化工技术与开发
化工技術與開髮
화공기술여개발
TECHNOLOGY & DVELOPMENT OF CHEMICAL INDUSTRY
2013年
11期
46-48,58
,共4页
红外光谱内标法%氯霉素片%氯霉素
紅外光譜內標法%氯黴素片%氯黴素
홍외광보내표법%록매소편%록매소
internal standard method of FTIR%chloramphenicol tablets%chloramphenicol
用红外光谱内标法(K3[Fe(CN)6]·6H2O为内标物)测定了氯霉素片中氯霉素的含量。实验表明,混合物红外光谱中氯霉素的测量峰(1686.4cm-1)和K3[Fe(CN)6]·6H2O的内标峰(2117.2cm-1)的峰高比(y=hi/hs)与两者质量比(x=mi/ms)有良好的线性关系,其线性回归方程为y=1.3127x+0.5705,相关系数r=0.9981。据此测得氯霉素片中氯霉素的含量为77.2%,相对标准偏差为1.8%,加标回收率分别为96.8%~103.8%,测定结果与药典规定的紫外分光光度法相近。该方法测量专属性强,无需分离提取,简便、快速、成本低,测定结果准确,特别适合快速批量检测,有应用价值。
用紅外光譜內標法(K3[Fe(CN)6]·6H2O為內標物)測定瞭氯黴素片中氯黴素的含量。實驗錶明,混閤物紅外光譜中氯黴素的測量峰(1686.4cm-1)和K3[Fe(CN)6]·6H2O的內標峰(2117.2cm-1)的峰高比(y=hi/hs)與兩者質量比(x=mi/ms)有良好的線性關繫,其線性迴歸方程為y=1.3127x+0.5705,相關繫數r=0.9981。據此測得氯黴素片中氯黴素的含量為77.2%,相對標準偏差為1.8%,加標迴收率分彆為96.8%~103.8%,測定結果與藥典規定的紫外分光光度法相近。該方法測量專屬性彊,無需分離提取,簡便、快速、成本低,測定結果準確,特彆適閤快速批量檢測,有應用價值。
용홍외광보내표법(K3[Fe(CN)6]·6H2O위내표물)측정료록매소편중록매소적함량。실험표명,혼합물홍외광보중록매소적측량봉(1686.4cm-1)화K3[Fe(CN)6]·6H2O적내표봉(2117.2cm-1)적봉고비(y=hi/hs)여량자질량비(x=mi/ms)유량호적선성관계,기선성회귀방정위y=1.3127x+0.5705,상관계수r=0.9981。거차측득록매소편중록매소적함량위77.2%,상대표준편차위1.8%,가표회수솔분별위96.8%~103.8%,측정결과여약전규정적자외분광광도법상근。해방법측량전속성강,무수분리제취,간편、쾌속、성본저,측정결과준학,특별괄합쾌속비량검측,유응용개치。
Potassium ferricyanide was added into chloramphenicol samples as internal reference and the mixtures were measured by Fou-rier transform infrared spectrophotometry (FT-IR). The peak of chloramphenicol at 1686.4 cm-1 was chosen as quantitative peak and the one of potassium ferricyanide at 2117.2 cm-1 was chosen as inside mark quantitative peak. The ratio of two peak’s absorbance (y=hi/hs) had good linear relationship with their mass ratio (x=mi/ms). The linear regression equation was y=1.3127x+0. 5705 with the correlation coef-ficient r=0.9981. The contents of chloramphenicol in the samples of chloramphenicol tablets was 77.2%, the relatively standard deviation was 1.8%, the recoveries of the method was 96.8%~103.8%. This method was highly specific measure, especially for fast batch testing.