Literature DB >> 7506653

Miocamycin. A review of its antimicrobial activity, pharmacokinetic properties and therapeutic potential.

S M Holliday1, D Faulds.   

Abstract

Miocamycin is an orally administered 16-membered macrolide antimicrobial drug. It has a spectrum of in vitro activity similar to that of erythromycin, inhibiting a range of Gram-positive and Gram-negative organisms, atypical microbes and some anaerobes. Importantly, miocamycin demonstrates greater in vitro potency than erythromycin against several pathogens including Legionella pneumophila, Mycoplasma hominis, and Ureaplasma urealyticum. Equally noteworthy is its activity against erythromycin-resistant staphylococcal and streptococcal species expressing inducible-type resistance. Miocamycin possesses poor overall activity against Haemophilus influenzae and is inactive against Enterobacteriaceae. Penetration of miocamycin into body tissues and fluids is both rapid and extensive. The 3 major metabolites of miocamycin possess antimicrobial activity and may contribute to the therapeutic efficacy of the drug. Clinical data indicate that miocamycin is useful in the treatment of upper and lower respiratory tract infections in both adult and paediatric patients. Miocamycin is also effective in the treatment of urogenital tract infections caused by Chlamydia trachomatis or U. urealyticum. Several studies suggest that miocamycin is at least as effective as erythromycin in these indications; however, comparisons with newer macrolide agents have yet to be performed. In other studies, miocamycin proved to be a useful agent in the treatment of periodontal infections and as anti-infective prophylaxis in dental surgery. Miocamycin appears to have a tolerability profile qualitatively similar to that of other macrolides, with gastrointestinal and skin disorders being the most commonly reported adverse events. Current data suggest that the potential for drug interactions with miocamycin is low, with the possible exceptions of carbamazepine and cyclosporin. Thus, although further confirmation and elaboration of various aspects of its efficacy and tolerability profile is needed, at this stage miocamycin offers a useful alternative oral therapy to erythromycin for the treatment of uncomplicated community-acquired respiratory tract infections and nongonococcal urethritis.

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Year:  1993        PMID: 7506653     DOI: 10.2165/00003495-199346040-00008

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  93 in total

1.  Some features of miocamycin in the gynecological field: pharmacokinetic data using preoperative administration and therapeutic aspects against chlamydial infections.

Authors:  P M Furneri; G Blandino; L Roccasalva; A Cianci; G Palumbo; G Tempera
Journal:  J Chemother       Date:  1989-07       Impact factor: 1.714

2.  Miokamycin penetration into oral cavity tissues and crevicular fluid.

Authors:  F Fraschini; F Scaglione; M Falchi; P Manzoni; S D'Orsi; S Badile; M Pignanelli
Journal:  Int J Clin Pharmacol Res       Date:  1989

3.  [Use of miocamycin in the acute exacerbation of chronic obstructive bronchopneumopathy. Case material contribution].

Authors:  C Miravalle; A Ardizzi; S Barberis; F Galietti; G E Giorgis; A Oliaro
Journal:  Minerva Med       Date:  1987-05-15       Impact factor: 4.806

4.  [Therapeutic activity and pharmacokinetic behavior of miokamycin in the respiratory system].

Authors:  M Fioretti; M Bandera; R Rimoldi
Journal:  G Ital Chemioter       Date:  1984 Jan-Aug

5.  [Clinical results of 9,3"-diacetylmidecamycin in the field of pediatrics (author's transl)].

Authors:  T Shinozaki; H Meguro; Y Koike; S Hashira; R Fujii
Journal:  Jpn J Antibiot       Date:  1982-01

6.  [Laboratory and clinical studies of 9,3"-diacetylmidecamycin in the pediatric field].

Authors:  Y Toyonaga; Y Kurosu; M Sugita; M Hori
Journal:  Jpn J Antibiot       Date:  1982-06

7.  Activities of human alveolar macrophages (HAMs). Note 1: Observations on phagocytosis and bacterial killing in the presence of miocamycin.

Authors:  A Capelli; O Capelli; L Azzolini; L Richeldi; E Prandi; G Velluti
Journal:  Chemioterapia       Date:  1988-04

8.  In vitro susceptibility of Ureaplasma urealyticum clinical isolates to new macrolides.

Authors:  Y Kanamoto; Y Miyake; H Suginaka; T Usui
Journal:  Chemotherapy       Date:  1991       Impact factor: 2.544

9.  Clinical efficacy of dirithromycin versus miocamycin in tonsillopharyngitis.

Authors:  G Ruggiero; R Utili; L E Adinolfi; V Attanasio; M P Scarano; A Mazzone; G Costa; L Califano; F Costa
Journal:  J Antimicrob Chemother       Date:  1993-03       Impact factor: 5.790

Review 10.  Pharmacokinetic drug interactions of macrolides.

Authors:  P Periti; T Mazzei; E Mini; A Novelli
Journal:  Clin Pharmacokinet       Date:  1992-08       Impact factor: 6.447

View more
  1 in total

Review 1.  Macrolide antibacterials. Drug interactions of clinical significance.

Authors:  N A von Rosensteil; D Adam
Journal:  Drug Saf       Date:  1995-08       Impact factor: 5.606

  1 in total

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