Results 11 to 20 of about 1,040,538 (251)

Cellulosic Polymers for Enhancing Drug Bioavailability in Ocular Drug Delivery Systems

open access: yesPharmaceuticals, 2021
One of the major impediments to drug development is low aqueous solubility and thus poor bioavailability, which leads to insufficient clinical utility. Around 70–80% of drugs in the discovery pipeline are suffering from poor aqueous solubility and poor ...
Bharti Gupta   +4 more
doaj   +1 more source

Micronization Techniques for Solubility Enhancement of Aceclofenac as a potential Solubility Enhancement Approach [PDF]

open access: yes, 2023
Aceclofenac is a BCS class II poorly aqueous soluble drug that has significant oral bioavailability limitations after intake. Numerous solubility enhancement techniques are available for the solubility enhancement, out of various techniques Micronization
Vishal Gupta   +2 more
core   +1 more source

Computing the aqueous solubility of organic drug-like molecules and understanding hydrophobicity [PDF]

open access: yes, 2015
This thesis covers a range of methodologies to provide an account of the current (2010-2014) state of the art and to develop new methods for solubility prediction.
McDonagh, James L.
core   +2 more sources

Cocrystals and Drug–Drug Cocrystals of Anticancer Drugs: A Perception towards Screening Techniques, Preparation, and Enhancement of Drug Properties

open access: yesCrystals, 2022
The most favored approach for drug administration is the oral route. Several anticancer drugs come under this category and mostly lack solubility and oral bioavailability, which are the most common causes of inadequate clinical efficiency. Enhancing oral
Divya Dhatri Kara, Mahalaxmi Rathnanand
doaj   +1 more source

Preparation and optimization of microemulsion of rosuvastatin calcium

open access: yesJournal of Pharmacy and Bioallied Sciences, 2012
Due to very less bioavailability (20%) of Rosuvastatin calcium, an attempt was made to develop and optimize microemulsion formulation. Capmul MCM, Tween 20 and PEG 400 were selected as oil, surfactant and cosurfactant respectively as the drug is having ...
B Zalak Patel   +3 more
doaj   +1 more source

Preparation and characterization of rilpivirine solid dispersions with the application of enhanced solubility and dissolution rate

open access: yesBeni-Suef University Journal of Basic and Applied Sciences, 2015
Rilpivirine (RPV) is a pharmaceutical drug used for the treatment of HIV infection. The drug is characterized with poor aqueous solubility and dissolution rate leading to low bioavailability of the drug.
Pavan kommavarapu   +3 more
doaj   +1 more source

Effect of a mixture of caffeine and nicotinamide on the solubility of vitamin (B2) in aqueous solution [PDF]

open access: yes, 2006
The effect of caffeine (CAF) and nicotinamide (NMD) on the solubility of a vitamin B2 derivative (FMN) has been evaluated for mixtures containing either a single hydrotrope (CAF or NMD) or the two hydrotropes simultaneously.
Davies, David B.   +3 more
core   +1 more source

Exploration of the Safety and Solubilization, Dissolution, Analgesic Effects of Common Basic Excipients on the NSAID Drug Ketoprofen

open access: yesPharmaceutics, 2023
Since its introduction to the market in the 1970s, ketoprofen has been widely used due to its high efficacy in moderate pain management. However, its poor solubility and ulcer side effects have diminished its popularity.
Heba A. Abou-Taleb   +4 more
doaj   +1 more source

Investigation of Solubility Enhancement Approaches of Ticagrelor

open access: yesIraqi Journal of Pharmaceutical Sciences, 2018
Ticagrelor is an orally administered antiplatelet medicine, direct-acting P2Y12-receptor antagonist. Ticagrelor binds reversibly and noncompetitively to the P2Y12 receptor at a site distinct from that of the endogenous agonist adenosine diphosphate (ADP).
Ihsan A. Mohammed, Mowafaq M. Ghareeb
doaj   +1 more source

Solubility and Bioavailability Enhancement of Oridonin: A Review

open access: yesMolecules, 2020
Oridonin (ORI), an ent-kaurene tetracyclic diterpenoid compound, is isolated from Chinese herb Rabdosia rubescens with various biological and pharmacological activities including anti-tumor, anti-microbial and anti-inflammatory effects.
Yuanyuan Zhang   +5 more
doaj   +1 more source

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