Chemometrics-Assisted UV-Vis Spectrophotometry for Quality Control of Pharmaceuticals: A Review

被引：8

作者：

Nurani, Laela Hayu ^{[1
]}

Edityaningrum, Citra Ariani ^{[1
]}

Irnawati, Irnawati ^{[2
]}

Putri, Anggita Rosiana ^{[3
]}

Windarsih, Anjar ^{[4
]}

Guntarti, Any ^{[1
]}

Rohman, Abdul ^{[5
,6
]}

机构：

[1] Univ Ahmad Dahlan, Fac Pharm, Jl Prof Soepomo, Janturan 55164, Yogyakarta, Indonesia

[2] Univ Halu Oleo, Fac Pharm, Kendari 93232, Indonesia

[3] Univ Brawijaya, Fac Med, Dept Pharm, Jl Vet, Malang 65145, Indonesia

[4] Natl Res & Innovat Agcy BRIN, Res Ctr Food Technol & Proc PRTPP, Yogyakarta 55861, Indonesia

[5] Univ Gadjah Mada, Ctr Excellence Inst Halal Ind & Syst, Yogyakarta 55281, Indonesia

[6] Univ Gadjah Mada, Fac Pharm, Dept Pharmaceut Chem, Yogyakarta 55281, Indonesia

来源：

INDONESIAN JOURNAL OF CHEMISTRY | 2023年 / 23卷 / 02期

关键词：

UV-Vis spectroscopy; chemometrics; API; degradation products; pharmaceutical dosage forms; PARTIAL LEAST-SQUARES; MULTIVARIATE CALIBRATION; BINARY-MIXTURE; PARACETAMOL; VALIDATION; HYDROCHLOROTHIAZIDE; SPECTROSCOPY; MODELS; HYDROCHLORIDE; CARBAMAZEPINE;

D O I：

10.22146/ijc.74329

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Spectroscopic method in the UV-Vis region is considered the most molecular spectrometric method for content determination of a single component. However, a lot of pharmaceutical dosage forms comprise two or more components which lead to peak overlapping. Moreover, in the chemical stability test, active pharmaceutical ingredient (API) was also found along with the degradation products, impurities, and adulterant compounds. UV-Vis spectroscopy is one of the methods of choice for the determination or quantification of a single component in pharmaceutical preparations. The pharmaceutical products typically contain two or more APIs having chromophoric agents capable of absorbing UV-Vis beams and the absorbance values are summative from the absorption of each UV-Vis active compound according to the additive nature of LambertBeer law. The main problem for the simultaneous determination of API along with impurities and the degradation products in pharmaceutical preparations is the presence of overlapping peaks of UV-Vis spectra. The chemometrics-assisted spectroscopy is one of the analytical efforts to solve these problems. This review highlighted the application of chemometrics in combination with UV-Vis spectroscopy for the assay of API, impurities, adulteration issues and degradation products present in pharmaceutical dosage forms.

引用

页码：542 / 567

页数：26

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