首页> 美国卫生研究院文献>AAPS PharmSciTech >Simultaneous Determination of Acetaminophen and Synthetic Color(s) by Derivative Spectroscopy in Syrup Formulations and Validation by HPLC: Exposure Risk of Colors to Children
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Simultaneous Determination of Acetaminophen and Synthetic Color(s) by Derivative Spectroscopy in Syrup Formulations and Validation by HPLC: Exposure Risk of Colors to Children

机译:通过糖浆配方中的导数光谱同时测定对乙酰氨基酚和合成色并通过HPLC进行验证:儿童接触颜色的风险

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摘要

Color additives are used in pediatric syrup formulations as an excipient; though not pre-requisite, but pediatric syrup formulations are normally colored. An attempt has been made to measure simultaneously the single drug, acetaminophen (AT), along with the colors, carmoisine (CA), erythrosine (ET), and sunset yellow FCF (SSY) added in it by three derivative spectroscopy methods namely, 1st order, ratio, and differential derivative methods. Moreover, evaluation has been made for the exposure assessment of the colors added as excipient because some colors have been reported to cause allergic reactions and hypersensitivity in children. The present methods provide simple, accurate, and reproducible quantitative determination of the drug, AT, along with the color in synthetic mixtures and commercial drug formulations without any interference. The limit of detection varied from 0.0001–0.31 μg/ml while limit of quantification ranged from 0.002–1.04 μg/ml in all the three methods. The calibration curve of all the three derivative methods exhibited good linear relationship with excellent regression coefficients (0.9986–1.000). Both intra-day and inter-day precisions showed %RSD value less than 2% while the percentage recovery was found between 96.8–103.8%. The sensitivity of the proposed methods is almost comparable to HPLC and thus, can be used for determination of drug AT, and color simultaneously in pharmaceutical formulation on routine basis. The present methods also showed that colors like SSY and ET are saturating more than 50% of acceptable daily intake (ADI) value which is alarming and needs to be considered for modification by regulatory authorities to safeguard the health of children.>Graphical Abstract
机译:着色剂在儿科糖浆配方中用作赋形剂。尽管不是前提条件,但儿科糖浆配方通常是有色的。尝试通过三种衍生光谱方法同时测量添加到其中的单一药物对乙酰氨基酚(AT)以及颜色,卡莫伊辛(CA),赤藓红(ET)和日落黄FCF(SSY),阶数,比率和微分导数方法。此外,由于据报道某些颜色会引起儿童过敏反应和超敏反应,因此已经对作为赋形剂添加的颜色的暴露评估进行了评估。本方法提供了简单,准确和可重现的药物AT定量测定方法,以及合成混合物和市售药物配方中的颜色,没有任何干扰。所有三种方法的检出限在0.0001–0.31μg/ ml之间,而定量限在0.002–1.04μg/ ml之间。所有三种导数方法的校准曲线均显示出良好的线性关系,并具有出色的回归系数(0.9986-1.000)。日内和日间精度均显示%RSD值小于2%,而回收率介于96.8–103.8%之间。所提出方法的灵敏度几乎与HPLC相当,因此可用于确定药物AT,并在常规基础上同时测定药物制剂的颜色。目前的方法还表明,像SSY和ET这样的颜色饱和度超过可接受的每日摄入量(ADI)值的50%以上,这令人震惊,需要监管机构考虑对其进行修改以保护儿童的健康。 ft0-> <!-fig @ position =“ anchor” mode = article f4-> <!-fig mode =“ anchored” f5-> >图形摘要<!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> <!-标题a7->ᅟ

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