Investigation of the Sensitivity of Transmission Raman Spectroscopy for Polymorph Detection in Pharmaceutical Tablets

被引:17
|
作者
Feng, Hanzhou [1 ]
Bondi, Robert W., Jr. [2 ]
Anderson, Carl A. [1 ]
Drennen, James K., III [1 ]
Igne, Benoit [2 ]
机构
[1] Duquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA 15219 USA
[2] GlaxoSmithKline, Analyt Sci & Dev, 709 Swedeland Rd, King Of Prussia, PA 19406 USA
关键词
Transmission Raman spectroscopy; polymorphs detection; sensitivity; multivariate detection limit; chemometrics; carbamazepine; DIFFERENTIAL SCANNING CALORIMETRY; RAY-POWDER DIFFRACTION; MULTIVARIATE DETECTION LIMITS; LEAST-SQUARES REGRESSION; SOLID-STATE FORMS; QUANTITATIVE-ANALYSIS; INFRARED-SPECTROSCOPY; CARBAMAZEPINE; QUANTIFICATION; MIXTURES;
D O I
10.1177/0003702817690407
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Polymorph detection is critical for ensuring pharmaceutical product quality in drug substances exhibiting polymorphism. Conventional analytical techniques such as X-ray powder diffraction and solid-state nuclear magnetic resonance are utilized primarily for characterizing the presence and identity of specific polymorphs in a sample. These techniques have encountered challenges in analyzing the constitution of polymorphs in the presence of other components commonly found in pharmaceutical dosage forms. Laborious sample preparation procedures are usually required to achieve satisfactory data interpretability. There is a need for alternative techniques capable of probing pharmaceutical dosage forms rapidly and nondestructively, which is dictated by the practical requirements of applications such as quality monitoring on production lines or when quantifying product shelf lifetime. The sensitivity of transmission Raman spectroscopy for detecting polymorphs in final tablet cores was investigated in this work. Carbamazepine was chosen as a model drug, polymorph form III is the commercial form, whereas form I is an undesired polymorph that requires effective detection. The concentration of form I in a direct compression tablet formulation containing 20% w/w of carbamazepine, 74.00% w/w of fillers (mannitol and microcrystalline cellulose), and 6% w/w of croscarmellose sodium, silicon dioxide, and magnesium stearate was estimated using transmission Raman spectroscopy. Quantitative models were generated and optimized using multivariate regression and data preprocessing. Prediction uncertainty was estimated for each validation sample by accounting for all the main variables contributing to the prediction. Multivariate detection limits were calculated based on statistical hypothesis testing. The transmission Raman spectroscopic model had an absolute prediction error of 0.241% w/w for the independent validation set. The method detection limit was estimated at 1.31% w/w. The results demonstrated that transmission Raman spectroscopy is a sensitive tool for polymorphs detection in pharmaceutical tablets.
引用
收藏
页码:1856 / 1867
页数:12
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