Skip to main content

Advertisement

Log in

Chlorophyllin sodium copper salt in hydrogel formulations: spectrophotometric stability studies and in vitro release

  • Original Paper
  • Published:
Chemical Papers Aims and scope Submit manuscript

Abstract

Commercial sodium copper chlorophyllin salt (SCC) is a green pigment, antioxidant and antimutagenic agent with numerous therapeutic applications. The aim of this study was to develop, characterize and evaluate stability and in vitro release of hydrogel containing SCC and SCC-loaded liposomes, in order to enhance the stability of SCC in the carrier-containing gels compared to the conventional gels. SCC-loaded liposomes were made of soy lecithin with phosphatidylcholine content of 90%, by the thin film hydration method. Hydrogel with SCC was prepared of poly(methyl vinyl ether/maleic anhydride decadiene) crosspolymer. The final SCC concentration in liposomes and hydrogel was set to 1 × 10–4 M. Hydrogel formulations were evaluated for physical stability during 6 months’ storage at 20 ± 2 °C. After SCC incorporation in liposomes, spectrophotometric studies have shown its improved stability compared to the aqueous environment. In vitro release study of SCC from developed liposomal suspensions and gel-type formulations was performed using direct dialysis bag technique, during 5 h. The results showed that formulation type—liposomes and hydrogel—affected the rate and amount of the released drug. SCC incorporation in liposomes gradually prolonged SCC release in comparison with SCC hydrogel and SCC solution. Poly(methyl vinyl ether/maleic anhydride decadiene) crosspolymer hydrogel formulations with and without liposomes met the requirements of physical stability based on the results of organoleptic, homogeneity, pH, viscosity and electrical conductivity tests, during 6 months.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Data availability

The paper presents original data which are not submitted to other journal.

References

Download references

Acknowledgements

Authors wish to express their gratitude to the Republic of Serbia—Ministry of Education, Science and Technological Development, Program for financing scientific research work, number 451-03-9/2021-14/200133 and Lipoid GmbH, Germany, for phospholipids gift. The authors are grateful for the professional support by M.Sc. Tech. Eng. Miroslav D. Milenković.

Author information

Authors and Affiliations

Authors

Contributions

All co-authors contributed to this work and they are aware of this submission.

Corresponding author

Correspondence to Sanja M. Petrovic.

Ethics declarations

Conflicts of interest

The authors declare that they have no potential conflicts of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 825 kb)

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Petrovic, S.M., Savic, S.M., Savic, S.R. et al. Chlorophyllin sodium copper salt in hydrogel formulations: spectrophotometric stability studies and in vitro release. Chem. Pap. 77, 2635–2645 (2023). https://doi.org/10.1007/s11696-022-02653-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11696-022-02653-8

Keywords

Navigation