Modeling of the In Vitro Release Kinetics of Sonosensitive Targeted Liposomes
Zeyad AlMajed1, Najla M Salkho2,3, Hana Sulieman4
1Biomedical Engineering Program, College of Engineering, American University of Sharjah, Sharjah P.O. Box 26666, United Arab Emirates.
Biomedicines
|December 23, 2022
Summary
Ultrasound-triggered targeted liposomes show potential for improved chemotherapy. Mathematical models accurately predict drug release profiles, aiding future in vitro studies.
Area of Science:
- Pharmacology
- Biomedical Engineering
- Materials Science
Background:
- Targeted liposomes offer a promising approach to enhance chemotherapy efficacy and minimize side effects.
- Ultrasound-triggered drug release from liposomes is an area of active research for improved therapeutic delivery.
Purpose of the Study:
- To perform comprehensive model fitting for liposomal release profiles under ultrasound stimulation.
- To evaluate the predictive accuracy of various mathematical models for drug release from targeted liposomes.
Main Methods:
- A large dataset of liposomal release profiles with seven targeting moieties and control liposomes was analyzed.
- Two ultrasound frequency levels (low: 20 kHz; high: 1.07 MHz and 3 MHz) and varying power densities were employed.
- Mathematical models including Hixson-Crowell, Korsmeyer-Peppas, Gompertz, Weibull, and Lu-Hagen were fitted to the release data.
Main Results:
- At low ultrasound frequencies, Hixson-Crowell, Korsmeyer-Peppas, Gompertz, Weibull, and Lu-Hagen models demonstrated good fits across all tested power densities.
- At high ultrasound frequencies, Hixson-Crowell, Korsmeyer-Peppas, and Gompertz models provided the best fit to the release profiles.
- Model fitting successfully characterized drug release kinetics under different ultrasound conditions.
Conclusions:
- Mathematical models are crucial for predicting drug release from ultrasound-triggered targeted liposomes.
- Selected kinetic models can accurately describe liposomal drug release, supporting the development of targeted chemotherapy delivery systems.
- These findings will facilitate the design and optimization of future in vitro studies for liposomal drug delivery.
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