化学分析计量
化學分析計量
화학분석계량
CHEMICAL ANALYSIS AND METERAGE
2014年
z1期
35-37
,共3页
离子色谱%抑制电导%伊班膦酸钠%亚磷酸%磷酸
離子色譜%抑製電導%伊班膦痠鈉%亞燐痠%燐痠
리자색보%억제전도%이반련산납%아린산%린산
ion chromatography%suppressor conductivity detection%ibandronate sodium%phosphate%phosphorous
建立了离子色谱–抑制电导法检测伊班膦酸钠中亚磷酸根和磷酸根离子的方法。实验采用SH–AC–1型离子交换色谱柱,3.6 mmol/L碳酸钠–4.5 mmol/L碳酸氢钠为淋洗液,流量为1.5 mL/min,进样体积为20μL。在此条件下,可同时分离亚磷酸和磷酸根离子,且色谱峰型对称。所测H2PO3–,H2PO4–离子的检出限(S/N=3)分别为0.027,0.053 mg/L。应用该方法测定H2PO3–,H2PO4–离子,加标回收率分别为95.7%~108.1%,99.8%~107.7%,测定结果的相对标准偏差分别为2.5%,5.6%(n=6)。该方法简单,测定结果准确、可靠,可以用于实际生产中监测伊班膦酸钠的质量。
建立瞭離子色譜–抑製電導法檢測伊班膦痠鈉中亞燐痠根和燐痠根離子的方法。實驗採用SH–AC–1型離子交換色譜柱,3.6 mmol/L碳痠鈉–4.5 mmol/L碳痠氫鈉為淋洗液,流量為1.5 mL/min,進樣體積為20μL。在此條件下,可同時分離亞燐痠和燐痠根離子,且色譜峰型對稱。所測H2PO3–,H2PO4–離子的檢齣限(S/N=3)分彆為0.027,0.053 mg/L。應用該方法測定H2PO3–,H2PO4–離子,加標迴收率分彆為95.7%~108.1%,99.8%~107.7%,測定結果的相對標準偏差分彆為2.5%,5.6%(n=6)。該方法簡單,測定結果準確、可靠,可以用于實際生產中鑑測伊班膦痠鈉的質量。
건립료리자색보–억제전도법검측이반련산납중아린산근화린산근리자적방법。실험채용SH–AC–1형리자교환색보주,3.6 mmol/L탄산납–4.5 mmol/L탄산경납위림세액,류량위1.5 mL/min,진양체적위20μL。재차조건하,가동시분리아린산화린산근리자,차색보봉형대칭。소측H2PO3–,H2PO4–리자적검출한(S/N=3)분별위0.027,0.053 mg/L。응용해방법측정H2PO3–,H2PO4–리자,가표회수솔분별위95.7%~108.1%,99.8%~107.7%,측정결과적상대표준편차분별위2.5%,5.6%(n=6)。해방법간단,측정결과준학、가고,가이용우실제생산중감측이반련산납적질량。
The method for determination of phosphate and phosphorous in ibandronate sodium by ion chromatography–suppressed conductivity detection was established. SH–AC–1 ion exchange column was used, 3.6 mmol/L sodium carbonate–4.5 mmol/L sodium bicarbonate was used as the eluent with theflow rate of 1.5 mL/min, and sample volume was 20μL. In these conditions,the separation of H2PO3–,H2PO4– was carried out with symmetric peak. The detection limit(S/N=3) of H2PO3– and H2PO4– was 0.027,0.053 mg/L, respectively. The recoveries of H2PO3–,H2PO4– were 95.7%–108.1%,99.8%–107.7%,respectively,and the relative standard deviation of determination results was 2.5%, 5.6%(n=6),respectively. This method is simple,accurate,reliable,and better practical applicability. It can be monitored quality of ibandronate sodium during product manufacturing.