固体制剂中的近紫外线和可见光光降解:柠檬酸盐缓冲液和铁(III)生成二氧化碳自由基阴离子。

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Pharmaceutics Pub Date : 2024-09-02 Epub Date: 2024-08-07 DOI:10.1021/acs.molpharmaceut.4c00513
Maribel Espinoza Ballesteros, Christian Schöneich
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引用次数: 0

摘要

在生产和储存过程中,近紫外线和可见光的光降解会对治疗蛋白质产生影响。虽然人们对光降解的基本途径往往不甚了解,但需要考虑的一个重要方面是制剂,特别是制剂缓冲液。柠檬酸盐是生物制药配方中常见的缓冲剂,它能与过渡金属(如铁(III))发生络合反应。在水溶液中,此类络合物遇光会形成二氧化碳自由基阴离子 (-CO2-),这是一种强力还原剂。然而,很少有研究对固体制剂中的此类过程进行描述。在这里,我们通过 DMPO 自旋捕获和 HPLC-MS/MS 分析表明,含有铁(III)的固体柠檬酸盐配方会导致 -CO2- 的光化学形成。我们评估了缓冲剂、氧气供应、辅料和固体制剂生产工艺等因素对 -CO2- 和其他自由基(如 -OH)形成的影响。
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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Near UV and Visible Light Photodegradation in Solid Formulations: Generation of Carbon Dioxide Radical Anions from Citrate Buffer and Fe(III).

Near UV and visible light photodegradation can target therapeutic proteins during manufacturing and storage. While the underlying photodegradation pathways are frequently not well-understood, one important aspect of consideration is the formulation, specifically the formulation buffer. Citrate is a common buffer for biopharmaceutical formulations, which can complex with transition metals, such as Fe(III). In an aqueous solution, the exposure of such complexes to light leads to the formation of the carbon dioxide radical anion (CO2-), a powerful reductant. However, few studies have characterized such processes in solid formulations. Here, we show that solid citrate formulations containing Fe(III) lead to the photochemical formation of CO2-, identified through DMPO spin trapping and HPLC-MS/MS analysis. Factors such as buffers, the availability of oxygen, excipients, and manufacturing processes of solid formulations were evaluated for their effect on the formation of CO2- and other radicals such as OH.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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