Significant research on meropenem cross-contamination management in a β-Lactam manufacturing unit: A high-performance liquid chromatography approach
- سال انتشار: 1403
- محل انتشار: فصلنامه روش های تجزیه در شیمی محیط زیست، دوره: 7، شماره: 3
- کد COI اختصاصی: JR_AMECJ-7-3_003
- زبان مقاله: انگلیسی
- تعداد مشاهده: 40
نویسندگان
ACME Laboratories Ltd., Dhulivita, Dhamrai, Dhaka, Bangladesh
Department of Pharmacy, Daffodil International University
Department of Pharmacy, Jahangirnagar University, Savar, Dhaka, Bangladesh
چکیده
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: ۲۰% tetrabutylammonium hydroxide adjusted to pH ۶.۵ ± ۰.۰۵ (۳۰:۷۰, v/v) on XTerra RP۱۸ column at a flow rate ۱.۰ mL min-۱ with an injection volume, ۲۰ μL and UV (۲۹۰ nm). HPLC-DAD method developed was found to be linear (R۲ ≥ ۰.۹۹۹), sensitive, precise (RSD < ۲.۷%), accurate (recovery between ۹۷% and ۱۰۹%), and LOD and LOQ were obtained at ۰.۰۵ and ۰.۱۰ mg L-۱, respectively. Teh area RSD (%) for six replicate injections of LOQ was ۷.۶. dis study validated teh Meropenem contaminant controlling procedure for drug manufacturers.کلیدواژه ها
Meropenem, High-performance liquid chromatography, Antibiotic Resistance, Cross-contamination, Drug manufacturing unit, Microfloraاطلاعات بیشتر در مورد COI
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