Lipid nanoparticles strategies to modify pharmacokinetics of central nervous system targeting drugs: Crossing or circumventing the blood–brain barrier (BBB) to …

AC Correia, AR Monteiro, R Silva, JN Moreira… - Advanced Drug Delivery …, 2022 - Elsevier
The main limitation to the success of central nervous system (CNS) therapies lies in the
difficulty for drugs to cross the blood–brain barrier (BBB) and reach the brain. Regarding its …

[HTML][HTML] Strategies to improve drug strength in nasal preparations for brain delivery of low aqueous solubility drugs

PC Pires, M Rodrigues, G Alves, AO Santos - Pharmaceutics, 2022 - mdpi.com
Intranasal administration is a promising route for brain drug delivery. However, it can be
difficult to formulate drugs that have low water solubility into high strength intranasal …

[HTML][HTML] Novel nasal niosomes loaded with lacosamide and coated with chitosan: A possible pathway to target the brain to control partial-onset seizures

AS Tulbah, MH Elkomy, RM Zaki, HM Eid… - International journal of …, 2023 - Elsevier
This work aimed to develop and produce lacosamide-loaded niosomes coated with chitosan
(LCA-CTS-NSM) using a thin-film hydration method and the Box-Behnken design. The effect …

Unravelling micro and nano vesicular system in intranasal drug delivery for epilepsy

S Salave, D Rana, R Pardhe, P Bule… - Pharmaceutical …, 2022 - ingentaconnect.com
Background: Epilepsy is one of the major neurological disorders, affecting about 50 million
people globally. Oral, intravenous and rectal delivery systems are available for the …

[HTML][HTML] Investigating the effect of surface hydrophilicity on the destiny of PLGA-poloxamer nanoparticles in an in vivo animal model

T Silvestri, L Grumetto, I Neri, M De Falco… - International Journal of …, 2023 - mdpi.com
This study aimed to examine the impact of different surface properties of poly (lactic-co-
glycolic) acid (PLGA) nanoparticles (P NPs) and PLGA-Poloxamer nanoparticles (PP NPs) …

Lyophilized SLN of Cinnacalcet HCl: BBD enabled optimization, characterization and pharmacokinetic study

SB Routray, CN Patra, R Raju… - Drug Development …, 2020 - Taylor & Francis
Objective: The objective of the present research is to formulate solid lipid nanoparticles
(SLN) of CH to improve its oral bioavailability. Methods: Cinnacalcet hydrochloride (CH) …

[HTML][HTML] Preparation and evaluation of carbamazepine solid lipid nanoparticle for alleviating seizure activity in pentylenetetrazole-kindled mice

M Qushawy, K Prabahar, M Abd-Alhaseeb, S Swidan… - Molecules, 2019 - mdpi.com
Objectives: The study aimed to prepare carbamazepine in solid lipid nanoparticle form (CBZ-
SLN) in order to enhance its anticonvulsant effect. Method: Eight formulations of CBZ-SLNs …

Nose-to-brain delivery of antiretroviral drug loaded lipidic nanocarriers to purge HIV reservoirs in CNS: a safer approach

S Mehrotra, PK Bg, NA Bhaskaran, JS Reddy… - Journal of Drug Delivery …, 2023 - Elsevier
Human immunodeficiency virus (HIV), which induces acquired immunodeficiency syndrome
(AIDS), is among the most lethal viral infections worldwide. Although the realm of highly …

Lamotrigine nanoparticle laden polymer composite oral dissolving films for improving therapeutic potential of the hydrophobic antiepileptic molecule

S Shankar Raman, VHB Narayanan… - ASSAY and Drug …, 2021 - liebertpub.com
Lamotrigine is used for neurological disorders and antiepileptic therapy at frequent dosing
due to its poor solubility. The present work aims to study the influence of combining the …

Molecularly Imprinted Drug Carrier for Lamotrigine—Design, Synthesis, and Characterization of Physicochemical Parameters

M Sobiech, SM Khamanga, K Synoradzki… - International Journal of …, 2024 - mdpi.com
This study presents the initial attempt at introducing a magnetic molecularly imprinted
polymer (MIP) designed specifically for lamotrigine with the purpose of functioning as a drug …