Efficacy of zincoderm G cream against wound infection by methicillin-resistant Staphylococcus Aureus in spraguedawley rats

S. M. Satyam, K. L. Bairy, S. Musharaf, D. Fernandes, V. Shashidhar

Research output: Contribution to journalArticle

Abstract

A fixed drug combinations (FDC) of clobetasol, gentamicin and Zinc namely Zincoderm G cream is available in the market. There are studies which shows the efficacy of each component in bacterial infections, but as FDC including Zinc has not been reported yet. A study was undertaken to evaluate the efficacy of Zincoderm G cream in burn wound infected with methicillin-resistant Staphylococcus aureus. Methods: A total of 18 Sprague-Dawley rats (male, pathogen free, 6-8 weeks old) were used in this study. The rats were divided into 3 groups of 6 rats each. 25-30 mg of test drugs (Zincoderm G cream with or without Zinc) was applied on S. aureus infected burn wound affected area of back of rats for two weeks. Degree of bacterial infection was assessed by quantification of bacteria. There was 30% mortality seen in both MRSA toxic control (cream base) and MRSA positive control (Zincoderm G cream without Zinc) groups. Only 10% mortality was observed in the MRSA group which was treated with Zincoderm G cream with Zinc. But, there was no significant difference found in MRSA bacterial concentration (number of CFU/ml wound fluid; after treatment) for both Zincoderm G with/without Zinc when compared with the MRSA toxic control (cream base) groupAddition of Zinc to Zincoderm G did not exhibit distinct killing profile against MRSA. We found that Zincoderm G cream with Zinc could not exhibit the distinct killing profiles against MRSA.

Original languageEnglish
Pages (from-to)P446-P449
JournalInternational Journal of Pharma and Bio Sciences
Volume6
Issue number2
Publication statusPublished - 01-01-2015

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Methicillin
Wound Infection
Methicillin-Resistant Staphylococcus aureus
Zinc
Rats
Poisons
Drug Combinations
Bacterial Infections
Wounds and Injuries
Clobetasol
Mortality
Pathogens
Gentamicins
Sprague Dawley Rats
Staphylococcus aureus
Bacteria
Fluids

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

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title = "Efficacy of zincoderm G cream against wound infection by methicillin-resistant Staphylococcus Aureus in spraguedawley rats",
abstract = "A fixed drug combinations (FDC) of clobetasol, gentamicin and Zinc namely Zincoderm G cream is available in the market. There are studies which shows the efficacy of each component in bacterial infections, but as FDC including Zinc has not been reported yet. A study was undertaken to evaluate the efficacy of Zincoderm G cream in burn wound infected with methicillin-resistant Staphylococcus aureus. Methods: A total of 18 Sprague-Dawley rats (male, pathogen free, 6-8 weeks old) were used in this study. The rats were divided into 3 groups of 6 rats each. 25-30 mg of test drugs (Zincoderm G cream with or without Zinc) was applied on S. aureus infected burn wound affected area of back of rats for two weeks. Degree of bacterial infection was assessed by quantification of bacteria. There was 30{\%} mortality seen in both MRSA toxic control (cream base) and MRSA positive control (Zincoderm G cream without Zinc) groups. Only 10{\%} mortality was observed in the MRSA group which was treated with Zincoderm G cream with Zinc. But, there was no significant difference found in MRSA bacterial concentration (number of CFU/ml wound fluid; after treatment) for both Zincoderm G with/without Zinc when compared with the MRSA toxic control (cream base) groupAddition of Zinc to Zincoderm G did not exhibit distinct killing profile against MRSA. We found that Zincoderm G cream with Zinc could not exhibit the distinct killing profiles against MRSA.",
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Efficacy of zincoderm G cream against wound infection by methicillin-resistant Staphylococcus Aureus in spraguedawley rats. / Satyam, S. M.; Bairy, K. L.; Musharaf, S.; Fernandes, D.; Shashidhar, V.

In: International Journal of Pharma and Bio Sciences, Vol. 6, No. 2, 01.01.2015, p. P446-P449.

Research output: Contribution to journalArticle

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