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Team:METU-Gene/Collagen Sponge
From 2009.igem.org
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== Characterization of the rhEGF-collagen sponges == | == Characterization of the rhEGF-collagen sponges == | ||
| - | <br align="center">[1]'''Determination of the degree of crosslinking''' | + | <br align="center">[1]'''Determination of the degree of crosslinking'''</br> |
The crosslinking degree could then be obtained from the | The crosslinking degree could then be obtained from the | ||
| Line 60: | Line 60: | ||
https://static.igem.org/mediawiki/2009/9/9b/Formul1.jpg | https://static.igem.org/mediawiki/2009/9/9b/Formul1.jpg | ||
| + | |||
| + | where s is the sample and ncl is non-crosslinked. | ||
| + | |||
| + | <br align="center">[2]'''Water-binding capacity'''</br> | ||
| + | |||
| + | The water uptake of the collagen sponges was calculated using | ||
| + | the following equation: | ||
| + | |||
| + | https://static.igem.org/mediawiki/2009/a/a3/Formul2.jpg | ||
| + | |||
| + | where Wd is the weight of the dry sponge and Ws is the | ||
| + | weight of the swollen sponge. | ||
| + | |||
| + | <br align="center">[3]'''Release kinetics'''</br> | ||
| + | |||
| + | To determine the possible release mechanism, drug release | ||
| + | from collagen sponges was fitted to the following power | ||
| + | model: | ||
| + | |||
| + | https://static.igem.org/mediawiki/2009/6/64/Formul3.jpg | ||
| + | |||
| + | where Mt/M is the fractional drug release percentage at | ||
| + | time t, and k is a constant related to the properties of the | ||
| + | drug delivery system and n is the diffusional exponent | ||
| + | which characterizes the drug transport mechanism. | ||
Revision as of 10:48, 13 October 2009
The release rate of bioactive hEGF from crosslinking collagen sponges ==
The purpose of this study was to prepare
recombinant human epidermal growth factor (rhEGF)
collagen sponges for topical applications and investigate
the effects of different types of crosslinked collagen
sponges as platforms for the controlled release of rhEGF.
The microstructure and the drug release rates of collagen
sponges were modified through treatment with different
types (glutaraldehyde (GTA), genipin and 1-ethyl-3-
(3-dimethylaminopropyl)carbodiimide (EDC)), different
concentrations of crosslinking agents and various preparation
conditions.
A good correlation was obtained for
in vitro release rates of rhEGF using the power model. The
crosslinked rhEGF collagen sponges showed a successful
delivery of rhEGF in bioactive form to stimulate cell
proliferation.
In addition, EGF can inhibit gastric
acid secretions in the stomach, enhance the proliferation
and keratinization of epithelial tissues and
accelerate wound healing. Due to its wound healing
properties, EGF is an attractive candidate for a therapeutic
drug. Studies have demonstrated that topical applications
of EGF promote wound healing in healthy and impaired
healing animals.
Since Carpenter and co-workers
first reported that for a mitogenic effect of EGF, a continuous
exposure of the target cells to EGF was required for
a minimum of 6–12 h, maintaining an effective topical
concentration at the wound site for a certain period of time
has become vital in the application of EGF. Indeed, we increased this continuous exposures by using Quaroum Sensing Mechanism of E.coli.
Collagen is a major constituent of the connective tissue
and is potentially a highly useful biomaterial. It has characteristics
that are suitable in medical application, such as
biodegradability and weak antigenicity, and it has been
used in resorbable surgical sutures, hemostatic agents, and
wound dressings for many years.
An in vitro controlled release study was conducted
to investigate the mechanism of recombinant human
epidermal growth factor (rhEGF) release from the different
degree of crosslinked collagen sponges.
Characterization of the rhEGF-collagen sponges
[1]Determination of the degree of crosslinking</br>
The crosslinking degree could then be obtained from the differences between the absorbance values before and after the crosslinking. The equation is as follows:
where s is the sample and ncl is non-crosslinked.
[2]Water-binding capacity</br>
The water uptake of the collagen sponges was calculated using the following equation:
where Wd is the weight of the dry sponge and Ws is the weight of the swollen sponge.
[3]Release kinetics</br>
To determine the possible release mechanism, drug release from collagen sponges was fitted to the following power model:
where Mt/M is the fractional drug release percentage at time t, and k is a constant related to the properties of the drug delivery system and n is the diffusional exponent which characterizes the drug transport mechanism.
