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Cefalonium Sale

(Synonyms: 头孢洛宁) 目录号 : GC49274

A cephalosporin antibiotic

Cefalonium Chemical Structure

Cas No.:5575-21-3

规格 价格 库存 购买数量
100 mg
¥1,799.00
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250 mg
¥4,266.00
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500 mg
¥8,103.00
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1 g
¥14,390.00
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Sample solution is provided at 25 µL, 10mM.

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Quality Control & SDS

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产品描述

Cefalonium is a cephalosporin antibiotic.1 It is active against pooled isolates of S. aureus from the milk of lactating dairy cows with subclinical mastitis (MIC90 = 2 µg/ml). Formulations containing cefalonium have previously been used in dry cow therapy in the treatment and prevention of mastitis.

1.Moroni, P., Pisoni, G., Antonini, M., et al.Short communication: Antimicrobial drug susceptibility of Staphylococcus aureus from subclinical bovine mastitis in ItalyJ. Dairy Sci.89(8)2973-2976(2006)

Chemical Properties

Cas No. 5575-21-3 SDF
别名 头孢洛宁
Canonical SMILES [H][C@]12SCC(C[N+]3=CC=C(C(N)=O)C=C3)=C(C([O-])=O)N1C([C@H]2NC(CC4=CC=CS4)=O)=O
分子式 C20H18N4O5S2 分子量 458.5
溶解度 DMSO: 25 mg/ml,DMSO:PBS (pH 7.2) (1:10): 0.09 mg/ml 储存条件 Store at -20°C,protect from light
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.181 mL 10.9051 mL 21.8103 mL
5 mM 0.4362 mL 2.181 mL 4.3621 mL
10 mM 0.2181 mL 1.0905 mL 2.181 mL
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Research Update

Assessment of the Usefulness of Cefapirin and Cefalonium Disks for Susceptibility Testing of Staphylococcus aureus Isolates from Bovine Mastitis

Antibiotics (Basel) 2020 Apr 21;9(4):197.PMID:32326215DOI:10.3390/antibiotics9040197.

Cefapirin (CEP) and Cefalonium (CNM) are first-generation cephalosporins widely used to treat bovine mastitis caused by Gram-positive bacteria including staphylococci. However, disks for susceptibility testing of those drugs in causative bacteria are not available. This study evaluated the efficacy of 10 µg and 30 µg pilot disks of CEP (CEP10 and CEP30) and CNM (CNM10 and CNM30) against 130 Staphylococcus aureus isolates from bovine mastitis. Scattergrams of minimum inhibitory concentrations (MICs) and zone diameters (ZDs) illustrated significant correlations between the MICs and ZDs of CEP10 (r = -0.912), CEP30 (r = -0.933), CNM10 (r = -0.847), and CNM30 (r = -0.807). The analysis by Normalized Resistance Interpretation indicated that the epidemiolocal cut-off value (ECV) of MIC for both cefapirin and Cefalonium is ≤ 0.5 µg/mL, and the ECV of ZD for CEP10, CEP30, CNM10, and CNM30 were ≥ 22 mm, ≥ 25 mm, ≥ 22 mm, and ≥ 29 mm, respectively. We believe that both 10 μg and 30 μg CEP and CNM susceptibility disks will be helpful for guiding the appropriate use of these antibiotics for bovine mastitis. Further studies toward the establishment of clinical breakpoint of CEP and CNM would be needed for their routine use.

[Determination of Cefalonium residue in milk by high performance liquid chromatography-tandem mass spectrometry]

Se Pu 2014 May;32(5):519-23.PMID:25185313DOI:10.3724/sp.j.1123.2013.12028.

An analytical method was developed for the determination of Cefalonium in milk by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). A total of 1 g milk was deproteinized by acetonitrile. The supernatant was transferred into a test tube to be blown dry with N2 at 37 degrees C. Then the residue was dissolved with methanol-0.1% formic acid in water (3:7, v/v). The sample was determined by HPLC-MS/MS after the purification. The chromatographic separation was achieved on a C18 column using 0.1% formic acid in water and acetonitrile as mobile phases with gradient elution. Qualitative and quantitative analyses were achieved by HPLC-MS/MS under positive ionization and multiple reaction monitoring (MRM) mode. Matrix-matched calibration curve was used for the quantification. Good correlation coefficients were obtained (r > 0. 999) in the mass concentration range of 2-200 microg/L. The limit of detection (LOD, S/N > or = 3) was 0.5 microg/kg in milk, and the limit of quantification (LOQ, S/N 10) was 2 microg/kg. The mean recoveries at the four levels of LOQ, 1/2MRL (maximum residue level), MRL, 2MRL were between 78.5% and 86.2%, with the intra-day relative standard deviations (RSDs) of 1.5% to 6.2% and inter-day RSDs of 2.9% to 5.6%. In conclusion, the established method can be applied for the determination of Cefalonium residue in milk.

Identification and quantification of multi-class veterinary drugs and their metabolites in beef using LC-MS/MS

Food Chem 2022 Jul 15;382:132313.PMID:35158273DOI:10.1016/j.foodchem.2022.132313.

The practice of abusing antibiotics to improve livestock growth poses a threat to food safety. To prevent and regulate this, accurate monitoring of residual veterinary drugs (VDs) is required. A method based on QuEChERS with dispersive solid-phase extraction for the determination of multi-class VDs was investigated using selected product ions under optimized multiple reaction monitoring conditions. During the clean-up procedure, chitosan, octadecyl silica, primary-secondary amine, and enhanced matrix removal (EMR)-lipid were evaluated for simultaneous analysis of multi-class VDs in beef matrix. The EMR sorbent was most advantageous (113/115) compared to others, and showed a satisfactory recovery range (70.7-117.9%) except cefquinome (67.3%) and Cefalonium (69.8%). This methodology can be used to detect oxolinic acid and ractopamine (27.4% and 88.0% of maximum residue limit, respectively) in real beef samples. We thus study propose a simple and fast analytical method for multi-class VDs for the future health of humans and animals.

The intramammary efficacy of first generation cephalosporins against Staphylococcus aureus mastitis in mice

Vet Microbiol 2012 Nov 9;160(1-2):141-50.PMID:22677480DOI:10.1016/j.vetmic.2012.05.017.

Staphylococcus aureus-induced mastitis in cattle causes important financial losses in the dairy industry due to lower yield and bad milk quality. Although S. aureus is susceptible to many antimicrobials in vitro, treatment often fails to cure the infected udder. Hence, comprehensive evaluation of antimicrobials against S. aureus mastitis is desirable to direct treatment strategies. The mouse mastitis model is an elegant tool to evaluate antimicrobials in vivo while circumventing the high costs associated with bovine experiments. An evaluation of the antimicrobial efficacy of the intramammary (imam) applied first generation cephalosporins cefalexin, Cefalonium, cefapirin and cefazolin, was performed using the S. aureus mouse mastitis model. In vivo determination of the effective dose 2log(10) (ED(2log10)), ED(4log10), protective dose 50 (PD(50)) and PD(100) in mouse mastitis studies, support that in vitro MIC data of the cephalosporins did not fully concur with the in vivo clinical outcome. Cefazolin was shown to be the most efficacious first generation cephalosporin to treat S. aureus mastitis whereas the MIC data indicate that Cefalonium and cefapirin were more active in vitro. Changing the excipient for imam application from mineral oil to miglyol 812 further improved the antimicrobial efficacy of cefazolin, confirming that the excipient can influence the in vivo efficacy. Additionally, statistical analysis of the variation of S. aureus-infected, excipient-treated mice from fourteen studies emphasizes the strength of the mouse mastitis model as a fast, cost-effective and highly reproducible screening tool to assess the efficacy of antimicrobial compounds against intramammary S. aureus infection.

Potential of ESBL-producing Escherichia coli selection in bovine feces after intramammary administration of first generation cephalosporins using in vitro experiments

Sci Rep 2022 Sep 5;12(1):15083.PMID:36065056DOI:10.1038/s41598-022-15558-z.

Selection and spread of Extended Spectrum Beta-Lactamase (ESBL) -producing Enterobacteriaceae within animal production systems and potential spillover to humans is a major concern. Intramammary treatment of dairy cows with first-generation cephalosporins is a common practice and potentially selects for ESBL-producing Enterobacteriaceae, although it is unknown whether this really occurs in the bovine fecal environment. We aimed to study the potential effects of intramammary application of cephapirin (CP) and Cefalonium (CL) to select for ESBL-producing Escherichia coli in the intestinal content of treated dairy cows and in manure slurry, using in vitro competition experiments with ESBL and non-ESBL E. coli isolates. No selection of ESBL-producing E. coli was observed at or below concentrations of 0.8 µg/ml and 4.0 µg/ml in bovine feces for CP and CL, respectively, and at or below 8.0 µg/ml and 4.0 µg/ml, respectively, in manure slurry. We calculated that the maximum concentration of CP and CL after intramammary treatment with commercial products will not exceed 0.29 µg/ml in feces and 0.03 µg/ml in manure slurry. Therefore, the results of this study did not find evidence supporting the selection of ESBL-producing E. coli in bovine feces or in manure slurry after intramammary use of commercial CP or CL-containing products.