The Influence of Operational Parameters on the Characterization of Tretinoin-Loaded Niosomes

A new pharmaceutical system was developed to integrate tretinoin into niosomes, optimizing drug encapsulation without increasing the niosome size. The aim of this study was to produce tretinoin-loaded niosomes by the thin film hydration method. The effects of three factors including the molar ratio of surfactants to cosurfactants (0.1, 0.3, 0.5), hydration process temperature (40, 50, 60 °C), and ultrasound intensity (100, 150, 200 kHz) on drug encapsulation, particle size, and zeta potential of niosomes were investigated. Span 60 and Tween 80 were used as nonionic surfactants, with 1-dodecanol as a stabilizer and cosurfactant, dichloromethane as the solvent, and a phosphate buffer (pH 5.5) for hydration. Drug loading efficiency varied from 41% to 83%, and niosome sizes ranged from 210 to 440 nm. The highest drug loading (83%) was achieved with a 0.1 molar ratio of surfactants, 40 °C hydration, and 100 kHz ultrasound, resulting in a particle size of 440 nm and zeta potential between -9 and -16 mV.

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Publication Details

Journal
ACS Omega
Published
2025-07-14
DOI
https://doi.org/10.1021/acsomega.4c11147
Citations
1
Primary Topic
Advancements in Transdermal Drug Delivery
Type
article
Field-Weighted Citation Impact
0.79

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article

The Influence of Operational Parameters on the Characterization of Tretinoin-Loaded Niosomes

Amir Jafarian, Kiana Peyvandi, Azam Shadloo, Samira Khalilabadi
1 citations
ACS Omega
Advancements in Transdermal Drug Delivery
0.79
article

The Influence of Operational Parameters on the Characterization of Tretinoin-Loaded Niosomes

Amir Jafarian, Kiana Peyvandi, Azam Shadloo, Samira Khalilabadi
article en
1 citations

Abstract

A new pharmaceutical system was developed to integrate tretinoin into niosomes, optimizing drug encapsulation without increasing the niosome size. The aim of this study was to produce tretinoin-loaded niosomes by the thin film hydration method. The effects of three factors including the molar ratio of surfactants to cosurfactants (0.1, 0.3, 0.5), hydration process temperature (40, 50, 60 °C), and ultrasound intensity (100, 150, 200 kHz) on drug encapsulation, particle size, and zeta potential of niosomes were investigated. Span 60 and Tween 80 were used as nonionic surfactants, with 1-dodecanol as a stabilizer and cosurfactant, dichloromethane as the solvent, and a phosphate buffer (pH 5.5) for hydration. Drug loading efficiency varied from 41% to 83%, and niosome sizes ranged from 210 to 440 nm. The highest drug loading (83%) was achieved with a 0.1 molar ratio of surfactants, 40 °C hydration, and 100 kHz ultrasound, resulting in a particle size of 440 nm and zeta potential between -9 and -16 mV.

ACS OmegaVol. 10(28)
Semnan University (IR)
Semnan University
Zero hunger
Openalex Percentile: Top 26%
Advancements in Transdermal Drug Delivery
0.79
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