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Development and validation of a RP-HPLC-PDA method for determination of curcuminoids in microemulsions

机译:RP-HPLC-PDA法测定微乳液中姜黄素的开发与验证

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A sensitive, specific and rapid high-performance liquid chromatography method was developed in an effort to quantify extremely low curcuminoid levels for the future transdermal experiments where the curcuminoids are incorporated with excipients such as microemulsion, liposomes, and micelles. The chromatographic separation was performed using a Symmetry~? C_ (18), 250 × 4.6 mm, 5-μm column, with a mobile phase composed of 5 mM acetonitrile:phosphoric acid (45:55, v/v) at a flow rate of 1.0 mL min~(-1), it was sensitive with a low limit of quantitation for curcuminoids (0.626 ng mL~(-1) for curcumin) and good linearity (r~ 2 ≥ 0.999) over the range 1-100 ng mL~(-1). All the validation data, such as accuracy and precision, were within the required limits from the ICH guideline. The assay method was successfully applied during forced degradation of curcuminoid solutions. The method retained its accuracy and precision when the standard addition technique was applied.
机译:开发了一种灵敏,特异且快速的高效液相色谱方法,旨在对未来的透皮实验(其中将姜黄素与微乳剂,脂质体和胶束等赋形剂结合在一起)进行定量分析,以测定极低的姜黄素含量。色谱分离使用Symmetry〜?进行。 C_(18),250×4.6 mm,5μm色谱柱,流动相由5 mM乙腈:磷酸(45:55,v / v)组成,流速为1.0 mL min〜(-1),对姜黄素类化合物的定量限很低(姜黄素为0.626 ng mL〜(-1)),在1-100 ng mL〜(-1)范围内具有良好的线性(r〜2≥0.999)。所有验证数据(例如准确性和精度)均在ICH指南要求的范围内。该测定方法已成功应用于姜黄素溶液的强制降解。当应用标准添加技术时,该方法保留了其准确性和精密度。

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