Efavirenz Dissolution Enhancement I: Co-Micronization

Improvement of some physicochemical properties of arundic acid, (R)-(−)-2-propyloctanonic acid, by complexation with hydrophilic cyclodextrins

(2011) Yuji Miyamoto et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

Oral pharmacokinetics of the anti-HIV efavirenz encapsulated within polymeric micelles

(2010) Diego A. Chiappetta et al.   BIOMATERIALS

Enhanced Dissolution and Bioavailability of Raloxifene Hydrochloride by Co-grinding with Different Superdisintegrants

(2010) Balasubramaniam Jagadish et al.   CHEMICAL & PHARMACEUTICAL BULLETIN

Glucosamine HCl as a new carrier for improved dissolution behaviour: Effect of grinding

(2010) Hiba Al-Hamidi et al.   COLLOIDS AND SURFACES B-BIOINTERFACES

New Solid State Forms of the Anti-HIV Drug Efavirenz. Conformational Flexibility and HighZ′Issues

(2010) Sudarshan Mahapatra et al.   CRYSTAL GROWTH & DESIGN

Solubilization of Sagopilone, a poorly water-soluble anticancer drug, using polymeric micelles for parenteral delivery

(2010) Annett Richter et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

Preparation of a chemically stable quercetin formulation using nanosuspension technology

(2010) Lei Gao et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

Quantum chemical and experimental studies on the structure and vibrational spectra of efavirenz

(2010) Soni Mishra et al.   VIBRATIONAL SPECTROSCOPY

Combination antiretroviral drugs in PLGA nanoparticle for HIV-1

(2009) Christopher J Destache et al.   BMC INFECTIOUS DISEASES

Advantages of celecoxib nanosuspension formulation and transformation into tablets

(2009) Andrej Dolenc et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

An improved kinetics approach to describe the physical stability of amorphous solid dispersions

(2009) Jiao Yang et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

Multi-drug loaded polymeric micelles for simultaneous delivery of poorly soluble anticancer drugs

(2009) Ho-Chul Shin et al.   JOURNAL OF CONTROLLED RELEASE

Efavirenz-loaded polymeric micelles for pediatric anti-HIV pharmacotherapy with significantly higher oral bioavailability

(2009) Diego A Chiappetta et al.   Nanomedicine

Cogrinding as an approach to enhance dissolution rate of a poorly water-soluble drug (gliclazide)

(2009) Mohammad Barzegar-Jalali et al.   POWDER TECHNOLOGY

Amorphization Alone Does Not Account for the Enhancement of Solubility of Drug Co-ground with Silicate: The Case of Indomethacin

(2008) Deepak Bahl et al.   AAPS PHARMSCITECH

Exploring the use of novel drug delivery systems for antiretroviral drugs

(2008) Elizabeth Ojewole et al.   EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS

Cyclodextrins as stabilizers for the preparation of drug nanocrystals by the emulsion solvent diffusion method

(2008) Abdallah Makhlof et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS

Cogrinding enhances the oral bioavailability of EMD 57033, a poorly water soluble drug, in dogs

(2007) Markus Vogt et al.   EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS

Effect of powder processing on performance of fenofibrate formulations

(2007) Rajeev A. Jain et al.   EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS

Dissolution enhancement of fenofibrate by micronization, cogrinding and spray-drying: Comparison with commercial preparations

(2007) Markus Vogt et al.   EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS

Amphotericin B-incorporated polymeric micelles composed of poly(d,l-lactide-co-glycolide)/dextran graft copolymer

(2007) Ki-Choon Choi et al.   INTERNATIONAL JOURNAL OF PHARMACEUTICS