Online citations, reference lists, and bibliographies.
← Back to Search

Oral Lipid-Based Formulations: Enhancing The Bioavailability Of Poorly Water-Soluble Drugs

J. Dressman
Published 2007 · Chemistry

Cite This
Download PDF
Analyze on Scholarcy
Share



This paper is referenced by
Mechanistic understanding of bioenabling formulation approaches to improve oral bioavailability using porcine in vivo and in silico models
Joseph P. O'Shea (2018)
Controlled Flow Cavitation Technology For Use In Pharmaceutical Processing Applications And Its Commercialization Plan
C. Chen (2012)
10.21608/ZJPS.2017.38120
Etodolac Softgels: Feasibility Assessment and Considerations for Lipid-Based Formulations of a highly hydrophobic drug
Ahmed N. Allam (2017)
Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer.
Bernard McDonald (2015)
Self-Emulsifying Drug Delivery Systems (SEDDS): An Update from Formulation Development to Therapeutic Strategies
A. K. Mahapatra (2014)
Mechanistic studies and modeling of effects of ingested lipids on oral drug absorption
S. D. Maio (2014)
10.1124/jpet.109.154542
Lymphatic Transport of Methylnortestosterone Undecanoate (MU) and the Bioavailability of Methylnortestosterone Are Highly Sensitive to the Mass of Coadministered Lipid after Oral Administration of MU
K. White (2009)
10.3109/03639045.2011.631548
Self-microemulsifying smaller molecular volume oil (Capmul MCM) using non-ionic surfactants: a delivery system for poorly water-soluble drug
Mithun Mohanraor Bandivadeka (2012)
10.3109/03639045.2012.669385
Atmospheric freeze drying for the reduction of powder electrostatics of amorphous, low density, high surface area pharmaceutical powders
K. O'donnell (2013)
Bio-relevant characterisation of lipidic formulations and prediction of in vivo exposure
Paloma Benito-Gallo (2017)
10.1016/j.ajps.2017.09.006
Formulation of self-nanoemulsifying drug delivery systems containing monoacyl phosphatidylcholine and Kolliphor® RH40 using experimental design
T. Tran (2018)
10.2147/IJN.S104187
Development of self-nanoemulsifying drug delivery systems for the enhancement of solubility and oral bioavailability of fenofibrate, a poorly water-soluble drug
K. Mohsin (2016)
10.1080/03639045.2020.1791164
A novel combination of Soluplus®/Poloxamer for Meloxicam solid dispersions via hot melt extrusion for rapid onset of action. Part 2: comparative bioavailability and IVIVC
N. F. Taha (2020)
10.1007/s11095-013-1107-3
Transforming Lipid-Based Oral Drug Delivery Systems into Solid Dosage Forms: An Overview of Solid Carriers, Physicochemical Properties, and Biopharmaceutical Performance
A. Tan (2013)
10.1016/j.nano.2008.09.001
Self-associated indisulam in phospholipid-based nanomicelles: a potential nanomedicine for cancer.
H. Cesur (2009)
A Review : Novel Oral Lipid Based Formulation for Poorly Soluble Drugs
Maulik J. Patel (2011)
10.1080/17425247.2018.1453804
Superparamagnetic lipid-based hybrid nanosystems for drug delivery
E. Millart (2018)
CODEN (USA): IJPSPP Formulation, Characterization and in vitro Evaluation of Entacapone Solid Dispersions with Lipid Carriers by Using Spray Drying Method
Madhusudan Rao (2015)
10.1016/J.AJPS.2014.12.006
Overview of milling techniques for improving the solubility of poorly water-soluble drugs
Z. H. Loh (2015)
10.5772/intechopen.88603
Self-Microemulsifying System
M. Shah (2019)
10.15406/JAPLR.2015.01.00001
Tackling the Challenges with Poorly Soluble Drugs
S. Ali (2015)
Silica-Lipid Hybrid Microparticles for Improved Bioavailability of Bcs Class IV Drugs
Vijay kumar Nagabandi (2013)
From Molecule to Dose Form – Accelerated Bioavailability Enhancement for Early Phase Molecules
Jean-Luc Veuthey (2015)
10.22159/IJAP.2019V11I1.29978
A SYSTEMATIC REVIEW ON SELF-MICRO EMULSIFYING DRUG DELIVERY SYSTEMS: A POTENTIAL STRATEGY FOR DRUGS WITH POOR ORAL BIOAVAILABILITY
G. V. Radha (2019)
10.15171/apb.2015.055
Furosemide Loaded Silica-Lipid Hybrid Microparticles: Formulation Development, in vitro and ex vivo Evaluation.
Swapna Sambaraj (2015)
10.1080/03639045.2017.1371739
Effect of semicrystalline polymers on self-emulsifying solid dispersions of nateglinide: in vitro and in vivo evaluation
R. P. Swain (2018)
10.1016/j.ejpb.2014.05.008
Characterization and pharmacokinetic analysis of crystalline versus amorphous rapamycin dry powder via pulmonary administration in rats.
S. R. Carvalho (2014)
10.1016/j.ejpb.2018.07.006
Solubilisation behaviour of poorly water‐soluble drugs during digestion of solid SMEDDS
K. Vithani (2018)
STUDIES ON DRUG SOLUBILIZATION MECHANISM IN SIMPLE MICELLE SYSTEMS
Shaoxin Feng (2009)
Self-nanoemulsifying drug delivery systems (SNEDDS) for the oral delivery of lipophilic drugs
Tianjing Zhao (2015)
10.25166/ijppr.2020.v19i02.45
Lipid Based Drug Delivery System: An Approach to Enhance Bioavailability ofPoorly Water Soluble Drugs
Sachin Aryal (2020)
10.1080/10717544.2016.1214990
Controversies with self-emulsifying drug delivery system from pharmacokinetic point of view
B. Chatterjee (2016)
See more
Semantic Scholar Logo Some data provided by SemanticScholar