反相高效液相色谱法同时定量制剂中扑热息痛和布洛芬的方法建立、验证及强制降解研究。

Analytical Chemistry Insights Pub Date : 2014-11-18 eCollection Date: 2014-01-01 DOI:10.4137/ACI.S18651
Md Sarowar Jahan, Md Jahirul Islam, Rehana Begum, Ruhul Kayesh, Asma Rahman
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引用次数: 27

摘要

建立了一种快速、稳定指示的反相高效液相色谱(RP-HPLC)方法,用于同时定量对乙酰氨基酚和布洛芬的联合剂型,特别是与已有的联合剂型方法相比,该方法具有更大的优势。根据美国药典(USP)指南对该方法进行了准确性、精密度、特异性、线性、溶液稳定性、鲁棒性、灵敏度和系统适用性等方面的验证。根据国际协调会议(ICH)验证了强制降解研究。为此,在常温下,在RP C18 (octadecylsilane (ODS), 150 × 4.6 mm, 5 μm, Phenomenex Inc.)色谱柱上,以pH 6.8的磷酸盐缓冲液和乙腈的比例为65:35,v/v,流速为0.7 mL/min的等温流动相条件下进行。对乙酰氨基酚和布洛芬的相关系数(R(2))分别为0.999和1.0,均在相关系数限定范围内(R(2) > 0.995),线性响应良好。两种药物的加样回收率均在可接受范围(97.0 ~ 103.0%)内。新方法日内、日间精密度研究均小于最大允许限度相对标准偏差百分比(%RSD)≤2.0。根据ICH指南对药品进行强制降解,目的是建立该方法的稳定性指示特性,并提供有关降解途径、降解产物以及在各种应力条件影响下原料药和药品质量如何随时间变化的有用信息。布洛芬的降解在限定范围内(根据ICH指南5-20%),扑热息痛则在限定范围内
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A Study of Method Development, Validation, and Forced Degradation for Simultaneous Quantification of Paracetamol and Ibuprofen in Pharmaceutical Dosage Form by RP-HPLC Method.

A rapid and stability-indicating reversed phase high-performance liquid chromatography (RP-HPLC) method was developed for simultaneous quantification of paracetamol and ibuprofen in their combined dosage form especially to get some more advantages over other methods already developed for this combination. The method was validated according to United States Pharmacopeia (USP) guideline with respect to accuracy, precision, specificity, linearity, solution stability, robustness, sensitivity, and system suitability. Forced degradation study was validated according to International Conference on Harmonisation (ICH). For this, an isocratic condition of mobile phase comprising phosphate buffer (pH 6.8) and acetonitrile in a ratio of 65:35, v/v at a flow rate of 0.7 mL/minute over RP C18 (octadecylsilane (ODS), 150 × 4.6 mm, 5 μm, Phenomenex Inc.) column at ambient temperature was maintained. The method showed excellent linear response with correlation coefficient (R (2)) values of 0.999 and 1.0 for paracetamol and ibuprofen respectively, which were within the limit of correlation coefficient (R (2) > 0.995). The percent recoveries for two drugs were found within the acceptance limit of (97.0-103.0%). Intra-and inter-day precision studies of the new method were less than the maximum allowable limit percentage of relative standard deviation (%RSD) ≤ 2.0. Forced degradation of the drug product was carried out as per the ICH guidelines with a view to establishing the stability-indicating property of this method and providing useful information about the degradation pathways, degradation products, and how the quality of a drug substance and drug product changes with time under the influence of various stressing conditions. The degradation of ibuprofen was within the limit (5-20%, according to the guideline of ICH), while paracetamol showed <20% degradation in oxidation and basic condition.

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