Identification, synthesis, and characterization of potential genotoxic impurities of sildenafil citrate drug substance

Author:

Rajesh Reddy P.,Musunuri Sivanadh,Rama Sekhara Reddy D.,Chittala V. Subrahmanyam,Murthy P V. N. S.,Krishnamohan K.

Abstract

Abstract Background Sildenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specifil phophodiesterase type 5 (PDE5). Sildenafil enhances the effect of nitric oxide by inhibiting phosphodiesterase type 5, which is responsible for the degradation of cGMP in the corpus cavernosum. The possible genotoxic impurities of sildenafil were synthesized, i.e., sildenafil sulfonyl methyl ester, sildenafil sulfonyl ethyl ester, and sildenafil sulfonyl isopropyl ester. The present work describes the synthesis and characterization of these sulfonyl ester compounds related to sildenafil. Results All the synthesized sildenafil sulfonyl esters have proved to be beneficial for the pharmaceutical industry in view of the regulatory importance. Conclusion A simple, efficient, and repeatable method was developed for the preparation of sildenafil sulfonyl esters in view of the regulatory importance of the potential genotoxic impurities in the active pharmaceutical ingredient. A detailed study of various impurities in sildenafil was conducted. Different process-related sulfonyl esters in sildenafil were identified, synthesized, and characterized by using various spectroscopic techniques like liquid chromatography-mass spectrometry (LCMS), mass, 1H NMR, and FT-IR. These efforts to synthesize and characterize them effectively have proved to be beneficial.

Publisher

Springer Science and Business Media LLC

Reference13 articles.

1. International Conference on Harmonization (ICH) guidelines Q3A (R) impurities in New Drug Substances (2002) ICH guidelines, Geneva

2. International Conference on Harmonization (ICH) guidelines Q2B validation of analytical Procedure (1996) Methodology, Geneva

3. M7(R1) assessment and control of DNA reactive (mutagenic) impurities in pharmaceuticals to limit potential carcinogenic risk; ICH guidelines: 2018

4. Raman NVSSS, Prasad AVSS, Ratnakar Reddy K (2011) Strategies for the identification, control and determination of genotoxic impurities in drug substances: a pharmaceutical perspective. J Pharm Biomed Anal 55:662–667. https://doi.org/10.1016/j.jpba.2010.11.039

5. European medicines agency. Guideline on the specification limits for residues of metal catalysts or metal reagents, Doc. Ref. EMEA/CHMP/SWP/4446/2000, European Medicines Agency, 2008.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3