Evaluation of Microbial Recovery from Raw Materials for Pharmaceutical Use
Mostafa Eissa(1*), Ahmed Mahmoud(2)
(1) HIKMA Pharma
(2) 
(*) Corresponding Author
Abstract
Microbiological quality of raw materials used in pharmaceutical manufacturing is critical attribute that affects the bioburden level of the final product. If the preliminary treatment for the microbiological analysis of the material is not suitable to recover actual microbial content, false estimation of microbial presence and/or count in raw materials may impact final product quality and safety. Accordingly a survey study was conducted on 12 selected materials that are used extensively in the manufacturing facility in order find suitable technique to recover low-level inoculums of standard strains. The basic processing and/or neutralization technique was dilution alone or in combination with chemical neutralization or less frequently filtration. Dill oil was the only raw material required combination of dilution and chemical neutralization for both of microbial enumeration and detection while this combination was necessary only in enumeration for Cetostearyl Alcohol. Although dilution method may be adopted alone for Sorbitol solution 70% yet filtration was done in combination to facilitate the visualization of commonly found yeast contaminant from the suppliers of the raw materials. Balsam Peru required the highest dilution among the tested materials for enumeration. The applied neutralization techniques were effective in detecting low level contamination in raw materials.
Full Text:
PDFReferences
Block, S.S. 1991. Disinfection, Sterilization, and Preservation. 4th ed. Malvern, PA, Lea and Febiger, USA.
Estridge, B.H., Reynolds, A.P. and Walters, N.J. 2000. Basic Medical Laboratory Techniques. 4th ed. Delmar Cengage Learning, Division of Thomson Learning, USA.
Clontz, L. 2008. Microbial Limit and Bioburden Tests: Validation Approaches and Global Requirements. 2nd ed. CRC Press, Taylor and Francis Group, USA. pp. 35–62.
Marshall, V., Poulson-Cook, S. and Moldenhaver, J. 1998. Comparative Mold and Yeast Recovery Analysis (the effect of differing incubation temperature ranges and growth media). PDA J. Pharm. Sci. Technol. 52(4): 165–9.
Cundell, A.M. 2002. Review of the Media Selection and Incubation Conditions for the Compendial Sterility and Microbial Limit Tests. Pharmacopeial Forum. 28(6).
Eissa, M.E., 2014. Studies Of Microbial Resistance Against Some Disinfectants: Microbial Distribution & Biocidal Resistance in Pharmaceutical Manufacturing Facility. 1st ed. LAP Lambert Academic Publishing GmbH & Co. KG, Saarbrücken, Germany.
Eissa, M.E. and Nouby, A.S., 2014. Validation of Spore-Forming Organisms Recovery from Peroxygen-Based Disinfectants. Journal of Pharmaceutical Research & Clinical Practice. 4(2):23-32.
Eissa, M.E., Naby, M.A., Nouby, A.S., 2014. ASSESSMENT OF ANTIMICROBIAL ACTIVITY OF NOVEL DISINFECTANT BASED ON PEROXYGEN/BIGUANIDE/ALCOHOL COMBINATION. Indonesian J. Pharm. 25 (3) : 153 – 163.
Jimenez, L. 2007. Microbial diversity in pharmaceutical product recalls and environments. PDA J. Pharm. Sci. Technol. 61(5):383-99.
USP36-NF31, Chapter <61> 2014. Microbiological Examination of Non sterile Products: Microbial Enumeration Tests. United States Pharmacopoeia 36/National Formulary 31, Baltimore, MD, USA.
USP36-NF31, Chapter <62> 2014. Microbiological Examination of Nonsterile Products: Tests for Specified Microorganisms. United States Pharmacopoeia 36/National Formulary 31, Baltimore, MD, USA.
USP36-NF31, Chapter <1227> 2014. Validation of Microbial Recovery from Pharmacopeial Articles. United States Pharmacopoeia 36/National Formulary 31, Baltimore, MD, USA.
DOI: https://doi.org/10.14499/jfps
Article Metrics
Abstract views : 1800 | views : 3932Refbacks
- There are currently no refbacks.
Journal of Food and Pharmaceutical Sciences (ISSN: 2339-0948) - Universitas Gadjah Mada, Indonesia.