Priyanshi Patel and Mitali Patel* Pages 1 - 11 ( 11 )
Background: Around 40% of newly discovered chemical entities in pharmaceutical industries have poor water solubility and hence they suffer from low oral bioavailability owing to undesirable physicochemical and pharmacokinetic properties. So, it is the challenge for the formulation scientists to develop the oral formulation that can mitigate the pitfalls associated with such lipophilic drugs.Methods: Lipid nanoparticles hold a promising tool to augment the pitfalls of lipophilic drugs as lipid component can effectively increases the absorption of drugs which leads to improvement in oral bioavailability. They are also considered as safe because they are made up of physiological lipids which are biocompatible and biodegradable in nature. Amongst the lipid nanoparticles, Nanostructured lipid carriers (NLCs) are the second-generation lipid nanoparticle and were developed to conquer the limitations of solid lipid nanoparticles. They increase the solubility, permeability, reduce metabolism, P-glycoprotein efflux and thereby increase the bioavailability of poorly soluble drugs. Conclusion: This review highlights the various aspects of NLCs such as formulation components, types, in vivo fate, Pharmacokinetic, toxicity, recent advances and patent review of NLCs in drug delivery.
In vivo fate, Lyophilization, Nanostructured lipid carrier, Oral delivery, Patents, Pharmacokinetic, Toxicity.
Maliba Pharmacy College, Uka Tarsadia University, Surat 394350, Gujarat, Maliba Pharmacy College, Uka Tarsadia University, Surat 394350, Gujarat