In the preclinical phase, formulation development is usually very standardized, limited in time and follows heuristic guidelines. The digital design approach to drug formulation developed by amofor offers a unique alternative for customers looking for more efficient approaches. This innovative method enables the development of highly potent preclinical formulations in just one day, allowing a […]

Overview & Capabilities What is the SOLCALC software? SOLCALC software is an Excel-based add-in specifically engineered for drug formulation applications. It facilitates a broad variety of PC-SAFT calculations, including classical phase equilibria and metastable states, and assesses the impact of humidity on formulation stability. Additionally, it enables the evaluation of glass transition temperature (Tg), wet

Predicting bioavailability is pivotal in drug development, directly influencing a drug’s effectiveness within the body. A key factor in this process is solubility, which enables the drug to be absorbed and distributed. However, a major challenge we face is the increasing complexity of drugs. A Historical Perspective Historically, achieving sufficient bioavailability was straightforward for molecules,

In the field of drug formulation, the path from concept to a market-ready product is full of challenges. Success in this field requires not only overcoming these obstacles, but also finding the right partners whose scientific expertise and technical capabilities can turn concepts into reality. Among this complex landscape, one innovative solution is still underutilized:

Picture polymers in drug formulation as the coating of a chocolate praline. They create a matrix for the active pharmaceutical ingredient (API), similar to how a praline’s outer shell encases its delicious center. This polymer « coating » does more than just bind the ingredients; it precisely regulates the release of the API, much like the controlled

Ensuring the stability and efficacy of drug formulations is of utmost importance. One often overlooked factor is storage humidity. Moisture uptake can significantly affect both the efficacy and the shelf life of drug formulations, especially that of amorphous formulations. The Dual Challenge of Humidity in Amorphous Drug Formulations Consider the all-too-common practice of storing medications

Solvents play a central but often invisible role in drug formulation. Although it might appear that solvents are irrelevant in the final product, as a tablet contains no solvents, there are several stages on the way to a final tablet where solvents are not only useful, but inevitably necessary. From Drug Synthesis to Tablet Production:

The pharmaceutical world is evolving rapidly and with it the complexity of drug formulation, especially in the field of amorphous solid dispersions (ASDs). One of the biggest challenges with ASDs lies in mastering crystallization, a crucial factor that determines the physical stability and efficacy of a drug. Challenges in Amorphous Solid Dispersions A major difficulty

Ever wondered how modern medicine addresses the challenge of drugs that don’t meet required bioavailability effectively? The solution is found in Amorphous Solid Dispersions (ASDs). ASDs have significantly transformed our approach to these drugs, enhancing their effectiveness. I am delighted having been invited to speak on this fascinating area of pharmaceutical science at the upcoming

Why do many promising newly designed drug molecules struggle in clinical trials? The key often lies in the hidden pitfalls of drug formulation. This is precisely why a clear and well-planned drug formulation strategy is crucial for successful clinical trials. Understanding Traditional Drug Formulation Methods The journey of drug formulation begins with an Active Pharmaceutical