<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JBNB</journal-id><journal-title-group><journal-title>Journal of Biomaterials and Nanobiotechnology</journal-title></journal-title-group><issn pub-type="epub">2158-7027</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbnb.2015.64022</article-id><article-id pub-id-type="publisher-id">JBNB-59643</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Chemistry&amp;Materials Science</subject></subj-group></article-categories><title-group><article-title>
 
 
  Natural ECM-Bacterial Cellulose Wound Healing—Dubai Study
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>afwat</surname><given-names>Mohd. El-Hoseny</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abdulwahid</surname><given-names>M. Alwahedi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Pierre</surname><given-names>Basmaji</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>José</surname><given-names>Domingos da Costa Oliveira</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Gabriel</surname><given-names>Molina de Olyveira</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ligia</surname><given-names>Maria Manzine Costa</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Gino</surname><given-names>Bruno Francozo</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff4"><addr-line>Department of Chemistry, USP, FFCLRP, Ribeir&amp;amp;atildeo Preto, Brazil</addr-line></aff><aff id="aff1"><addr-line>Al Qassimi Hospital, Sharjah, United Arab Emirates</addr-line></aff><aff id="aff3"><addr-line>Department of Physical Chemistry, UNESP, Araraquara, Brazil</addr-line></aff><aff id="aff2"><addr-line>Innovatec’s-Biotechnology Research and Development, S&amp;amp;atildeo Carlos, Brazil</addr-line></aff><pub-date pub-type="epub"><day>16</day><month>09</month><year>2015</year></pub-date><volume>06</volume><issue>04</issue><fpage>237</fpage><lpage>246</lpage><history><date date-type="received"><day>31</day>	<month>July</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>13</month>	<year>September</year>	</date><date date-type="accepted"><day>16</day>	<month>September</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Bacterial cellulose (BC) can be used in wide area of applied scientific, especially for tissue regeneration and regenerative medicine, lately, bacterial cellulose mats are used in the treatment of skin conditions such as burns and ulcers, because of the morphology of fibrous biopolymers serving as a support for cell proliferation, its pores allow gas exchange between the organism and the environment. Moreover, the nanostructure and morphological similarities with collagen make BC attractive for cell immobilization, cell support and Natural Extracellular Matrix (ECM) Scaffolds. In this scope, Natural ECM is the ideal biological scaffold since it contains all the components of the tissue. The development of mimicking biomaterials and hybrid biomaterial can further advance directed cellular differentiation without specific induction. The extracellular matrix (ECM) contains several signals that are received by cell surface receptors and contribute to cell adhesion and cell fate which control cellular activities such as proliferation, migration and differentiation. As such, regenerative medicine studies often rely on mimicking the natural ECM to promote the formation of new tissue by host cells, and characterization of natural ECM components is vital for the development of new biomimetic approaches. In this work, the bacterial cellulose fermentation process is modified by the addition of vegetal stem cell to the culture medium and natural materials before the bacteria are inoculated. In vivo behavior using natural ECM for regenerative medicine is presented.
 
</p></abstract><kwd-group><kwd>Bacterial Cellulose (Nanoskin)</kwd><kwd> Natural Nanocomposites</kwd><kwd> Regenerative Medicine</kwd><kwd> Stem Cells</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Patients with chronic wounds are treated successfully (80%) by the district nurse or practice nurse staff [<xref ref-type="bibr" rid="scirp.59643-ref1">1</xref>] .</p><p>After a certain time, often self-determined by the community nurse team, the non-healing patient is referred to a “wound care specialist” who will initially assess the wound care policy and patient records of how they have been treated to date. If the treatment was deemed to be poor or sub optimal, the wound care specialist will initially instigate a “gold standard” regime of advanced wound care therapy. If this therapy is successful, they will continue to healing with advanced wound care alone [<xref ref-type="bibr" rid="scirp.59643-ref2">2</xref>] .</p><p>If the previous treatment undertaken was deemed to be good or gold standard care, the wound care specialist would assess the wound and recommend/use a series of advanced therapies which would be needed to promote the ultimate healing of the wound [<xref ref-type="bibr" rid="scirp.59643-ref3">3</xref>] .</p><p>The improved understanding of the physiology of wounds and the processes involved in wound healing have resulted in a change of understanding as regards the wound environment and healing [<xref ref-type="bibr" rid="scirp.59643-ref3">3</xref>] .</p><p>Previous non-healing wounds were assumed to have a deficiency in the epithelial cells, it was excepted a problem of Extra Cellular Matrix (ECM) which is the major issue in static non healing chronic wounds [<xref ref-type="bibr" rid="scirp.59643-ref4">4</xref>] .</p><p>In this scope, Natural ECM is the ideal biological scaffold since it contains all the components of the tissue. Constructive remodeling can be performed using such natural ECM scaffolds and vegetal/animal stem cells, since the cells can be delivered to the site of infraction and then cells help wound healing process. The development of niche mimicking biomaterials and hybrid biomaterial can further advance directed differentiation without specific induction [<xref ref-type="bibr" rid="scirp.59643-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.59643-ref6">6</xref>] .</p><p>The extracellular matrix (ECM) contains an abundant variety of signals that are received by cell surface receptors and contribute to cell adhesion and cell fate, via regulation of cellular activities such as proliferation, migration and differentiation. As such, regenerative medicine studies often rely on mimicking the natural ECM to promote the formation of new tissue by host cells, and characterization of natural ECM components is vital for the development of new biomimetic approaches [<xref ref-type="bibr" rid="scirp.59643-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.59643-ref8">8</xref>] .</p><p>Bacterial cellulose (BC) is natural cellulose produced by bacterial synthesis, by biochemical steps and self- assembling of the secreted cellulose fibrils on the medium. Shaping of BC materials in the culture medium can be controlled by the type of cultivation that changes chain size, origin of strains which produces different proportions of crystalline phase of BC and the kind of bioreactor. BC hydrogel or BC in dry state is then obtained by methods, such as freeze-drying [<xref ref-type="bibr" rid="scirp.59643-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.59643-ref10">10</xref>] . The structural features of microbial cellulose, its properties and compatibility as a biomaterial for regenerative medicine can be changed by modifying its culture medium [<xref ref-type="bibr" rid="scirp.59643-ref11">11</xref>] or surface modification by physical [<xref ref-type="bibr" rid="scirp.59643-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.59643-ref13">13</xref>] ; chemical methods [<xref ref-type="bibr" rid="scirp.59643-ref14">14</xref>] and genetic modifications [<xref ref-type="bibr" rid="scirp.59643-ref15">15</xref>] to obtain a biomaterial with less rejection when in contact to the body [<xref ref-type="bibr" rid="scirp.59643-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.59643-ref17">17</xref>] .</p><p>Bacterial cellulose fibers mimics Collagen in creating an extra cellular matrix in the wound, which is neither originating from animals (e.g. SIS matrix) nor synthetic (man-made), and it therefore must be described as Artificial Biology. This artificial biological ECM replaces the body’s own lost or damaged ECM and also stimulates the body to produce more of its own collagen, which supports the body’s wound healing closure mechanism. Stimulating fibroblast production and subsequently TGF-b (Transforming growth factor beta) production will also be stimulated. Then granulation and epithelialization will start due to the presence of fibroblasts, endothelial cells are attracted to the wound producing growth factors, fibroblasts will release the body’s own collagen and glycosaminoglycans. The combination of collagen and fibronectin forms the new ECM, ECM synthesis and new vessels, granulation tissue formation and epithelialization by keratinocyte migration, resulting in and increasing in the dermis volume and accelerating the healing. Besides, BC like Natural ECM also activates NK killer cells (same sized cells) T and B cells. The body then understands when to produce positive items (collagen etc.) and when to stop. Correcting wound modulation and kick starting correct cellular communication. The body then auto regulates the delivery of the necessary components necessary to promote wound repair and these fibers have high concentration of flavonoid compounds, diterpene, triterpene, lignans, phenylpropanoids and prenylated acetophenones which strengthen our immunity cells and improve our immune system [<xref ref-type="bibr" rid="scirp.59643-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.59643-ref19">19</xref>] .</p><p>However, the success of the scaffold to be used in tissue engineering depends, in part, on the adhesion and growth of cells of interest on its surface. The surface chemistry of the material may define the cellular material and thus affect the adhesion, proliferation, migration and cell function [<xref ref-type="bibr" rid="scirp.59643-ref20">20</xref>] -[<xref ref-type="bibr" rid="scirp.59643-ref24">24</xref>] .</p><p>In this work, novel studies of natural nanocomposites with Bacterial cellulose (Nanoskin&#174;) for functional materials are reported. In order to produce scaffolds with drug delivery ability, porous structure and better cell adhesion, fermentation changes in gel bacterial cellulose with chondroitin sulfate, hyaluronic acid and vegetal stem cells were performed and its in vivo cell behavior is presented.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Materials</title><p>The Bacterial cellulose (Nanoskin&#174;) raw material was provided from Innovatec’s (S&#227;o Carlos SP, Brazil). Chondroitin sulfate and hyaluronic acid sodium salt from Streptococcus equi (bacterial glycosaminoglycan polysaccharide) were purchased from Sigma Aldrich. Vegetal stem cells were obtained from Brazillian environment, Carapa guianensis and Copaifera langsdorffii Desf.</p></sec><sec id="s2_2"><title>2.2. Methods</title><sec id="s2_2_1"><title>2.2.1. Synthesis of Bacterial Cellulose and Bacterial Cellulose/Chondroitin Sulfate/Hyaluronic Acid</title><p>The acetic fermentation process was achieved by using glucose as a carbohydrate source. Results of this process are vinegar and a nanobiocellulose biomass. The modifying process is based on the addition of hyaluronic acid and chondroitin sulfate (1% w/w) to the culture medium before the bacteria is inoculated. Bacterial cellulose (BC) is produced by Gram-negative bacteria Gluconacetobacter xylinus, which can be obtained from the culture medium in the pure 3-D structure, consisting of an ultra fine network of cellulose nanofibers [<xref ref-type="bibr" rid="scirp.59643-ref19">19</xref>] .</p></sec><sec id="s2_2_2"><title>2.2.2. Bionanocomposite Preparation</title><p>In the present study, a novel biomaterial has been explored and different bacterial cellulose nanocomposites have been prepared; BC/chondroitin sulfate and hyaluronic acid. Samples were washed and its medium was changed with cells culture medium as illustrate in <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p></sec></sec><sec id="s2_3"><title>2.3. Vegetal Stem Cells</title><p>The material of the plant of interest is collected and induced damage to causing the formation of scar tissue called callus. This tissue consists of totipotent cells, undifferentiated (stem cells) are collected and grown on agar plates to complete differentiation and generation of a homogeneous culture (2 - 10 days).</p><p>Cultures of these stem cells are grown in bioreactors and the batch is collected after all the sugar was metabolized. The cells are washed and homogenized to release secondary metabolites. Soluble metabolites in oil and water are collected and, if you need the isomalt-based spraying are performed.</p></sec><sec id="s2_4"><title>2.4. Characterization</title><p>Scanning Electron Microscopy (SEM) images were performed on a PHILIPS XL30 FEG. The samples were covered with gold and silver paint for electrical contact and to perform the necessary images.</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Materials and methods draft</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x5.png"/></fig><p>Transmission infrared spectroscopy (FTIR, Perkin Elmer Spectrum 1000)-Influences of hyaluronic acid (HA) and chondroitin sulfate (CS) in bacterial cellulose were analyzed in the range between 250 and 4000 cm<sup>−1</sup> and with 2 cm<sup>−1</sup> resolution with samples.</p><p>In vivo analysis-Evaluation-Clinical study was done at Al Qassimi Hospital under supervision of Dr. Safwat Mohd. El-Hoseny. Evaluation model-patient with 3<sup>rd</sup> degree burn by hot water; patient with car accident (rolled over).</p></sec></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. Morphological Behavior</title><sec id="s3_1_1"><title>3.1.1. Bacterial Cellulose Sample</title><p>Bacterial cellulose mats were obtained by fermentation change and results showed bacterial cellulose bionanocomposites surface as illustrated in <xref ref-type="fig" rid="fig2">Figure 2</xref>.</p></sec><sec id="s3_1_2"><title>3.1.2. Hyaluronic Acid/Bacterial Cellulose Mats</title><p>Hyaluronic acid/bacterial cellulose mats were modified with hyaluronic acid and results showed bacterial cellulose bionanocomposites surface as illustrated in <xref ref-type="fig" rid="fig3">Figure 3</xref>.</p></sec><sec id="s3_1_3"><title>3.1.3. Chondroitin Sulfate/Bacterial Cellulose Mats</title><p>Chondroitin sulfate/bacterial cellulose mats were modified with chondroitin sulfate and results showed bacterial cellulose bionanocomposites surface as illustrated in <xref ref-type="fig" rid="fig4">Figure 4</xref>.</p><p>It can be observed that bacterial cellulose was successfully modified by changing the fermentation medium and sample with hyaluronic acid has little differences in surface morphology than tested others mainly because there is higher hydrogen bond between bacterial cellulose groups (hydroxyl) and hyaluronic acid (acetyl) which changes bacterial cellulose fibers formation and surface morphology.</p></sec></sec><sec id="s3_2"><title>3.2. FTIR-Interaction between Bacterial Cellulose with Hyaluronic Acid and Chondroitin Sulfate</title><p>Influences of hyaluronic acid (HA) and chondroitin sulfate (CS) in bacterial cellulose were analyzed in the range between 250 and 4000 cm<sup>−1</sup> and with resolution of 2 cm<sup>−1</sup> with FTIR analysis. The main features of the bacterial cellulose in infrared spectroscopy is: 3500 cm<sup>−1</sup>: OH stretching, 2900 cm<sup>−1</sup>: CH stretching of alkane and asymmetric CH<sub>2</sub> stretching, 2700 cm<sup>−1</sup>: CH<sub>2</sub> symmetric stretching, 1640 cm<sup>−1</sup>: OH deformation, 1400 cm<sup>−1</sup>: CH<sub>2</sub> deformation, 1370 cm<sup>−1</sup>: CH<sub>3</sub> deformation, 1340 cm<sup>−1</sup>: OH deformation and 1320 - 1030 cm<sup>−1</sup>: CO deformation [<xref ref-type="bibr" rid="scirp.59643-ref23">23</xref>] -[<xref ref-type="bibr" rid="scirp.59643-ref26">26</xref>] .</p><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> SEM images of bacterial cellulose mats</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x6.png"/></fig><fig id="fig3"  position="float"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> SEM images of bacterial cellulose/hyaluronic acid mats</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x7.png"/></fig><fig id="fig4"  position="float"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> SEM images of bacterial cellulose/chondroitin sulfate mats</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x8.png"/></fig><p>In the case of FT-IR spectra of bacterial cellulose/chondroitin sulfate (BC/CS) nanocomposites, there were no shifts in the bands of carboxylate 1640 cm<sup>−1</sup> and sulfate groups that appear at 1250 cm<sup>−1</sup> and 1230 cm<sup>−1</sup> in bac- terial cellulose/chondroitin sulfate nanocomposites (<xref ref-type="fig" rid="fig5">Figure 5</xref>). However, it has exhibited broad overlapping bands at 1640 cm<sup>−1</sup> (primary amide bond stretching) and 1564 cm<sup>−1</sup> (aromatic C=C stretching vibrations), as well as N-H bending vibrations at 1508 cm<sup>−1</sup> [<xref ref-type="bibr" rid="scirp.59643-ref24">24</xref>] -[<xref ref-type="bibr" rid="scirp.59643-ref26">26</xref>] . Besides, it was assigned an increase of intensity absorp- tion bands at 1250 cm<sup>−1</sup> and 1230 cm<sup>−1</sup> due to sulphate-related modes, corresponding to antisymmetric and sym- metric stretching of the sulphate group, respectively. The intensity of the antisymmetric bridge oxygen stret- ching band at 1163 cm<sup>−1</sup> was reduced after formation of BC/CS nanocomposite, indicating a change in the hy- drogen-bonding of the bridge oxygen after the addition of chondroitin sulfate in the system. The visible spectral profile changes observed at 897 cm<sup>−1</sup>, corresponding to characteristic of β-anomers or β-linked glucose poly- mers, assigned as C-O-C stretching of the β-(1→4)-glycosidic linkage. This band becomes sharp and strong in the BC/CS nanocomposite. It can be explained from participation of the oxygen atom attached to C1 in this vi- bration and changes in the hydrogen bonding in cellulose [<xref ref-type="bibr" rid="scirp.59643-ref23">23</xref>] -[<xref ref-type="bibr" rid="scirp.59643-ref26">26</xref>] . Therefore, the results clearly show one possible interaction between bacterial cellulose and chondroitin sulfate, mainly by hydrogen interactions between</p><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> FTIR spectra of bacterial cellulose/chondroitin sulfate nanocomposites</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x9.png"/></fig><p>hydroxyl and carbonyl groups.</p><p>It can be observed similar OH stretching (at 2900 cm<sup>−1</sup>) in bacterial cellulose/hyaluronic acid nanocomposites (BC/HA), mainly because of the NH<sub>2</sub> interaction with hydroxyl groups (<xref ref-type="fig" rid="fig6">Figure 6</xref>). Besides, it can be observed a shift from (H-O-H) absorption band at 1640 cm<sup>−1</sup> of bacterial cellulose structures and amide I absorption from HA at 1620 cm<sup>−1</sup>, indicating an integrated HA/BC molecules. Another absorption peak was obtained in the range of 1490 cm<sup>−1</sup> on both samples, which shows the presence of a carbonyl group in the bacterial cellulose together with bonds corresponding to those of glycoside, including C-O-C at 1162 cm<sup>−1</sup> (as in the case of natural cellulose) [<xref ref-type="bibr" rid="scirp.59643-ref23">23</xref>] -[<xref ref-type="bibr" rid="scirp.59643-ref26">26</xref>] . These results clearly show one possible interaction between bacterial cellulose and hyaluronic acid, mainly by hydrogen interactions between hydroxyl and carbonyl groups.</p></sec><sec id="s3_3"><title>3.3. In Vivo Analysis</title><p>Patient (M. A. A. A.) enters in Al Qassimi Hospital on 08/20/2013 under supervision of Dr. Safwat Mohd. El-Hoseny, diagnosed with 3rd degree burns by hot water. It was performed immediate intervention with antibiotics and clinical protocols for this disease. In 2013 September started treatment of thick slough and debridement. In October 2013, treatment with Bacterial cellulose membranes (Nanoskin&#174;).</p><p>After using the Bacterial cellulose material in alternate days, it can be observed an excellent recovery of the edge and bottom of the wound and wound area reduction (70% extension) in 3 weeks as illustrated in <xref ref-type="fig" rid="fig7">Figure 7</xref> (a-before and b-after). The aesthetic gain of the lesion was excellent. In November 2013, burns healing completely.</p><p>The simple application of dressing only required the association of saline, gauze and bandage, decrease patient stay and operating room use, resulting in a better cost-benefit.</p><p>Patient (Y. S. S. A.) enters in Al Qassimi Hospital on 10/07/2014 under supervision of Dr. Safwat Mohd. El-Hoseny, diagnosed with hand skin loss wound by car accident. In the beginning, there were deep full thickness skin loss and multiple thickness friction burns on hand and fingers. All wounds were cleaned with Betadine solution, then covered with flamazine cream dressing, patient still complain several pain at all times as illustrated in <xref ref-type="fig" rid="fig8">Figure 8</xref>(a). In 10/15/2014 started Bacterial cellulose (Nanoskin&#174;) Dressing, all wounds gets better with (Nanoskin&#174;) dressing, dramatic changes was noted after application of (Nanoskin&#174;) dressing, patient rarely complain of pain. In 12/21/2014 completely healing using (Nanoskin&#174;) dressing as illustrated in <xref ref-type="fig" rid="fig8">Figure 8</xref>(b).</p></sec></sec><sec id="s4"><title>4. Conclusions</title><p>Bacterial cellulose (Nanoskin&#174;) was successfully modified by changing the fermentation medium as shown by FTIR and SEM, which produced suitable scaffolds for use in surface morphology applications with promising cell viability/attachment.</p><p>Bacterial cellulose (BC) is used in the treatment of skin conditions such as burns and ulcers, because of the</p><fig id="fig6"  position="float"><label><xref ref-type="fig" rid="fig6">Figure 6</xref></label><caption><title> FTIR spectra of bacterial cellulose/hyaluronic acid nanocomposites</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x10.png"/></fig><fig-group id="fig7"><label><xref ref-type="fig" rid="fig7">Figure 7</xref></label><caption><title> Wound healing evolution in 3 months and Bacterial cellulose (Nanoskin&#174;) impact use in biological wound dressing.</title></caption><fig id ="fig7_1"><label>(b)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x12.png"/></fig><fig id ="fig7_2"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x11.png"/></fig><fig id ="fig7_3"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x14.png"/></fig><fig id ="fig7_4"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x13.png"/></fig></fig-group><fig-group id="fig8"><label><xref ref-type="fig" rid="fig8">Figure 8</xref></label><caption><title> Wound healing evolution in 2 months and Bacterial cellulose impact use in biological wound dressing.</title></caption><fig id ="fig8_1"><label>(b)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x15.png"/></fig><fig id ="fig8_2"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x16.png"/></fig><fig id ="fig8_3"><label></label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/1-3200408x17.png"/></fig></fig-group><p>morphology of fibrous biopolymers serving as a support for cell proliferation, moreover, the nanostructure and morphological similarities with collagen make BC attractive for cell immobilization, cell support and Natural Extracellular Matrix (ECM) Scaffolds, then vegetal stem cells are natural choice in regenerative medicine.</p><p>In conclusion, Bacterial cellulose (Nanoskin&#174;) membrane applies to the protective cover and sutures, with or without exudate lesions, in unfavorable healing and with large areas until decubitus sores, its uses can be for all age people.</p></sec><sec id="s5"><title>Cite this paper</title><p>Safwat Mohd.El-Hoseny,Abdulwahid M.Alwahedi,PierreBasmaji,Jos&#233; Domingos da CostaOliveira,Gabriel Molina deOlyveira,Ligia Maria ManzineCosta,Gino BrunoFrancozo, (2015) Natural ECM-Bacterial Cellulose Wound Healing—Dubai Study. Journal of Biomaterials and Nanobiotechnology,06,237-246. doi: 10.4236/jbnb.2015.64022</p></sec></body><back><ref-list><title>References</title><ref id="scirp.59643-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Canavan, R., Connolly, V., Mcintosh, J., Airey, M. and Unwin, N. (2003) Geographic Variation in Lower Extremity Amputation Rates. Diabetic Foot, 6, 82-89.</mixed-citation></ref><ref id="scirp.59643-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Vowden, K.R. and Vowden, P. (1996) Peripheral Arterial Disease. Journal of Wound Care, 5, 23-26.</mixed-citation></ref><ref id="scirp.59643-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Van Gent,W.B., Wilschut, E.D. and Wittens, C. (2010) Management of Venous Ulcer Disease. 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