dc.contributor.advisor | Professor Dr. Rakibul Islam | |
dc.contributor.author | OSMAN, AHMED-WELI HUSSEIN | |
dc.date.accessioned | 2022-04-27T04:26:25Z | |
dc.date.available | 2022-04-27T04:26:25Z | |
dc.date.issued | 2020-06 | |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/1125 | |
dc.description | A Thesis
By
AHMED-WELI HUSSEIN OSMAN
Registration No. 1905310
Semester: January- June. 2020
Session: 2019-2020
Submitted to the
Department of Physiology and Pharmacology
Hajee Mohammad Danesh Science and Technology University, Dinajpur
In partial fulfillment of the requirements
For the degree of
MASTER OF SCIENCE (M.S.)
IN
PHARMACOLOGY | en_US |
dc.description.abstract | Oral delivery of insulin may significantly improve the quality of life of diabetes patients
who routinely receive insulin by the subcutaneous route. However, the oral delivery of
insulin remains a challenge because its oral absorption is limited. The main barriers
faced by insulin in the gastrointestinal tract are degradation by proteolytic enzymes and
lack of transport across the intestinal epithelium. Polymeric nanoparticles are suitable
colloidal carriers for insulin delivery and many investigations have been performed for
the administration of oral route. The present study was carried out to evaluate the
nanoparticle tactics for the oral delivery of insulin in the alloxan-induced hyperglycemic
rat model. Twenty male rats at the age of four months were randomly assigned into four
groups (T0, T1, T2, and T3). After acclimatization diabetes was induced in three groups of
rats (T1, positive control, T2, was treated insulin T3 was treated insulin with
nanoparticles) by administered alloxan injection a dose of 120mg/kg body weight
intraperitoneally. Group T0 was kept for negative control while T1 was kept positive
control. T2 was considered as insulin-treated group @ 21.I.U/kg and T3 is treated of
insulin with nanoparticles of the same dose as insulin. Throughout the trial, observations
were recorded for blood glucose level, body weight, and glycosylated hemoglobin.
Blood glucose levels were increased significantly (P ≤ 0.05) in all treated groups
compared to the negative control group. Similarly, body weight was decreased
significantly (P ≤ 0.05) in all alloxan treated groups compared to the negative control.
There was a significant decrease in blood glucose level in insulin with nanoparticle
treated group (T3) compared to only the insulin-treated group (T2) and (T1) that was
received alloxan. The present study shows that oral administration of insulin with
nanoparticles was significantly decreased blood glucose levels and increased body
weight. It can be concluded that oral insulin supplementation with nanoparticles may
have a significant effect on hyperglycemic control. | en_US |
dc.language.iso | en | en_US |
dc.publisher | HAJEE MOHAMMOD DANESH SCIENCE AND TECHNOLOGY UNIVERSITY, DINAJPUR | en_US |
dc.subject | Polymeric nanoparticles | en_US |
dc.subject | Alloxan, Diabetes | en_US |
dc.subject | Insulin | en_US |
dc.subject | Rat | en_US |
dc.title | NANOPARTICLE TACTICS FOR THE ORAL DELIVERY OF INSULIN IN ALLOXAN INDUCED HYPERGLYCEMIC RAT MODEL | en_US |
dc.type | Thesis | en_US |