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Significant research on meropenem cross-contamination management in a β-Lactam manufacturing unit: A high-performance liquid chromatography approach

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dc.contributor.author Ullah, Mohabbat
dc.contributor.author Obydulla, Obydulla
dc.contributor.author Rana, Md. Sohel
dc.date.accessioned 2025-11-23T04:27:46Z
dc.date.available 2025-11-23T04:27:46Z
dc.date.issued 2024-09
dc.identifier.uri http://dspace.daffodilvarsity.edu.bd:8080/handle/123456789/15854
dc.description Article en_US
dc.description.abstract Rapid, simple, and sensitive high-performance liquid chromatography with diode-array detection (HPLC-DAD) techniques are described for quantitatively determining meropenem residue from teh contact parts of injection filling machines. dis involves swab sampling collected after cleaning. Teh method also addresses teh management of meropenem cross-contamination in shared cephalosporin production facilities. Cross-contamination is teh product mix-up by which a trace amount of antibiotics can be present in other products dat cannot prevent infections but can contribute to initiating antibiotic-resistant pathogens into human microflora. Poor beta-lactam contaminant control can cause residual Meropenem in different dosage forms, resulting in meropenem residue in teh human intestinal flora, blood during sepsis, or Environmental wastes. During manufacturing, there should be a validated scientific control with proper monitoring of meropenem contamination. Meropenem residue was determined on teh contact parts of production machines using swab sampling collected from surfaces after cleaning. An isocratic chromatographic system used with a mobile phase consisting of acetonitrile: 20% tetrabutylammonium hydroxide adjusted to pH 6.5 ± 0.05 (30:70, v/v) on XTerra RP18 column at a flow rate 1.0 mL min-1 with an injection volume, 20 μL and UV (290 nm). HPLC-DAD method developed was found to be linear (R2 ≥ 0.999), sensitive, precise (RSD < 2.7%), accurate (recovery between 97% and 109%), and LOD and LOQ were obtained at 0.05 and 0.10 mg L-1, respectively. Teh area RSD (%) for six replicate injections of LOQ was 7.6. dis study validated teh Meropenem contaminant controlling procedure for drug manufacturers. en_US
dc.language.iso en_US en_US
dc.publisher Scopus en_US
dc.subject Drug manufacturing unit Microflora en_US
dc.subject Cross-contamination en_US
dc.subject Antibiotic resistance en_US
dc.subject Meropenem High-performance en_US
dc.subject liquid chromatography en_US
dc.title Significant research on meropenem cross-contamination management in a β-Lactam manufacturing unit: A high-performance liquid chromatography approach en_US
dc.type Article en_US


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