DescriptionCurator's Comment: description was created based on several sources, including
http://reference.medscape.com/drug/neo-fradin-myciguent-neomycin-po-342515
Curator's Comment: description was created based on several sources, including
http://reference.medscape.com/drug/neo-fradin-myciguent-neomycin-po-342515
Neomycin is an aminoglycoside antibiotic found in many topical medications such as creams, ointments, and eye drops. In vitro tests have demonstrated that neomycin is bactericidal and acts by inhibiting the synthesis of protein in susceptible bacterial cells. It is effective primarily against gram-negative bacilli but does have some activity against gram-positive organisms. Neomycin is active in vitro against Escherichia coli and the Klebsiella-Entero. Topical uses include treatment for superficial eye infections caused by susceptible bacteria (used in combination with other anti-infective), treatment of otitis externa caused by susceptible bacteria, treatment or prevention of bacterial infections in skin lesions, and use as a continuous short-term irrigant or rinse to prevent bacteriuria and gram negative rod bacteremia in bacteriuria patients with indwelling catheters. May be used orally to treat hepatic encephalopathy, as a perioperative prophylactic agent, and as an adjunct to fluid and electrolyte replacement in the treatment of diarrhea caused to enter pathogenic E. coli (EPEC). Neomycin sulfate has been shown to be effective adjunctive therapy in hepatic coma by reduction of the ammonia forming bacteria in the intestinal tract. The subsequent reduction in blood ammonia has resulted in neurologic improvement. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Neomycin Sulfate Oral Solution and other antibacterial drugs, susceptible bacteria should use Neomycin Sulfate Oral Solution only to treat or prevent infections that are proven or strongly suspected to be caused. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Neomycin binds to four nucleotides of 16S rRNA and a single amino acid of protein S12. This interferes with decoding site near nucleotide 1400 in 16S rRNA of 30S subunit. This region interacts with the wobble base in the anticodon of tRNA. This leads to interference with the initiation complex, misreading of mRNA so incorrect amino acids are inserted into the polypeptide leading to nonfunctional or toxic peptides and the breakup of polysomes into nonfunctional monosomes
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2363135 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18060665 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Preventing | CVP TRIPLE ANTIBIOTIC Approved UseUses: first aid to help prevent infection in minor: cuts, scrapes, burns Launch Date1995 |
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Palliative | NEO-FRADIN Approved UseHepatic coma (portal-systemic encephalopathy): Neomycin sulfate has been shown to be effective adjunctive therapy in hepatic coma by reduction of the ammonia forming bacteria in the intestinal tract. The subsequent reduction in blood ammonia has resulted in neurologic improvement. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Neomycin Sulfate Oral Solution and other antibacterial drugs, Neomycin Sulfate Oral Solution should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Launch Date2001 |
PubMed
Title | Date | PubMed |
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Aluminum is a weak agonist for the calcium-sensing receptor. | 1999 May |
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A simple classification method for residual antibiotics using E. coli cells transformed by the calcium chloride method and drug resistance plasmid DNA. | 2001 |
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Split-thickness skin graft donor site dressing: preliminary results of a controlled, clinical comparative study of MEBO and Sofra-Tulle. | 2001 Jan |
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Agenesis of the skull bones. | 2001 Jul |
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Inhibition of the HIV-1 rev-RRE complex formation by unfused aromatic cations. | 2001 May |
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A hole in the drum. An overview of tympanic membrane perforations. | 2002 Aug |
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[Synthesis of biomimetic analogs of neomycin B]. | 2002 Jul |
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Inhibition of protein synthesis by aminoglycoside-arginine conjugates. | 2002 Oct |
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Delayed hypersensitivity reaction to topical aminoglycosides in patients undergoing middle ear surgery. | 2002 Oct |
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Insulin induces cobalt uptake in a subpopulation of rat cultured primary sensory neurons. | 2003 Nov |
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A new class of branched aminoglycosides: pseudo-pentasaccharide derivatives of neomycin B. | 2003 Oct 2 |
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A peptide inhibitor of c-Jun N-terminal kinase protects against both aminoglycoside and acoustic trauma-induced auditory hair cell death and hearing loss. | 2003 Sep 17 |
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Aminoglycoside antibiotics reduce glucose reabsorption in kidney through down-regulation of SGLT1. | 2003 Sep 5 |
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Inhibition of the proteolytic activity of anthrax lethal factor by aminoglycosides. | 2004 Apr 21 |
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Efficacy and safety of topical ciprofloxacin/dexamethasone versus neomycin/polymyxin B/hydrocortisone for otitis externa. | 2004 Aug |
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The use of perioperative Sofradex eardrops in preventing tympanostomy tube blockage: a prospective double-blinded randomized-controlled trial. | 2004 Dec |
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Lipoprotein lipase in hemodialysis patients: indications that low molecular weight heparin depletes functional stores, despite low plasma levels of the enzyme. | 2004 Nov 3 |
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[The effectiveness of some methods in eliminating bacteria from the root canal of a tooth with chronic apical periodontitis]. | 2005 |
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Neamine inhibits xenografic human tumor growth and angiogenesis in athymic mice. | 2005 Dec 15 |
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Targeted infection of HIV-1 Env expressing cells by HIV(CD4/CXCR4) vectors reveals a potential new rationale for HIV-1 mediated down-modulation of CD4. | 2005 Dec 21 |
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Introduction of a substituent at the 5"-position of N-Boc neomycin B under Mitsunobu reaction conditions. | 2005 Jun 7 |
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Contact allergy to neomycin sulfate: results of a multifactorial analysis. | 2005 Oct |
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Analysis of neomycin sulfate and framycetin sulfate by high-performance liquid chromatography using evaporative light scattering detection. | 2005 Sep 16 |
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Neamine derivatives having a nucleobase with a lysine or an arginine as a linker, their synthesis and evaluation as potential inhibitors for HIV TAR-Tat. | 2006 Apr 15 |
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Rapid analysis of native neomycin components on a portable capillary electrophoresis system with potential gradient detection. | 2006 Aug |
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Mixed-type noncompetitive inhibition of anthrax lethal factor protease by aminoglycosides. | 2006 Jul |
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Neonatal deafness results in degraded topographic specificity of auditory nerve projections to the cochlear nucleus in cats. | 2006 Jul 1 |
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Prevalence of methicillin-resistant Staphylococcus aureus (MRSA) in community-acquired primary pyoderma. | 2006 Mar-Apr |
Sample Use Guides
Hepatic coma: 4-12 grams per day given in the following regimen:
1. Withdraw protein from diet. Avoid use of diuretic agents.
2. Give supportive therapy including blood products, as indicated.
3. Give NEO-FRADIN Oral Solution in doses of four to twelve grams of neomycin sulfate per day in divided doses. Treatment should be continued over a period of five to six days during which time protein should be returned incrementally to the diet.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27405449
Curator's Comment: TRMU, tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase, is expressed in both hair cells and HEI-OC-1 cells, and its expression is significantly decreased after 24 h neomycin treatment. Downregulated TRMU expression with siRNA and found that cell death and apoptosis were significantly increased after neomycin injury.
Unknown
Substance Class |
Mixture
Created
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Record UNII |
057Y626693
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Record Status |
Validated (UNII)
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Classification Tree | Code System | Code | ||
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CFR |
21 CFR 333.120
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CFR |
21 CFR 522.1484
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NCI_THESAURUS |
C2363
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EPA PESTICIDE CODE |
6313
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CFR |
21 CFR 333.110
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CFR |
21 CFR 558.364
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Code System | Code | Type | Description | ||
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CHEMBL2109089
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C66227
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7300
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PRIMARY | RxNorm | ||
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215-773-1
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057Y626693
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057Y626693
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m7809
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PRIMARY | Merck Index | ||
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NEOMYCIN SULFATE
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PRIMARY | Description: A white or yellowish white powder; odourless or almost odourless. Solubility: Freely soluble in water; very slightly soluble in ethanol (~750 g/l) TS; practically insoluble in acetone R and ether R. Category: Antiinfective drug. Storage: Neomycin sulfate should be kept in a tightly closed container and protected from light. Additional information: Neomycin sulfate is hygroscopic. Even in the absence of light, it is gradually degraded on exposure to ahumid atmosphere, the decomposition being faster at higher temperatures. An aqueous solution is dextrorotatory. Definition: Neomycin sulfate is a mixture of sulfate salts of substances produced by the growth of Streptomyces fradiae, the maincomponents of which are neomycin B and its stereoisomer neomycin C.Neomycin sulfate contains not less than 600 International Units of neomycin per mg, calculated with reference to the driedsubstance. | ||
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DTXSID4041074
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DBSALT000472
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1458009
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1405-10-3
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SUB22344
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31635
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SUB03409MIG
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757240
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CHEMBL184618
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PRIMARY |
All of the following components must be present:
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PARENT -> SALT/SOLVATE |
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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ACTIVE MOIETY |