Department

Chemistry

Major

Biological Sciences

Research Advisor

Sotiriou-Leventis, Chariklia

Advisor's Department

Chemistry

Funding Source

National Science Foundation (NSF); OURE

Abstract

This study explores the potential to predict the drug loading and release profiles of aerogels based on their morphologies: a milestone in drug delivery research which can help save time and cost invested in formulating new aerogel drug carriers and cut-down evaluation of the drug delivery capabilities of aerogels to a few experimental runs. Polyurea (PUA) and poly (isocyanurate-urethane) (PIR-PUR) aerogels were used as model systems while 5-fluorouracil (5-FU) and paracetamol (PM) were used as model drugs. These model systems were chosen because they can be synthesized into different morphologies identified by the so-called K-index (contact angle:porosity). The model drugs were loaded onto the aerogels using a physical adsorption method, and the drug-loaded aerogels were characterized with FT-IR, SEM, DSC, XPS and UV spectroscopy. Drugs could fill the porous network of the aerogels up to about 10% v/v and their release mechanism was predominantly through Fickian diffusion. Comparing all the morphologies studied, aerogels with K-indexes 1.2-1.6 could load larger amounts of drug, those with K-indexes 1.5 and 2.2 were more suitable for immediate-release formulations, those with K-indexes 1.2, 1.3 and 1.6- 2.0 were more suitable for sustained release formulations, and nanofibrous morphology (K-index = 1.6) was more suitable for controlled release formulations.

Biography

Kamden George is a Junior majoring in Biological Sciences and minoring in Chemistry working as an OURE student in Dr. Chariklia Sotiriou-Leventis' chemistry lab. His research focuses on the effect of morphology on two aerogels, polyurea and poly (isocyanurate-urethane), and how different morphologies affect the ability of the aerogels to hold and release drugs, e.g. 5-fluorouracil and Paracetemol. Outside of the lab, Kamden works as a scribe in the Emergency Department at Phelps Health and enjoys football. Kamden plans to apply to PA school after attaining his baccalaureate degree.

Research Category

Sciences

Presentation Type

Poster Presentation

Document Type

Poster

Award

Sciences Poster Session - First Place

Location

Innovation Forum - 1st Floor Innovation Lab

Presentation Date

10 April 2024, 9:00 am - 12:00 pm

Share

COinS
 
Apr 10th, 9:00 AM Apr 10th, 12:00 PM

Effect of Morphology as a Function of the K-index on the Drug Loading and Release Profiles in Polyurea and Poly(isocyanurate-urethane) Aerogels

Innovation Forum - 1st Floor Innovation Lab

This study explores the potential to predict the drug loading and release profiles of aerogels based on their morphologies: a milestone in drug delivery research which can help save time and cost invested in formulating new aerogel drug carriers and cut-down evaluation of the drug delivery capabilities of aerogels to a few experimental runs. Polyurea (PUA) and poly (isocyanurate-urethane) (PIR-PUR) aerogels were used as model systems while 5-fluorouracil (5-FU) and paracetamol (PM) were used as model drugs. These model systems were chosen because they can be synthesized into different morphologies identified by the so-called K-index (contact angle:porosity). The model drugs were loaded onto the aerogels using a physical adsorption method, and the drug-loaded aerogels were characterized with FT-IR, SEM, DSC, XPS and UV spectroscopy. Drugs could fill the porous network of the aerogels up to about 10% v/v and their release mechanism was predominantly through Fickian diffusion. Comparing all the morphologies studied, aerogels with K-indexes 1.2-1.6 could load larger amounts of drug, those with K-indexes 1.5 and 2.2 were more suitable for immediate-release formulations, those with K-indexes 1.2, 1.3 and 1.6- 2.0 were more suitable for sustained release formulations, and nanofibrous morphology (K-index = 1.6) was more suitable for controlled release formulations.