Scientific Reports · 2024 · 28 citations · 85 references
PharmacyPharmaceuticsPharmacologyBioavailabilityDrug DeliveryNanoparticle Drug DeliveryDrug EncapsulationLipid-based NanoparticlesNanomaterials For Drug DeliveryNanomedicineNanoparticle CharacterizationNanoparticle FormulationsAntidiabetic Drug TherapyChitosanChitosan NanocarriersEntrapmentIn Vivo StudiesLipid Nanoparticle DeliveryLipid NanoparticlesLipid-based Nanoparticle Formulation
The aim of the present study was to prepare and evaluate Piperine (PP) loaded chitosan lipid nanoparticles (PP-CLNPs) to evaluate its biological activity alone or in combination with the antidiabetic drug Metformin (MET) in the management of cognitive deficit in diabetic rats. Piperine was successfully loaded on CLNPs prepared using chitosan, stearic acid, Tween 80 and Tripolyphosphate (TPP) at different concentrations. The developed CLNPs exhibited high entrapment efficiency that ranged from 85.12 to 97.41%, a particle size in the range of 59.56-414 nm and a negatively charged zeta potential values (- 20.1 to - 43.9 mV). In vitro release study revealed enhanced PP release from CLNPs compared to that from free PP suspensions for up to 24 h. In vivo studies revealed that treatment with the optimized PP-CLNPs formulation (F2) exerted a cognitive enhancing effect and ameliorated the oxidative stress associated with diabetes. PP-CLNPs acted as an effective bio-enhancer which increased the potency of metformin in protecting brain tissue from diabetes-induced neuroinflammation and memory deterioration. These results suggested that CLNPs could be a promising drug delivery system for encapsulating PP and thus can be used as an adjuvant therapy in the management of high-risk diabetic cognitive impairment conditions.
85
Kinetic modeling on drug release from controlled drug delivery systems.
Suvakanta Dash, P. N. Murthy, Lilakanta Nath et al. · PubMed · 2010 · 2.7K citations