海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2014年
12期
245-246,247
,共3页
张涛%陈楚雄%余晓霞%温预关
張濤%陳楚雄%餘曉霞%溫預關
장도%진초웅%여효하%온예관
液相色谱-质谱联用法%帕珠沙星%血药浓度
液相色譜-質譜聯用法%帕珠沙星%血藥濃度
액상색보-질보련용법%파주사성%혈약농도
LC-MS/MS%Pazufloxacin%Plasma centration
目的:建立一种快速灵敏检测帕珠沙星血药物浓度的液相色谱-串联质谱方法。方法色谱柱为 Agilent Eclipse XDB-C18(4.6mm ×150mm,5μm);流动相为乙腈:水(0.005mol? L-1甲酸铵,0.1%甲酸)=(30∶70);流速:0.5mL? min -1;质谱条件为电喷雾电离源(ESI);采用选择反应监测(SRM)对帕珠沙星(m/z 319.0→301.1)和环丙沙星(m/z 332.2→314.2)进行测定。样本处理采用乙腈沉淀蛋白法,吸取上清液1μL进样。结果帕珠沙星的线性范围为0.02~20μg? mL -1,提取回收率为82%~92%,日内和日间精密度均小于15%。结论本方法简便、灵敏,该方法经考察符合血浆样品的测定要求,可以应用于临床药物浓度的测定和药代动力学的研究。
目的:建立一種快速靈敏檢測帕珠沙星血藥物濃度的液相色譜-串聯質譜方法。方法色譜柱為 Agilent Eclipse XDB-C18(4.6mm ×150mm,5μm);流動相為乙腈:水(0.005mol? L-1甲痠銨,0.1%甲痠)=(30∶70);流速:0.5mL? min -1;質譜條件為電噴霧電離源(ESI);採用選擇反應鑑測(SRM)對帕珠沙星(m/z 319.0→301.1)和環丙沙星(m/z 332.2→314.2)進行測定。樣本處理採用乙腈沉澱蛋白法,吸取上清液1μL進樣。結果帕珠沙星的線性範圍為0.02~20μg? mL -1,提取迴收率為82%~92%,日內和日間精密度均小于15%。結論本方法簡便、靈敏,該方法經攷察符閤血漿樣品的測定要求,可以應用于臨床藥物濃度的測定和藥代動力學的研究。
목적:건립일충쾌속령민검측파주사성혈약물농도적액상색보-천련질보방법。방법색보주위 Agilent Eclipse XDB-C18(4.6mm ×150mm,5μm);류동상위을정:수(0.005mol? L-1갑산안,0.1%갑산)=(30∶70);류속:0.5mL? min -1;질보조건위전분무전리원(ESI);채용선택반응감측(SRM)대파주사성(m/z 319.0→301.1)화배병사성(m/z 332.2→314.2)진행측정。양본처리채용을정침정단백법,흡취상청액1μL진양。결과파주사성적선성범위위0.02~20μg? mL -1,제취회수솔위82%~92%,일내화일간정밀도균소우15%。결론본방법간편、령민,해방법경고찰부합혈장양품적측정요구,가이응용우림상약물농도적측정화약대동역학적연구。
OBJECTIVE To establish a specific and sensitive HPLC-MS/MS method for determining the con-centration of pazufloxacin in human plasma .METHODS Pazufloxacin was extracted with acetonitrile .The drugs from plasma were separated on a Agilent Eclipse XDB-C18 (4.6mm ×150mm,5μm) column by using mobile phase consisted of acetonitrile (0.1%formic acid)-0.005mol? L-1 ammonium formate (30:70 V/V);the flow rate was 0.5 mL? min-1;an electrospray ionization ion-trap sourse was used as the detector and operated in the positive ion mode.Selected reacted monitoring ( SRM) was used to dectct pazufloxacin ( m/z 319.0→301.1 ) and ciprofloxacin ( m/z 332.2→314.2 ) .After protein sediment by acetonitrile ,1μL supernatantwas injected .RESULTS The cali-bration curves were linear in the range of 0.02~20μg? mL-1 .The extraction recovery was 82%~92%.The intra-day and inter-day variations (RSD) were less than 15%.CONCLUSION The method is sensitive,accurate,simple and quick ,it can be used for clinical drug monitoring and pharmacokinetics studies of pazufloxacin .