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    <Identifier>dgkh000108</Identifier>
    <ArticleType>Research Article</ArticleType>
    <TitleGroup>
      <Title language="en">In vivo analysis of wound healing by optical methods</Title>
      <TitleTranslated language="de">In-vivo-Analyse der Wundheilung mit optischen Methoden</TitleTranslated>
    </TitleGroup>
    <CreatorList>
      <Creator>
        <PersonNames>
          <Lastname>Alborova</Lastname>
          <LastnameHeading>Alborova</LastnameHeading>
          <Firstname>Alena</Firstname>
          <Initials>A</Initials>
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        <Address>
          <Affiliation>Center of Applied Cutaneous Physiology (CCP), Department of Dermatology and Allergology, Charit&#233; - Universit&#228;tsmedizin, Berlin, Germany</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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        <PersonNames>
          <Lastname>Lademann</Lastname>
          <LastnameHeading>Lademann</LastnameHeading>
          <Firstname>J&#252;rgen</Firstname>
          <Initials>J</Initials>
          <AcademicTitle>Prof. Dr. Dr. Ing.</AcademicTitle>
        </PersonNames>
        <Address>Charit&#233; - Universit&#228;tsmedizin Berlin, Klinik f&#252;r Dermatologie, Venerologie und Allergologie, Bereich Hautphysiologie, Charit&#233;platz 1, 10117 Berlin, Tel.: 030&#47;450 518 100, Fax: 030&#47;450 518 918<Affiliation>Center of Applied Cutaneous Physiology (CCP), Department of Dermatology and Allergology, Charit&#233; - Universit&#228;tsmedizin, Berlin, Germany</Affiliation></Address>
        <Email>juergen.lademann&#64;charite.de</Email>
        <Creatorrole corresponding="yes" presenting="no">author</Creatorrole>
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        <PersonNames>
          <Lastname>Kramer</Lastname>
          <LastnameHeading>Kramer</LastnameHeading>
          <Firstname>Axel</Firstname>
          <Initials>A</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Institute of Hygiene and Environmental Medicine, Ernst-Moritz-Arndt-University, Greifswald, Germany</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
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          <Lastname>Richter</Lastname>
          <LastnameHeading>Richter</LastnameHeading>
          <Firstname>Heike</Firstname>
          <Initials>H</Initials>
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        <Address>
          <Affiliation>Center of Applied Cutaneous Physiology (CCP), Department of Dermatology and Allergology, Charit&#233; - Universit&#228;tsmedizin, Berlin, Germany</Affiliation>
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        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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        <PersonNames>
          <Lastname>Patzelt</Lastname>
          <LastnameHeading>Patzelt</LastnameHeading>
          <Firstname>Alexa</Firstname>
          <Initials>A</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Center of Applied Cutaneous Physiology (CCP), Department of Dermatology and Allergology, Charit&#233; - Universit&#228;tsmedizin, Berlin, Germany</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Sterry</Lastname>
          <LastnameHeading>Sterry</LastnameHeading>
          <Firstname>Wolfram</Firstname>
          <Initials>W</Initials>
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        <Address>
          <Affiliation>Center of Applied Cutaneous Physiology (CCP), Department of Dermatology and Allergology, Charit&#233; - Universit&#228;tsmedizin, Berlin, Germany</Affiliation>
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        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Koch</Lastname>
          <LastnameHeading>Koch</LastnameHeading>
          <Firstname>Stefan</Firstname>
          <Initials>S</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Institute of Pathology, Helios Klinikum, Bad Saarow, Germany</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
    </CreatorList>
    <PublisherList>
      <Publisher>
        <Corporation>
          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
        </Corporation>
        <Address>D&#252;sseldorf</Address>
      </Publisher>
    </PublisherList>
    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
      <Keyword language="en">in vivo laser scanning microscopy</Keyword>
      <Keyword language="en">optical coherent tomography</Keyword>
      <Keyword language="en">transepidermal water loss</Keyword>
      <Keyword language="en">suction blister technique</Keyword>
      <Keyword language="en">wound healing analysis</Keyword>
      <Keyword language="de">In-vivo-Laser-Scan-Mikroskopie</Keyword>
      <Keyword language="de">transepidermaler Wasserverlust</Keyword>
      <Keyword language="de">Wundheilungsanalyse</Keyword>
      <Keyword language="de">Saugblasentechnik</Keyword>
    </SubjectGroup>
    <DatePublishedList>
      <DatePublished>20080311</DatePublished>
    </DatePublishedList>
    <Language>engl</Language>
    <SourceGroup>
      <Journal>
        <ISSN>1863-5245</ISSN>
        <Volume>3</Volume>
        <Issue>1</Issue>
        <JournalTitle>GMS Krankenhaushygiene Interdisziplin&#228;r</JournalTitle>
        <JournalTitleAbbr>GMS Krankenhaushyg Interdiszip</JournalTitleAbbr>
        <IssueTitle>Plasma Medicine - its perspective for wound therapy</IssueTitle>
      </Journal>
    </SourceGroup>
    <ArticleNo>10</ArticleNo>
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  <OrigData>
    <Abstract language="de" linked="yes">
      <Pgraph>Die Analyse der Wundheilung ist wichtig zur Therapiekontrolle und f&#252;r die Entwicklung von Arzneimitteln zur Wundheilungsf&#246;rderung. Wunden verursachen eine Sch&#228;digung der Hautbarriere. Ein gesch&#228;digtes Stratum corneum verursacht einen erh&#246;hten Wasserverlust durch die Hautbarriere. Daher ist das Standardverfahren zur Charakterisierung von Wundheilungsprozessen die Messung des transepidermalen Wasserverlusts (TEWL). Der Nachteil dieser Methode ist die St&#246;ranf&#228;lligkeit durch die Perspiration der Probanden sowie durch topisch applizierte Substanzen, z.B. Wundheilungscremes. </Pgraph>
      <Pgraph>In der vorliegenden Studie werden die In-vivo-Laser-Scan-Mikroskopie und die optische Koher&#228;nztomographie in ihrer Aussagekraft, Wundheilungsprozesse zu charakterisieren, verglichen. Die In-vivo-Laser-Scan-Mikroskopie erm&#246;glicht die Darstellung des Heilungsprozesses auf zellul&#228;rer Ebene. Mit Bewertungskriterien, die die Stadien des Wundheilungsprozesses beschreiben, l&#228;sst sich der Heilungsprozess numerisch beschreiben.</Pgraph>
    </Abstract>
    <Abstract language="en" linked="yes">
      <Pgraph>The analysis of wound healing is important for the therapy control and for the development of drugs stimulating the healing process. Wounds cause damage to the skin barrier. A damaged stratum corneum leads to an increased water loss through the skin barrier. The standard measuring procedure for characterization of wound healing is the measurement of transepidermal water loss (TEWL). The disadvantage of this method is that it can be easily disturbed by the perspiration of the volunteers and by topically applied substances, for instance wound healing creams. </Pgraph>
      <Pgraph>In the study presented, in vivo laser scanning microscopy and optical coherent tomography were compared concerning the application for their analysis of wound healing processes. The laser scanning microscopy allows the analysis of the healing process on a cellular level. The course of wound healing determined by laser scanning microscopy was correlated with numerical values, allowing the numerical characterization of the wound healing process.</Pgraph>
    </Abstract>
    <TextBlock linked="yes" name="Introduction">
      <MainHeadline>Introduction</MainHeadline>
      <Pgraph>The skin is the largest organ of our body and represents a barrier to the environment.  It protects the organism from water loss and penetration of harmful substances. The barrier can be damaged by mechanical and thermal action or by UV light and different diseases, such as psoriasis and atopic dermatitis <TextLink reference="1"></TextLink>, <TextLink reference="2"></TextLink>. If the skin barrier is disturbed, the skin starts repair mechanisms <TextLink reference="3"></TextLink>. The kinetic of the wound healing processes is influenced by endogenous and exogenous factors <TextLink reference="4"></TextLink>. The analysis of the kinetic is important for therapy control and for the development of efficient drugs and cosmetic products, stimulating the wound healing <TextLink reference="5"></TextLink>. </Pgraph>
      <Pgraph>In all cases of damaged skin, the transepidermal water loss (TEWL) through the barrier is increased. Therefore, TEWL measurements are used for the characterization of the barrier properties <TextLink reference="6"></TextLink>. The disadvantage of TEWL measurement is that it can be easily influenced by the perspiration of the volunteers and by topically applied drugs and cosmetic products <TextLink reference="7"></TextLink>. </Pgraph>
      <Pgraph>In the present study, laser scanning microscopy (LSM) <TextLink reference="8"></TextLink>, <TextLink reference="9"></TextLink> and optical coherent tomography (OCT) <TextLink reference="10"></TextLink>, <TextLink reference="11"></TextLink> were compared concerning the application for the characterization of wound healing processes. </Pgraph>
    </TextBlock>
    <TextBlock linked="yes" name="Materials and methods">
      <MainHeadline>Materials and methods</MainHeadline>
      <SubHeadline>Volunteers</SubHeadline>
      <Pgraph>The investigations were carried out on 6 volunteers aged between 22 and 38 years. Approval for the investigations had been obtained from the Ethics Committee of the Charit&#233;.</Pgraph>
      <SubHeadline>Suction blister formation</SubHeadline>
      <Pgraph>Suction blisters were induced on the untreated forearms of the volunteers. The blisters were produced using the tube of a syringe, pressed upside down onto the skin. The needle nipple was connected to a vacuum pump. A vacuum of 0.3 bar was applied for approximately 1 h, until the suction blister was generated. Subsequently, the vacuum pump was disconnected <TextLink reference="12"></TextLink>. </Pgraph>
      <SubHeadline>TEWL-measurements</SubHeadline>
      <Pgraph>The measurements of the transepidermal water loss (TEWL) were performed using the TEWA-meter TM 210 (Courage &#43; Khazaka Electronics, GmbH, Cologne, Germany) <TextLink reference="6"></TextLink>.</Pgraph>
      <SubHeadline>Optical methods</SubHeadline>
      <Pgraph>In principle, two optical methods are suitable for the characterization of wound healing &#8211; the optical coherent tomography (OCT) and the laser scanning microscopy (LSM). Both techniques are non-invasive online methods. The OCT produces images of vertical sections of the skin, analogical to biopsies, whereas, the LSM produces images of horizontal sections. </Pgraph>
      <SubHeadline>Laser scanning microscopy (LSM)</SubHeadline>
      <Pgraph>The investigations were carried out using the in vivo laser scanning microscope &#8220;Stratum&#8221; (OptiScan, Ltd., Melbourne, Australia) <TextLink reference="8"></TextLink>. The hand piece of the laser scanning microscope contains the optical scanning system and is connected by optical fibers to the base station, containing the Argon laser (&#955;&#61;488 nm) and the detector system. By the application of the hand piece on the skin surface, images of 200x200 &#181;m are obtained online. Furthermore, the focus can be moved to a depth of approx. 250 &#181;m. In the meantime, the skin can be analyzed layer by layer.</Pgraph>
      <SubHeadline>Optical coherent tomography (OCT)</SubHeadline>
      <Pgraph>OCT measurements were performed utilizing the SkinDex 300 (Isis Optronics, GmbH, Mannheim, Germany) <TextLink reference="10"></TextLink>. With this system a depth and lateral resolution in tissue can be achieved of approx. 5 &#181;m and 3 &#181;m, respectively. </Pgraph>
    </TextBlock>
    <TextBlock linked="yes" name="Results and discussion">
      <MainHeadline>Results and discussion</MainHeadline>
      <Pgraph>In Figure 1 <ImgLink imgNo="1" imgType="figure"/>, the vertical section of an OCT image obtained in the non-invasive manner of intact human skin is compared to a histological section obtained from a biopsy likewise of intact human skin. The stratum corneum (SC), the epidermis (EP) and the dermis (DE) can be clearly recognized in both cases. Unfortunately, the resolution of the OCT is not sufficient to determine the real thickness of the barrier (SC). The determination of the real thickness of the stratum corneum on the histological section is also not possible, because the structure and thickness of the stratum corneum changed during the preparation of the histological section, on account of mechanical stress and hydration. </Pgraph>
      <Pgraph>In Figure 2 <ImgLink imgNo="2" imgType="figure"/>, a histological section of intact human skin (Figure 2 a <ImgLink imgNo="2" imgType="figure"/>) is compared to an image obtained by non-invasive in vivo LSM measurements of likewise intact human skin. The LSM measurement produced horizontal sections in contrast to histology and OCT. In order to determine the thickness of the barrier, the laser focus has to be moved from the skin surface (Figure 2 b <ImgLink imgNo="2" imgType="figure"/>) down to the boundary between the stratum corneum (SC) and the stratum granulosum (SG) (Figure 2 c <ImgLink imgNo="2" imgType="figure"/>). This boundary can be clearly recognized, because the size and the structure of the cells in the SC and the SG are significantly different. In Figure 2 c <ImgLink imgNo="2" imgType="figure"/>, the smaller cells of the SG can be seen in the upper part of the image, whilst the relatively larger cells of the SC are located in the lower part. The distance which the focus has to be moved from the skin surface down to the boundary layer, corresponds to the thickness of the SC.</Pgraph>
      <Pgraph>The SC has a thickness between 15 and 25 &#181;m. Only on the palms and feet, it is much thicker up to 150 &#181;m. Therefore, the OCT measurements are unsuitable for the determination of the thickness of the skin barrier, because of the low depth resolution. In contrast to OCT, the application of LSM can achieve a depth resolution of about 250 &#181;m. Therefore, this method is well suited for the determination of the barrier properties. </Pgraph>
      <Pgraph>In the second part of this study, laser scanning microscopy was compared with TEWL measurements, analyzing the wound healing process after application of the suction blister technique. The disadvantage of the TEWL measurement was that it could not be applied during the first stage of the wound healing process, because the skin surface of the lesion was covered by wound secretion. The corresponding high water evaporation disturbs the TEWL measurement. Furthermore, the application of a wound healing cream is able to disturb the TEWL measurement. On the contrary, the application of in vivo laser scanning microscopy allows the determination of the formation of single cell layers during the healing process. The formation of the first cell layer of the SC is demonstrated in Figure 3 <ImgLink imgNo="3" imgType="figure"/>. It can be seen that the formation of the new cells starts from the outer edge of the lesion and around the hair follicles. In some volunteers, a colonization of the wounds with fungi was observed; mainly in the case of a wound healing cream being applied to stimulate the wound healing. The fungi spores could be clearly recognized by LSM. One reason for the colonization of fungi in some lesions could be that the applied wound healing cream disturbs the natural formation of a protection film by the wound secretion on the surface of the lesion, which has antibacterial and antimycotic properties <TextLink reference="13"></TextLink>.</Pgraph>
      <Pgraph>There are hints that the infection of wounds can be reduced or even prevented by a combined application of a wound healing cream and plasma techniques, because electrical signals stimulating the wound healing <TextLink reference="14"></TextLink> and plasma posses antimicrobial properties. </Pgraph>
      <Pgraph>The LSM is the method most suited for analyzing the wound healing process, non-invasively and online on a cellular level. This method is less sensitive to endogenous or exogenous interferences and, additionally, it can be used for the analysis of wound colonization by fungi.</Pgraph>
      <Pgraph>Taking into consideration the new developments in the field of laser electroscopic techniques, it can be expected that in the near future efficient and low-cost optical systems will be available, which can be used as a standard tool for therapy control of wound healing and infection processes. </Pgraph>
    </TextBlock>
    <TextBlock linked="yes" name="Acknowledgements">
      <MainHeadline>Acknowledgements</MainHeadline>
      <Pgraph>We would like to thank the Foundation &#8220;Skin Physiology&#8221; of the Donor Association for German Science and Humanities for financial support. </Pgraph>
    </TextBlock>
    <References linked="yes">
      <Reference refNo="1">
        <RefAuthor>Lipozencic J</RefAuthor>
        <RefAuthor>Wolf R</RefAuthor>
        <RefTitle>Atopic dermatitis: an update and review of the literature</RefTitle>
        <RefYear>2007</RefYear>
        <RefJournal>Dermatol Clin</RefJournal>
        <RefPage>605-12</RefPage>
        <RefTotal>Lipozencic J, Wolf R. Atopic dermatitis: an update and review of the literature. Dermatol Clin. 2007;25:605-12.</RefTotal>
      </Reference>
      <Reference refNo="2">
        <RefAuthor>Lebwohl M</RefAuthor>
        <RefAuthor>Herrmann LG</RefAuthor>
        <RefTitle>Impaired skin barrier function in dermatologic disease and repair with moisturization</RefTitle>
        <RefYear>2005</RefYear>
        <RefJournal>Cutis</RefJournal>
        <RefPage>7-12</RefPage>
        <RefTotal>Lebwohl M, Herrmann LG. Impaired skin barrier function in dermatologic disease and repair with moisturization. Cutis. 2005;76:7-12.</RefTotal>
      </Reference>
      <Reference refNo="3">
        <RefAuthor>Fu X</RefAuthor>
        <RefAuthor>Fang L</RefAuthor>
        <RefAuthor>Li H</RefAuthor>
        <RefAuthor>Li X</RefAuthor>
        <RefAuthor>Cheng B</RefAuthor>
        <RefAuthor>Sheng Z</RefAuthor>
        <RefTitle>Adipose tissue extract enhances skin wound healing</RefTitle>
        <RefYear>2007</RefYear>
        <RefJournal>Wound Repair Regen</RefJournal>
        <RefPage>540-8</RefPage>
        <RefTotal>Fu X, Fang L, Li H, Li X, Cheng B, Sheng Z. Adipose tissue extract enhances skin wound healing. Wound Repair Regen. 2007;15(4):540-8.</RefTotal>
      </Reference>
      <Reference refNo="4">
        <RefAuthor>Stadelmann W</RefAuthor>
        <RefAuthor>Greenwald D</RefAuthor>
        <RefAuthor>Stevens L</RefAuthor>
        <RefAuthor>Shumway S</RefAuthor>
        <RefAuthor>Leoni K</RefAuthor>
        <RefAuthor>Krizek T</RefAuthor>
        <RefTitle>Mechanical analysis of the effects of bacteria and aprotinin on skin wound healing in adult guinea pigs</RefTitle>
        <RefYear>1993</RefYear>
        <RefJournal>Wound Repair Regen</RefJournal>
        <RefPage>187-93</RefPage>
        <RefTotal>Stadelmann W, Greenwald D, Stevens L, Shumway S, Leoni K, Krizek T. Mechanical analysis of the effects of bacteria and aprotinin on skin wound healing in adult guinea pigs. Wound Repair Regen. 1993;1(3):187-93.</RefTotal>
      </Reference>
      <Reference refNo="5">
        <RefAuthor>Alborova A</RefAuthor>
        <RefAuthor>Lademann J</RefAuthor>
        <RefAuthor>Meye L</RefAuthor>
        <RefAuthor></RefAuthor>
        <RefAuthor>Kramer A</RefAuthor>
        <RefAuthor>Patzelt A</RefAuthor>
        <RefAuthor>Sterry W</RefAuthor>
        <RefAuthor>Antoniou C</RefAuthor>
        <RefTitle>Application of laser scanning microscopy for the characterization of wound healing</RefTitle>
        <RefYear>2007</RefYear>
        <RefJournal>GMS Krankenhaushygiene Interdisziplin&#228;r</RefJournal>
        <RefArticleNo>37</RefArticleNo>
        <RefTotal>Alborova A, Lademann J, Meye L,, Kramer A, Patzelt A, Sterry W, Antoniou C. Application of laser scanning microscopy for the characterization of wound healing. GMS Krankenhaushygiene Interdisziplin&#228;r. 2007;2(2):Doc37. Available from: http:&#47;&#47;www.egms.de&#47;en&#47;journals&#47;dgkh&#47;2007-2&#47;dgkh000070.shtml.</RefTotal>
        <RefLink>http:&#47;&#47;www.egms.de&#47;en&#47;journals&#47;dgkh&#47;2007-2&#47;dgkh000070.shtml</RefLink>
      </Reference>
      <Reference refNo="6">
        <RefAuthor>Weigmann HJ</RefAuthor>
        <RefAuthor>Ulrich J</RefAuthor>
        <RefAuthor>Schanzer S</RefAuthor>
        <RefAuthor>Jacobi U</RefAuthor>
        <RefAuthor>Schaefer H</RefAuthor>
        <RefAuthor>Sterry W</RefAuthor>
        <RefAuthor>Lademann J</RefAuthor>
        <RefTitle>Comparison of transepidermal water loss and spectroscopic absorbance to quantify changes of the stratum corneum after tape stripping</RefTitle>
        <RefYear>2005</RefYear>
        <RefJournal>Skin Pharmacol Physiol</RefJournal>
        <RefPage>180-5</RefPage>
        <RefTotal>Weigmann HJ, Ulrich J, Schanzer S, Jacobi U, Schaefer H, Sterry W, Lademann J. Comparison of transepidermal water loss and spectroscopic absorbance to quantify changes of the stratum corneum after tape stripping. Skin Pharmacol Physiol. 2005;18:180-5.</RefTotal>
      </Reference>
      <Reference refNo="7">
        <RefAuthor>Siebert J</RefAuthor>
        <RefTitle></RefTitle>
        <RefYear>2005</RefYear>
        <RefBookTitle>Bestimmung der individuellen Hornschichtdicke &#252;ber die Abrissmethode - Vergleich des transepidermalen Wasserverlustes und der Pseudoabsorption der Korneozyten</RefBookTitle>
        <RefPage></RefPage>
        <RefTotal>Siebert J. Bestimmung der individuellen Hornschichtdicke &#252;ber die Abrissmethode - Vergleich des transepidermalen Wasserverlustes und der Pseudoabsorption der Korneozyten &#91;Doctor Thesis&#93;. Berlin: Med Fac Charit&#233; Universit&#228;tsmed; 2005.</RefTotal>
      </Reference>
      <Reference refNo="8">
        <RefAuthor>Teichmann A</RefAuthor>
        <RefAuthor>Sadeyh Pour Saleh H</RefAuthor>
        <RefAuthor>Schanzer S</RefAuthor>
        <RefAuthor>Richter H</RefAuthor>
        <RefAuthor>Schwarz A</RefAuthor>
        <RefAuthor>Lademann J</RefAuthor>
        <RefTitle>Evaluation of the efficacy of skin care products by laser scanning microscopy</RefTitle>
        <RefYear>2006</RefYear>
        <RefJournal>Laser Phys Lett</RefJournal>
        <RefPage>507-9</RefPage>
        <RefTotal>Teichmann A, Sadeyh Pour Saleh H, Schanzer S, Richter H, Schwarz A, Lademann J. Evaluation of the efficacy of skin care products by laser scanning microscopy. Laser Phys Lett. 2006;3(10):507-9.</RefTotal>
      </Reference>
      <Reference refNo="9">
        <RefAuthor>Jacobi U</RefAuthor>
        <RefAuthor>Waibler E</RefAuthor>
        <RefAuthor>Sterry W</RefAuthor>
        <RefAuthor>Lademann J</RefAuthor>
        <RefTitle>In vivo determination of the long-term reservoir of the horny layer using laser scanning microscopy</RefTitle>
        <RefYear>2005</RefYear>
        <RefJournal>Laser Phys</RefJournal>
        <RefPage>565-9</RefPage>
        <RefTotal>Jacobi U, Waibler E, Sterry W, Lademann J. In vivo determination of the long-term reservoir of the horny layer using laser scanning microscopy. Laser Phys. 2005;15(4):565-9.</RefTotal>
      </Reference>
      <Reference refNo="10">
        <RefAuthor>Lademann J</RefAuthor>
        <RefAuthor>Otberg N</RefAuthor>
        <RefAuthor>Richter H</RefAuthor>
        <RefAuthor>Meyer L</RefAuthor>
        <RefAuthor>Audring H</RefAuthor>
        <RefAuthor>Teichmann A</RefAuthor>
        <RefAuthor>Thomas S</RefAuthor>
        <RefAuthor>Knuettel A</RefAuthor>
        <RefAuthor>Sterry W</RefAuthor>
        <RefTitle>Application of optical non-invasive methods in skin physiology: a comparison of laser scanning microscopy and optical coherent tomography with histological analysis</RefTitle>
        <RefYear>2007</RefYear>
        <RefJournal>Skin Res Technol</RefJournal>
        <RefPage>119-23</RefPage>
        <RefTotal>Lademann J, Otberg N, Richter H, Meyer L, Audring H, Teichmann A, Thomas S, Knuettel A, Sterry W. Application of optical non-invasive methods in skin physiology: a comparison of laser scanning microscopy and optical coherent tomography with histological analysis. Skin Res Technol. 2007;13:119-23.</RefTotal>
      </Reference>
      <Reference refNo="11">
        <RefAuthor>Lademann J</RefAuthor>
        <RefAuthor>Kn&#252;ttel A</RefAuthor>
        <RefAuthor>Richter H</RefAuthor>
        <RefAuthor>Otberg N</RefAuthor>
        <RefAuthor>v Pelchrzim R</RefAuthor>
        <RefAuthor>Audring H</RefAuthor>
        <RefAuthor>Meffert H</RefAuthor>
        <RefAuthor>Sterry W</RefAuthor>
        <RefAuthor>Hoffmann K</RefAuthor>
        <RefTitle>Application of optical coherent tomography for skin diagnostics</RefTitle>
        <RefYear>2005</RefYear>
        <RefJournal>Laser Phys</RefJournal>
        <RefPage>1-7</RefPage>
        <RefTotal>Lademann J, Kn&#252;ttel A, Richter H, Otberg N, v Pelchrzim R, Audring H, Meffert H, Sterry W, Hoffmann K. Application of optical coherent tomography for skin diagnostics. Laser Phys. 2005;15(2):1-7.</RefTotal>
      </Reference>
      <Reference refNo="12">
        <RefAuthor>Lademann J</RefAuthor>
        <RefAuthor>Jacobi U</RefAuthor>
        <RefAuthor>Richter H</RefAuthor>
        <RefAuthor>Otberg N</RefAuthor>
        <RefAuthor>Weigmann HJ</RefAuthor>
        <RefAuthor>Meffert H</RefAuthor>
        <RefAuthor>Schaefer H</RefAuthor>
        <RefAuthor>Blume-Peytavi U</RefAuthor>
        <RefAuthor>Sterry W</RefAuthor>
        <RefTitle>In vivo determination of UV-photons entering into human skin</RefTitle>
        <RefYear>2004</RefYear>
        <RefJournal>Laser Phys</RefJournal>
        <RefPage>234-7</RefPage>
        <RefTotal>Lademann J, Jacobi U, Richter H, Otberg N, Weigmann HJ, Meffert H, Schaefer H, Blume-Peytavi U, Sterry W. In vivo determination of UV-photons entering into human skin. Laser Phys. 2004;14(2):234-7.</RefTotal>
      </Reference>
      <Reference refNo="13">
        <RefAuthor>Davis JL</RefAuthor>
        <RefAuthor>Salmon JH</RefAuthor>
        <RefAuthor>Papich MG</RefAuthor>
        <RefTitle>Pharmacokinetics and tissue fluid distribution of cephalexin in the horse after oral and i.v. administration</RefTitle>
        <RefYear>2005</RefYear>
        <RefJournal>J Vet Pharm Ther</RefJournal>
        <RefPage>425-31</RefPage>
        <RefTotal>Davis JL, Salmon JH, Papich MG. Pharmacokinetics and tissue fluid distribution of cephalexin in the horse after oral and i.v. administration. J Vet Pharm Ther. 2005;28:425-31.</RefTotal>
      </Reference>
      <Reference refNo="14">
        <RefAuthor>McCaig C</RefAuthor>
        <RefTitle>Electrical control of cell behavior and wound healing</RefTitle>
        <RefYear>2008</RefYear>
        <RefJournal>GMS Krankenhaushyg Interdiszip</RefJournal>
        <RefArticleNo>03</RefArticleNo>
        <RefTotal>McCaig C. Electrical control of cell behavior and wound healing. GMS Krankenhaushyg Interdiszip. 2008;3(1):Doc03. Available from: http:&#47;&#47;www.egms.de&#47;en&#47;journals&#47;dgkh&#47;2008-3&#47;dgkh000101.shtml.</RefTotal>
        <RefLink>http:&#47;&#47;www.egms.de&#47;en&#47;journals&#47;dgkh&#47;2008-3&#47;dgkh000101.shtml</RefLink>
      </Reference>
    </References>
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              <Mark1>Figure 1: Comparison between a histological section (left picture) and an image obtained by OCT (right picture); the stratum corneum (SC), the epidermis (EP) and the dermis (DE) can be clearly recognized.</Mark1>
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              <Mark1>Figure 3: LSM image showing the formation of a new cell layer of corneocytes during the wound healing process</Mark1>
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              <Mark1>Figure 2: Comparison between a histological section (a) and an image obtained by LSM; in the LSM image the skin surface (b) and the boundary of the SC to the SG (c) can be clearly recognized.</Mark1>
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