Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/32449
Title: Polyelectrolytes Formulated with Primary Unconjugated Bile Acid Optimised Pharmacology of Bio-engineered Implant
Authors: Armin Mooranian
Corina Mihaela Ionescu
Susbin Raj Wagle
Božica Kovačević
Daniel Walker
Melissa Jones
Jacqueline Chester
Thomas Foster
Edan Johnston
Sanja Kojić 
Goran Stojanović 
Momir Mikov 
Hani Al-Salami
Keywords: poly-(4styrene)-sulphonate;poly-(allyl)-amine;primary bile acids;chenodeoxycholic acid;pharmacology;transplants;in vivo studies
Issue Date: 16-Oct-2021
Publisher: MDPI
Project: H2020 SALSETH
Journal: Pharmaceutics
Abstract: Several studies have shown that different biomaterials and hydrogels comprising various bile acids such as chenodeoxycholic acid (CDCA), as well as excipients such as poly-(styrene)-sulphonate (PSS) and poly-(allyl)-amine (PAA), exhibited positive biological effects on encapsulated viable pancreatic -cells. Hence, this study aimed to investigate whether incorporating CDCA with PSS and PAA will optimise the functions of encapsulated pancreatic islets post-transplantation in Type 1 diabetes (T1D). Methods. Mice were made T1D, divided into two equal groups, and transplanted with encapsulated islets in PSS-PAA (control) or with CDCA-PSS-PAA (treatment) microcapsules. The effects of transplanted microcapsules on blood glucose, inflammation and the bile acid profile were measured post-transplantation. Results and Conclusion. Compared with control, the treatment group showed better survival rate, improved glycaemic control, and lower inflammatory profile, illustrated by # interleukin 1- , interleukin-6, interleukin-12, and tumournecrosis factor-, and # levels of the bile acid, as well as lithocholic acid in the plasma, liver, large intestine and faeces. The results suggest that CDCA incorporation with PSS-PAA microcapsules exerted beneficial effects on encapsulated islets and resulted in enhanced diabetes treatment, posttransplantation, at the local and systemic levels.
URI: https://open.uns.ac.rs/handle/123456789/32449
ISSN: 1999-4923
DOI: https://doi.org/ 10.3390/pharmaceutics13101713
Rights: Attribution-NonCommercial-NoDerivs 3.0 United States
Appears in Collections:FTN Publikacije/Publications

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