pH Sensitive Interpenetrating Network Bio Containers of Gum Ghatti for Sustained Release of Glipizide.
Animals
Blood Glucose
/ drug effects
Cell Survival
/ drug effects
Cells, Cultured
Delayed-Action Preparations
/ administration & dosage
Diabetes Mellitus, Experimental
/ blood
Drug Delivery Systems
Drug Liberation
Glipizide
/ administration & dosage
Humans
Hypoglycemic Agents
/ administration & dosage
Leukocytes, Mononuclear
/ drug effects
Male
Microspheres
Plant Gums
/ administration & dosage
Rats, Wistar
Gum ghatti
anti diabetic effect
glipizide
hydrogel
interpenetrating network
microspheres.
Journal
Current drug delivery
ISSN: 1875-5704
Titre abrégé: Curr Drug Deliv
Pays: United Arab Emirates
ID NLM: 101208455
Informations de publication
Date de publication:
2019
2019
Historique:
received:
20
02
2019
revised:
17
09
2019
accepted:
29
09
2019
pubmed:
19
10
2019
medline:
21
4
2020
entrez:
19
10
2019
Statut:
ppublish
Résumé
A novel natural polymer, Gum Ghatti (GG) was explored to develop a new polymeric system that will combine the biodegradable and biocompatible properties of GG and mechanical properties of poly vinyl alcohol (PVA) for drug delivery application. Smart pH sensitive, porous, glutaraldehyde (GA) crosslinked interpenetrating network (IPN) microspheres loaded with glipizide were developed by the emulsion crosslinking method. The drug entrapment efficiency was 92.85±1.5%. FTIR confirmed the formation of IPN structure. Drug release can be extended upto 7 hours by modulating the concentration of crosslinking agent. Swelling study and diffusion co-efficient (D) of water transport were performed in order to understand the phenomenon of water penetration through the microsphere. In vivo antidiabetic activity performed on alloxane induced diabetic rats indicated that in case of pure glipizide sudden reduction of elevated blood glucose was observed after 3 hours. In case of rats treated with glipizide loaded IPN microparticles, the initial percentage reduction of blood glucose level was slow within the first 3 hours of administration, as compared to pure glipizide but after 6 hours 90% reduction was observed which confirmed sustained release nature of microspheres. Thus IPN microparticles were found suitable for sustained delivery of BCS class II drug glipizide.
Identifiants
pubmed: 31625476
pii: CDD-EPUB-101586
doi: 10.2174/1567201816666191017154719
doi:
Substances chimiques
Blood Glucose
0
Delayed-Action Preparations
0
Hypoglycemic Agents
0
Plant Gums
0
gum ghatti
X1N78DL020
Glipizide
X7WDT95N5C
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
849-861Informations de copyright
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