Two-photon fluorescence microscopy for determination of the riboflavin concentration in the anterior corneal stroma when using the dresden protocol

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Theo Seiler
  • Tobias Ehmke
  • Isaak Fischinger
  • Daniel Zapp
  • Oliver Stachs
  • Theo Seiler
  • Alexander Heisterkamp

Organisationseinheiten

Externe Organisationen

  • Institut für Refraktive und Ophthalmo-Chirurgie (IROC)
  • Laser Zentrum Hannover e.V. (LZH)
  • Universität Rostock
  • Technische Universität München (TUM)
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Details

OriginalspracheEnglisch
Seiten (von - bis)6740-6746
Seitenumfang7
FachzeitschriftInvestigative Ophthalmology and Visual Science
Jahrgang56
Ausgabenummer11
PublikationsstatusVeröffentlicht - Okt. 2015

Abstract

PURPOSE. To determine the riboflavin concentration gradient in the anterior corneal stroma when using the Dresden protocol with different dextran solutions. METHODS. Three different groups of porcine corneas, five each, were compared regarding the riboflavin concentration in the anterior stroma. Before all experiments, stable hydration conditions were established for the corresponding solution. All groups were treated with 0.1% riboflavin in different dextran solutions (15%, 16%, 20%). After imbibition, two-photon microscopy was used to determine fluorescence intensity. For signal attenuation and concentration determination corneas were saturated and measured a second time by twophoton microscopy. Additionally, the distribution was calculated mathematically and compared to the empiric results. RESULTS. Riboflavin concentration is decreasing with depth for all dextran solutions. A nearly constant concentration could be determined over the first 75 lm. Analysis of the fit functions leads to diffusion coefficients of D = 2.97 × 10-7 cm2/s for the 15% dextran solution, D = 2.34 × 10-7 cm2/s for the 16% dextran solution, and D = 1.28 × 10-7 cm2/s for the 20% dextran solution. The riboflavin gradients of the 20% dextran group were statistically significantly different from 15% dextran starting at a depth of 220 mm and deeper (P = 0.047). The 16% dextran group differed statistically at a depth of 250 µm and deeper (P = 0.047). These results show a significant difference to those published previously. CONCLUSIONS. With correct settings two-photon microscopy is a precise way to determine the concentration of riboflavin in cornea. The measured gradient is excellently fit by a Gaussian distribution, which comes out as a solution of Fick’s second law.

ASJC Scopus Sachgebiete

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Two-photon fluorescence microscopy for determination of the riboflavin concentration in the anterior corneal stroma when using the dresden protocol. / Seiler, Theo; Ehmke, Tobias; Fischinger, Isaak et al.
in: Investigative Ophthalmology and Visual Science, Jahrgang 56, Nr. 11, 10.2015, S. 6740-6746.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Two-photon fluorescence microscopy for determination of the riboflavin concentration in the anterior corneal stroma when using the dresden protocol",
abstract = "PURPOSE. To determine the riboflavin concentration gradient in the anterior corneal stroma when using the Dresden protocol with different dextran solutions. METHODS. Three different groups of porcine corneas, five each, were compared regarding the riboflavin concentration in the anterior stroma. Before all experiments, stable hydration conditions were established for the corresponding solution. All groups were treated with 0.1% riboflavin in different dextran solutions (15%, 16%, 20%). After imbibition, two-photon microscopy was used to determine fluorescence intensity. For signal attenuation and concentration determination corneas were saturated and measured a second time by twophoton microscopy. Additionally, the distribution was calculated mathematically and compared to the empiric results. RESULTS. Riboflavin concentration is decreasing with depth for all dextran solutions. A nearly constant concentration could be determined over the first 75 lm. Analysis of the fit functions leads to diffusion coefficients of D = 2.97 × 10-7 cm2/s for the 15% dextran solution, D = 2.34 × 10-7 cm2/s for the 16% dextran solution, and D = 1.28 × 10-7 cm2/s for the 20% dextran solution. The riboflavin gradients of the 20% dextran group were statistically significantly different from 15% dextran starting at a depth of 220 mm and deeper (P = 0.047). The 16% dextran group differed statistically at a depth of 250 µm and deeper (P = 0.047). These results show a significant difference to those published previously. CONCLUSIONS. With correct settings two-photon microscopy is a precise way to determine the concentration of riboflavin in cornea. The measured gradient is excellently fit by a Gaussian distribution, which comes out as a solution of Fick{\textquoteright}s second law.",
keywords = "Concentration, Cornea, Cross-linking, Riboflavin distribution, Two-photon microscopy",
author = "Theo Seiler and Tobias Ehmke and Isaak Fischinger and Daniel Zapp and Oliver Stachs and Theo Seiler and Alexander Heisterkamp",
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doi = "10.1167/iovs.15-17656",
language = "English",
volume = "56",
pages = "6740--6746",
journal = "Investigative Ophthalmology and Visual Science",
issn = "0146-0404",
publisher = "Association for Research in Vision and Ophthalmology Inc.",
number = "11",

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Download

TY - JOUR

T1 - Two-photon fluorescence microscopy for determination of the riboflavin concentration in the anterior corneal stroma when using the dresden protocol

AU - Seiler, Theo

AU - Ehmke, Tobias

AU - Fischinger, Isaak

AU - Zapp, Daniel

AU - Stachs, Oliver

AU - Seiler, Theo

AU - Heisterkamp, Alexander

PY - 2015/10

Y1 - 2015/10

N2 - PURPOSE. To determine the riboflavin concentration gradient in the anterior corneal stroma when using the Dresden protocol with different dextran solutions. METHODS. Three different groups of porcine corneas, five each, were compared regarding the riboflavin concentration in the anterior stroma. Before all experiments, stable hydration conditions were established for the corresponding solution. All groups were treated with 0.1% riboflavin in different dextran solutions (15%, 16%, 20%). After imbibition, two-photon microscopy was used to determine fluorescence intensity. For signal attenuation and concentration determination corneas were saturated and measured a second time by twophoton microscopy. Additionally, the distribution was calculated mathematically and compared to the empiric results. RESULTS. Riboflavin concentration is decreasing with depth for all dextran solutions. A nearly constant concentration could be determined over the first 75 lm. Analysis of the fit functions leads to diffusion coefficients of D = 2.97 × 10-7 cm2/s for the 15% dextran solution, D = 2.34 × 10-7 cm2/s for the 16% dextran solution, and D = 1.28 × 10-7 cm2/s for the 20% dextran solution. The riboflavin gradients of the 20% dextran group were statistically significantly different from 15% dextran starting at a depth of 220 mm and deeper (P = 0.047). The 16% dextran group differed statistically at a depth of 250 µm and deeper (P = 0.047). These results show a significant difference to those published previously. CONCLUSIONS. With correct settings two-photon microscopy is a precise way to determine the concentration of riboflavin in cornea. The measured gradient is excellently fit by a Gaussian distribution, which comes out as a solution of Fick’s second law.

AB - PURPOSE. To determine the riboflavin concentration gradient in the anterior corneal stroma when using the Dresden protocol with different dextran solutions. METHODS. Three different groups of porcine corneas, five each, were compared regarding the riboflavin concentration in the anterior stroma. Before all experiments, stable hydration conditions were established for the corresponding solution. All groups were treated with 0.1% riboflavin in different dextran solutions (15%, 16%, 20%). After imbibition, two-photon microscopy was used to determine fluorescence intensity. For signal attenuation and concentration determination corneas were saturated and measured a second time by twophoton microscopy. Additionally, the distribution was calculated mathematically and compared to the empiric results. RESULTS. Riboflavin concentration is decreasing with depth for all dextran solutions. A nearly constant concentration could be determined over the first 75 lm. Analysis of the fit functions leads to diffusion coefficients of D = 2.97 × 10-7 cm2/s for the 15% dextran solution, D = 2.34 × 10-7 cm2/s for the 16% dextran solution, and D = 1.28 × 10-7 cm2/s for the 20% dextran solution. The riboflavin gradients of the 20% dextran group were statistically significantly different from 15% dextran starting at a depth of 220 mm and deeper (P = 0.047). The 16% dextran group differed statistically at a depth of 250 µm and deeper (P = 0.047). These results show a significant difference to those published previously. CONCLUSIONS. With correct settings two-photon microscopy is a precise way to determine the concentration of riboflavin in cornea. The measured gradient is excellently fit by a Gaussian distribution, which comes out as a solution of Fick’s second law.

KW - Concentration

KW - Cornea

KW - Cross-linking

KW - Riboflavin distribution

KW - Two-photon microscopy

UR - http://www.scopus.com/inward/record.url?scp=84944734416&partnerID=8YFLogxK

U2 - 10.1167/iovs.15-17656

DO - 10.1167/iovs.15-17656

M3 - Article

C2 - 26567785

AN - SCOPUS:84944734416

VL - 56

SP - 6740

EP - 6746

JO - Investigative Ophthalmology and Visual Science

JF - Investigative Ophthalmology and Visual Science

SN - 0146-0404

IS - 11

ER -