兽药绿色和白色评价方法中的惩罚和颜色代码技术方法:妥曲珠利悬浮剂的检测。

Miranda F Kamal, Rasha M Youssef, Nehal W El-Sayed, Samir Morshedy, Haydi S Elbordiny
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引用次数: 0

摘要

背景:肠球虫病是一种使家禽和牲畜衰弱的疾病,在全球范围内造成经济影响。在饲料中添加抗球虫药物可预防和治疗肉鸡球虫病。在饮用水中添加 Toltrazuril 可治疗球虫病:目的:开发了三种可靠的分析方法,用于定量检测纯药和药物制剂中的妥曲珠利。此外,还采用了生态学指标、基于惩罚或颜色编码的技术来评估检测方法:首先,采用二次衍生(Δλ;5 nm)分光光度法;在 5-25 μg/mL 的线性范围内,在 244-260 nm 波长处测量oltrazuril 的峰值。第二种方法是在硅胶铝片上进行高效薄层色谱分析,以乙酸乙酯、甲醇、氯化铵缓冲液和水(8:1:0.5:0.5)(%V/V)为洗脱相。在 243 纳米波长下,托曲唑在 1-9 μg/spot 范围内线性测定,延迟因子为 0.66 ± 0.01。第三种是反相-高效液相色谱二极管阵列检测法,采用安捷伦 C18 色谱柱(5 μm,4.6 x 150 mm),等度洗脱模式,流动相为乙腈和水,比例分别为 80:20(v/v),流速为 1 mL/min。妥曲珠利的洗脱保留时间为 2.58 ± 0.1 分钟,在 0.25-25 μg/mL 范围内于 243 纳米波长下线性测定:计算出的二维值和峰面积与相应的药物浓度高度相关,相关系数r>0.999。所有方法均通过 ICH 验证,并应用于剂型,回收率令人满意(97-103%)。使用 t 检验和 F 检验进行的统计比较显示,差异不明显。在绿色和白度标准方面,对所提出的方法进行了评估,并将其与四种不同的报告方法进行了排名:结论:所提出的方法绿色、准确,可用于常规质量控制,测定药物制剂中的妥曲珠利。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Penalization and Color Code Technical Approaches for Method Greenness and Whiteness Appraisal in Veterinary Medication: Assay of Toltrazuril Suspension.

Background: Intestinal coccidiosis is a debilitating disease in poultry and livestock, leading to economic impact worldwide. Coccidiosis is prevented and treated in broilers by the inclusion of anticoccidials in feed. Toltrazuril is administered in potable water to treat coccidiosis.

Objective: Three robust analytical methods for the quantitation of toltrazuril in pure and pharmaceutical formulations are developed. Furthermore, ecological metrics, either penalization- or color-code-based techniques, are applied for the appraisal of assays.

Methods: First, second-derivative (Δλ; 5 nm) spectrophotometric method is used. Toltrazuril is measured from peak to peak at 244-260 nm within a linearity range of 5-25 μg/mL. The second method is an HPTLC analysis performed on an aluminum sheet of silica gel using ethyl acetate-methanol-ammonium chloride buffer-water (8:1:0.5:0.5, by volume respectively) as the elution phase. Toltrazuril, at a retardation factor of 0.66 ± 0.01, is linearly determined in the range of 1-9 μg/spot at 243 nm. The third method is reversed-phase HPLC with diode array detection, using an Agilent C18 column (5 μm, 4.6 × 150 mm) in isocratic elution mode at 1 mL/min flow rate with a mobile phase of acetonitrile and water in a ratio of 80:20 (v/v). Toltrazuril elutes at a retention time of 2.58 ± 0.1 min and is linearly determined at 243 nm in the range of 0.25-25 μg/mL.

Results: Calculated 2D-values and peak areas are highly correlated to their corresponding drug concentrations at coefficients: r > 0.999. All methods were International Council of Harmonization (ICH) validated and applied to the dosage form with satisfactory % recoveries (97-103%). Statistical comparisons versus reported one using t-test and F-test disclose insignificant variation. In examining greenness and whiteness norms, the proposed methods were evaluated and ranked alongside four different reported methods.

Conclusions: The proposed methods are green, accurate, and can be applied in routine QC for the determination of toltrazuril in pharmaceutical formulations.

Highlights: Intestinal coccidiosis substantially affects the chicken intestinal tract leading to reduced growth. Toltrazuril is used for the treatment and prevention of intestinal coccidiosis. Three robust, accurate, and precise analytical methods are developed for toltrazuril determination in pure and pharmaceutical formulations. All proposed methods were ecologically assessed and compared with published ones.

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