Purpose
To determine whether high-fluence photoactivated chromophore for keratitis cross-linking (PACK-CXL) can be accelerated.
Methods
Solutions of
Staphylococcus aureus
and
Pseudomonas aeruginosa
with 0.1% riboflavin were prepared and exposed to 365 nm ultraviolet (UV)-A irradiation of intensities and fluences from 9 to 30 mW/cm
2
and from 5.4 to 15.0 J/cm
2
, respectively, representing nine different accelerated PACK-CXL protocols. Irradiated solutions and unirradiated controls were diluted, plated, and inoculated on agar plates so that the bacterial killing ratios (BKR) could be calculated. Additionally, strains of
Achromobacter xylosoxidans, Staphylococcus epidermidis
, and
Stenotrophomonas maltophilia
were exposed to a single accelerated PACK-CXL protocol (intensity: 30 mW/cm
2
, total fluence: 15.0 J/cm
2
).
Results
With total fluences of 5.4, 10.0, and 15.0 J/cm
2
, the range of mean BKR for
S. aureus
was 45.78% to 50.91%, 84.13% to 88.16%, and 97.50% to 99.90%, respectively; the mean BKR for
P. aeruginosa
was 69.09% to 70.86%, 75.37% to 77.93%, and 82.27% to 91.44%, respectively. The mean BKR was 41.97% for
A. xylosoxidans
, 65.38% for
S. epidermidis
, and 78.04% for
S. maltophilia
for the accelerated PACK-CXL protocol (30 mW/cm
2
, 15 J/cm
2
).
Conclusions
The BKR of high-fluence PACK-CXL protocols can be accelerated while maintaining a high, but species-dependent, BKR. The Bunsen to Roscoe law is respected in fluences up to 10 J/cm
2
in
S. aureus
and
P. aeruginosa
, whereas fluences above 10 J/cm
2
show strain dependence.
Translational Relevance
The high-fluence PACK-CXL protocols can be accelerated in clinical practice while maintaining high levels of BKR.