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Shin-Etsu
Miscibility, phase behavior, and mechanical properties of copovidone/HPMC ASLF and…
Abstract
Currently, most amorphous solid dispersion (ASD) formulations contain a single polymer to stabilize an amorphous drug. However, a single polymer has a limited ability to form strong drug-polymer interactions, resulting in poor drug loading (<30 % w/w) and a high pill burden. This…
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Release-modulating mechanism and comparative pharmacokinetics in beagle dogs of bethanechol-loaded…
Abstract
Bethanechol chloride (BTC), a quaternary ammonium compound used in bladder dysfunction treatment, requires challenges in developing optimal oral dosage forms due to its high water-solubility, short half-life, rapid elimination and four times a day administration. The aim of this study…
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A new strategy for enhancing S-Adenosyl-L-Methionine (SAMe) oral bioavailability: Preparation of…
Abstract
S-Adenosylmethionine (SAMe) is a crucial endogenous molecule in vital biochemical processes such as DNA, RNA, and protein methylation. It has been found beneficial in the treatment of liver disease, osteoarthritis, and particularly depression. However, SAMe's therapeutic potential is…
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The effect of filler particle size on API homogeneity of controlled release formulations via…
Abstract
Previous research has shown that controlled release (CR) formulations with hydrox- ypropyl methylcellulose (HPMC) as hydrophilic matrix former produced via twin-screw wet granulation (TSWG) yield granules with an inhomogeneous active pharmaceutical ingredient (API) distribution (Denduyver…
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Exploring granulation in pharmaceuticals: the role of cellulose ethers
Solid pharmaceutical dosage forms, such as tablets and capsules, are the most used drug delivery systems, favored for their ease of production and patient preference. These forms combine active pharmaceutical ingredients (APIs) with excipients that are carefully selected and processed to ensure…
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Understanding the effect of plasticizers in film coat materials on the physical stability of…
Abstract
Amorphous solid dispersions (ASDs) have been extensively utilized to improve the bioavailability of drugs that have low aqueous solubility. The influence of different excipients on the conversion of amorphous drugs into their crystalline forms in ASDs has been extensively researched.…
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Development and Evaluation of Lactose-Free Single-Unit and Multiple-Unit Preparations of a BCS Class…
Abstract
Background/Objectives: The aim of the present study was to develop lactose-free formulations of rivaroxaban, a novel oral anticoagulant used for the treatment and prevention of blood clotting. As a BCS Class II drug, rivaroxaban is characterized by poor solubility in aqueous media, posing…
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Posaconazole nanocrystals dry powder inhalers for the local treatment of invasive pulmonary…
Abstract
Invasive pulmonary aspergillosis poses a significant threat to immunocompromised patients, characterized by high mortality rates. Posaconazole (PSZ), a second-generation triazole antifungal, exhibits broad-spectrum activity but suffers from limited pulmonary concentrations and notable…
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Homogeneity and mechanical properties of orodispersible films loaded with pellets
Abstract
Orodispersible films (ODFs) have served as an emerging platform for the delivery of drugs in a convenient way. The production of ODFs with incorporated pellets may still be a challenging process due to problems to obtain proper homogeneity and deteriorating mechanical properties of the…
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Fluid bed granulation – Process optimization
Abstract
Fluidized bed granulation is a single unit operation that integrates several process transformations including powder transfer and fluidization, atomization of binder solution and wetting of the fluidized powder, growth and consolidation of granules, drying, and discharge of the granular…
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