Studies on allantoin topical formulations: in vitro drug release studies and rheological characteristics

The extent and rate of release of active substances from topical products must be sufficient to ensure their effectiveness, which depends on selecting the most appropriate formulation. This study examined allantoin emulsions and gel formulations. In water-in-oil (W/O) and oil-in-water (O/W) emulsions, the main emulsifier was varied, while the same gelling agent was used in all formulations to test the effects of oil phase presence and emulsifier type on allantoin release, as well as the formulations' rheological and textural characteristics. O/W emulsions exhibited similar release rates and the overall amount released over six hours (11-14.8%), while the highest amount of allantoin (20.9%) was released from the gel formulation. Conversely, the amount of allantoin released from the W/O emulsion (0.77%) was insufficient. Experimental data generally fit best with the Higuchi model kinetics. The formulations demonstrated shear-thinning thixotropic behavior. The greatest deviation from the Newtonian type of flow, with the smallest value of constant n (0.106-0.13) and the largest thixotropic loop area (6602.67-8140 Pas<sup>-1</sup>) were shown by O/W emulsions. The W/O emulsion exhibited the highest constant n (0.70) and smaller hysteresis area (991.23 Pas<sup>-1</sup>). Firmness and consistency values increased in the order: gel < W/O emulsion < O/W emulsions. The O/W emulsions showed similarity in microstructure and textural characteristics, likely explaining their similar release behavior.

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Publication Details

Journal
Pharmaceutical Development and Technology
Published
2024-10-18
DOI
https://doi.org/10.1080/10837450.2024.2414938
Citations
3
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
Field-Weighted Citation Impact
0.62
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article

Studies on allantoin topical formulations: in vitro drug release studies and rheological characteristics

Alisa Elezović, Miroslav Hadnađev, Ervina Bečić, Adna Džemat et al.
3 citations
Pharmaceutical Development and Technology
Advancements in Transdermal Drug Delivery
0.62
article

Studies on allantoin topical formulations: in vitro drug release studies and rheological characteristics

Alisa Elezović, Miroslav Hadnađev, Ervina Bečić, Adna Džemat, Belma Imamović, Veljko S. Krstonosic, Amar Elezović, Emina Hrnčić
article en
3 citations

Abstract

The extent and rate of release of active substances from topical products must be sufficient to ensure their effectiveness, which depends on selecting the most appropriate formulation. This study examined allantoin emulsions and gel formulations. In water-in-oil (W/O) and oil-in-water (O/W) emulsions, the main emulsifier was varied, while the same gelling agent was used in all formulations to test the effects of oil phase presence and emulsifier type on allantoin release, as well as the formulations' rheological and textural characteristics. O/W emulsions exhibited similar release rates and the overall amount released over six hours (11-14.8%), while the highest amount of allantoin (20.9%) was released from the gel formulation. Conversely, the amount of allantoin released from the W/O emulsion (0.77%) was insufficient. Experimental data generally fit best with the Higuchi model kinetics. The formulations demonstrated shear-thinning thixotropic behavior. The greatest deviation from the Newtonian type of flow, with the smallest value of constant n (0.106-0.13) and the largest thixotropic loop area (6602.67-8140 Pas<sup>-1</sup>) were shown by O/W emulsions. The W/O emulsion exhibited the highest constant n (0.70) and smaller hysteresis area (991.23 Pas<sup>-1</sup>). Firmness and consistency values increased in the order: gel < W/O emulsion < O/W emulsions. The O/W emulsions showed similarity in microstructure and textural characteristics, likely explaining their similar release behavior.

Pharmaceutical Development and TechnologyVol. 29(9)
University of Sarajevo (BA), University of Novi Sad (RS), Academy of Medical Sciences of Bosnia and Herzegovina (BA)
Zero hunger
Openalex Percentile: Top 36%
Advancements in Transdermal Drug Delivery
0.62
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