1999
DOI: 10.1117/12.350041
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Selective RPE photodestruction: mechanism of cell damage by pulsed-laser irradiance in the ns to μm time regime

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Cited by 10 publications
(24 citation statements)
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“…Consequently the thresholds for cell death (412 mJ/cm ) and for bubble detection (456 mJ/cm^) are both higher than for 12 nsec pulses. However, this increase in threshold is not as dramatic as the values predicted for bubble formation around a single, isolated melanosome [4]. Mutual heating among the closely-spaced melanosome particles within the RPE cell can be a significant cause for the temperature increase during the microsecond laser pulses, leading to higher temperatures than an isolated melanosome would reach [4].…”
Section: Significancementioning
confidence: 86%
See 3 more Smart Citations
“…Consequently the thresholds for cell death (412 mJ/cm ) and for bubble detection (456 mJ/cm^) are both higher than for 12 nsec pulses. However, this increase in threshold is not as dramatic as the values predicted for bubble formation around a single, isolated melanosome [4]. Mutual heating among the closely-spaced melanosome particles within the RPE cell can be a significant cause for the temperature increase during the microsecond laser pulses, leading to higher temperatures than an isolated melanosome would reach [4].…”
Section: Significancementioning
confidence: 86%
“…However, this increase in threshold is not as dramatic as the values predicted for bubble formation around a single, isolated melanosome [4]. Mutual heating among the closely-spaced melanosome particles within the RPE cell can be a significant cause for the temperature increase during the microsecond laser pulses, leading to higher temperatures than an isolated melanosome would reach [4]. Mutual heating is insignificant for 12 nsec pulses because there is much less heat diffiision outside the particles.…”
Section: Significancementioning
confidence: 88%
See 2 more Smart Citations
“…15 We have demonstrated using a slit lamp adapted laser scanner that SRT can also be achieved in vivo in rabbits by scanning the spot ͑diameter of about one RPE cell͒ of a cw laser across the retina so as to produce microsecond-short exposure at each targeted RPE cell. 16,17 However, accurate dosimetry in a clinical setting will be complicated partly because the absorption coefficient of ocular melanosomes is not well described; available values in the literature [18][19][20][21][22] vary from about 0.2 m −1 to 1.3 m −1 . Furthermore, the number of absorbing melanosomes per RPE cell differs among individuals and is not necessarily uniformly distributed within an individual eye.…”
Section: Introductionmentioning
confidence: 99%