Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/54669
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dc.contributor.authorNguyễn, Quốc Vượng-
dc.contributor.authorTrần, Thị Bích Vân-
dc.contributor.authorNguyễn, Thị Liên-
dc.contributor.authorVũ, Văn Chiến-
dc.contributor.authorPhạm, Thị Hằng-
dc.contributor.authorNguyễn, Thị Huế-
dc.date.accessioned2021-06-09T07:47:55Z-
dc.date.available2021-06-09T07:47:55Z-
dc.date.issued2018-
dc.identifier.issn0866-7861-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/54669-
dc.description.abstractLinezolid was synthesized, purified, and evaluated for acute toxicity. The purity of the synthesized linezolid was analyzed by HPLC as follows: Column - Phenomenex Rp18(5 pm, 150 mm x 4.6 mm); Flow rate -1.0 ml/min; Detector- UV (251 nm): Mobile phase - Monobasic ammonium phosphate buffer (0.23 g/1000 mL)/Methanol 75/25 (v/v). By calibration curves, the purity of the obtained linezolid was found to attain 99.7%, with two impurities in quite low percentages (0.012% and 0.021%). /4s thus, synthesized linezolid showed well meet the requirments by USP 2012. Acute toxicity of the linezolid in mouse was performed at the dose level of 5000 - 8000 mg/kgP of mouse and observed for 7 consecutive days. The LD^value (6.32 ± 0.24) g/1 kg of mouse proved low toxicity of linezolid.vi_VN
dc.language.isovivi_VN
dc.relation.ispartofseriesTạp chí Dược học;Số 510 .- Tr.52-55-
dc.subjectLinezolidvi_VN
dc.subjectPurificationvi_VN
dc.subjectHPLCvi_VN
dc.subjectAcute toxicityvi_VN
dc.titleTinh chế, xác định hàm lượng và đánh giá độc tính cấp của tác nhân kháng khuẩn linezolidvi_VN
dc.typeArticlevi_VN
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