Determination of Atropine Enantiomers in Ophthalmic Solutions by Liquid Chromatography Using a Chiral AGP® Column

被引:0
|
作者
Soares, Renata [1 ]
Singh, Anil Kumar [1 ]
Maria Kedor-Hackmann, Erika Rosa [1 ]
Rocha Miritello Santoro, Maria Ines [1 ]
机构
[1] Univ Sao Paulo, Dept Pharm, Fac Pharmaceut Sci, BR-05315970 Sao Paulo, Brazil
关键词
HUMAN ALPHA(1)-ACID GLYCOPROTEIN; BONDED STATIONARY PHASE; CAPILLARY-ELECTROPHORESIS; ALPHA-1-ACID GLYCOPROTEIN; TROPANE ALKALOIDS; EXPERIMENTAL-DESIGN; CIRCULAR-DICHROISM; GENETIC-VARIANTS; BINDING; ROBUSTNESS;
D O I
暂无
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Many therapeutic agents are commercialized under their racemic form. The enantiomers can show differences in the pharmacokinetic and pharmacodynamic profile. The use of a pure enantiomer in pharmaceutical formulations may result in a better therapeutic index and fewer adverse effects. Atropine, an alkaloid of Atropa belladonna, is a racemic mixture of l-hyoscyamine and d-hyoscyamine. It is widely used to dilate the pupil. To quantify these enantiomers in ophthalmic solutions, an HPLC method was developed and validated using a Chiral AGP (R) column at 20 degrees C. The mobile phase consisted of a buffered phosphate solution (containing 10 mM 1-octanesulfonic acid sodium salt and 7.5 mM triethylamine, adjusted to pH 7.0 with orthophosphoric acid) and acetonitrile (99 + 1, v/v). The flow rate was 0.6 mL/min, with UV detection at 205 nm. In the concentration range of 14.0-26.0 mu g/mL, the method was found to be linear (r > 0.9999), accurate (with recovery of 100.1-100.5%), and precise (RSD system: <= 0.6%; RSD intraday: <= 1.1%; RSD interday: <= 0.9%). The method was specific, and the standard and sample solutions were stable for up to 72 h. The factorial design assures robustness with a variation of +/-10% in the mobile phase components and 2 degrees C of column temperature. The complete validation, including stress testing and factorial design, was studied and is presented in this research.
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页码:1663 / 1672
页数:10
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