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一种用于普拉佐米星的双功能显色和荧光苯并呋喃嗪探针及其在开发两种高通量微孔分析方法以分析原料药和药物制剂方面的创新应用。

A dual-function chromogenic and fluorogenic benzofurazan probe for plazomicin and its innovative utility for development of two microwell assays with high throughput for analysis of drug substance and pharmaceutical formulations.

作者信息

Alkathiri Fai A, Al-Outaibi Majed, Darwish Ibrahim A

机构信息

Department of Pharmaceutics, College of Pharmacy, King Saud University P. O. Box 2457 Riyadh 11451 Saudi Arabia falkathire@@ksu.edu.sa +966-114677200 +966-118052392.

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University P. O. Box 2457 Riyadh 11451 Saudi Arabia.

出版信息

RSC Adv. 2024 Aug 27;14(37):27215-27226. doi: 10.1039/d4ra04882b. eCollection 2024 Aug 22.

DOI:10.1039/d4ra04882b
PMID:39193289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11348761/
Abstract

Plazomicin (PLZ) is a novel aminoglycoside which has been recently approved by The US Food and Drug Administration for the treatment of complicated urinary tract infections including acute pyelonephritis, caused by certain Enterobacteriaceae, in adult patients with limited or no options for alternative treatment. This study focuses on the development of microwell-based photometric and fluorometric assays for the quantitative determination of PLZ in its bulk drug substance and commercial pharmaceutical formulations (Zemedri® injections). Both assays utilize the dual-function chromogenic and fluorogenic properties of the 4-fluoro-7-nitrobenzofurazan (NBD-F) probe. The reaction between PLZ and NBD-F, conducted in a borate buffer at pH 8, resulted in the formation of a colored and fluorescent reaction product. The product exhibited maximum light absorption at 473 nm and emitted fluorescence at 541 nm when excited at 473 nm. Factors influencing the reaction between PLZ and NBD-F were thoroughly investigated, and optimal conditions were determined. Under the optimized reaction conditions, calibration curves were generated to establish the relationship between absorbance and fluorescence intensities of the reaction product with the corresponding PLZ concentrations. The absorbance-concentration relation was linear in a PLZ concentration range of 20-800 μg mL with a limit of quantitation of 25 μg mL, while the fluorescence-concentration relation was linear in the concentration range of 0.05-1.5 μg mL with a limit of quantitation of 0.08 μg mL. Both assays underwent validation and were successfully applied to the quantitation of PLZ in its bulk drug substance and pharmaceutical formulations (injections) with satisfactory accuracy and precision. The eco-friendliness/greenness assessment of the assays demonstrated that both assays comply with the requirements of green analytical chemistry approaches. Furthermore, the proposed microwell assay plates allowed for the simultaneous handling of numerous samples with micro-volumes, enabling high-throughput analysis. In conclusion, this study represents the first evaluation of NBD-F as a dual-function probe for the microwell-based photometric and fluorometric determination of PLZ. The developed assays serve as valuable analytical tools for the quality control of PLZ's bulk drug substance and pharmaceutical formulations.

摘要

普拉佐米星(PLZ)是一种新型氨基糖苷类药物,最近已获美国食品药品监督管理局批准,用于治疗由某些肠杆菌科细菌引起的复杂性尿路感染,包括急性肾盂肾炎,适用于替代治疗选择有限或没有替代治疗选择的成年患者。本研究重点在于开发基于微孔板的光度法和荧光法,用于定量测定原料药和商业药物制剂(Zemedri®注射液)中的PLZ。两种方法均利用了4-氟-7-硝基苯并呋喃(NBD-F)探针的双功能显色和荧光特性。PLZ与NBD-F在pH 8的硼酸盐缓冲液中进行反应,生成有色且有荧光的反应产物。该产物在473 nm处有最大吸光度,在473 nm激发时于541 nm处发射荧光。对影响PLZ与NBD-F反应的因素进行了全面研究,并确定了最佳条件。在优化的反应条件下,绘制校准曲线以建立反应产物的吸光度和荧光强度与相应PLZ浓度之间的关系。吸光度与浓度的关系在PLZ浓度范围为20 - 800 μg/mL时呈线性,定量限为25 μg/mL,而荧光与浓度的关系在浓度范围为0.05 - 1.5 μg/mL时呈线性,定量限为0.08 μg/mL。两种方法均经过验证,并成功应用于原料药和药物制剂(注射液)中PLZ的定量,具有令人满意的准确度和精密度。对这些方法的生态友好性/绿色度评估表明,两种方法均符合绿色分析化学方法的要求。此外,所提出的微孔板检测方法允许同时处理大量微量样品,实现高通量分析。总之,本研究首次评估了NBD-F作为基于微孔板的光度法和荧光法测定PLZ的双功能探针。所开发的方法是用于PLZ原料药和药物制剂质量控制的有价值的分析工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/29b3d668ca5c/d4ra04882b-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/598a4f690bbb/d4ra04882b-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/6e3fa606c069/d4ra04882b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/750f13268289/d4ra04882b-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/c1b5b4d5f0a2/d4ra04882b-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/d3b3731ab80e/d4ra04882b-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/29b3d668ca5c/d4ra04882b-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/598a4f690bbb/d4ra04882b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/6ff9925be673/d4ra04882b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/6e3fa606c069/d4ra04882b-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/750f13268289/d4ra04882b-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/c1b5b4d5f0a2/d4ra04882b-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/d3b3731ab80e/d4ra04882b-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5893/11348761/29b3d668ca5c/d4ra04882b-f7.jpg

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Plazomicin: a new aminoglycoside in the fight against antimicrobial resistance.普拉佐米星:一种对抗抗菌药物耐药性的新型氨基糖苷类药物。
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