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首页> 外文期刊>Chemical Science International Journal >Application of HPTLC-densitometry byDerivatization and Stability Indicating LC forSimultaneous Determination of MefloquineHydrochloride and Artesunate in CombinedDosage form
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Application of HPTLC-densitometry byDerivatization and Stability Indicating LC forSimultaneous Determination of MefloquineHydrochloride and Artesunate in CombinedDosage form

机译:衍生化和稳定性指示LC的HPTLC密度测定法在联合剂型同时测定盐酸甲氟喹和青蒿琥酯中的应用

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摘要

This paper presents simultaneous quantification of mefloquine hydrochloride (MEFQ) and artesunate (ARTS) by HPTLC and RP-HPLC methods in combined tablet formulation. In RP-HPLC method, the drugs were resolved using a mobile phase of methanol-phosphate buffer (70:30, v/v) with pH adjusted to 3.2 using phosphoric acid on Symmetry C_(18) (250 × 4.6 mm and 5 μm) column in isocratic mode. Quantification was achieved with UV detection at 220 nm for MEFQ and 313 nm for ARTS based on peak area with linear calibration curves at concentration ranges of 12.5–75.0 and 2.5–15 μg/mL for MEFQ and ARTS respectively. In HPTLC method, the chromatograms were developed using a mobile phase of toluene-ethyl acetate-acetone (2.5:1.0:0.5, v/v/v) in pre-coated plate of silica gel 60 F_(254). It is a single method with two steps in which after the development of chromatogram, MEFQ was detected at 285 nm. Then ARTM was derivatized and detected at 525 nm. Recovery values of 97.36–98.80%, %RSD 0.9994 shows that the developed methods were accurate and precise. In HPLC, the binary drug mixture was exposed to thermal, photolytic, acid, alkali and oxidative stress. The methods distinctly separated the drugs and degradation products even in actual samples. In conclusion, the proposed HPLC and HPTLC methods were simple, precise, rapid and accurate. Both methods have the potential to determine these drugs simultaneously from dosage forms without any interference of excipients.
机译:本文介绍了通过HPTLC和RP-HPLC方法同时测定片剂组合中盐酸甲氟喹(MEFQ)和青蒿琥酯(ARTS)的含量。在RP-HPLC方法中,使用对称磷酸盐C_(18)(250×4.6 mm和5μm)上的甲醇-磷酸盐缓冲液(70:30,v / v)的流动相将pH值调节至3.2,用磷酸将药物拆分)列在等度模式下。基于峰面积的线性检测曲线,分别在MEFQ和ARTS的浓度范围分别为12.5–75.0和2.5–15μg/ mL的条件下,对MEFQ和ARTS分别在220 nm和313 nm处进行紫外检测,从而实现了定量。在HPTLC方法中,色谱图是在硅胶60 F_(254)的预涂板上使用甲苯-乙酸​​乙酯-丙酮(2.5:1.0:0.5,v / v / v)的流动相绘制的。这是一个包含两个步骤的单一方法,其中在色谱图显影后,在285 nm处检测到MEFQ。然后将ARTM衍生化并在525 nm处检测。回收率为97.36–98.80%,%RSD为0.9994,表明所开发的方法准确而精确。在HPLC中,二元药物混合物暴露于热,光解,酸,碱和氧化应激。该方法甚至在实际样品中也能明显分离药物和降解产物。总之,所提出的HPLC和HPTLC方法简便,准确,快速且准确。两种方法都有可能从剂型中同时确定这些药物,而不会对赋形剂产生任何干扰。

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