 29(6):1079-1087 PMID 2425732

    Montenez JP, Kishore BK, Maldaque P and Tulkens PM (1984) Leupeptin and E-64, inhibitors of cysteine proteinases, prevent gentamicin-induced lysosomal phospholipidosis in cultured rat fibroblasts. Toxicol Lett. 73(3):201-208 PMID 8091428

    Rudin A, Healey A, Phillips CA, Gump DW and Forsyth BR (1970) Antibacterial activity of gentamicin sulfate in tissue culture. Appl. Microbiol. 20(6):989-990. PMID 4992660

    Sood AK (2001) Molecular determinants of ovarian cancer plasticity. Am. J. Pathol. 158(4):1279-1288. PMID 11290546

    Temel Y, Ayna A, Shafeeq IH and Ciftci M (2018) In vitro effects of some antibiotics on glucose-6-phosphate dehydrogenase from rat (Rattus norvegicus) erythrocyte. Drug and Chemical Toxicol. DOI: 10.1080/01480545.2018.1481083

    Wan J et al (1994) Intravesical instillation of gentamicin sulfate: In vitro, rat, canine, and human studies. Urology 43(4):531-536. PMID 8154077

Other Items In This Category