From 23fb09ef3f4ee5644f7cd512573da762e5a38347 Mon Sep 17 00:00:00 2001 From: Lucas Attia <43359170+lucasattia@users.noreply.github.com> Date: Thu, 8 Aug 2024 14:08:30 -0400 Subject: [PATCH] Update 1_project.md --- _projects/1_project.md | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/_projects/1_project.md b/_projects/1_project.md index 2efcb6b..94a6bcd 100644 --- a/_projects/1_project.md +++ b/_projects/1_project.md @@ -10,7 +10,7 @@ related_publications: Attia2023-bc This project, the first in my PhD, focused on figuring out a clever way to engineer core-shell hydrogel drug carrier particles. Core-shell particles are extremely useful in oral drug delivery. They can unlock sustained and delayed release profiles, which is important for instestinal and colonic targeting applications. They can also formulate fixed dosage combination (FDC) products, structuring different active ingredients in the core and the shell. Despite these useful applications, conventional methods for engineering core-shell carriers for pharmaceutical applications are limited, relying on organic solvents, high processing temperatures, and are often unable to structure drugs in the shell (see below).