Literature DB >> 18611587

Cefuroxime axetil.

P Dellamonica1.   

Abstract

Cefuroxime is the first commercially-available second-generation cephalosporine to be widely used in therapy; it is a semi-synthetic cephalosporin obtained from the 7-cephalosporanic acid nucleus of cephalosporin C. Cefuroxime axetil is the acetoxyethyl ester of cefuroxime. The majority of micro-organisms associated with respiratory infections are highly sensitive to cefuroxime. These include Haemophilus influenzae, Streptococcus pneumoniae, Streptococcus pyogenes and the other streptococci (excluding group D streptococci), and Moraxella catarrhalis. Bacteria sensitive to cefuroxime include the enterobacteria (Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, and Salmonella and Shigella and Straphylococcus aureus (methicillin-sensitive strains). The pharmacokinetic studies show that the maximum plasma concentration of cefuroxime after oral administration of 250 mg and 500 mg of cefuroxime axetil after a meal are respectively 4.6 and 7.9 mg/l. The absolute bioavailability of tablets is 68% (extremes 63-73%) after oral administration of 500 mg cefuroxime axetil. The protein binding is 33+/-5.7%. Tissue diffusion was studied in the interstitial fluid, the bronchial mucosa, the tonsils, and the bronchial secretions. Cefuroxime axetil is available as capsule-shaped tablets containing 125, 250 or 500 mg. An oral suspension dosage form for paediatric purposes is also available as granules in multidose bottles and sachets. Constitution gives a suspension containing 125 mg or 250 mg cefuroxime (as cefuroxime axetil). Cefuroxime axetil is indicated for the treatment of infections caused by susceptible bacteria. Indications include: lower respiratory tract infections (e.g., acute and chronic bronchitis and pneumonia); upper respiratory tract infections (e.g., ear, nose and throat infections such as otitis media, sinusitis tonsillitis and pharyngitis); genito-urinary tract infections (e.g., pyelonephritis, cystitis and urethritis, gonorrhoea, acute uncomplicated gonococcal urethritis and cervicitis); and skin and soft tissue infections (e.g., furunculosis, pyoderma and impetigo). For most infections, a dose of 250 mg twice daily is appropriate. In some urinary tract infections, 125 mg twice daily has been shown to be effective. If pneumonia is suspected or in more severe lower respiratory tract infection, doses of 500 mg bd should be used. Uncomplicated gonorrhoea has been shown to respond to a single 1-g dose of cefuroxime axetil. Adverse reactions to cefuroxime have generally been mild and transient in nature (gastrointestinal disturbances, including diarrhoea, nausea and vomiting).

Entities:  

Year:  1994        PMID: 18611587     DOI: 10.1016/0924-8579(94)90061-2

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  10 in total

1.  Stability of cefuroxime axetil oral suspension at different temperature storage conditions.

Authors:  Alija Uzunović; Edina Vranić
Journal:  Bosn J Basic Med Sci       Date:  2008-02       Impact factor: 3.363

2.  Concentrations of Cefuroxime in Brain Tissue of Neurointensive Care Patients.

Authors:  A Hosmann; L C Ritscher; H Burgmann; Z Oesterreicher; W Jäger; S Poschner; E Knosp; A Reinprecht; A Gruber; M Zeitlinger
Journal:  Antimicrob Agents Chemother       Date:  2018-01-25       Impact factor: 5.191

Review 3.  Cefuroxime axetil: an updated review of its use in the management of bacterial infections.

Authors:  L J Scott; D Ormrod; K L Goa
Journal:  Drugs       Date:  2001       Impact factor: 9.546

4.  Optimization of a Cefuroxime Axetil-Loaded Liquid Self-Nanoemulsifying Drug Delivery System: Enhanced Solubility, Dissolution and Caco-2 Cell Uptake.

Authors:  Arshad Ali Khan; Akhtar Atiya; Safia Akhtar; Yogesh Yadav; Kamal A Qureshi; Mariusz Jaremko; Syed Mahmood
Journal:  Pharmaceutics       Date:  2022-04-01       Impact factor: 6.525

5.  Cefuroxime-induced lupus.

Authors:  Ebru Uz; Nuket Bavbek; Faruk Hilmi Turgut; Mehmet Kanbay; Arif Kaya; Ali Akcay
Journal:  J Natl Med Assoc       Date:  2007-09       Impact factor: 1.798

Review 6.  Cefuroxime axetil. A review of its antibacterial activity, pharmacokinetic properties and therapeutic efficacy.

Authors:  C M Perry; R N Brogden
Journal:  Drugs       Date:  1996-07       Impact factor: 9.546

7.  Prospective Cohort Study Investigating the Safety and Efficacy of Ambulatory Treatment With Oral Cefuroxime-Axetil in Febrile Children With Urinary Tract Infection.

Authors:  Elise Hennaut; Hong P Duong; Benedetta Chiodini; Brigitte Adams; Ksenija Lolin; Sophie Blumental; Karl M Wissing; Khalid Ismaili
Journal:  Front Pediatr       Date:  2018-08-31       Impact factor: 3.418

8.  Preparation and characterization of cefuroxime axetil solid dispersions using hydrophilic carriers.

Authors:  Adinarayana Gorajana; Adhiyaman Rajendran; Lee Mun Yew; Kamal Dua
Journal:  Int J Pharm Investig       Date:  2015 Jul-Sep

9.  Evaluation of Acquired Antibiotic Resistance in Escherichia coli Exposed to Long-Term Low-Shear Modeled Microgravity and Background Antibiotic Exposure.

Authors:  Madhan R Tirumalai; Fathi Karouia; Quyen Tran; Victor G Stepanov; Rebekah J Bruce; C Mark Ott; Duane L Pierson; George E Fox
Journal:  mBio       Date:  2019-01-15       Impact factor: 7.867

Review 10.  FDA-Approved Oximes and Their Significance in Medicinal Chemistry.

Authors:  Jyothi Dhuguru; Eugene Zviagin; Rachid Skouta
Journal:  Pharmaceuticals (Basel)       Date:  2022-01-04
  10 in total

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