4.7 Article

Drug Release from Nanoparticles (Polymeric Nanocapsules and Liposomes) Mimed through a Multifractal Tunnelling-Type Effect

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POLYMERS
卷 15, 期 4, 页码 -

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MDPI
DOI: 10.3390/polym15041018

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drug release; nanocapsules; liposomes; multifractal tunnelling-type effect

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The present study examines the drug release process from nanoparticles and its inclusion in cream-type formulations. The cream allows for targeted delivery of the drug to tumor epithelial cells, reducing side effects and improving treatment effectiveness. The process of obtaining these formulations is simple and reproducible. The theoretical model considers the system as complex, utilizing multifractal dimensions and functions to analyze microscopic characteristics and system complexity.
The present study analyzes (theoretically and experimentally) a drug release process from nanoparticles (polymeric nanocapsules and liposomes). This process is functionalized on the surface with an aptamer. These types of drug release processes can also be included in cream-type formulations. The obtained cream ensures the active targeting of tumor epithelial cells, in the case of skin cancer, because it can be easily administered to the skin by spreading, thus avoiding side effects caused by the toxicity of the drug to healthy cells, increasing both patient compliance and the effectiveness of the treatment. The process of obtaining these formulations is a simple one, easy to use and highly reproductible. The theoretical model, based on the multifractal tunnel effect within the Scale Relativity Theory, considers the system as a complex one. In this model, complexity is replaced with system multifractality, quantified in physical quantities as multifractal dimensions and multifractal functions. The main advantage of this approach consists in the fact that it allows us to obtain information on system behavior at a microscopic level and to evaluate microscopic characteristics of the system, such as intrinsic transparences of the drug molecules, multifractal constants as indicators of the system's complexity, the frequency of interactions within the system and the energy ratio between potential barrier energy and the energy of drug molecules.

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