{"title":"尼日利亚西南部拉各斯一家制药厂环境质量的微生物评价","authors":"Ojo-Omoniyi OA, Akinnola OO, Adeduro MR, Mmadu CP","doi":"10.53346/wjbpr.2022.2.2.0031","DOIUrl":null,"url":null,"abstract":"The evaluation of predominant microorganisms distributed in the air of the critical rooms in the production plant of a pharmaceutical company in Agege Local Government area, Lagos-Nigeria was investigated using settle- plate method. A total of seven critical rooms in the production facility that is, Dispensary, Granulation, Blending, Blistering, Tableting, Syrup, and Syrup filling rooms were sampled respectively under aseptic conditions. These samples were processed in duplicates on Sabouraud Dextrose Agar (SDA) and Tryptone Soya Agar (TSA) and incubated at 25ºC and 37 ºC respectively. Thereafter, microorganisms were isolated and identified using standard and conventional methods. The data obtained were analyzed to find the microbial distributions in the environment of the pharmaceutical facility. Eight bacterial species were isolated from different locations in the pharmaceutical facility, they were of the following genera; Staphylococcus (12.5%), Micrococcus (50%) and Bacillus (37.5%). Most of the microorganisms found in this study belong to the genus Micrococcus (four species) and three Bacillus species and one Staphylococcus species. Despite the compliance of this company with international standards, the above mentioned microbial species were still found within the facility. Hence, compliance with the international specified standard alone, that is, Good Manufacturing Practice (GMP) does not guarantee sterile pharmaceutical product from the industry. Therefore, other microbial quality assurance procedures must be strictly adhered to in order to have products that comply with international specifications. The microbial isolates from the pharmaceutical facility include: Bacillus subtilis, Bacillus badius, Staphyloccocus aureus, Proteus mirabilis, Microccocus sp. Pseudomonas aeruginosa, Enterobacter aerogenes, Citrobacter sp. Talaromyces sp. Aspergillus tamari.","PeriodicalId":267430,"journal":{"name":"World Journal of Biological and Pharmaceutical Research","volume":"37 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Microbiological evaluation of the environmental quality of a pharmaceutical plant in Lagos, Southwest Nigeria\",\"authors\":\"Ojo-Omoniyi OA, Akinnola OO, Adeduro MR, Mmadu CP\",\"doi\":\"10.53346/wjbpr.2022.2.2.0031\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The evaluation of predominant microorganisms distributed in the air of the critical rooms in the production plant of a pharmaceutical company in Agege Local Government area, Lagos-Nigeria was investigated using settle- plate method. 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引用次数: 0
摘要
采用平板沉降法对尼日利亚拉各斯阿格格地方政府区某制药公司生产车间关键房间空气中的优势微生物进行了评价。在无菌条件下,生产设施中共有7个关键房间,即药房、制粒室、调配室、起泡室、压片室、糖浆室和糖浆灌装室分别取样。这些样品在Sabouraud Dextrose Agar (SDA)和Tryptone soy Agar (TSA)上重复处理,分别在25ºC和37ºC孵育。然后,用标准和常规方法分离和鉴定微生物。对所获得的数据进行分析,找出制药设施环境中的微生物分布。从制药设施的不同地点分离到8种细菌,它们属于以下属;葡萄球菌(12.5%)、微球菌(50%)和芽孢杆菌(37.5%)。本研究中发现的微生物大部分属于微球菌属(4种)、芽孢杆菌属3种、葡萄球菌属1种。尽管该公司符合国际标准,但在该设施内仍发现上述微生物种类。因此,仅符合国际规定的标准,即良好生产规范(GMP)并不能保证无菌药品来自工业。因此,其他微生物质量保证程序必须严格遵守,以使产品符合国际规范。从制药厂分离出的微生物包括:枯草芽孢杆菌、坏芽孢杆菌、金黄色葡萄球菌、神奇变形杆菌、微球菌、铜绿假单胞菌、产气肠杆菌、柠檬酸杆菌、塔尔芳香菌、tamari曲霉。
Microbiological evaluation of the environmental quality of a pharmaceutical plant in Lagos, Southwest Nigeria
The evaluation of predominant microorganisms distributed in the air of the critical rooms in the production plant of a pharmaceutical company in Agege Local Government area, Lagos-Nigeria was investigated using settle- plate method. A total of seven critical rooms in the production facility that is, Dispensary, Granulation, Blending, Blistering, Tableting, Syrup, and Syrup filling rooms were sampled respectively under aseptic conditions. These samples were processed in duplicates on Sabouraud Dextrose Agar (SDA) and Tryptone Soya Agar (TSA) and incubated at 25ºC and 37 ºC respectively. Thereafter, microorganisms were isolated and identified using standard and conventional methods. The data obtained were analyzed to find the microbial distributions in the environment of the pharmaceutical facility. Eight bacterial species were isolated from different locations in the pharmaceutical facility, they were of the following genera; Staphylococcus (12.5%), Micrococcus (50%) and Bacillus (37.5%). Most of the microorganisms found in this study belong to the genus Micrococcus (four species) and three Bacillus species and one Staphylococcus species. Despite the compliance of this company with international standards, the above mentioned microbial species were still found within the facility. Hence, compliance with the international specified standard alone, that is, Good Manufacturing Practice (GMP) does not guarantee sterile pharmaceutical product from the industry. Therefore, other microbial quality assurance procedures must be strictly adhered to in order to have products that comply with international specifications. The microbial isolates from the pharmaceutical facility include: Bacillus subtilis, Bacillus badius, Staphyloccocus aureus, Proteus mirabilis, Microccocus sp. Pseudomonas aeruginosa, Enterobacter aerogenes, Citrobacter sp. Talaromyces sp. Aspergillus tamari.