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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >ESI-MSn and LC-ESI-MS studies to characterize forced degradation products of bosentan and a validated stability-indicating LC-UV method
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ESI-MSn and LC-ESI-MS studies to characterize forced degradation products of bosentan and a validated stability-indicating LC-UV method

机译:ESI-MSn和LC-ESI-MS研究以表征波生坦的强制降解产物和经过验证的稳定性表明LC-UV方法

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摘要

The present study reports the characterization of forced degradation products of bosentan and a validated stability-indicating HPLC method for the stability testing of bosentan tablets. The forced degradation was carried out under the conditions of hydrolysis, oxidation, dry heat and photolysis. The drug was found unstable in acid, alkali and oxidative media whereas stable to the hydrolysis in water, to dry heat and to photolysis. In total, six degradation products were formed in all conditions which were resolved in a single run on a C-18 column with gradient elution using ammonium acetate buffer (pH 4.5, 5.0mM), methanol and acetonitrile. Structures of all the degradation products were characterized through +ESI-MSn and LC-ESI-MS spectral data of bosentan as well as LC-ESI-MS spectral data of the products. The products II-VI were characterized as 6-amino-[2,2']bipyrimidinyl-4,5-diol, 6-amino-5-(2-methoxyphenoxy)-[2,2']-bipyrimidinyl-4-ol, 2-[6-amino-5-(2-methoxyphenoxy)-[2,2']-bipyrimidinyl-4-yloxy]-ethanol, 4-tert-butyl-N-[6-(1-methoxyethoxy)-5-(2-methoxyphenoxy)-[2,2']-bipyrimidinyl-4-yl]-benzenesulfonamide and 4-tert-butyl-N-[6-hydroxy-5-(2-methoxyphenoxy)-[2,2']bipyrimidinyl-4-yl]-benzenesulfonamide, respectively. The peak of the product I was found to be due to two secondary degradation products which co-eluted and were characterized as β-hydroxyethyl p-tert-butylphenylsulfonate (Ia) and 2-[2-(2-hydroxyethoxy)-phenoxy]-ethanol (Ib). These products were formed due to hydrolysis of sulfonamide and alkylaryl ether and the diaryl ether linkages as well as dehydration of the primary alcohol group. The most probable degradation mechanisms were proposed. The HPLC method was found to be stability-indicating, linear (2-100μgml-1), accurate, precise, sensitive, specific, rugged and robust for quantitation of the drug. The method was applied to the stability testing of the commercially available bosentan tablets successfully.
机译:本研究报告了波生坦片剂的强制降解产物的表征以及用于波生坦片剂稳定性测试的经过验证的稳定性指示HPLC方法。在水解,氧化,干热和光解的条件下进行强制降解。发现该药物在酸,碱和氧化介质中不稳定,而对在水中水解,对干热和对光解稳定。在所有条件下,总共形成了六种降解产物,将它们在C-18色谱柱上一次运行即可分离,并使用乙酸铵缓冲液(pH 4.5,5.0mM),甲醇和乙腈进行梯度洗脱。通过波生坦的+ ESI-MSn和LC-ESI-MS光谱数据以及产物的LC-ESI-MS光谱数据表征了所有降解产物的结构。产物II-VI的特征是6-氨基-[2,2']联嘧啶基-4,5-二醇,6-氨基-5-(2-甲氧基苯氧基)-[2,2']-联嘧啶基-4-醇,2- [6-氨基-5-(2-甲氧基苯氧基)-[2,2']-双嘧啶基-4-基氧基]-乙醇,4-叔丁基-N- [6-(1-甲氧基乙氧基)-5 -(2-甲氧基苯氧基)-[2,2']-联嘧啶基-4-基]-苯磺酰胺和4-叔丁基-N- [6-羟基-5-(2-甲氧基苯氧基)-[2,2']双嘧啶基-4-基]-苯磺酰胺。发现产物I的峰是由于两个次级降解产物,它们共同洗脱,并表征为β-羟乙基对叔丁基苯基磺酸盐(Ia)和2- [2-(2-(2-羟基乙氧基)-苯氧基]-乙醇(Ib)。这些产物是由于磺酰胺和烷基芳基醚的水解以及二芳基醚键的水解以及伯醇基团的脱水而形成的。提出了最可能的降解机理。 HPLC方法被证明具有稳定性指示,线性(2-100μgml-1),准确,精确,灵敏,特异,坚固耐用且对药物定量的鲁棒性。该方法成功应用于市售波生坦片的稳定性测试。

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