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Solvent-driven stability: UV spectroscopy study of phenolic substances

Year 2025, Volume: 12 Issue: 3, 657 - 668, 04.09.2025
https://doi.org/10.21448/ijsm.1590240

Abstract

In contemporary industry, the analysis of various substances often requires handling samples with appropriate solvents, relying on stock solutions for research purposes. This study investigates the stability of gallic acid, ellagic acid, and quercetin naturally occurring polyphenolic compounds with potential pharmaceutical applications. The study explored the stability of these materials in different solvent environments and at varied temperatures, highlighting the critical role of solvent choice and temperature in preserving compound integrity. Gallic acid, quercetin, and ellagic acid were each dissolved at a concentration of 5 µg/mL in different solvents. UV spectroscopic analysis was conducted periodically over one month, with samples stored in controlled environments. Stability was assessed by examining UV absorption spectra, and data were analyzed using statistical methods. The results indicated that the choice of solvent significantly impacted compound stability. Gallic acid showed the highest stability in ethanol (100%) and DMSO (10%) at both room and refrigerated temperatures. Ellagic acid demonstrated optimal stability in DMSO (10%), with variability in other solvents. Quercetin exhibited the highest stability in DMSO (10%), while ethanol showed significant variability. Refrigeration enhanced stability across all solvents. These findings underscore the importance of selecting appropriate solvents and storage conditions to preserve the quality of active pharmaceutical ingredients (API). The results offer valuable insights for improving the stability of stock solutions in pharmaceutical development and quality control, providing crucial information for enhancing the preservation of APIs.

References

  • Ambhore, N.J.P., Adhao, N.V.S., Cheke, N.R.S., Cheke, N.R.S., Popat, N.R.R., & Gandhi, N. S.J. (2021). Futuristic review on progress in force degradation studies and stability indicating assay method for some antiviral drugs. GSC Biological and Pharmaceutical Sciences, 16(1), 133–149. https://doi.org/10.30574/gscbps.2021.16.1.0172
  • Babich, H., Schuck, A.G., Weisburg, J.H., & Zuckerbraun, H.L. (2011). Research strategies in the study of the pro-oxidant nature of polyphenol nutraceuticals. Journal of Toxicology, 2011, 1–12. https://doi.org/10.1155/2011/467305
  • Badhani, B., Sharma, N., & Kakkar, R. (2015a). Gallic acid: a versatile antioxidant with promising therapeutic and industrial applications. RSC Advances, 5(35), 27540–27557. https://doi.org/10.1039/c5ra01911g
  • Badhani, B., Sharma, N., & Kakkar, R. (2015b). Gallic acid: a versatile antioxidant with promising therapeutic and industrial applications. RSC Advances, 5(35), 27540–27557. https://doi.org/10.1039/c5ra01911g
  • Baek, K., & Patra, J.K. (2015). Novel green synthesis of gold nanoparticles using Citrullus lanatus rind and investigation of proteasome inhibitory activity, antibacterial, and antioxidant potential. International Journal of Nanomedicine, 7253. https://doi.org/10.2147/ijn.s95483
  • Bhaskar, R., Ola, M., Agnihotri, V., Chavan, A., & Girase, H. (2020). Current trend in performance of forced degradation studies for drug substance and drug product’s. Journal of Drug Delivery and Therapeutics, 10(2-s), 149–155. https://doi.org/10.22270/jddt.v10i2-s.4040
  • Blessy, M., Patel, R.D., Prajapati, P.N., & Agrawal, Y. (2014). Development of forced degradation and stability indicating studies of drugs-A review. Journal of Pharmaceutical Analysis, 4(3), 159–165. https://doi.org/10.1016/j.jpha.2013.09.003
  • Chakraborty, S., Sharmin, S., Rony, S.R., Ahmad, S.a.I., & Sohrab, M.H. (2018). Stability-indicating UV/Vis spectrophotometric method for diazepam development and validation. Indian Journal of Pharmaceutical Sciences, 80(2). https://doi.org/10.4172/pharmaceutical-sciences.1000366
  • Daniel, E.M., Krupnick, A.S., Heur, Y., Blinzler, J.A., Nims, R.W., & Stoner, G.D. (1989). Extraction, stability, and quantitation of ellagic acid in various fruits and nuts. Journal of Food Composition and Analysis, 2(4), 338–349. https://doi.org/10.1016/0889-1575(89)90005-7
  • Görög, S. (2018). Ultraviolet-visible spectrophotometry in pharmaceutical analysis. In CRC Press eBooks. https://doi.org/10.1201/9781351077422
  • Jakkam, N.N.R., Chintakula, N.S., & Battula, N S.R. (2021). Studies on forced degradation and solid state stability of tenofovir disoproxil orotate. International Journal of Research in Pharmaceutical Sciences, 12(4), 2485–2491. https://doi.org/10.26452/ijrps.v12i4.4891
  • Karinen, R., Oiestad, E.L., Andresen, W., Smith-Kielland, A., & Christophersen, A. (2011). Comparison of the stability of stock solutions of drugs of abuse and other drugs stored in a freezer, refrigerator, and at ambient temperature for up to one year. Journal of Analytical Toxicology, 35(8), 583–590. https://doi.org/10.1093/anatox/35.8.583
  • Polaka, S., Vitore, J., & Tekade, R.K. (2021). Factors affecting the stability of drugs and their metabolites in biological matrices. In Elsevier eBooks (pp. 517 537). https://doi.org/10.1016/b978-0-12-814425-1.00022-x
  • Robnik, B., Likozar, B., Wang, B., Ljubin, T.S., & Časar, Z. (2019). Understanding and kinetic modeling of complex degradation pathways in the solid dosage form: The case of saxagliptin. Pharmaceutics, 11(9), 452. https://doi.org/10.3390/pharmaceutics11090452
  • Salazar-Orbea, G.L., García-Villalba, R., Bernal, M.J., Hernández-Jiménez, A., Egea, J.A., Tomás-Barberán, F.A., & Sánchez-Siles, L.M. (2023). Effect of storage conditions on the stability of polyphenols of apple and strawberry purees produced at ındustrial scale by different processing techniques. Journal of Agricultural and Food Chemistry, 71(5), 2541–2553. https://doi.org/10.1021/acs.jafc.2c07828
  • Singh, A., & Singh, P. (2018). Technical considerations of forced degradation studıes of new drug substances and product: Regulatory perspectives. Journal of Drug Delivery and Therapeutics, 8(2). https://doi.org/10.22270/jddt.v8i2.1681
  • Srivastava, R.K. (2017). An updated review: forced degradation study. World Journal of Pharmacy and Pharmaceutical Sciences, 709–726. https://doi.org/10.20959/wjpps20176-9329
  • Verma, A., Singla, S., & Palia, P. (2022). The development of forced degradation and stability ındicating studies of drugs - A review. Asian Journal of Pharmaceutical Research and Development, 10(2), 83–89. https://doi.org/10.22270/ajprd.v10i2.1104

Solvent-driven stability: UV spectroscopy study of phenolic substances

Year 2025, Volume: 12 Issue: 3, 657 - 668, 04.09.2025
https://doi.org/10.21448/ijsm.1590240

Abstract

In contemporary industry, the analysis of various substances often requires handling samples with appropriate solvents, relying on stock solutions for research purposes. This study investigates the stability of gallic acid, ellagic acid, and quercetin naturally occurring polyphenolic compounds with potential pharmaceutical applications. The study explored the stability of these materials in different solvent environments and at varied temperatures, highlighting the critical role of solvent choice and temperature in preserving compound integrity. Gallic acid, quercetin, and ellagic acid were each dissolved at a concentration of 5 µg/mL in different solvents. UV spectroscopic analysis was conducted periodically over one month, with samples stored in controlled environments. Stability was assessed by examining UV absorption spectra, and data were analyzed using statistical methods. The results indicated that the choice of solvent significantly impacted compound stability. Gallic acid showed the highest stability in ethanol (100%) and DMSO (10%) at both room and refrigerated temperatures. Ellagic acid demonstrated optimal stability in DMSO (10%), with variability in other solvents. Quercetin exhibited the highest stability in DMSO (10%), while ethanol showed significant variability. Refrigeration enhanced stability across all solvents. These findings underscore the importance of selecting appropriate solvents and storage conditions to preserve the quality of active pharmaceutical ingredients (API). The results offer valuable insights for improving the stability of stock solutions in pharmaceutical development and quality control, providing crucial information for enhancing the preservation of APIs.

References

  • Ambhore, N.J.P., Adhao, N.V.S., Cheke, N.R.S., Cheke, N.R.S., Popat, N.R.R., & Gandhi, N. S.J. (2021). Futuristic review on progress in force degradation studies and stability indicating assay method for some antiviral drugs. GSC Biological and Pharmaceutical Sciences, 16(1), 133–149. https://doi.org/10.30574/gscbps.2021.16.1.0172
  • Babich, H., Schuck, A.G., Weisburg, J.H., & Zuckerbraun, H.L. (2011). Research strategies in the study of the pro-oxidant nature of polyphenol nutraceuticals. Journal of Toxicology, 2011, 1–12. https://doi.org/10.1155/2011/467305
  • Badhani, B., Sharma, N., & Kakkar, R. (2015a). Gallic acid: a versatile antioxidant with promising therapeutic and industrial applications. RSC Advances, 5(35), 27540–27557. https://doi.org/10.1039/c5ra01911g
  • Badhani, B., Sharma, N., & Kakkar, R. (2015b). Gallic acid: a versatile antioxidant with promising therapeutic and industrial applications. RSC Advances, 5(35), 27540–27557. https://doi.org/10.1039/c5ra01911g
  • Baek, K., & Patra, J.K. (2015). Novel green synthesis of gold nanoparticles using Citrullus lanatus rind and investigation of proteasome inhibitory activity, antibacterial, and antioxidant potential. International Journal of Nanomedicine, 7253. https://doi.org/10.2147/ijn.s95483
  • Bhaskar, R., Ola, M., Agnihotri, V., Chavan, A., & Girase, H. (2020). Current trend in performance of forced degradation studies for drug substance and drug product’s. Journal of Drug Delivery and Therapeutics, 10(2-s), 149–155. https://doi.org/10.22270/jddt.v10i2-s.4040
  • Blessy, M., Patel, R.D., Prajapati, P.N., & Agrawal, Y. (2014). Development of forced degradation and stability indicating studies of drugs-A review. Journal of Pharmaceutical Analysis, 4(3), 159–165. https://doi.org/10.1016/j.jpha.2013.09.003
  • Chakraborty, S., Sharmin, S., Rony, S.R., Ahmad, S.a.I., & Sohrab, M.H. (2018). Stability-indicating UV/Vis spectrophotometric method for diazepam development and validation. Indian Journal of Pharmaceutical Sciences, 80(2). https://doi.org/10.4172/pharmaceutical-sciences.1000366
  • Daniel, E.M., Krupnick, A.S., Heur, Y., Blinzler, J.A., Nims, R.W., & Stoner, G.D. (1989). Extraction, stability, and quantitation of ellagic acid in various fruits and nuts. Journal of Food Composition and Analysis, 2(4), 338–349. https://doi.org/10.1016/0889-1575(89)90005-7
  • Görög, S. (2018). Ultraviolet-visible spectrophotometry in pharmaceutical analysis. In CRC Press eBooks. https://doi.org/10.1201/9781351077422
  • Jakkam, N.N.R., Chintakula, N.S., & Battula, N S.R. (2021). Studies on forced degradation and solid state stability of tenofovir disoproxil orotate. International Journal of Research in Pharmaceutical Sciences, 12(4), 2485–2491. https://doi.org/10.26452/ijrps.v12i4.4891
  • Karinen, R., Oiestad, E.L., Andresen, W., Smith-Kielland, A., & Christophersen, A. (2011). Comparison of the stability of stock solutions of drugs of abuse and other drugs stored in a freezer, refrigerator, and at ambient temperature for up to one year. Journal of Analytical Toxicology, 35(8), 583–590. https://doi.org/10.1093/anatox/35.8.583
  • Polaka, S., Vitore, J., & Tekade, R.K. (2021). Factors affecting the stability of drugs and their metabolites in biological matrices. In Elsevier eBooks (pp. 517 537). https://doi.org/10.1016/b978-0-12-814425-1.00022-x
  • Robnik, B., Likozar, B., Wang, B., Ljubin, T.S., & Časar, Z. (2019). Understanding and kinetic modeling of complex degradation pathways in the solid dosage form: The case of saxagliptin. Pharmaceutics, 11(9), 452. https://doi.org/10.3390/pharmaceutics11090452
  • Salazar-Orbea, G.L., García-Villalba, R., Bernal, M.J., Hernández-Jiménez, A., Egea, J.A., Tomás-Barberán, F.A., & Sánchez-Siles, L.M. (2023). Effect of storage conditions on the stability of polyphenols of apple and strawberry purees produced at ındustrial scale by different processing techniques. Journal of Agricultural and Food Chemistry, 71(5), 2541–2553. https://doi.org/10.1021/acs.jafc.2c07828
  • Singh, A., & Singh, P. (2018). Technical considerations of forced degradation studıes of new drug substances and product: Regulatory perspectives. Journal of Drug Delivery and Therapeutics, 8(2). https://doi.org/10.22270/jddt.v8i2.1681
  • Srivastava, R.K. (2017). An updated review: forced degradation study. World Journal of Pharmacy and Pharmaceutical Sciences, 709–726. https://doi.org/10.20959/wjpps20176-9329
  • Verma, A., Singla, S., & Palia, P. (2022). The development of forced degradation and stability ındicating studies of drugs - A review. Asian Journal of Pharmaceutical Research and Development, 10(2), 83–89. https://doi.org/10.22270/ajprd.v10i2.1104
There are 18 citations in total.

Details

Primary Language English
Subjects Natural Products and Bioactive Compounds
Journal Section Articles
Authors

Manoj Madanahalli Ramesh 0009-0009-0104-464X

Annegowda Hardur Venkatappa 0000-0003-1542-6154

Richard Lobo 0000-0003-3202-1108

Early Pub Date June 11, 2025
Publication Date September 4, 2025
Submission Date November 23, 2024
Acceptance Date April 13, 2025
Published in Issue Year 2025 Volume: 12 Issue: 3

Cite

APA Madanahalli Ramesh, M., Hardur Venkatappa, A., & Lobo, R. (2025). Solvent-driven stability: UV spectroscopy study of phenolic substances. International Journal of Secondary Metabolite, 12(3), 657-668. https://doi.org/10.21448/ijsm.1590240
International Journal of Secondary Metabolite

e-ISSN: 2148-6905