[PDF][PDF] Solubility enhancement of aripiprazole by solid-self emulsifying drug delivery systems
A Chennuri, D Prasanthi - International Journal of Pharmaceutical …, 2018 - researchgate.net
Self-emulsifying drug delivery systems are a promising approach for the formulation of drug
compounds with poor aqueous solubility. The main objective of this work was to formulate …
compounds with poor aqueous solubility. The main objective of this work was to formulate …
Design and Evaluation of a Self-Emulsifying Drug Delivery System of Aripiprazole.
AR Ramya, P Sudheer… - Indian Journal of …, 2019 - search.ebscohost.com
The present investigation is aimed at enhancing the solubility and the dissolution rate of
aripiprazole by formulating a self-micro emulsifying drug delivery system. The preliminary …
aripiprazole by formulating a self-micro emulsifying drug delivery system. The preliminary …
Formulation development and bioavailability assessment of aripiprazole by self-nanoemulsifying drug delivery systems
SK Sahoo - Asian Journal of Pharmaceutics (AJP), 2018 - asiapharmaceutics.info
Aim: The aim of the present study was to develop a self-nanoemulsifying drug delivery
system (SNEDDS) for the oral delivery of aripiprazole (APZ), an antipsychotic drug used in …
system (SNEDDS) for the oral delivery of aripiprazole (APZ), an antipsychotic drug used in …
pH-independent dissolution and enhanced oral bioavailability of aripiprazole-loaded solid self-microemulsifying drug delivery system
The present study pursued the systematic development of a stable solid self-emulsifying
drug delivery system (SMEDDS) of an atypical antipsychotic drug, aripiprazole (APZ), which …
drug delivery system (SMEDDS) of an atypical antipsychotic drug, aripiprazole (APZ), which …
[PDF][PDF] Solubility enhancement of lurasidone hydrochloride by preparing SMEDDS
F Jangipuria, V Londhe - Int J Pharm Pharm Sci, 2015 - academia.edu
Objective: The objective of the study was to enhance solubility of Lurasidone HCl, an
atypical antipsychotic drug, by formulating self-micro emulsifying drug delivery system …
atypical antipsychotic drug, by formulating self-micro emulsifying drug delivery system …
Formulation and evaluation of solid self nano emulsifying drug delivery system of olanzapine to enhance aqueous solubility and dissolution rate
MS Reddy, B Sravani - Asian Journal of Pharmaceutical …, 2021 - indianjournals.com
Present research work was aimed to enhance aqueous solubility and dissolution rate of
olanzapine by solid self nano emulsifying drug delivery system (S-SNEDDS). Olanzapine is …
olanzapine by solid self nano emulsifying drug delivery system (S-SNEDDS). Olanzapine is …
[HTML][HTML] Twin screw melt granulation: a single step approach for developing self-emulsifying drug delivery system for lipophilic drugs
D Nyavanandi, P Mandati, S Narala, A Alzahrani… - Pharmaceutics, 2023 - mdpi.com
The current research aims to improve the solubility of the poorly soluble drug, ie, ibuprofen,
by developing self-emulsifying drug delivery systems (SEDDS) utilizing a twin screw melt …
by developing self-emulsifying drug delivery systems (SEDDS) utilizing a twin screw melt …
[HTML][HTML] Formulation, optimization, and evaluation of self-emulsifying drug delivery systems of nevirapine
R Chintalapudi, T Murthy, KR Lakshmi… - International journal of …, 2015 - ncbi.nlm.nih.gov
Background: The aim of the present study was to formulate and optimize the self-emulsifying
drug delivery systems (SEDDS) of nevirapine (NVP) by use of 2 2 factorial designs to …
drug delivery systems (SEDDS) of nevirapine (NVP) by use of 2 2 factorial designs to …
Formulation and statistical optimization of clozapine solid self emulsification system for improving the dissolution properties
R Pethani, K Dudhat, MM Soniwala… - Journal of Dispersion …, 2024 - Taylor & Francis
Clozapine is an atypical antipsychotic drug that exhibits low bioavailability (> 27%) due to
poor solubility and higher hepatic metabolism. The present investigation was aimed to …
poor solubility and higher hepatic metabolism. The present investigation was aimed to …
Development of self-microemulsifying tablets containing dutasteride for enhanced dissolution and pharmacokinetic profile
KM Hwang, MS Choi, SH Seok, ES Park - International Journal of …, 2022 - Elsevier
This study aimed to develop self-microemulsifying tablets containing the hydrophobic drug
dutasteride for easy administration and high in vivo absorption. The candidate lipids and …
dutasteride for easy administration and high in vivo absorption. The candidate lipids and …