Li Jingyi, Shao Shan, Solorzano Mauro, Allmaier Gary J, Kurtulik Paul T
Analytical Research and Development, Celgene Corporation, Summit, NJ 07091, USA.
J Chromatogr A. 2009 Apr 10;1216(15):3328-36. doi: 10.1016/j.chroma.2009.02.029. Epub 2009 Feb 21.
Static headspace gas chromatography (HS-GC) with immiscible binary solvents is described to quantitatively determine the residual ethanol used to seal the hard gelatin capsules by liquid encapsulated and microspray sealing (LEMS; cfs 1200, Greenwood, SC, USA). The effects of decane, dodecane, heptane, 0.1M HCl, N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone and dimethyl sulfoxide on the method sensitivity are compared. It is observed that the ethanol headspace concentrations can be increased by fourfolds when aliphatic hydrocarbon solvents are added into the aqueous sample solutions in a HS vial. In addition, a mathematic model based on the concentration equilibriums of liquid-liquid and liquid-gas phases is derived to quantitatively describe the ethanol headspace concentrations versus the volumes of the aliphatic hydrocarbon solvents. The proposed model fits well to the experimental data. The impacts of the oven temperatures and vial equilibration times on the ethanol headspace concentrations are also investigated. Furthermore, the potential interferences of the capsule placebo and hard gelatin capsule shells on the selectivity and quantitation of the method are discussed. The linearity is validated from 5 microg/mL to 500 microg/mL. The limit of quantitation is 5 microg/mL. The accuracy is determined to be 100.8+/-6%. Finally, this method is successfully used to determine the residual ethanol in the sealed capsules of 5mg and 10mg developmental Drug A, and 100mg and 200mg developmental Drug B.
描述了使用不混溶二元溶剂的静态顶空气相色谱法(HS-GC)来定量测定通过液体封装和微喷雾密封(LEMS;cfs 1200,美国南卡罗来纳州格林伍德)用于密封硬明胶胶囊的残留乙醇。比较了癸烷、十二烷、庚烷、0.1M盐酸、N,N-二甲基甲酰胺、N,N-二甲基乙酰胺、N-甲基-2-吡咯烷酮和二甲基亚砜对方法灵敏度的影响。观察到,当在顶空瓶的水性样品溶液中加入脂肪烃溶剂时,乙醇顶空浓度可增加四倍。此外,基于液-液和液-气相传质平衡推导了一个数学模型,以定量描述乙醇顶空浓度与脂肪烃溶剂体积的关系。所提出的模型与实验数据拟合良好。还研究了柱温箱温度和顶空瓶平衡时间对乙醇顶空浓度的影响。此外,讨论了胶囊安慰剂和硬明胶胶囊壳对该方法选择性和定量的潜在干扰。线性范围在5μg/mL至500μg/mL之间得到验证。定量限为5μg/mL。准确度测定为100.8±6%。最后,该方法成功用于测定5mg和10mg研发药物A以及100mg和200mg研发药物B的密封胶囊中的残留乙醇。