Quantitative analysis of cephalexin in solid dosage form by Raman spectroscopy and chemometric tools.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-01-01 Epub Date: 2024-01-30 DOI:10.1080/03639045.2023.2290021
Nida Ghafoor, Naeema Kanwal, Haq Nawaz, Muhammad Irfan Majeed, Nosheen Rashid, Shazra Ishtiaq, Rabiah Tariq, Kiran Kainat, Arslan Ali, Ayesha Anwar, Zainab Shoukat, Aiman Amir, Muhammad Imran
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引用次数: 0

Abstract

Objective: To use Raman Spectroscopy for qualitative and quantitative evaluation of pharmaceutical formulations of active pharmaceutical ingredient (API) of Cephalexin.

Significance: Raman Spectroscopy is a noninvasive, nondestructive, reliable and rapid detection technique used for various pharmaceutical drugs quantification. The present study explores the potential of Raman Spectroscopy for quantitative analysis of pharmaceutical drugs.

Method: For qualitative and quantitative analysis of Cephalexin API, various standard samples containing less and more concentration of API than commercial tablet was prepared. To study spectral differences, the mean plot of all the samples was prepared. For qualitative analysis, Principal Component Analysis (PCA) and for quantitative analysis Partial Least Square Regression analysis (PLSR) was used. Both of these are Multivariate data analysis techniques and give reliable results as published in previous literature.

Results: PCA model distinguished all the Raman Spectral data related to the various Cephalexin solid dosage formulations whereas the PLSR model was used to calculate the concentration of different unknown formulations. For the PLSR model, RMSEC and RMSEP were determined to be 3.3953 and 3.8972, respectively. The prediction efficiency of this built PLSR model was found to be very good with a goodness of the model value (R2) of 0.98. The PLSR model also predicted the concentrations of Cephalexin formulations in the blind or unknown sample.

Conclusion: These findings demonstrate that the Raman spectroscopy coupled to PLSR analysis could be regarded as a fast and effectively reliable tool for quantitative analysis of pharmaceutical drugs.

利用拉曼光谱和化学计量学工具对固体制剂中的头孢氨苄进行定量分析。
目的:利用拉曼光谱对头孢氨苄的活性药物成分(API)进行定性和定量评估:利用拉曼光谱对头孢氨苄有效成分(API)的药物制剂进行定性和定量评估:拉曼光谱是一种非侵入性、非破坏性、可靠且快速的检测技术,可用于各种药物的定量分析。本研究探讨了拉曼光谱在定量分析药物方面的潜力:方法:为了对头孢氨苄原料药进行定性和定量分析,制备了不同的标准样品,这些样品中的原料药浓度比商品片剂低,也比商品片剂高。为研究光谱差异,绘制了所有样品的平均图。定性分析采用主成分分析法(PCA),定量分析采用部分最小平方回归分析法(PLSR)。这两种方法都是多变量数据分析技术,可提供可靠的结果,这已在以前的文献中发表过:结果:PCA 模型区分了与各种头孢氨苄固体制剂有关的所有拉曼光谱数据,而 PLSR 模型则用于计算不同未知制剂的浓度。PLSR 模型的 RMSEC 和 RMSEP 分别为 3.3953 和 3.8972。所建立的 PLSR 模型的预测效率非常高,模型优度(R2)为 0.98。PLSR 模型还预测了盲样或未知样品中头孢氨苄制剂的浓度:这些研究结果表明,拉曼光谱与 PLSR 分析相结合,可被视为一种快速、有效、可靠的药物定量分析工具。
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
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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