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Predicting Calcein Release from Ultrasound-Targeted Liposomes: A Comparative Analysis of Random Forest and Support

Ibrahim Shomope1, Kelly M Percival1, Nabil M Abdel Jabbar1

  • 1Department of Chemical and Biological Engineering, American University of Sharjah, Sharjah 26666, United Arab Emirates.

Technology in Cancer Research & Treatment
|November 14, 2024
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Random Forest (RF) models outperform Support Vector Machines (SVM) in predicting drug release from targeted liposomes triggered by low-frequency ultrasound (LFUS). RF models demonstrated superior accuracy across various power densities.

Keywords:
artificial intelligencecalceindrug deliverydrug releasemachine learningpower densityrandom forestsupport vector machineultrasound

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Area of Science:

  • Biomedical Engineering
  • Drug Delivery Systems
  • Machine Learning Applications

Background:

  • Targeted liposomes offer precise drug delivery.
  • Ultrasound-triggered release allows for spatiotemporal control.
  • Predictive models are crucial for optimizing drug delivery parameters.

Purpose of the Study:

  • To compare the predictive performance of Random Forest (RF) and Support Vector Machine (SVM) algorithms.
  • To evaluate these models for predicting calcein release from ultrasound-triggered, targeted liposomes.
  • To assess model performance under varying low-frequency ultrasound (LFUS) power densities.

Main Methods:

  • Synthesis and characterization of liposomes loaded with calcein and targeted with seven different moieties.
  • Utilized Dynamic Light Scattering and Bicinchoninic Acid assays for characterization.
  • Trained and evaluated RF and SVM models using metrics like MAE, MSE, R², and a20 index.

Main Results:

  • Random Forest (RF) models consistently showed superior performance compared to SVM.
  • RF achieved R² scores exceeding 0.96 across all tested LFUS power densities.
  • RF demonstrated a strong correlation with experimental data, especially at higher power densities.

Conclusions:

  • Random Forest (RF) is a more effective algorithm than Support Vector Machine (SVM) for predicting drug release from targeted liposomes.
  • Both models have potential applications depending on specific predictive requirements.
  • The findings support the use of machine learning for optimizing ultrasound-mediated drug delivery.