Results 41 to 50 of about 30,050 (289)

Tailoring supersaturation from amorphous solid dispersions [PDF]

open access: yesJournal of Controlled Release, 2018
The maximum achievable concentration of a drug in solution is dictated by the chemical potential of the solid form. Because an amorphous solid has a higher chemical potential than the corresponding crystal form, in the absence of phase transformations, a higher transient solubility is expected.
Na Li, Lynne S. Taylor
openaire   +2 more sources

Modelling phase separation in amorphous solid dispersions [PDF]

open access: yesActa Biomaterialia, 2019
Much work has been devoted to analysing thermodynamic models for solid dispersions with a view to identifying regions in the phase diagram where amorphous phase separation or drug recrystallization can occur. However, detailed partial differential equation non-equilibrium models that track the evolution of solid dispersions in time and space are ...
Meere Martin   +2 more
openaire   +5 more sources

Solid-state characterization of Felodipine–Soluplus amorphous solid dispersions [PDF]

open access: yesDrug Development and Industrial Pharmacy, 2015
The aim of the current study is to develop amorphous solid dispersion (SD) via hot melt extrusion technology to improve the solubility of a water-insoluble compound, felodipine (FEL). The solubility was dramatically increased by preparation of amorphous SDs via hot-melt extrusion with an amphiphilic polymer, Soluplus® (SOL).
Jiannan, Lu   +7 more
openaire   +2 more sources

Use of Solid Dispersion Systems in Pharmacy

open access: yesКонденсированные среды и межфазные границы, 2020
An overview of the use of solid dispersion systems in pharmacy is presented. The main techniques of obtaining solid dispersions were considered. The simplest one is the solvent removal technique: the medicinal drug and the carrier are dissolved in the ...
Sof ’ya Yu. Silaeva   +6 more
doaj   +1 more source

The characterization and dissolution performances of spray dried solid dispersion of ketoprofen in hydrophilic carriers

open access: yesAsian Journal of Pharmaceutical Sciences, 2015
Solid dispersion is one of the most promising strategies to improve oral bioavailability of poorly soluble API. However, there are inconsistent dissolution performances of solid dispersion reported which entails further investigation.
Siok-Yee Chan   +4 more
doaj   +1 more source

Thermal stability of amorphous sugar matrix, dried from methanol, as an amorphous solid dispersion carrier [PDF]

open access: yes, 2018
[EN] Developing a technique to disperse hydrophobic ingredients homogeneously in a water-soluble solid matrix (solid dispersion) is one of the topics that have been extensively investigated in the pharmaceutical and food industries.
Takeda, K.   +9 more
core   +1 more source

Design and Characterization of Phosphatidylcholine-Based Solid Dispersions of Aprepitant for Enhanced Solubility and Dissolution

open access: yesPharmaceutics, 2020
This study aimed to improve the solubility and dissolution of aprepitant, a drug with poor aqueous solubility, using a phosphatidylcholine (PC)-based solid dispersion system.
Sooho Yeo   +4 more
doaj   +1 more source

Solid Dispersion Technology for Improving the Solubility of Antiviral Drugs

open access: yesPharmaceutical Sciences and Research, 2023
Most drugs, including antiviral drugs, show low solubility in water, which affects dissolution, bioavailability, and therapeutic effectiveness. Therefore, many antiviral drugs are given in very large doses.
Maria Elvina Tresia Butar-Butar   +3 more
doaj   +1 more source

Manufacturing strategies to develop amorphous solid dispersions: An overview [PDF]

open access: yesJournal of Drug Delivery Science and Technology, 2020
Since the past several decades, poor water solubility of existing and new drugs in the pipeline have remained a challenging issue for the pharmaceutical industry. Literature describes several approaches to improve the overall solubility, dissolution rate, and bioavailability of drugs with poor water solubility.
Nicole, Mendonsa   +6 more
openaire   +2 more sources

Exploring the Solubility and Bioavailability of Sodium Salt and Its Free Acid Solid Dispersions of Dolutegravir

open access: yesAdvances in Pharmacological and Pharmaceutical Sciences, 2023
Amorphous salt solid dispersion (ASSD) of Dolutegravir amorphous salt (DSSD) was generated using quench cooling and compared to its Dolutegravir free acid solid dispersion (DFSD) to improve the solubility and bioavailability. Soluplus (SLP) was used as a
Dani Lakshman Yarlagadda   +3 more
doaj   +1 more source

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