Nanosuspensions as carriers of active ingredients: Chemical composition, development methods, and their biological activities

Nanosuspensions (NSps) are colloidal dispersions of particles that have the potential to solve the delivery problems of active ingredients associated with their low solubility in water or instability due to environmental factors. It is essential to consider their chemical composition and preparation methods because they directly influence drug loading, size, morphology, solubility, and stability; these characteristics of nanosuspensions influence the delivery and bioavailability of active ingredients. NSps provides high loading of drugs, protection against degrading agents, rapid dissolution, high particle stability, and high bioavailability of active ingredients across biological membranes.

Highlights

  • Nanosuspensions are a cost-effective alternative to carrier lipophilic drugs.
  • Nanosuspensions improve drug bioavailability compared to other carriers.
  • Nanosuspensions are excellent carriers of active ingredients with potential therapeutic applications.

In addition, they provide lower toxicity compared to other nanocarriers, such as liposomes or polymeric nanoparticles, and can modify the pharmacokinetic profiles, thus improving their safety and efficacy. The present review aims to address all aspects related to the composition of NSps, the different methods for their production, and the main factors affecting their stability. Moreover, recent studies are described as carriers of active ingredients and their biological activities.

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Gabriela Aguilar-Hernández, Brandon A. López-Romero, Mayra Nicolás-García, Yolanda Nolasco-González, Hugo S. García-Galindo, Efigenia Montalvo-González, Nanosuspensions as carriers of active ingredients: Chemical composition, development methods, and their biological activities, Food Research International, Volume 174, Part 1, 2023, 113583, ISSN 0963-9969, https://doi.org/10.1016/j.foodres.2023.113583.


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Rational Selection of Cyclodextrins for the Solubilization of Poorly Soluble Oral Drugs
Rational Selection of Cyclodextrins for the Solubilization of Poorly Soluble Oral Drugs
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