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Grace
Development and Characterization of Celecoxib Solid Self-nanoemulsifying Drug Delivery Systems…
Self-nanoemulsifying drug delivery systems (SNEDDS) represent an interesting platform for improving the oral bioavailability of poorly soluble lipophilic drugs. While Liquid-SNEDDS (L-SNEDDS) effectively solubilize the drug in vivo, they have several drawbacks, including poor storage stability.…
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Implementation of a New Electronic Liquid Dispensing System for Individualized Compounding of Hard…
An automated compounding device can be a useful tool for the rapid and accurate production of small batches for personalized medicine as well as for clinical batches. A novel electronic liquid dispensing system (ELDS) was investigated to produce hard capsules with individualized dose strengths. An…
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PLGA-modified Syloid®-based microparticles for the ocular delivery of terconazole: in-vitro and…
The eye is an invulnerable organ with intrinsic anatomical and physiological barriers, hindering the development of a pioneer ocular formulation. The aim of this work was to develop an efficient ocular delivery system that can augment the ocular bioavailability of the antifungal drug, terconazole.…
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Pharma Account Executive, US – Job opportunity with Grace
Built on talent, technology, and trust, Grace is a leading global supplier of catalysts and engineered materials. The company’s two industry-leading business segments—Catalysts Technologies and Materials Technologies—provide innovative products, technologies, and services that enhance the products…
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Comparative Study of Powder Carriers Physical and Structural Properties
High specific surface area (SSA), porous structure, and suitable technological characteristics (flow, compressibility) predetermine powder carriers to be used in pharmaceutical technology, especially in the formulation of liquisolid systems (LSS) and solid self-emulsifying delivery systems…
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An Improved 2-Step Process for Moisture Sensitive Drugs Using Syloid® FP Silicas
Introduction: Several APIs are sensitive to moisture, and formulating these drugs into stable oral dosage forms can pose quite a challenge to formulators. There are several potential problems associated with moisture sensitive drugs, such as caking and poor flow properties, chemical degradation,…
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Study of solid-state transitions and its impact on solubility and stability of Repaglinide
The aim of this research was to study the impact of melting and quenching approach on solid-state characteristics of amorphous dispersion and its impact on dissolution and solubility of Repaglinide, a BCS Class II drug. Solid dispersions of Repaglinide were prepared separately by quench cooling…
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Effect of Carrier Type and Tween® 80 Concentration on the Release of Silymarin from Amorphous Solid…
Silymarin is a mixture of flavonolignans obtained from the seeds of milk thistle (Silybum marianum L. Gaertner). Silymarin behaves as a weak acid and is categorised as a class IV drug substance in accordance with biopharmaceutics drug disposition classification system, possessing low solubility, as…
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Exploring the role of mesoporous silica nanoparticle in the development of novel drug delivery…
The biocompatible nature of mesoporous silica nanoparticles (MSN) attracted researchers’ attention to deliver therapeutic agents in the treatment of various diseases, where their porous nature, high drug loading efficiency, and suitability to functionalize with a specific ligand of MSN helped to…
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Silica-filled methacrylic composites with extremely high compressive strength
SYLOID® 244 has never been applied as a filler in composites with potential dental application. Therefore, the aim of research was to apply this silica in its unmodified and diazonium salt-modified forms in different mass ratios as fillers in light-cured methacrylic composites.
The effectiveness…
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