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Journal ArticleDOI

Bottom-up design of hydrogels for programmable drug release.

Cally Owh, +6 more
- 01 Sep 2022 - 
- Vol. 141, pp 213100 - 213100
TLDR
In this paper , the authors present a review of physical models of hydrogel release and discuss the interesting potential and challenges for programming release, and potential implications with the advent of machine learning.
Abstract
Hydrogels are a promising drug delivery system for biomedical applications due to their biocompatibility and similarity to native tissue. Programming the release rate from hydrogels is critical to ensure release of desired dosage over specified durations, particularly with the advent of more complicated medical regimens such as combinatorial drug therapy. While it is known how hydrogel structure affects release, the parameters that can be explicitly controlled to modulate release ab initio could be useful for hydrogel design. In this review, we first survey common physical models of hydrogel release. We then extensively go through the various input parameters that we can exercise direct control over, at the levels of synthesis, formulation, fabrication and environment. We also illustrate some examples where hydrogels can be programmed with the input parameters for temporally and spatially defined release. Finally, we discuss the exciting potential and challenges for programming release, and potential implications with the advent of machine learning.

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Citations
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Journal ArticleDOI

Solute diffusion and partitioning in multi-arm poly(ethylene glycol) hydrogels.

TL;DR: In this paper , the Richbourg-Peppas swollen polymer network (SPN) model was used to model the influence of the hydrogel structure on solute transport.
Journal ArticleDOI

Sustained release of GLP-1 analog from γ-PGA-PAE copolymers for management of type 2 diabetes.

TL;DR: In this article , a drug delivery system based on self-assembling polymer-amino acid conjugates (γ-PGA-PAE) was developed to provide sustained release of GLP-1 analog (DLG3312).
References
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Journal ArticleDOI

Mechanisms of solute release from porous hydrophilic polymers

TL;DR: In this article, the role of dynamic swelling and the dissolution of the polymer matrix on the release mechanism was discussed, as well as the effect of the tracer/excipient ratio on the poly(vinyl alcohol) release profile.
Journal ArticleDOI

Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matrices

TL;DR: The analyses suggest that for the latter system the time required to release 50% of the drug would normally be expected to be approximately 10 per cent of that required to dissolve the last trace of the solid drug phase in the center of the pellet.
Journal ArticleDOI

A simple equation for description of solute release II. Fickian and anomalous release from swellable devices

TL;DR: In this paper, an exponential relation M t /M ∞ = kt n may be used to describe the Fickian and non-Fickian release behavior of release systems which are prepared by incorporation of a drug in a hydrophilic, initially glassy polymer.
Journal ArticleDOI

A simple equation for description of solute release I. Fickian and non-fickian release from non-swellable devices in the form of slabs, spheres, cylinders or discs

TL;DR: In this paper, a simple exponential relation Mt/M∞ = ktn is introduced to describe the general solute release behavior of controlled release polymeric devices, where Mt is the fractional release, t is the release time, k is a constant, and n is the diffusional exponent characteristic of the release mechanism.
Journal ArticleDOI

Designing hydrogels for controlled drug delivery.

TL;DR: This Review discusses how different mechanisms interact and can be integrated to exert fine control in time and space over the drug presentation, and collects experimental release data from the literature and presents quantitative comparisons between different systems to provide guidelines for the rational design of hydrogel delivery systems.
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