Background:
The oral application of drugs is the most popular route through which the systemic effect can be
achieved. Nevertheless, oral administration is limited by difficulties related to physicochemical properties of the drug molecule, including low aqueous solubility, instability, low permeability, and rapid metabolism, all of which result in low and irregular oral bioavailability.
Objective:
The enhancement of oral bioavailability of drug molecules with such properties could lead to extreme complications in drug preparations. Oral lipid based nanoparticles seems to possess extensive advantages due to their ability to increase the solubility, simplifying intestinal absorption and decrease or eradicate the effect of food on the absorption of low
soluble, lipophilic drugs and therefore improving the oral bioavailability.
Method:
The present review provides a summary of the general theory of lipid based nanoparticles, their preparation methods as well as their oral applications. Moreover, the oral drug delivery challenges are discussed.
Results:
According to this review, the most frequent types of lipid-based nanoparticle, the solid lipid nanoparticles and
nanostructured lipid carriers are potent oral carriers due to their ability to penetrate the oral drug adsorption barriers. Moreover, such lipid nanoparticles can be beneficial drug carriers against cardiovascular risk disorders as diabetes, hypertension
etc.
Conclusion:
In this review, the most current and promising studies involving Solid Lipid Nanoparticles and Nanostructured
Lipid Carriers as oral drug carriers are reported aiming to assist researchers who focus their research on lipid based nanoparticles.
A concise review on preparation methods used for the development of solid lipid nanoparticles
