Investigation on the Stability of New Biologically Active Thiosemicarbazone- Derived Compounds by a Validated HPLC-PDA Method

Author:

Secci Daniela1,Locatelli Marcello2,Kabir Abuzar3,Salvatorelli Erika2,Macedonio Giorgia2,Mollica Adriano2,Carradori Simone2

Affiliation:

1. Dipartimento di Chimica e Tecnologie del Farmaco, Sapienza University of Rome, p.le A. Moro 5, 00185 Rome, Italy

2. Department of Pharmacy, , Italy

3. International Forensic Research Institute, Department of Chemistry and Biochemistry, Florida International University, Miami, FL, United States

Abstract

Background: New Chemical Entities (NCEs) could be generally exposed to several stress conditions of hydrolysis, oxidation, photolysis and thermal degradation in order to better characterize the compounds and to know if the degradation processes lead to generate undesired (or toxic) products. Objective: This paper reports the development and validation of an HPLC-PDA method for the qualiquantitative profiles determination and chemical-physical stability evaluation after forced decomposition studies of thiosemicarbazone-derived compounds endowed with interesting pharmacological activities. Methods: All compounds and two possible degradation products were resolved by using a Grace® C-18 (ODS) column (250 mm × 4.6 mm; 5 mm particle size) in gradient elution mode. The chromatographic analysis was run in 28 min. The analytical method was correctly validated using weighted-matrix matched standard curves in the following ranges: 1-100 µg mL-1 for the lead compounds, and 0.1-8 μg mL-1 for the two possible degradation products showing a good correlation coefficients (≥0.9756). Precision and trueness comply with International Guidelines on method validation. Results: The obtained results demonstrated an excellent stability of the thiosemicarbazone-derived products following the treatment with UV set at 254 nm and heat (at 80°C). In solution, however, the compounds showed different stability profiles. Conclusion: The results obtained through the forced degradation studies provided important information not only for handling, formulation and storage of the substances, but also for the possible chemical changes in order to increase the stability. Given the importance of the non-conventional dosage forms, the stability of the substances was also analyzed in the presence of widely used surfactants.

Funder

University of Chieti - Pescara “G. d’Annunzio”, Chieti, Italy

Publisher

Bentham Science Publishers Ltd.

Subject

Analytical Chemistry

Reference29 articles.

1. Tamizi E, Jouyban A. Eur J Pharm Biopharm, Forced degradation studies of biopharmaceuticals: Selection of stress conditions.,, 2016, 98,, 26-46,

2. Blessy M, Ruchi DP, Prajesh NP, Agrawal YK. J Pharm Anal, Development of forced degradation and stability indicating studies of drugs.,, 2014, 4,, 159-165,

3. International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. Harmonised Tripartite Guideline: Validation of Analytical Procedures: Text and Methodology. ICH Q2(R1)., , 2005

4. International Conference of Harmonisation of Technical Requirements for registration of pharmaceuticals for human use; "Stability testing: photostability testing of new drug substances and products. ICH Q1B., , 1996

5. International Conference of Harmonisation of Technical Requirements for registration of pharmaceuticals for human use; "Stability Testing of New Drug Substances and Products. ICH Q1A(R2)., , 2006

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

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