مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

2,330
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

USE OF ALAMAR BLUE ASSAY AS A COLORIMETRIC METHOD FOR DETECTION OF MULTIDRUG-RESISTANT MYCOBACTERIUM TUBERCULOSIS

Pages

  47-51

Abstract

 Background and Aim: In recent years, tuberculosis (TB) has acquired a growing importance in developed and developing countries. The spread of multidrug-resistant (MDR) strains of MYCOBACTERIUM TUBERCULOSIS is an increasing public health concern in many parts of the world, especially in low- income countries. Standard methods for drug susceptibility testing of M. tuberculosis are time-consuming. In this study, we have evaluated the possibility of using colorimetric method by means of ALAMAR BLUE, to detect susceptibility of M. tuberculosis strains as less expensive and easier-to-read methods.Materials and Methods: For this study 23 isolates of MYCOBACTERIUM TUBERCULOSIS were obtained from Iranian National Research Institute of Tuberculosis and Long Diseases. 11 isolates were resistant to rifampin and isoniazid and 12 isolates were susceptible to rifampin and isoniazid. The colorimetric method in this study was performed with a critical concentration of 0.2 mg/ml for isoniazid and 2 mg/ml for rifampin in 7H9GC broth. The tubes were incubated at 3TC for 4 weeks.Results: For both rifampin and isoniazid, the sensitivity and specificity of ALAMAR BLUE method was %100 and %90 respectively. In this study, the results for ALAMAR BLUE were available in average 6 days.Conclusion: Medical laboratories in developing countries have to adapt a simple method, which does not require expensive equipment materials. In conclusion, this colorimetric method is simple, reliable and inexpensive methods to evaluate drug susceptibility of MYCOBACTERIUM TUBERCULOSIS, especially in laboratories with low- income. In this regard, ALAMAR BLUE culture tubes have the optional to become the method of choice for assessing drug susceptibility of M. tuberculosis in countries like Iran.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    MOHAMMADZADEH, ALI REZA, MOHAMMADZADEH, ALI REZA, FARNIA, P., RASHED, T., GHAZVINI, K., BEHDANI, M., & GHANAAT, J.. (2007). USE OF ALAMAR BLUE ASSAY AS A COLORIMETRIC METHOD FOR DETECTION OF MULTIDRUG-RESISTANT MYCOBACTERIUM TUBERCULOSIS. OFOGH-E-DANESH, 13(3), 47-51. SID. https://sid.ir/paper/68803/en

    Vancouver: Copy

    MOHAMMADZADEH ALI REZA, MOHAMMADZADEH ALI REZA, FARNIA P., RASHED T., GHAZVINI K., BEHDANI M., GHANAAT J.. USE OF ALAMAR BLUE ASSAY AS A COLORIMETRIC METHOD FOR DETECTION OF MULTIDRUG-RESISTANT MYCOBACTERIUM TUBERCULOSIS. OFOGH-E-DANESH[Internet]. 2007;13(3):47-51. Available from: https://sid.ir/paper/68803/en

    IEEE: Copy

    ALI REZA MOHAMMADZADEH, ALI REZA MOHAMMADZADEH, P. FARNIA, T. RASHED, K. GHAZVINI, M. BEHDANI, and J. GHANAAT, “USE OF ALAMAR BLUE ASSAY AS A COLORIMETRIC METHOD FOR DETECTION OF MULTIDRUG-RESISTANT MYCOBACTERIUM TUBERCULOSIS,” OFOGH-E-DANESH, vol. 13, no. 3, pp. 47–51, 2007, [Online]. Available: https://sid.ir/paper/68803/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button