Correction to “Primaquine Analysis in Pharmaceutical Formulation Using Multiple and Short-End Injections by Capillary Zone Electrophoresis-Ultraviolet Detection”

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
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引用次数: 0

Abstract

J. C. Q. de Souza, P. R. Chellini, M. V. N. de Souza, and M. A. L. de Oliveira, “Primaquine Analysis in Pharmaceutical Formulation Using Multiple and Short-End Injections by Capillary Zone Electrophoresis-Ultraviolet Detection,” Journal of Separation Science 47, no. 22 (2024): 1–11, https://doi.org/10.1002/jssc.70026.

The corrections to the article entitled “Primaquine Analysis in Pharmaceutical Formulation Using Multiple and Short-End Injections by Capillary Zone Electrophoresis-Ultraviolet Detection,” published in the Journal of Separation Science, DOI: 10.1002/jssc.70026 were considered. Thus, the corrections took into account errors in the following sections: Introduction, paragraph 2, and BGE Optimization, paragraph 2. Additionally, a correction was performed in Figure 1. The explanations for each corrected item have been described in detail.

In paragraph 2 of the “Introduction” section, the text “[…] the pKa2 belongs to the nitrogen of pyridine moiety; […]” was incorrect. This should have read: “[…] the pKa2 belongs to the nitrogen of the quinoline ring; […].”

In paragraph 2 of the “BGE Optimization” section, the text “The effective mobility versus pH curves in Figure 1B showed that the PQN is ionized up to pH 3.0, has a neutral behavior in the range of 4.0–10.0, and the anionic form becomes predominant at a pH above 11.0. So, PQN at pH values lower than pKa2 behaves as a Lewis acid; at pH values between 4.5 and 9.5, approximately, it will have neutral behavior. Finally, above pH 10.4, it will behave as a Lewis base.” was incorrect. This should have read: “The effective mobility versus pH curves in Figure 1B show that PQN is doubly positively charged up to pH 3.2 (pKa1), exhibits cationic behavior with a single positive charge in the pH range 4.0–10.0, and its neutral form becomes predominant at pH values above 10.4 (pKa3). The expanded region of the first inflection point of the PQN curve, between 19.6 and 20.6 cm2 V−1 s−1, is shown in Figure 1C.”

In Figure 1, Figure 1B is incorrect because the effective mobility versus pH curve of primaquine is incorrect. After recalculating the data, new mobility values were obtained, and the updated curve presents a very subtle inflection region. Therefore, the new Figure 1 should be divided into three parts: 1A—Primaquine structure and its pKa values; 1B—effective mobility versus pH curves for primaquine and background electrolyte components; and 1C—the expanded region of the first inflection point of the primaquine curve.″ The correct Figure 1 is shown below.

We apologize for these errors.

Abstract Image

Abstract Image

Abstract Image

对“用毛细管带电泳-紫外检测法分析多端和短端注射剂制剂中的伯氨喹”的修正
J. C. Q. de Souza, P. R. Chellini, M. V. N. de Souza, M. A. L. de Oliveira,“用毛细管带电泳-紫外检测法分析多端和短端注射药物配方中的伯氨喹”,《分离科学》第47期,第4期。22 (2024): 1-11, https://doi.org/10.1002/jssc.70026.The对题为“通过毛细管带电泳-紫外检测使用多个和短端注射的药物配方中的伯氨喹分析”的文章的更正,发表在《分离科学杂志》上,DOI: 10.1002/jssc。70026被考虑。因此,修正考虑了以下部分的错误:引言,第2段和BGE优化,第2段。此外,在图1中执行了更正。每一项修正的解释都有详细的描述。在“引言”部分的第2段中,文本“[…]pKa2属于吡啶部分的氮;[…]是不正确的。这应该是:“[…]pKa2属于喹啉环的氮;[…]”。在“BGE优化”部分的第2段中,文本“图1B的有效迁移率随pH曲线显示PQN在pH为3.0时电离,在4.0-10.0范围内具有中性行为,并且在pH高于11.0时阴离子形式成为主导。”因此,PQN在pH值低于pKa2时表现为路易斯酸;在pH值大约在4.5和9.5之间时,它将具有中性行为。最后,当pH值高于10.4时,它会表现为路易斯碱。这应该是这样写的:“图1B中的有效迁移率与pH曲线表明,PQN在pH 3.2 (pKa1)时具有双正电荷,在pH 4.0-10.0范围内具有单正电荷的阳离子行为,而在pH高于10.4 (pKa3)时,其中性形式占主导地位。PQN曲线第一个拐点的扩展区域在19.6 ~ 20.6 cm2 V−1 s−1之间,如图1C所示。在图1中,图1B是不正确的,因为伯氨喹的有效迁移率随pH值的曲线是不正确的。重新计算数据后,得到了新的迁移率值,更新后的曲线呈现出一个非常微妙的拐点区域。因此,新的图1应分为三部分:1a -伯氨喹结构及其pKa值;伯氨喹和本底电解质组分的有效迁移率随pH曲线;和1c -伯氨喹曲线第一个拐点的扩展区域。″正确的图1如下所示。我们为这些错误道歉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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