Abstract

Nanoparticles (NPs) hold great potential as therapeutics, particularly in the realm of drug delivery. They are effective at functional cargo delivery and offer a great degree of amenability that can be used to offset toxic side effects or to target drugs to specific regions in the body. However, there are many challenges associated with the development of NP-based drug formulations that hamper their successful clinical translation. Arguably, the most significant barrier in the way of efficacious NP-based drug delivery systems is the tedious and time-consuming nature of NP formulation—a process that needs to account for downstream effects, such as the onset of potential toxicity or immunogenicity, in vivo biodistribution and overall pharmacokinetic profiles, all while maintaining desirable therapeutic outcomes. Computational and AI-based approaches have shown promise in alleviating some of these restrictions. Via predictive modeling and deep learning, in silico approaches have shown the ability to accurately model NP-membrane interactions and cellular uptake based on minimal data, such as the physicochemical characteristics of a given NP. More importantly, machine learning allows computational models to predict how specific changes could be made to the physicochemical characteristics of a NP to improve functional aspects, such as drug retention or endocytosis. On a larger scale, they are also able to predict the in vivo pharmacokinetics of NP-encapsulated drugs, predicting aspects such as circulatory half-life, toxicity, and biodistribution. However, the convergence of nanomedicine and computational approaches is still in its infancy and limited in its applicability. The interactions between NPs, the encapsulated drug and the body form an intricate network of interactions that cannot be modeled with absolute certainty. Despite this, rapid advancements in the area promise to deliver increasingly powerful tools capable of accelerating the development of advanced nanoscale therapeutics. Here, we describe computational approaches that have been utilized in the field of nanomedicine, focusing on approaches for NP design and engineering.

Highlights

  • Nanoparticle (NP)-based therapeutics have gained increased popularity in recent years. This is attributed to the many advantages that nano-formulated therapeutics such as nanoscale drug delivery systems can offer over free drugs, including the ability to bypass biological barriers with ease, improved amenability without having to chemically alter the drug and the option to direct NPs to desired target sites [1]

  • Exploiting technological advancements such as in silico modeling can help direct the design of better nanomedicine platforms while the application of novel computational approaches can expedite the process of NP development

  • Most currently used modeling approaches are unable to take into account a holistic view of NP physicochemical characteristics, with highly complicated structures such as biologically derived extracellular vesicles (EVs) that consist of a complex milieu of proteins, lipids, and glycans with diverse patterns of organization

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Summary

INTRODUCTION

Nanoparticle (NP)-based therapeutics have gained increased popularity in recent years. The plethora of associated variables make it impractical to use high throughput methods to determine optimal in vivo treatment conditions in most cases Exploiting technological advancements such as in silico modeling can help direct the design of better nanomedicine platforms while the application of novel computational approaches can expedite the process of NP development. It is possible to predict physiochemical properties of targets, biodistribution and quantitative assessment of NPs on the spatial scale [10, 11] In this way, many aspects of NP-based drug delivery platforms such as physicochemical-functional relationships, dose quantification for determining therapeutic and side effects and evaluation of drug efficacy over time can be predicted.

Silica NP Quantum dots Carbon nanotubes
Completed Completed Completed Completed
COMPUTATIONAL APPROACHES FOR NP DESIGN
Size of NPs
Surface Modification of NPs
Shapes of NPs
Surface Chemistry of NPs
Concentration of NPs
Elasticity of NPs
Hydrophobicity of NPs
Safety of NPs
COMPUTATIONAL APPROACHES TO PREDICT IN VIVO BEHAVIOR OF NPS
Modeling Circulation and Clearance
Open Open Open
Modeling Extravasation and Tissue
Modeling Cell Membrane Permeability
CONCLUSION AND FUTURE DIRECTIONS
AUTHOR CONTRIBUTIONS
Full Text
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