posted on 2018-07-27, 00:00authored byDulari Jayawardena
Vasoactive intestinal peptide (VIP) is an endogenous neuropeptide with a wide
array of immunomodulatory properties. VIP has shown beneficial effects in managing
multiple inflammatory disorders, including inflammatory bowel disease (IBD). IBD
includes chronic disorders of the gastro intestinal tract, namely Crohn’s disease (CD) and
ulcerative colitis (UC). The usage of VIP is hindered by its short biological half-life and off
target effects (hypotension). To overcome these delivery challenges, we have developed
a biocompatible nano-carrier (SSM), which can successfully deliver active VIP to the
target tissue to treat IBD. The studies herein were designed to determine the therapeutic
benefit of intra peritoneally (ip) administered VIP nanomedicine, VIP-SSM in managing
IBD, utilizing mouse models of colitis resembling both CD (2,4,6-trinitrobenzene sulfonic
acid/TNBS induced colitis) and UC (dextran sulfate sodium/DSS induced colitis). Since
IBD is an intestinal disease, delivering VIP-SSM via oral route would be more beneficial.
To this end, we have tested the effectiveness of administering the nanomedicine intra
luminally to the colon. Finally, we tested the prospects of scaling up the nanomedicine for
clinical use via oral formulation by incorporating the nanomedicine into enteric-coated
capsules. Our results demonstrate that ip administered VIP-SSM is effective in alleviating
inflammation associated with both DSS and TNBS colitis. VIP-SSM significantly reduced
the inflammation and associated diarrhea in colitis by affecting pro-inflammatory cytokine
mRNA expression, histology, tight junction proteins, secreted mucus and ion transporter
expression in the distal colon. These beneficial effects were also apparent when the
nanomedicine was administered intra rectally to the colonic lumen, showing potential for
oral delivery. Furthermore, in vitro studies show that freeze-dried powder of the
nanomedicine gives rise to micelles with active VIP, released from capsules in solution.
Together, our data indicate the effectiveness of VIP-SSM as a therapeutic agent in
managing IBD, and shows proof of concept of its use as a novel oral product.
History
Advisor
Onyuksel, HayatDudeja, Pradeep K
Chair
Onyuksel, Hayat
Department
Biopharmaceutical Sciences
Degree Grantor
University of Illinois at Chicago
Degree Level
Doctoral
Committee Member
Jeong, Hyun-Young
Johnson, Jeremy
Gill, Ravinder K