Literature DB >> 28235722

Current trend in drug delivery considerations for subcutaneous insulin depots to treat diabetes.

Jayakrishnapillai P V1, Shantikumar V Nair1, Kaladhar Kamalasanan2.   

Abstract

Diabetes mellitus (DM) is a metabolic disorder due to irregularities in glucose metabolism, as a result of insulin disregulation. Chronic DM (Type 1) is treated by daily insulin injections by subcutaneous route. Daily injections cause serious patient non-compliance and medication non-adherence. Insulin Depots (ID) are parenteral formulations designed to release the insulin over a specified period of time, to control the plasma blood glucose level for intended duration. Physiologically, pancreas produces and secretes insulin in basal and pulsatile mode into the blood. Delivery systems mimicking basal release profiles are known as open-loop systems and current marketed products are open-loop systems. Future trend in open-loop systems is to reduce the number of injections per week by enhancing duration of action, by modifying the depot properties. The next generation technologies are closed-loop systems that mimic the pulsatile mode of delivery by pancreas. In closed-loop systems insulin will be released in response to plasma glucose. This review focuses on future trend in open-loop systems; by understanding (a) the secretion of insulin from pancreas, (b) the insulin regulation normal and in DM, (c) insulin depots and (d) the recent progress in open-loop depot technology particularly with respect to nanosystems.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Biomaterials; Chronic disease; Diabetes; Drug delivery; Insulin therapy; PK/PD; Pancreas; Type 1

Mesh:

Substances:

Year:  2017        PMID: 28235722     DOI: 10.1016/j.colsurfb.2017.02.017

Source DB:  PubMed          Journal:  Colloids Surf B Biointerfaces        ISSN: 0927-7765            Impact factor:   5.268


  2 in total

1.  Identification of N-Terminally Truncated Derivatives of Insulin Analogs Formed in Pharmaceutical Formulations.

Authors:  Joanna Zielińska; Jacek Stadnik; Anna Bierczyńska-Krzysik; Dorota Stadnik
Journal:  Pharm Res       Date:  2018-05-16       Impact factor: 4.200

2.  Zinc oxide nanoparticles augment CD4, CD8, and GLUT-4 expression and restrict inflammation response in streptozotocin-induced diabetic rats.

Authors:  Norhan Elassy; Shady El-Dafrawy; Amira O Abd El-Azim; Om Ali Y El-Khawaga; Amr Negm
Journal:  IET Nanobiotechnol       Date:  2020-10       Impact factor: 1.847

  2 in total

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