HYBRID EVENT: You can participate in person at Rome, Italy or Virtually from your home or work.
Speaker at Applied Microbiology 2022 - Rolee Sharma
C. S. J. M. University, India
Title : Particulate Glucan from Yeast : Novel Application as Delivery vehicles

Abstract:

A biocompatible, biodegradable β-1,3-D-glucan based macrophage targeting delivery system has been developed in our lab as 1–4 µm spherical, hollow shells extracted from the cell wall of Saccharomyces cerevisiae (Baker’s yeast). Macrophage are the first line of defense against infections, as they phagocytose any bacilli or foreign particles they encounter. Yeast derived particulate 1,3-β-glucan thus provides for receptor-mediated uptake by phagocytic cells expressing β-glucan receptors, making GPs an ideal drug delivery vehicle to target phagocytic cells in the immune system. These also act as “natural polysaccharide immunomodulators,” and activate the immune system. 
We report here, the preparation of β-glucan particles (GP) from yeast cells, their characterization and demonstration of their rapid phagocytic uptake by the macrophage. The beta glucan structure of particles was validated by fourier transform infrared spectroscopy (FTIR), and NMR. The particles were loaded with an anti-tuberculosis drug, Rifabutin and sealed with alginate. Electron microscopy revealed the porous nature of these particles with drug nano-precipitates. The drug entrapment and drug loading was seen up to 81.46 ± 4.9 % and ~40.5 ± 1.9 %, respectively. These results indicate that these yeast derived glucan particles have the potential to be used as an effective agent for delivery of Rifabutin and targeting to macrophage. 
Additionally, these particles have been seen to induce phagosomal maturation and autophagy induction within M.tb. infected macrophage. The particles thus not only act as effective delivery vehicles but also activate anti-microbial defence mechanism within host cells. Thus, the intracellular drug delivery supplements the innate response in M. tuberculosis infected macrophage, thereby accounting for the enhanced efficacy observed for this delivery system and holding promise for their use as formulations against TB.
What will audience learn from your presentation? 
• The audience shall learn about the various applications of this delivery system. 
• The audience shall learn about the preparation of these particles from yeast cells.
• The audience shall come to understand that these particles can be applied for the delivery of a diverse array of small molecules including prophylactics and therapeutics. 
• The presentation shall explain the benefits of using this delivery system against intracellular infections, particularly M.tb.

 

Biography:

Dr. Rolee Sharma received M.Sc. degree in Biochemistry from Lucknow University, Lucknow. She then joined the research group of Dr Amit Misra at the Central Drug Research Institute, Lucknow, India and earned her doctoral degree from the same Institute in 2006. Thereafter, she joined the Department of Biosciences, Integral University, Lucknow, and is currently working as Professor at the School of Life Sciences and Biotechnology, C.S.J.M. University, Kanpur. Her research interests lie in area of targeted drug delivery, innate responses and host defence. She has around 50 publications of National and International repute and has five international patents.

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