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Table 1 Summary of experimental results for diffusion coefficient, D, from recent studies using fluorescent dye.

From: Measurement of diffusion in articular cartilage using fluorescence correlation spectroscopy

Fluorescent dye

Method

Specimen

Temp. (°C)

D(×10-10m2/s)

Ref.

Fluorecein (332 Da)

Fluorescence recovery after photobleaching (FRAP)

Human intervertebral discs

22

0.38 ± 0.25 ~ 2.68 ± 0.84

[18]

  

   Inner, middle and outer regions of annulus fibrosus

   

Fluorecein (376 Da)

Fluorescence loss induced by photobleaching (FLIP).

Murine (C57BL6J) distal humurs

4

 

[19]

  

   Subchondral bone

 

0.0002 ~ 0.012 (0.0007 ± 0.0003)

 
  

   Calcified cartilage

 

0.0005 ~ 0.009 (0.0026 ± 0.0022)

 

Fluorescein isothiocyante (FITC)-tagged dextran (3, 40, 70, and 500 kDa)

Fluorescence recovery after photobleaching (FRAP)

Tissue engineered cartilage from human adipose-derived stem cell with or without scaffold (alginate, agarose, fibrin and gelatin)

37

0.16 ± 0.08 (Day 28, cultured within fibrin in control media using 500 kDa)

[20]

   

or

~ 18.10 ± 3.94 (Day 1, cultured within gelatine in chondrogenic media using 3 kDa)

 
   

?

  

Fluorescein isothiocyante (FITC)-tagged dextran (70 kDa)

Scanning microphotolysis (SCAMP).

Porcine femoral condyle

?

 

[21]

  

   Healthy cartilage

   
  

Extracellular matrix

 

0.23 ± 0.02

 
  

Pericellular matrix

 

0.19 ± 0.02

 
  

   Osteoarthritic cartilage

   
  

Extracellular matrix

 

0.23 ± 0.02

 
  

Pericellular matrix

 

0.23 ± 0.02

 

Fluorescein isothiocyante (FITC)-tagged dextran (70 kDa)

Scanning microphotolysis (SCAMP) and Fluorescence imaging of continuous point photobleaching (FICOPP)

Porcine femoral condyle

?

 

[22]

  

   Normal cartilage

 

0.33

 
  

   Compressed cartilage

 

0.07

 

Fluorescein isothiocyante (FITC)-tagged dextran (3 and 500 kDa)

Fluorescence imaging of continuous point photobleaching (FICOPP)

Collagenous tissues

4

Inexpressible because authors explain diffusivity by not diffusion coefficient but by diffusivity ratio for comparisons

[23]

  

   3% agarose gel

or

  
  

   Lateral collateral ligaments (Porcine)

?

  

Rhodamine B (443 Da, cationic), Rhodamine B (479 Da, neutral but polar), Fluorecein (332 Da), and Na-fluorecein (376 Da)

Quantitative fluorescence microscopy on histological sections

Equine forelimb

4

0.0098 ± 0.0013 ~ 0.037 ± 0.003

[24]

  

   Subchondral bone

   
  

   Calcified cartilage

   

Bovine serum albumin labeled with rhodamine - maleimide and Nitrobenz -2-oxa-1,3-diazole (NBD) -labelled lauric acid (378 Da) bound to the fluorescent albumin

Quantitative fluorescence microscopy on histological sections

Equine metacarpal-phalangeal joints

4

9.0 ± 2.0 (48 h-incubation, using albumin)

[25]

    

~

 
    

290.0 ± 10.0 (2 h-incubation, using lauric acid)

 

Fluorescein-conjugated bovine serum albumin (66 kDa).

Fluorescence recovery after photobleaching (FRAP)

3~8% agarose gel

24

0.164 ± 0.018 ~ 0.411 ± 0.008

[26]

  

Porcine growth plate

 

0.0387 ~ 0.4922

 

Tetramethylrhodamine (TMR) -tagged dextran (3,10, and 40 kDa) and tetramethylrhodamine (430 Da) itself,

Novel experimental apparatus and desorption fluorescence method.

Bovine femurs

4

0.19 ± 0.02 (8% compression, using 40 kDa dextran)

[27, 28]

  

   Compressed cartilage

 

~

 
    

0.52 ± 0.06 (8% compression, using 430 Da TMR)

 
  1. For studies investigating anisotropic diffusivity, the smallest to the largest value of the diffusion coefficient is reported. (Temp.: Temperature, Ref.: Reference)