AI Article Synopsis

  • Mucoadhesion-based drug delivery systems are gaining traction for their ability to enhance the duration of drug action at mucosal surfaces, improving patient compliance and convenience.
  • However, testing mucoadhesion is complicated due to a lack of standardized methods and difficulties in conducting multiple measurements simultaneously, often leading to subjective results.
  • The study introduces a new technique called MUCO-DIS, using AFM to measure mucoadhesion force, surface topography, polymer dissolution, and drug release characteristics together, demonstrating its effectiveness with pectin microparticles and various gastrointestinal mucosal surfaces.

Article Abstract

Mucoadhesion-based drug delivery systems have recently gained interest because of their bio-adhesion capability, which results in enhanced residence time leading to prolonged duration of action with the mucosal surface, potentially improving compliance and convenience. Mucoadhesion testing of these formulations is widely reported; however, this is technically challenging due to the absence of any standard methods and difficulty in conducting mucoadhesion, formulation-mucosal surface interaction, mucosal surface topography and drug release in a single experiment. As these measurements are currently conducted separately, on replicate formulations, results can often be subjective and difficult to correlate. Hence, the aim of the present study was to develop a new AFM-based single-entity ex vivo muco-dissolution (MUCO-DIS) technique to simultaneously evaluate mucoadhesion force, 3D surface topography, polymer dissolution and drug release characteristics. To demonstrate the potential of the current technique, the interactions between model pectin microparticles containing metformin HCl and a range of gastrointestinal mucosal surfaces (gastric, small intestine, large intestine and buccal) were studied. This novel system has not only successfully determined the mucoadhesion force, polymer dissolution and drug release information but has also highlighted the difference in microparticle performance with different mucosal targets. The current work has highlighted the potential of this newly developed MUCO-DIS system and we believe this will be a valuable tool for characterising these popular pharmaceutical formulations. This technique could also provide an opportunity to other scientific fields to evaluate materials, substrate behaviour and their interactions in their hydrated state at nanoscale with real-time chemical and surface mapping.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7231801PMC
http://dx.doi.org/10.1208/s12249-020-01697-xDOI Listing

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