Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems
J Cui, B Yu, Y Zhao, W Zhu, H Li, H Lou… - International journal of …, 2009 - Elsevier
Curcumin is a poorly water-soluble drug and its oral bioavailability is very low. A new self-
microemulsifying drug delivery system (SMEDDS) has been successfully developed to …
microemulsifying drug delivery system (SMEDDS) has been successfully developed to …
Enhancement of curcumin oral absorption and pharmacokinetics of curcuminoids and curcumin metabolites in mice
L Zhongfa, M Chiu, J Wang, W Chen, W Yen… - Cancer chemotherapy …, 2012 - Springer
Purpose Curcumin has shown a variety of biological activity for various human diseases
including cancer in preclinical setting. Its poor oral bioavailability poses significant …
including cancer in preclinical setting. Its poor oral bioavailability poses significant …
Exemestane loaded self-microemulsifying drug delivery system (SMEDDS): development and optimization
AK Singh, A Chaurasiya, M Singh, SC Upadhyay… - Aaps Pharmscitech, 2008 - Springer
The purpose of this research work was to formulate and characterize self-micro emulsifying
drug delivery system containing exemestane. The solubility of exemestane was determined …
drug delivery system containing exemestane. The solubility of exemestane was determined …
A critical appraisal of microemulsions for drug delivery: part II
Microemulsions are thermodynamically stable, optically transparent isotropic solutions of oil
and water successfully formulated by using a combination of suitable surfactant and …
and water successfully formulated by using a combination of suitable surfactant and …
Lipid Nanoparticles Improve the Uptake of α-Asarone Into the Brain Parenchyma: Formulation, Characterization, In Vivo Pharmacokinetics, and Brain Delivery
Abstract Treatment of brain-related diseases is one of the most strenuous challenges in drug
delivery research due to numerous hurdles, including poor blood-brain barrier penetration …
delivery research due to numerous hurdles, including poor blood-brain barrier penetration …
Preparation and characterization of novel self nano emulsifying drug delivery system of allopurinol
The aim of research was to develop self nanoemulsifying drug delivery technology
containing low aqueous soluble drug allopurinol for improving solubility, dissolution and …
containing low aqueous soluble drug allopurinol for improving solubility, dissolution and …
High performance liquid chromatography method for the pharmacokinetic study of bicalutamide SMEDDS and suspension formulations after oral administration to rats
Bicalutamide is a non-steroidal antiandrogen and is an oral medication that is used for
treating prostate cancer. To evaluate the bioavailability of bicalutamide from bicalutamide …
treating prostate cancer. To evaluate the bioavailability of bicalutamide from bicalutamide …
Microemulsions: pharmaceutical applications
VB Patravale, AA Date - Microemulsions: Background, New …, 2009 - Wiley Online Library
Pharmaceutical research is aimed at delivery of the active pharmaceutical ingredient (API) to
the target organ at therapeutically relevant levels, with negligible discomfort and side effects …
the target organ at therapeutically relevant levels, with negligible discomfort and side effects …
Dissolution and bioavailability enhancement of alpha-asarone by solid dispersions via oral administration
L Deng, Y Wang, T Gong, X Sun… - Drug development and …, 2017 - Taylor & Francis
Abstract Alpha (α)-asarone (1-propenyl-2, 4, 5-methoxybenzol)(ARE) has been extensively
used to treat chronic obstructive pulmonary diseases (COPD), bronchial asthma …
used to treat chronic obstructive pulmonary diseases (COPD), bronchial asthma …
A Comprehensive Insight on Self Emulsifying Drug Delivery Systems
R Kadian, A Nanda - Recent Advances in Drug Delivery and …, 2022 - ingentaconnect.com
Background: The oral route is a highly recommended route for the delivery of a drug. But
most lipophilic drugs are difficult to deliver via this route due to their low aqueous solubility …
most lipophilic drugs are difficult to deliver via this route due to their low aqueous solubility …