Non-invasive determination of ethanol, propylene glycol and water in a multi-component pharmaceutical oral liquid by direct measurement through amber plastic bottles using Fourier transform near-infrared spectroscopy

被引:46
作者
Broad, NW
Jee, RD
Moffat, AC
Eaves, MJ
Mann, WC
Dziki, W
机构
[1] Univ London, Sch Pharm, Ctr Pharmaceut Anal, London WC1N 1AX, England
[2] Abbott Labs, Queenborough ME11 5EL, Kent, England
[3] Abbott Labs, Pharmaceut & Analyt Res & Dev, N Chicago, IL 60064 USA
关键词
D O I
10.1039/b006789j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Fourier transform near-infrared (FT-NIR) spectroscopy was used to quantify rapidly the ethanol (34-49% v/v), propylene glycol (20-35% v/v) and water (11-20% m/m) contents within a multi-component pharmaceutical oral liquid by measurement directly through the amber plastic bottle packaging. Spectra were collected in the range 7302-12000 cm(-1) and calibration models set-up using partial least-squares regression (PLSR) and multiple linear regression. Reference values for the three components were measured using capillary gas chromatography (ethanol and propylene glycol) and Karl Fischer (water) assay procedures. The calibration and test sets consisted of production as well as laboratory batches that were made to extend the concentration ranges beyond the natural production variation. The PLSR models developed gave standard errors of prediction (SEP) of 1.1% v/v for ethanol, 0.9% v/v for propylene glycol and 0.3% m/m for water. For each component the calibration model was validated in terms of: linearity, repeatability, intermediate precision and robustness. All the methods produced statistically favourable outcomes. Ten production batches independent of the calibration and test sets were also challenged against the PLSR models, giving SEP values of 1.3% v/v (ethanol), 1.0% v/v (propylene glycol) and 0.2% m/m (water). NIR transmission spectroscopy allowed all three liquid constituents to be non-invasively measured in under 1 min.
引用
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页码:2054 / 2058
页数:5
相关论文
共 13 条
[1]  
ADAMS MJ, 1995, CHEMOMETRICS ANAL SP, P126
[2]   STANDARD NORMAL VARIATE TRANSFORMATION AND DE-TRENDING OF NEAR-INFRARED DIFFUSE REFLECTANCE SPECTRA [J].
BARNES, RJ ;
DHANOA, MS ;
LISTER, SJ .
APPLIED SPECTROSCOPY, 1989, 43 (05) :772-777
[3]   DETERMINATION OF 5 COMPONENTS IN A PHARMACEUTICAL FORMULATION USING NEAR-INFRARED REFLECTANCE SPECTROPHOTOMETRY [J].
DUBOIS, P ;
MARTINEZ, JR ;
LEVILLAIN, P .
ANALYST, 1987, 112 (12) :1675-1679
[4]  
Halsey SA, 1998, QUANTITATIVE NIR CAL
[5]  
HALSEY SA, 1994, TECHNICAL NOTE
[6]   NEAR-INFRARED SPECTROSCOPIC DETERMINATION OF RESIDUAL MOISTURE IN LYOPHILIZED SUCROSE THROUGH INTACT GLASS VIALS [J].
KAMAT, MS ;
LODDER, RA ;
DELUCA, PP .
PHARMACEUTICAL RESEARCH, 1989, 6 (11) :961-965
[7]   JCAMP-DX - A STANDARD FORM FOR EXCHANGE OF INFRARED-SPECTRA IN COMPUTER READABLE FORM [J].
MCDONALD, RS ;
WILKS, PA .
APPLIED SPECTROSCOPY, 1988, 42 (01) :151-162
[8]   Assay of effervescent tablets by near-infrared spectroscopy in transmittance and reflectance mode: acetylsalicylic acid in mono and combination formulations [J].
Merckle, P ;
Kovar, KA .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 17 (03) :365-374
[9]  
MILLER JC, 1993, E HORWOOD SERIES ANA
[10]  
N?s T., 1994, NIR NEWS, V5, P4