Drug release kinetics and transport mechanisms of doxorubicin from core-shell delivery systems

Authors

  • í–zlem Gí¶kçe Kocabay Yildiz Technical University / Istanbul Restoration and Conservation Center and Regional Laboratory Directorate https://orcid.org/0000-0003-4352-3453
  • Osman İsmail Yildiz Technical University

DOI:

https://doi.org/10.4025/actascitechnol.v47i1.70363

Keywords:

diffusion; dissolution; drug release mechanism; drug release modeling; erosion; swelling

Abstract

In the current research drug release kinetics and transport mechanisms of doxorubicin (DOX) from DOX, DOX/valspodar (PSC 833) and DOX/ᴅ-α- tocopheryl polyethylene glycol 1000 succinate (TPGS 1000) loaded polymeric micelle (PM) delivery systems were studied. Mathematical modeling has shown that the best suitability for release at pH 5.0 medium (R2 > 0.98) is provided by Korsmeyer-Peppas model and drug release kinetics are both anomalous transport (non-Fickian) and Super case II transport. The drug release was considered to fits in both the Korsmeyer-Peppas and Weibull models for DOX release from DOX-PM, DOX/PSC 833-PM, DOX/TPGS 1000-PM at pH 6.5 and pH 7.4 medium.

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Published

2025-03-25

How to Cite

Kocabay, í–zlem G. ., & İsmail, O. . (2025). Drug release kinetics and transport mechanisms of doxorubicin from core-shell delivery systems. Acta Scientiarum. Technology, 47(1), e70363. https://doi.org/10.4025/actascitechnol.v47i1.70363

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Section

Chemical Engineering