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Determination of ethinylestradiol and levonorgestrel in oral contraceptives with HPLC methods with UV detection and UV/fluorescence detection

机译:用UV检测和UV /荧光检测用HPLC方法测定口腔避孕药中乙乙烯雌二醇和左旋烯醇酮

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摘要

Oral contraceptives are pharmaceutical formulations containing an estrogen in a small amount and a synthetic progestin in 5-30 times bigger amount. A sensitive, accurate and rapid method for determination of active compounds is required.udWe have developed HPLC methods for determination of ethinylestradiol (EED) and levonorgestrel (LNG) in commercially available tablets. Chromatographic separation was performed on a Purospher® STAR RP-18e reversed-phase column (150 X 4.0 mm I.D.; particle size 5 μm) in an isocratic mode with a mobile phase constituted of 47% acetonitrile: 53% water (V/V) for both methods. The elution was carried out at a flow rate of 1.50 ml /min. All analyses were performed at room temperature (24 +/- 2°C). In the HPLC method with UV detection (internal standard method) both compounds were detected at 215 nm. Drospirenone was used as an internal standard. In HPLC method with UV/fluorescence detection (external standard method) LNG was monitored at 242 nm, while EED was detected with fluorescence detector at 310 nm (excitation 285 nm).udThe methods’ performances were fully validated by a determination of linearity, reproducibility, accuracy and sensitivity. Both methods were applied for determination of Uniformity of Dosage Units. The results obtained with both methods were highly comparable. However, the HPLC method with UV/ fluorescence detection has showed superior sensitivity for EED indicated by 83 times loweruddetection limit.udHPLC method with UV/ fluorescence detection could be recommended as a method of choice for determination of ethinylestradiol, present at a very low dosage level in low-dose oral contraceptives, that also contain bigger amount of synthetic progestin.
机译:口服避孕药是包含在小的量的雌激素和在5-30倍大量的合成的孕激素的药物制剂。需要确定活性化合物的灵敏,准确和快速的方法。 udWe具有用于判定炔雌醇(EED)的和左炔诺孕酮(LNG)在商购的片剂发达的HPLC方法。 (150×4.0毫米内径;粒径为5μm)上的Purospher®STAR RP-18E进行色谱分离反相柱中结合移动相等度模式构成的47%乙腈:53%水(V / V)对于这两种方法。洗脱物在1.50毫升/分钟的流速进行。所有分析均在室温(24 +/- 2℃)下进行。在用UV检测(内标法)HPLC法在215nm检测两种化合物。屈螺酮被用作内标。在HPLC方法用UV /荧光检测(外标法)LNG在242处监测,而EED在310纳米(激发285纳米)。 udThe方法性能进行了充分的线性度的确定验证用荧光检测器检测,再现性,精确度和灵敏度。这两种方法被应用为确定剂量单位的均匀性。这两种方法得到的结果是高度相当的。为EED然而,用UV /荧光检测的HPLC方法已经显示了优良的灵敏度表示通过83倍降低 uddetection限制。 udHPLC方法用UV /荧光检测可被推荐为在非常测定炔雌醇的选择的方法,本在低剂量水平的低剂量口服避孕药,还包含合成的孕激素的量更大。

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