Search Results - "Halbert, Gavin"
-
1
Mefenamic acid solid dispersions: Impact of formulation composition on processing parameters, product properties and performance
Published in International journal of pharmaceutics (25-03-2022)“…[Display omitted] The objective of this study was to develop an immediate release (IR), crystalline solid dispersion (CSD) formulation of Mefenamic acid (MFA)…”
Get full text
Journal Article -
2
Manufacturing Considerations for the Development of Lipid Nanoparticles Using Microfluidics
Published in Pharmaceutics (15-11-2020)“…In the recent of years, the use of lipid nanoparticles (LNPs) for RNA delivery has gained considerable attention, with a large number in the clinical pipeline…”
Get full text
Journal Article -
3
Characterisation of colloidal structures and their solubilising potential for BCS class II drugs in fasted state simulated intestinal fluid
Published in International journal of pharmaceutics (15-11-2024)“…[Display omitted] A suite of fasted state simulated intestinal fluid (SIF), based on variability observed in a range of fasted state human intestinal fluid…”
Get full text
Journal Article -
4
Improving Consistency for a Mefenamic Acid Immediate Release Formulation
Published in Journal of pharmaceutical sciences (01-11-2020)“…The objective of this study was to develop an immediate release dose form containing 250 mg Mefenamic acid (MFA) presented as a crystalline solid dispersion in…”
Get more information
Journal Article -
5
Structured solubility behaviour in fed simulated intestinal fluids
Published in European journal of pharmaceutics and biopharmaceutics (01-12-2023)“…Intestinal drug solubility is a key parameter controlling absorption after the administration of a solid oral dosage form. The ability to measure fed state…”
Get full text
Journal Article -
6
Fed intestinal solubility limits and distributions applied to the Developability classification system
Published in European journal of pharmaceutics and biopharmaceutics (01-05-2023)“…[Display omitted] For solid oral dosage forms drug solubility in intestinal fluid is an important parameter influencing product performance and…”
Get full text
Journal Article -
7
Fasted intestinal solubility limits and distributions applied to the biopharmaceutics and developability classification systems
Published in European journal of pharmaceutics and biopharmaceutics (01-01-2022)“…[Display omitted] After oral administration, a drug’s solubility in intestinal fluid is an important parameter influencing bioavailability and if the value is…”
Get full text
Journal Article -
8
Structured solubility behaviour in bioequivalent fasted simulated intestinal fluids
Published in European journal of pharmaceutics and biopharmaceutics (01-07-2022)“…[Display omitted] Drug solubility in intestinal fluid is a key parameter controlling absorption after the administration of a solid oral dosage form. To…”
Get full text
Journal Article -
9
Small scale in vitro method to determine a bioequivalent equilibrium solubility range for fasted human intestinal fluid
Published in European journal of pharmaceutics and biopharmaceutics (01-11-2021)“…[Display omitted] Drug solubility is a key parameter controlling oral absorption, but intestinal solubility is difficult to assess in vitro. Human intestinal…”
Get full text
Journal Article -
10
Small scale in vitro method to determine a potential bioequivalent equilibrium solubility range for fed human intestinal fluid
Published in European journal of pharmaceutics and biopharmaceutics (01-08-2022)“…[Display omitted] Intestinal drug solubility is a key parameter controlling oral absorption but varies both intra and inter individuals and between the fasted…”
Get full text
Journal Article -
11
An Additive Manufacturing MicroFactory: Overcoming Brittle Material Failure and Improving Product Performance through Tablet Micro-Structure Control for an Immediate Release Dose Form
Published in Polymers (11-09-2024)“…Additive manufacturing of pharmaceutical formulations offers advanced micro-structure control of oral solid dose (OSD) forms targeting not only customised…”
Get full text
Journal Article -
12
Rapid scale-up and production of active-loaded PEGylated liposomes
Published in International journal of pharmaceutics (30-08-2020)“…[Display omitted] Manufacturing of liposomal nanomedicines (e.g. Doxil®/Caelyx®) is a challenging and slow process based on multiple-vessel and batch…”
Get full text
Journal Article -
13
Statistical investigation of simulated fed intestinal media composition on the equilibrium solubility of oral drugs
Published in European journal of pharmaceutical sciences (01-03-2017)“…Gastrointestinal fluid is a complex milieu and it is recognised that gut drug solubility is different to that observed in simple aqueous buffers. Simulated…”
Get full text
Journal Article -
14
A novel hot-melt extrusion formulation of albendazole for increasing dissolution properties
Published in International journal of pharmaceutics (29-02-2016)“…[Display omitted] The main aim of the research focused on the production of hot-melt extrusion (HME) formulations with increased dissolution properties of…”
Get full text
Journal Article -
15
Topography of Simulated Intestinal Equilibrium Solubility
Published in Molecular pharmaceutics (06-05-2019)“…Oral administration of a solid dosage form requires drug dissolution in the gastrointestinal tract before absorption. Solubility is a key factor controlling…”
Get full text
Journal Article -
16
A novel simulated media system for in vitro evaluation of bioequivalent intestinal drug solubility
Published in European journal of pharmaceutics and biopharmaceutics (01-06-2024)“…[Display omitted] Orally administered solid drug must dissolve in the gastrointestinal tract before absorption to provide a systemic response. Intestinal…”
Get full text
Journal Article -
17
Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs
Published in European journal of pharmaceutical sciences (16-06-2014)“…Preformulation measurements are used to estimate the fraction absorbed in vivo for orally administered compounds and thereby allow an early evaluation of the…”
Get full text
Journal Article -
18
Influence of Physiological Gastrointestinal Surfactant Ratio on the Equilibrium Solubility of BCS Class II Drugs Investigated Using a Four Component Mixture Design
Published in Molecular pharmaceutics (04-12-2017)“…The absorption of poorly water-soluble drugs is influenced by the luminal gastrointestinal fluid content and composition, which control solubility. Simulated…”
Get full text
Journal Article -
19
Use of Terahertz-Raman Spectroscopy to Determine Solubility of the Crystalline Active Pharmaceutical Ingredient in Polymeric Matrices during Hot Melt Extrusion
Published in Molecular pharmaceutics (07-10-2019)“…Polymer-based amorphous solid dispersions (ASDs) comprise one of the most promising formulation strategies devised to improve the oral bioavailability of…”
Get full text
Journal Article -
20
Excipient Impact on Fenofibrate Equilibrium Solubility in Fasted and Fed Simulated Intestinal Fluids Assessed Using a Design of Experiment Protocol
Published in Pharmaceutics (01-10-2023)“…Solubility is a critical parameter controlling drug absorption after oral administration. For poorly soluble drugs, solubility is influenced by the complex…”
Get full text
Journal Article