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Abstract

Forced Degradation Studies on Agents of Therapeutic Interest †

Department of Quality Assurance, SVKM’S Dr. Bhanuben Nanavati College of Pharmacy, Mumbai 400056, India
*
Authors to whom correspondence should be addressed.
Presented at the 8th International Electronic Conference on Medicinal Chemistry, 1–30 November 2022; Available online: https://ecmc2022.sciforum.net/.
Med. Sci. Forum 2022, 14(1), 22; https://doi.org/10.3390/ECMC2022-13233
Published: 1 November 2022
(This article belongs to the Proceedings of The 8th International Electronic Conference on Medicinal Chemistry)

Abstract

:
Chalcones possessing potential anti-Alzheimer’s activity were synthesised in our lab using the Claisen Schmidt reaction. FDS (Forced degradation protocols) protocols in accordance with ICH (International Conference on Harmonization) guidelines were applied to three thiophene chalcones TC1, TC2, and TC3. The method was developed using Thermo Scientific C18 column (Agilent Technologies India Ltd., Mumbai, India 250 × 4.6 mm, 5 µm) as stationary phase and sodium acetate buffer (pH 3.0), with acetonitrile (40:60, v/v; 40:60, v/v; 25:75, v/v, respectively) as the mobile phase at 1 mL/min flow rate and 280 nm as detection wavelength. The developed method was successful in resolving TC1, TC2 and TC3 from its degradation products. TC1, TC2 and TC3 were eluted at a retention time of 10.5 min, 27.4 min and 10.2 min, respectively. HPLC (High Performance Liquid Chromatography) method was developed and validated for the individual untreated molecules and was found to be specific, selective, precise, reproducible, robust and linear in the range of about 5–15 ppm of the working standard concentration. The chalcones were stable under thermal and thermal-humidity stress, but degraded to different extents under acid-and base-catalysed hydrolysis, oxidative stress and photolytic conditions, as seen by HPLC analysis. The degradation of TC1 was studied by LC-MS and predictions of the mechanism of degradation were attempted.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/ECMC2022-13233/s1.

Author Contributions

Conceptualization, A.P. and R.R.; methodology, N.P.P. and R.R.; validation, A.P. and R.R.; formal analysis, A.P. and R.R.; investigation, N.P.P., A.P. and R.R.; resources, A.P.; data curation, R.R.; writing—original draft preparation, N.P.P.; writing—review and editing, A.P. and R.R.; visualization, N.P.P.; supervision, R.R. and A.P.; project administration, A.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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MDPI and ACS Style

Pise, N.P.; Prabhu, A.; Raheja, R. Forced Degradation Studies on Agents of Therapeutic Interest. Med. Sci. Forum 2022, 14, 22. https://doi.org/10.3390/ECMC2022-13233

AMA Style

Pise NP, Prabhu A, Raheja R. Forced Degradation Studies on Agents of Therapeutic Interest. Medical Sciences Forum. 2022; 14(1):22. https://doi.org/10.3390/ECMC2022-13233

Chicago/Turabian Style

Pise, Nikita Pravin, Arati Prabhu, and Radhika Raheja. 2022. "Forced Degradation Studies on Agents of Therapeutic Interest" Medical Sciences Forum 14, no. 1: 22. https://doi.org/10.3390/ECMC2022-13233

APA Style

Pise, N. P., Prabhu, A., & Raheja, R. (2022). Forced Degradation Studies on Agents of Therapeutic Interest. Medical Sciences Forum, 14(1), 22. https://doi.org/10.3390/ECMC2022-13233

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