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Research ArticleResearch

Quantitative and Qualitative Evaluation of Microorganism Profile Identified in Bioburden Analysis in a Biopharmaceutical Facility in Brazil: Criteria for Classification and Management of Results

Josiane Machado Vieira Mattoso, Luciana Veloso da Costa, Bruna de Almeida do Vale, Cristhiane Falavina dos Reis, Joyce Modesto de Andrade, Lygia Maria Paulo da Silva Braga, Greice Maria Silva da Conceição, Paulo Borges Mathias Costa, Igor Barbosa da Silva, Letícia de Alencar Pereira Rodrigues, Jeancarlo Pereira dos Anjos and Marcelo Luiz Lima Brandão
PDA Journal of Pharmaceutical Science and Technology March 2025, 79 (2) 125-156; DOI: https://doi.org/10.5731/pdajpst.2023.012883
Josiane Machado Vieira Mattoso
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Luciana Veloso da Costa
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Bruna de Almeida do Vale
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Cristhiane Falavina dos Reis
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Joyce Modesto de Andrade
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Lygia Maria Paulo da Silva Braga
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Greice Maria Silva da Conceição
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Paulo Borges Mathias Costa
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Igor Barbosa da Silva
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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Letícia de Alencar Pereira Rodrigues
3Centro Universitário SENAI CIMATEC, Salvador/BA, Brazil
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Jeancarlo Pereira dos Anjos
3Centro Universitário SENAI CIMATEC, Salvador/BA, Brazil
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Marcelo Luiz Lima Brandão
1Laboratory of Microbiology Control, Department of Quality Control, Bio-Manguinhos/Fiocruz, Rio de Janeiro/RJ, Brazil;
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  • For correspondence: marcelo.brandao@bio.fiocruz.br
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Abstract

Microbiological contamination may cause microbial proliferation and consequently additional problems for pharmaceutical companies through production stoppage, product contamination, investigations of process deviations, out-of-specification results, and product disposal. This is one of the major concerns of the regulatory health agencies. Microbiological load (bioburden) may represent a potential risk for patients if the sterilization process is not effective and/or due to the production of toxins. Although bioburden can be eliminated by terminal sterilization or filtration processes, it is important to monitor the amount and determine the identity and characteristics of the microorganisms present prior to final processing. The application of microorganism identification systems is crucial for identifying the type of contamination, which can be extremely useful for investigating. The aim of this study was to evaluate the profiles of microorganisms identified in bioburden assays from solutions, culture media, and products (SCP) from a pharmaceutical industry facility. From 2018–2020, a total of 1078 samples from 857 different lots of SCP were analyzed and the isolated microorganisms were identified. A prefiltering step was included after March 2020 in order to reduce the bioburden before sterilizing filtration. Criteria for the definition and management of the microorganisms identified were evaluated after an integrative bibliographic review, and three groups were proposed (critical, objectionable, and nonobjectionable microorganisms). For the samples that did not include prefiltering (n = 636), 227 (35.7%) presented microbial growth. For those that included prefiltering, before prefiltering (n = 221), 60.6% presented microbial growth, and after prefiltering, this value was reduced to 4.1%. Microbial growth recovered after prefiltration is likely to be attributed to contamination during sample collection or filtration. From the samples that presented microbial growth, 678 microorganisms were identified as bacteria and 59 as molds and yeasts. A total of 120 microorganisms (56 and 27 Gram-positive and Gram-negative bacteria, respectively, 31 yeasts, and 6 filamentous molds) could not be identified, and the remaining microorganisms were classified as objectionable (n = 507; 82.2%), nonobjectionable (n = 103; 16.7%), and critical (n = 7; 1.1%). Most of the bioburden species (>80.0%) were considered objectionable microorganisms. A process for classification and management of bioburden analysis results based on a literature review of pathogenic and physiological characteristics of the microorganisms was proposed.

  • Pharmaceutical facility
  • Bioburden
  • Quality control
  • Microbial contamination
  • Contamination control strategy
  • Identification
  • © PDA, Inc. 2025
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PDA Journal of Pharmaceutical Science and Technology: 79 (2)
PDA Journal of Pharmaceutical Science and Technology
Vol. 79, Issue 2
March/April 2025
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Quantitative and Qualitative Evaluation of Microorganism Profile Identified in Bioburden Analysis in a Biopharmaceutical Facility in Brazil: Criteria for Classification and Management of Results
Josiane Machado Vieira Mattoso, Luciana Veloso da Costa, Bruna de Almeida do Vale, Cristhiane Falavina dos Reis, Joyce Modesto de Andrade, Lygia Maria Paulo da Silva Braga, Greice Maria Silva da Conceição, Paulo Borges Mathias Costa, Igor Barbosa da Silva, Letícia de Alencar Pereira Rodrigues, Jeancarlo Pereira dos Anjos, Marcelo Luiz Lima Brandão
PDA Journal of Pharmaceutical Science and Technology Mar 2025, 79 (2) 125-156; DOI: 10.5731/pdajpst.2023.012883

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Quantitative and Qualitative Evaluation of Microorganism Profile Identified in Bioburden Analysis in a Biopharmaceutical Facility in Brazil: Criteria for Classification and Management of Results
Josiane Machado Vieira Mattoso, Luciana Veloso da Costa, Bruna de Almeida do Vale, Cristhiane Falavina dos Reis, Joyce Modesto de Andrade, Lygia Maria Paulo da Silva Braga, Greice Maria Silva da Conceição, Paulo Borges Mathias Costa, Igor Barbosa da Silva, Letícia de Alencar Pereira Rodrigues, Jeancarlo Pereira dos Anjos, Marcelo Luiz Lima Brandão
PDA Journal of Pharmaceutical Science and Technology Mar 2025, 79 (2) 125-156; DOI: 10.5731/pdajpst.2023.012883
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Keywords

  • Pharmaceutical facility
  • Bioburden
  • Quality control
  • Microbial Contamination
  • Contamination Control Strategy
  • Identification

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