BLOOD GLUCOSE LOWERING EFFECT OF GLIBENCLAMIDE TRANSFERSOME IN RATS (RATTUS NORVEGICUS)
Introduction and objectives: Glibenclamide has been reported as a therapeutic agent for type 2 DM with side effects of severe to fatal hypoglycemia and gastrointestinal disturbances, including nausea, vomiting and heartburn after oral administration. The transfersome is an ultradeformable arti...
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Format: | Theses |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/80324 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | Introduction and objectives: Glibenclamide has been reported as a therapeutic
agent for type 2 DM with side effects of severe to fatal hypoglycemia and
gastrointestinal disturbances, including nausea, vomiting and heartburn after oral
administration. The transfersome is an ultradeformable artificial vesicle that is well
known for its potential in topical drug delivery. This vesicle has been selected as a
carrier in Trandermal Drug Delivery System to avoid side effects of Glibenclamide
drug during oral administration. Methods: The transfersome was prepared by thinlayer hydration method. The transfersome suspension was then characterized for
particle size, polydispersity index, entrapment efficiency, and vesicle morphology.
Gel containing glibeclamide transfersome was prepared with Carbopol 940 base at
a concentration of 1% for activity test to reduce blood sugar level of rats. Results:
The transfersome suspension has produced a particle size of 379.9, polydispersity
index of 0.321, % entrapment efficiency of 98.03%. The results of activity tests on
reducing blood sugar levels of rats showed that the transfersome gel treatment
group was able to reduce the blood sugar levels of rats to normal values within 2
weeks without any rats experiencing hypoglycemia while in the oral glibenclamide
group reduced sugar levels was profound with one rat having blood sugar levels of
40 mg/dL. Conclusion: Transfersome gel is able to provide activity to reduce blood
sugar levels in rats (Rattus norvegicus) during 15 days of administration without
experiencing hypoglycemia.
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