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HomeWebinarsUnlocking Bioavailability: Mesoporous Drug Carrier for Stable Amorphous Formulations

Unlocking Bioavailability: Mesoporous Drug Carrier for Stable Amorphous Formulations



WEBINAR

Drug solubility is a critical issue in formulation development, with many compounds facing risks due to poor oral bioavailability. Enhancing solubility is a major challenge for both new chemical entities and existing drugs. Mesoporous silica offers a solution by utilizing molecular adsorption and steric stabilization within its nanoconfined pores, to create stable and effective amorphous formulations. This approach is promising for improving the bioavailability of poorly soluble active pharmaceutical ingredients (APIs). The session will cover the mechanistic foundations of mesoporous silica, including lab-scale loading and scale-up potential, along with in vitro and in vivo case studies demonstrating its effectiveness for typical BCS II compounds.

In this webinar, you will learn:

  • An overview how mesoporous silica technology result in stable and effective amorphous formulations
  • Loading methods on mesoporous silica and their performance
  • Case studies of in vitro and in vivo performance of mesoporous silica formulations
  • How mesoporous silica can reduce the risk of re-crystallization of poor glass formers.

Speakers

Markus Lubda, Ph.D.

Markus Lubda, Ph.D.

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Strategic Business Manager

Markus is a biomolecular engineer. He is responsible for the strategic development and positioning of an excipient portfolio for oral solid dosage form applications. Thereby, the focus is to enhance solubility and bioavailability of the most challenging APIs with specifically engineered excipients for oral solid application. He holds a Ph.D. in biology/chemistry from the Technical University of Darmstadt and is a biomolecular engineer. 

Rimson Muara Jaya

Rimson Muara Jaya

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Customer Application Expert SEATWO

Rimson is a technical application expert, specializing in small to large molecules.  Rimson holds a pharmacist's degree and a master's in business administration. He has more than 10 years of extensive experience in the pharmaceutical industry, with a strong focus on project management, production, and GMP assurance for various small molecule pharmaceutical dosage forms.

Webinar Information

Pharma and biopharma manufacturing

  • Liquid Formulation Strategies
  • Duration:1h

  • Language:English

  • Session 1:presented January 21, 2025

    Register Now


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