Theoretical and experimental studies on theophylline release from hydrophilic alginate nanoparticles

Abstract Background Mathematical modelling may be able to reduce the number of in vitro experiments and provide an insight into the elementary physical and chemical mechanisms that regulate the rate and degree of drug release. The aim of the present examination was to develop a simple mathematical m...

Full description

Saved in:
Bibliographic Details
Main Authors: Deepa Thomas (Author), Vinish V. Nair (Author), M. S. Latha (Author), K. Kurien Thomas (Author)
Format: Book
Published: SpringerOpen, 2019-09-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_30f30c12850d4bd3aba93cc68a7ab3b2
042 |a dc 
100 1 0 |a Deepa Thomas  |e author 
700 1 0 |a Vinish V. Nair  |e author 
700 1 0 |a M. S. Latha  |e author 
700 1 0 |a K. Kurien Thomas  |e author 
245 0 0 |a Theoretical and experimental studies on theophylline release from hydrophilic alginate nanoparticles 
260 |b SpringerOpen,   |c 2019-09-01T00:00:00Z. 
500 |a 10.1186/s43094-019-0002-0 
500 |a 2314-7253 
520 |a Abstract Background Mathematical modelling may be able to reduce the number of in vitro experiments and provide an insight into the elementary physical and chemical mechanisms that regulate the rate and degree of drug release. The aim of the present examination was to develop a simple mathematical model to portray drug release from the alginate-type hydrophilic matrix, taking into account the Fickian diffusion of drug and swelling of the matrix using theophylline as the model drug. Results The nanoparticles show a remarkable swelling in the simulated intestinal fluid. The theoretical drug release values were validated with experimental values by considering diffusion and diffusion with swelling. The experimental value fitted well with the theoretical value predicted based on diffusion. It was found that after 3 h, the entire drug release followed a pure diffusion transport. Conclusions The numerical model was found to be sufficiently accurate in guessing the drug release from the alginate matrix. The developed model could be extended to quantitatively prognosticate the drug release from hydrophilic spherical matrices. 
546 |a EN 
690 |a Matrix 
690 |a Diffusion 
690 |a Swelling 
690 |a Modelling 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Future Journal of Pharmaceutical Sciences, Vol 5, Iss 1, Pp 1-7 (2019) 
787 0 |n http://link.springer.com/article/10.1186/s43094-019-0002-0 
787 0 |n https://doaj.org/toc/2314-7253 
856 4 1 |u https://doaj.org/article/30f30c12850d4bd3aba93cc68a7ab3b2  |z Connect to this object online.