TY - JOUR
T1 - Oral insulin delivery by self-assembled chitosan nanoparticles
T2 - In vitro and in vivo studies in diabetic animal model
AU - Mukhopadhyay, Piyasi
AU - Sarkar, Kishor
AU - Chakraborty, Mousumi
AU - Bhattacharya, Sourav
AU - Mishra, Roshnara
AU - Kundu, P. P.
PY - 2013/1/1
Y1 - 2013/1/1
N2 - We have developed self-assembled chitosan/insulin nanoparticles for successful oral insulin delivery. The main purpose of our study is to prepare chitosan/insulin nanoparticles by self-assembly method, to characterize them and to evaluate their efficiency in vivo diabetic model. The size and morphology of the nanoparticles were analyzed by dynamic light scattering (DLS), atomic force microscopy (AFM) and scanning electron microscopy (SEM). The average particle size ranged from 200 to 550 nm, with almost spherical or sub spherical shape. An average insulin encapsulation within the nanoparticles was ~ 85%. In vitro release study showed that the nanoparticles were also efficient in retaining good amount of insulin in simulated gastric condition, while significant amount of insulin release was noticed in simulated intestinal condition. The oral administrations of chitosan/insulin nanoparticles were effective in lowering the blood glucose level of alloxan-induced diabetic mice. Thus, self-assembled chitosan/insulin nanoparticles show promising effects as potential insulin carrier system in animal models.
AB - We have developed self-assembled chitosan/insulin nanoparticles for successful oral insulin delivery. The main purpose of our study is to prepare chitosan/insulin nanoparticles by self-assembly method, to characterize them and to evaluate their efficiency in vivo diabetic model. The size and morphology of the nanoparticles were analyzed by dynamic light scattering (DLS), atomic force microscopy (AFM) and scanning electron microscopy (SEM). The average particle size ranged from 200 to 550 nm, with almost spherical or sub spherical shape. An average insulin encapsulation within the nanoparticles was ~ 85%. In vitro release study showed that the nanoparticles were also efficient in retaining good amount of insulin in simulated gastric condition, while significant amount of insulin release was noticed in simulated intestinal condition. The oral administrations of chitosan/insulin nanoparticles were effective in lowering the blood glucose level of alloxan-induced diabetic mice. Thus, self-assembled chitosan/insulin nanoparticles show promising effects as potential insulin carrier system in animal models.
KW - Chitosan
KW - Insulin
KW - Nanoparticles
KW - Oral delivery
KW - Self-assembly
UR - https://www.scopus.com/pages/publications/84869087095
U2 - 10.1016/j.msec.2012.09.001
DO - 10.1016/j.msec.2012.09.001
M3 - Article
C2 - 25428084
AN - SCOPUS:84869087095
SN - 0928-4931
VL - 33
SP - 376
EP - 382
JO - Materials Science and Engineering C
JF - Materials Science and Engineering C
IS - 1
ER -