The global aim of this research was to develop and evaluate self-microemulsifying drug
delivery system (SMEDDS) to improve oral bioavailability of Lurasidone Hydrochloride (LH) …

Purpose The aims of this study were to prepare a baicalein self-microemulsion with
baicalein-phospholipid complex as the intermediate (BAPC-SMEDDS) and to compare its …

Background: Raloxifene, a second-generation selective estrogen receptor modulator
(SERM) used to prevent osteoporosis in postmenopausal women is administered orally in …

Asenapine maleate (AM)-loaded self-microemulsifying drug delivery system (AM-SMEDDS)
was prepared to increase its oral bioavailability. AM-SMEDDS was developed using Capryol …

Objective: The aim of this study was to develop a formulation for lymphatic uptake with
enhanced solubility of antifungal drug, terbinafine by use of self-microemulsifying drug …

The therapeutic potential of saquinavir, a specific inhibitor of human immunodeficiency virus
(HIV)-1 and HIV-2 protease enzymes, has been largely limited because of a low solubility …

Poor aqueous solubility and dissolution limit the oral bioavailability of Biopharmaceutics
Classification System (BCS) class II drugs. In this study, we aimed to improve the aqueous …

The objective of our investigation was to design a self-microemulsifying drug-delivery
system (SMEDDS) to improve the bioavailability of probucol. SMEDDS was composed of …

The objective was to study the phase behavior of different formulations, to identify the micro
emulsion area and to prepare solid SMEDDS particles (SSMED) of loratadine (LOR) for …

The aim of this study was to improve the oral absorption of loratadine, a pH-sensitive drug,
by self-microemulsifying drug delivery systems (SMEDDSs). The optimal SMEDDS was …