1 September 2008 In-vivo singlet oxygen dosimetry of clinical 5-aminolevulinic acid photodynamic therapy
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J. of Biomedical Optics, 13(5), 050504 (2008). doi:10.1117/1.2981813
Photodynamic therapy (PDT) is a viable treatment option for a wide range of applications, including oncology, dermatology, and ophthalmology. Singlet oxygen is believed to play a key role in the efficacy of PDT, and on-line monitoring of singlet oxygen during PDT could provide a methodology to establish and customize the treatment dose clinically. This work is the first report of monitoring singlet oxygen luminescence in vivo in human subjects during PDT, demonstrating the correlation of singlet oxygen levels during PDT with the post-PDT photobiological response.
Laubach, Chang, Lee, Rizvi, Zurakowski, Davis, Taylor, and Hasan: In-vivo singlet oxygen dosimetry of clinical 5-aminolevulinic acid photodynamic therapy

Photodynamic therapy (PDT) is a viable treatment option for a variety of applications, including oncology, dermatology, and ophthalmology.1 In particular, 5-aminolevulinic acid (ALA)-PDT is widely used to treat a range of dermatologic conditions.2 PDT is based on the interaction of a photosensitizer (PS), light, and oxygen, in which photoactivation of PS generates cytotoxic molecular species. Customized dosimetry could, in principle, impact the efficacy of treatment outcome and of the effective use of resources. Dosimetry in PDT is complex, as the treatment effect is generated by an interaction of multiple components.

A number of dose metrics have been evaluated to monitor the outcome of ALA-PDT in dermatological treatment.3, 4 Since singlet oxygen (O21) , which phosphoresces to the ground triplet state, is believed to be a key cytotoxic species in PDT,1 its direct monitoring is of great interest. Until now, in-vivo optical detection of O21 luminescence at 1270nm remained elusive because of its low signal yield. In recent pioneering works, Niedre 5 and Yamamoto 6 measured PDT-generated O21 luminescence in vivo in mice, and demonstrated its correlation with treatment outcome. Recently, we have developed a fiber-based O21 monitoring device7 that is compatible with human studies. We present the first clinical trial measuring PDT-generated O21 levels in skin of healthy volunteers before and after ALA application, and correlating the O21 luminescence signal with the photobiological effects of ALA-PDT, possibly indicating treatment outcome.

A total of 18 healthy subjects (14 males and 4 females) were enrolled with written, informed consent in the clinical study approved by our internal Institutional Review Board to ensure adherence to the Declaration of Helsinki protocols. Power analysis indicated that the sample size of 18 subjects provided 80% power ( α=0.05 , β=0.20 ) to detect a significant linear relationship between the change in O21 luminescence signal and photobiological skin response following PDT using repeated-measures mixed model regression analysis (version 6.0, nQuery Advisor, Statistical Solutions, Saugus, Massachusetts). A newly developed, entirely fiber-based O21 dosimeter was used to detect O21 luminescence in vivo.7 The device uses a low power, time-resolved diode laser of 635nm ( 10-kHz repetition rate, 5-μs pulse duration, less than 1μJ /pulse) for PS activation. O21 signal was measured at the end of each laser pulse to reduce background fluorescence signal. Simultaneously, three optical signal strengths at 1.22, 1.27, and 1.315μm are recorded using narrow bandpass filters and a photon multiplier tube (PMT) (Hamamatsu H9170-45) with a fast photon counter (model MSA-300, Becker and Hickl, Berlin). The average signal from 1.22 and 1.315 is used to estimate the background signal and then subtracted from the O21 signal at 1.27μm to eliminate background noise. Measurements typically take only a few seconds.

Each subject had two treatment sites on the right upper arm outlined and randomly assigned for ALA-PDT (Levulan Kerastick, DUSA Pharmaceuticals, Wilmington, Massachusetts) with either one-hour (Ishort) or three-hour (Ilong) incubation periods. ALA incubation time was varied to control PS accumulation, keeping in mind that longer incubation times result in increased PpIX levels,8 leading to different O21 production and treatment outcomes. O21 measurements were done before ALA application (pre-ALA) when no exogenous PS was administered and immediately before the therapeutic light dose (pre-PDT) following PpIX production from ALA application.

Following O21 measurements, each treatment site was irradiated with a therapeutic light dose of 20Jcm2 (irradiance 100mWcm2 ) with a separate fiber-based continuous diode laser at 635nm (HPD 7401, High Power Devices, North Brunswick, New Jersey).

Standardized digital photographs of the treatment sites were taken within 15min and at 24h after this treatment and used for the evaluation of phototoxic reactions by four blinded investigators. Each investigator rated the degree of erythema and edema between a scale of 0 (no response) to 10 (most pronounced). Median of the four readings is reported to minimize any potential interobserver variability. The photobiological response to the Ilong treatment sites were more pronounced and more clinically significant compared to Ishort treatment sites (Fig. 1 ). Consistent with Ref. 9, edema and erythema response peaked at 15min and 24h following PDT, respectively. Subsequent analysis was performed using the maximal photobiological skin response: acute edema at 15-min post-PDT and erythema at follow-up 24-h post-PDT. PS-induced O21 signal was defined by change in O21 luminescence between pre-ALA (time of minimum PpIX concentration) and pre-PDT (time of maximum PpIX concentration) time points.

Fig. 1

Representative images of treatment sites with 1h (Ishort) or 3h (Ilong) of ALA application time. The phototoxic reaction in Ilong sites (edema immediately after PDT and erythema 24h afterward) is more intense than in Ishort sites.


Several researchers have shown that the degree of erythema and edema following ALA-PDT is predictive of clinical outcome in various dermatologic conditions.4, 10 To evaluate the relationship between O21 signal and photobiological skin responses (edema and erythema), we applied repeated-measures linear mixed model analysis.11 Using this model, the O21 luminescence signal significantly correlated with acute edema in Ilong sites (P=0.01) and 24-h follow-up erythema for Ilong and Ishort combined (P=0.028) (Table 1 ).

Table 1

Effect of O21 signal on photobiological responses based on a linear mixed model regression analysis of the data. Slope of the linear correlation between O21 signal and photobiological response in either Ishort sites, Ilong sites, or the combined data are reported. Edema is measured at post-PDT; erythema is measured at follow-up. The slope test shows the comparison of slopes estimated from Ishort sites and Ilong sites using an F-test. ST is statistically significant. CI=confidence interval.

O21 signal Edema+ Erythema×
Slope (95% CI) P valueSlope (95% CI) P value
Slope 0.009 (ST)0.527
Ishort −0.002 0.747
Ilong 0.035(0.011, 0.059)0.010 (ST)
Combined sites0.017(0.002, 0.031)0.028 (ST)

Equality of slopes for Ishort and Ilong sites was assessed with an F-test to decide whether a common slope parameter could be modeled to describe this correlation.12 The relationship between erythema and O21 signal showed no significant difference in slopes between Ishort and Ilong sites (P=0.527) . As a result, correlation between follow-up erythema and O21 signal was investigated with a common slope fitted to the combined dataset for the Ishort and Ilong sites (Fig. 2 ). The interpretation is that the percent change in O21 signal from baseline is positively correlated for both sites in a similar way, and thus can be described using a common slope.

Fig. 2

Scatter plots illustrating the relationship between O21 luminescence signal versus (a) acute edema rating and (b) erythema rating 24h after PDT. Regression-based fits to the Ishort , Ilong , and combined data are shown by the red dashed line, the blue dotted line, and the solid green line, respectively. (Color online only.)


On the other hand, the correlation between acute edema and O21 signal was modeled separately for Ishort and Ilong sites because they had unequal slopes (P=0.009) (Fig. 2). In fact, greater edema was significantly correlated with greater percent change from baseline in O21 signal but only for the Ilong sites (P=0.01) , not Ishort sites (P=0.747) (Table 1). Interestingly, only Ilong sites showed a significant correlation between O21 signal and acute edema (Fig. 2). It is possible that the minor acute edema at the Ishort sites (median score of 0.25 out of 10) may not have been clearly discernable by the blinded investigators in a 2-D photograph, and thus may not have correlated significantly with the quantitative O21 signal.

Unexpectedly, a decrease in O21 signal after the incubation period was observed in some treatment sites. This might be related to modification of skin optical properties by ALA and its carrier.13 A carrier-only control treatment site could potentially provide additional information when incorporated in future studies.

This is the first study showing the feasibility of monitoring PS-generated O21 signal in vivo in human subjects. O21 signal measured immediately prior to PDT light irradiation correlated significantly with the photobiological response to ALA-PDT in normal skin. As a result, monitoring O21 production in the skin is predictive of the clinical ALA-PDT outcome and is a helpful tool for customizing the clinical ALA-PDT treatment.


This work was supported by NIH SBIR Phase II grant R44 CA096243 and in part by NIH grant P01 CA84203. We also thank Oleg Akilov, Mehron Puoris’haag, Fernanda Sakamoto, and Kana Watanabe for evaluating the phototoxic response from the clinical photographs.



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Hans Laubach, Sung K. Chang, Seonkyung Lee, Imran Rizvi, David Zurakowski, Steven J. Davis, Charles R. Taylor, Tayyaba Hasan, "In-vivo singlet oxygen dosimetry of clinical 5-aminolevulinic acid photodynamic therapy," Journal of Biomedical Optics 13(5), 050504 (1 September 2008). http://dx.doi.org/10.1117/1.2981813

Photodynamic therapy



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