Research Papers: Imaging

Tumor bracketing and safety margin estimation using multimodal marker seeds: a proof of concept

[+] Author Affiliations
Tessa Buckle, Patrick T. K. Chin, Nynke S. van den Berg, Claudette E. Loo, Wim Koops, Kenneth G. A. Gilhuijs, Fijs W. B. van Leeuwen

Departments of Radiology and Nuclear Medicine, Division of Diagnostic Oncology at the Netherlands Cancer Institute—Antoni van Leeuwenhoek Hospital, 1066 CX Amsterdam, The Netherlands

J. Biomed. Opt. 15(5), 056021 (October 27, 2010). doi:10.1117/1.3503955
History: Received June 16, 2010; Revised August 31, 2010; Accepted August 31, 2010; Published October 27, 2010; Online October 27, 2010
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* Address all correspondence to: Fijs W. B. van Leeuwen, Departments of Radiology and Nuclear Medicine, Division of Diagnostic Oncology at the Netherlands Cancer Institute—Antoni van Leeuwenhoek Hospital, 1066 CX Amsterdam, The Netherlands. Tel:31-205-126-084; E-mail: fw.v.leeuwen@nki.nl

Accurate tumor excision is crucial in the locoregional treatment of cancer, and for this purpose, surgeons often rely on guide wires or radioactive markers for guidance toward the lesion. Further improvement may be obtained by adding optical guidance to currently used methods, in the form of intra-operative fluorescence imaging. To achieve such a multimodal approach, we have generated markers that can be used in a pre-, intra-, and post-operative setting, based on a cocktail of a dual-emissive inorganic dye, lipids, and pertechnetate. Phantom experiments demonstrate that these seeds can be placed accurately around a surrogate tumor using ultrasound. Three-dimensional bracketing provides delineation of the entire lesion. Combined with the multimodal nature, this provides the opportunity to predetermine the resection margins by validating the placement accuracy using multiple imaging modalities (namely, x ray, MRI, SPECT/CT, and ultrasound). The dual-emissive fluorescent properties of the dye provide the unique opportunity to intra-operatively estimate the depth of the seed in the tissue via multispectral imaging: emission green λmax=520nm5mm penetration versus emission red λmax=660nm12mm penetration. By using particles with different colors, the original geographic orientation of the excised tissue can be determined.

Figures in this Article

One of the main reasons for locoregional treatment failure in oncology is the inability to fully excise the (primary) tumor during surgery. For example, complete resection of cancer is particularly difficult when the tumor is nonpalpable. In such instances, surgical guidance techniques that help optimize the excision are expected to have a positive influence on the clinical outcome.

Initial detection of nonpalpable lesions at pre-operative imaging [Fig. 1] is often followed by image-guided markation of the lesion [Fig. 1]. These procedures typically aim to mark the center of the lesion using guide-wire localization (WL), radio-guided occult lesion localization (ROLL), or radioactive seed localization (RSL). In WL, a hook is placed in the center of the tumor and attached to a guide-wire12 along which the surgeon can excise the tissue. In ROLL, a nonspecific radiotracer (Tc99m-NanoColl or sulfur-colloid) is injected into the tumor prior to surgery.3 The radioactive signal is then used to acoustically localize the lesion intra-operatively using a gamma probe. Radioactive seed localization (RSL) provides an alternative radio guidance method to ROLL using titanium marker seeds filled with a small amount of radioactive iodine (I125).47

Graphic Jump LocationF1 :

Schematic representation of the combined pre-, intra-, and post-operative imaging paradigm that can be achieved with multimodal marker seeds. (a) Tumor diagnosing imaging procedure. (b) Image-guided placement of bracketing tumor marker seeds. (c) Pre-operative validation of the marker placement accuracy. (d) Optical intra-operative detection of the tumor markers. (e) Geographical (re)orientation of the excised tissue section at pathology.

Image-guided localization is typically carried out using x-ray imaging [such as (stereotactic) mammography (XM)], ultrasonography (US), or magnetic resonance imaging (MRI).4,68 Although WL, ROLL, and RSL all aid in the localization of cancer during surgery, accurate marker placement remains crucial. Hence, accurate verification of the marker relative to the tumor location in one or multiple preoperative imaging modalities may be useful. This strategy requires the localization markers to be visible in the same modality that was used to visualize the tumor. Clearly, the latter may vary for different tumor types and sites.

Intra-operative fluorescence imaging is emerging as an optical detection method in surgical oncology. Fluorescent dyes such as fluorescein and indocyanine green (ICG) are used in several different applications in patients, mostly for superficial imaging of blood flow or lymph node detection.912 Surprisingly, the potential of this optical modality in tumor-localization applications is currently unexplored. Nevertheless, it can be used to overcome an important shortcoming of the current acoustic radioguidance methods—namely, by providing real-time optical guidance.

To eliminate the need for margin re-excision, it is vital that surgical resection margins do not contain any residual tumor tissue. For this reason, an additional small tumor-free margin around the tumor, the so-called surgical safety margin, is often excised.1314 Different fluorescent wavelengths have different degrees of tissue penetration. While visual dyes (emission 400to600nm) can be detected only superficially, far-red and near-infrared dyes (emissions 650nm) give a much higher degree of tissue penetration, but can be detected only with a light-sensitive camera system.15 This difference in tissue penetration can be used to provide a rough estimate of the depth of the marker in the tissue. Multispectral fluorescence imaging thereby enables differentiation between simultaneous emissions at different wavelengths.1617 Specifically for this purpose, we have previously developed dual-emissive (inorganic) dyes that have a visible green emission and a far-red emission that can be accurately detected without autofluorescence.18

Improved macroscopic localization methods may also be beneficial post-operatively at pathology. To report the presence of cancer on the resection edges back to the surgeon for potential re-excision, the pathologist typically indicates the direction in which the positive edge was observed. Commonly, India ink and sutures are used to mark the original orientation of the excised tissue in the patient.19 Three-dimensional bracketing of a lesion with differently “colored” marker seeds may provide an opportunity to record the relative location and orientation of the tumor in individual patients.

The technical challenge we have set out to solve is the development of marker seeds that (1) can be accurately placed at different positions surrounding the lesion and thereby implementing a safety margin [Fig. 1]; (2) can be pre-operatively detected using the same imaging technique employed to diagnose the lesion rather than only with the modality used for bracketing [Fig. 1]; (3) can be optically located during surgical procedures [Fig. 1]; and (4) will provide information about specimen orientation for pathologists [Fig. 1] after excision of the lesion. To incorporate all these properties into a single marker, we have generated multimodal marker seeds that are visible with fluorescence imaging, XM, US, MRI, computed tomography (CT), and single-photon emission computed tomography (SPECT). We have studied their potential in providing surgical guidance in pre-, intra-, and post-operative phantom experiments and in experiments in dead surplus mice.

Dual-Emissive Dyes

Lipid-coated InPZnS particles were synthesized and irradiated as described previously.18 These particles have two separate emissions—namely, an exciton emission at λem=520nm, 600nm, or 660nm (short lifetime) and a defect emission at λmax=660nm [long lifetime >60min; see Figs. 2]. The latter emission can be preilluminated (λem=366nm) and detected without real-time excitation.

Graphic Jump LocationF2 :

Dual-emissive InPZnSn particles and generation of multimodal marker seeds. (a) Schematic representation of dual-emissive InPZnS particles. (b) Normalized fluorescent emission spectra with λem=520nm (exciton green) and λem=660nm (defect; red). (c) Schematic generation of multimodal marker seeds that incorporate dual-emissive dyes and Tc99m lipids. (Color online only.)

For safety margin estimation, green particles (λem=520nm) were used. For geographic tissue orientation, green, orange (λem=600nm), and red (λem=660nm) particles were used. Herein, the colors were used for visual detection.

Creation of Multimodal Marker Seeds

Marker seeds were made of glass capillaries, which were melted and thereby closed at one end. The seed was then filled with a mixture of the dual-emissive InPZnS QDs [see Fig. 2], triton X-100 (10%), and pertechnetate solution (Tc99m; 40MBq50μl). The seed was closed with a small drop of epoxy resin, leaving a small air bubble inside. Total dimension of the seed was 1.0×8.0mm so that it fits in a hollow implantation needle.

Generation Tumor Phantom and Seed Placement

A I125 seed (STM1251, Bard Brachytherapy), situated in a tiny amount of silicone gel, was placed in the center of a piece of tenderloin to act as a tumor phantom. After preillumination, the multimodal marker seeds were placed at different positions surrounding the surrogate tumor under US guidance using a hollow implantation needle (AccuNeedle; 18 gauge, 20cm; Oncura). Alternatively, a seed was placed in the prostate of a surplus dead male mouse.

Imaging Modalities
US

Placement of the multimodal marker in the tissue phantom was conducted under US guidance by an experienced radiologist, using a Hitachi E7U-MT27-S1 US scanning device equipped with a linear probe (6to14MHz) typically used for breast scanning.

X-ray mammography

The phantom tissue was positioned on a Perspex plate (3mm thick). The sample was imaged on an x-ray mammograph (Selenia, Lorad) at 25kV and 85mAs, to provide anatomical detail and to visualize the multimodal seeds and surrogate tumor.

MRI

For MR imaging, the phantom was placed in a clinical Philips Achieva 3.0T MRI scanner (Philips). A standard scanning sequence was used to acquire T2-weighted images using a Flex Small wrist coil. The imaging data was reconstructed using the Achieva scanner software. Kodak viewing software (Kodak) was used to analyze the images.

SPECT/CT

For visualization of the radioactivity inside the seeds, the phantom was placed in an animal holder (Equipment Veterinaire MINERVE) before performing a SPECT/CT scan on the nanoSPECT/CT (Bioscan, Inc.) A region of interest incorporating the whole phantom was selected, based on a (sagittal) tomographic planning x-ray image, and a dual-isotope SPECT scan (I125: 30keV; Tc99m: 140keV) of the same field of view was initialized. Directly after the SPECT imaging sequence, a helical 3-D CT acquisition of the phantom was performed. After acquisition, the CT data was reconstructed with HiSPECT software (Scivis GmbH). The SPECT and CT data sets were automatically co-registered, and the images were analyzed using the InVivoScope post-processing software (Bioscan, Inc.).

Optical spectroscopy and imaging

UV-VIS spectra were recorded using a Perkin Elmer Lambda 900 or Lambda 3b spectrophotometer. Steady state fluorescence spectra were measured with an Edinburgh Instruments FS920 spectrophotometer (λex=450nm; λem=520nm). Long-term decay of the InPZnS defect emission λem=660nm was recorded using the IVIS 200 camera (Xenogen Corp.) using open filter settings (λem=515to885nm). The narrow bandpass filter set of the IVIS 200 system was used to record the defect spectrum of InPZnS QDs in 1-octadecene (λex=366nm, 4-W electrical power, UV light).

Tissues and mice were placed in the temperature-controlled (37°C) imaging chamber of the IVIS 200. The exciton emission was measured with the standard GFP excitation and emission settings (λex=445to490nm; λem=515to575nm; acquisition time: 30s). The defect emission was imaged with open filters (acquisition time: 120s). To determine the tissue penetration of the different emissions, the distance of the seed to the edge of the phantom was decreased by approximately 2mm after every scan. The signal intensities (photonscm2s) were quantified with Living Image 3-D software (Xenogen Corp.). Signal-to-background ratios (SBRs) were calculated using the following formula: SBR=IQDIbackground, where IQD and Ibackground are, respectively, the signal intensities from the exciton/defect emission of the InPZnS QDs and the background signal from surrounding tissue at the respective imaging settings. An SBR ratio >2 was considered to be useful for diagnostic purposes. Tissue penetration experiments were conducted in triplicate.

To combine the ability to pre-operatively set and validate preferred resection margins with optical detection and safety margin estimation, multimodal and dual-emissive marker seeds were generated. The potential of these marker seeds for pre-operative tumor bracketing, intra-operative surgical guidance, and post-operative geographic reorientation was studied.

To illustrate the multimodal seed concept and the potential of these seeds in vivo, seeds were first implanted into the prostate of a dead surplus mouse. After implantation with a hollow needle into the prostate, a SPECT/CT image was made, clearly visualizing the location of the radioactive seed with respect to the anatomy of the mouse (Fig. 3; SPECT/CT). Following the pre-operative SPECT/CT, intra-operative multispectral fluorescence imaging enabled detection of the seed (Fig. 3). Here, the defect emission allows detection without autofluorescence.18 In addition, the visual exciton emission of the InPZnS-particles in the seed could also be detected by eye after excitation with a UV light source [flashlight; Fig. 3]. Due to the small size of the animal and relatively large size of the marker seed, these experiments unfortunately did not enable a form of surgical safety margin estimation.

Graphic Jump LocationF3 :

Imaging of multimodal marker seeds: (a) Schematic representation of the placement of the seed in a mouse prostate. (b) 3-D SPECT/CT image visualizes the seed localization (color-coding: fire) with respect to the mouse anatomy, followed by (c) 660nm emission (color-coding: glow), (d) 520nm emission (color-coding: rainbow) and (e) a visual fluorescent (orange) image of the exposed marker seed. (Color online only.)

The potential use of multimodal marker seeds in surgical safety margin estimation was further investigated in a tissue phantom using a surrogate tumor. After placement under US guidance [Figs. 4 and 4(bI)], the distinctive contrast-generating properties of the seeds could be exploited to differentiate the seeds from their environment. T2-weighted MR imaging provided a clear distinction between the glass seed itself (black) and the lipid content of the seed [white; see Fig. 4(bII)]. With x ray, the difference in density provides a clear distinction between the tissue, the silicone rubber, the titanium shell of the I125-seed, and the glass of the multimodal marker seeds [Fig. 4(bIII)]. Dual-isotope SPECT/CT allowed differentiation between the I125-seed and the Tc99m-containing multimodal marker seeds [see Fig. 4(bIV)].

Graphic Jump LocationF4 :

“Pre-operative” multimodal seed bracketing and placement delineation in a tumor phantom. (a) 3-D tumor bracketing with multimodal marker seeds. Phantom contains a surrogate tumor in a fresh piece of tenderloin. (b) Pre-operative assessment of the marker seed localization using (I) ultrasound—the marker seeds deflect the ultrasound signal enabling accurate detection; (II) T2-weighted MRI—the marker seeds can be accurately discriminated from the surrounding by the lack of signal from the seed and the white signal from its contents; (III) a planar x-ray image—the high attenuation of the seed material is easily detected; and (IV) SPECT/CT—dual-isotope SPECT enables differentiation between Tc99m-containing multimodal marker seeds (color-coding: green) and the I125 containing iodine seed (color-coding: fire). (Color online only.)

To mimic intra-operative surgical safety margin estimation, the phantom was imaged in a multispectral manner at different stages during the resection. For a representation of the tissue penetration at the different emissions, see Fig. 5. Signal-to-background ratios (SBRs) were used to present the ability to detect the different emissions at a different distance from the seed to the surface. The preilluminated defect emission could already be detected while the seed was situated at a distance of 12mm(SBR=2.2), followed by a ten-fold increased SBR at a distance of 5mm [Fig. 5]. In contrast, the exciton signal could be detected only starting at a distance to the surface of 5mm(SBR=2.5).

Graphic Jump LocationF5 :

Margin estimation based on multispectral imaging of dual-emissive seeds. (a) Schematic representation of the tissue penetration depth of the different optical emissions from the marker seeds; fluorescence excitation (λex=366nm; blue) and the emissions λmax=520nm (green) and λmax=660nm (red). (b) Detection of 660nm (color-coding: glow) and 520nm (color-coding; rainbow) emissions during the layer-by-layer exposure of the marker seeds. Fluorescent signal intensities are depicted as signal-to-background ratio (SBR). (Color online only.)

To exploit the value of the fluorescence detection in geographical pathologic guidance, seeds filled with differently colored InPZnS particles were used. These particles emit light at different wavelengths and thus have different visual colors: green: 520nm; orange: 600nm; and red: 660nm [see Fig. 6]. To prove the concept of using 3-D bracketing with marker seeds in geographic tissue (re)orientation, the differently colored seeds were placed on the different sides of a dice. Seeds filled with red particles were placed at position one and six, seeds filled with orange particles were placed at the two and five position, and seeds filled with green particles were placed at position three and four of the dice [Figs. 6]. When placed under a UV light source, it was possible to visually discriminate between the different orientations. The same differentiation is of course possible using different settings on a (multispectral) fluorescence camera.

Graphic Jump LocationF6 :

3-D tumor bracketing for (re)orientation at pathology: (a) Differences in emission peaks of the different InPZnS particles. (b) Schematic representation of 3-D tumor bracketing with differently colored seeds (green/orange/red). (c) Proof of concept on a die allowing accurate visual identification and differentiation of the marker seeds. (Color online only.)

In the clinic, tumor-lesions are often marked before surgical removal. Multimodal markers may extend the use of current tumor marking approaches, as they are applicable during the entire pre-, intra-, and post-operative trajectory. The different properties of our experimental multimodal seeds can be used for (1) accurate seed placement, (2) verification of the placement accuracy, (3) fluorescence guided excision with surgical safety-margins, and (4) ex vivo verification of original specimen orientation.

Clinical Application Seed-Based Tumor Bracketing

Pleijhuis et al. 1 have stated that the restricted visibility of the lesion during excision could explain the high rate of positive resection margins reported in the literature. Although not yet widely applied, one approach to better delineate the outline of larger and more complex lesions is pre-operative placement of markers bracketing the tumor in three dimensions (3-D).2,5 Without increasing the need for re-excision, tumor bracketing can reduce the amount of healthy breast tissue that is unnecessarily removed during tumor excision.20 Bracketing with radioactive seeds has been reported to be of value for nonpalpable breast tumors such as invasive ductal/lobular carcinoma, ductal carcinoma in situ, and papillary carcinoma.45,7 Evidently, the here-reported multimodal seeds can potentially be used in previously reported applications for RSL. An advantage of marker seeds and guidewires over ROLL is that the first two do not suffer from tracer spillage and migration.1 We envision that marker seeds also have more potential in abdominal applications where WL-bracketing is cumbersome; WL-bracketing restricts the surgical access and can be manipulated during patient handling.1,4,7 Furthermore, the use of, e.g., brachytherapy I125-seeds in the prostate is already widely applied.21

Image-Guided Bracketing and Verification of the Placement Accuracy

In the phantom experiments described, seeds were placed at a predetermined position under US guidance. US is one of the modalities frequently used for placement of (bracketing) markers under real-time guidance [Fig. 1].4,6 Although not studied by us, placement under guidance of x ray (CT), SPECT/CT, and MRI is also a possibility with these seeds, as their multimodal character also provides contrast in these modalities (see Fig. 4). Detection of the marker seeds using the same modality that was used to detect the tumor itself [XM, MRI, or SPECT/CT; Fig. 1] can also be achieved due to the multimodal nature of the marker seeds described here (see Fig. 4). This allows for accurate validation of their placement with respect to the tumor edge and surgical margins. For example, when one of the markers is misplaced, the surgical procedure can be slightly redirected during the planning phase [see Fig. 1].

Surgical Guidance

The dual-emissive optical properties of the seeds provide the unique opportunity to optically determine the position of the marker seed during the intervention via real-time multispectral fluorescence imaging [Fig. 1]. The differences in tissue penetration between the separate emissions also offer information about the obtained surgical safety margin (see Fig. 5). Here, sole detection of the 660nm emission suggests that the tumor is located 12mm below the surface, whereas detection of both emissions (520 and 660nm) suggests that the seed is located 5mm below the surface. Hence, when only the 660nm emission is detected, a surgical safety margin of >5mm is retained. This “traffic light approach” underlines the potential of dual-emissive optical properties in a single marker seed.

Post-Operative Geographic Guidance

After surgical planning and excision, histological analysis is performed to assess possible presence of tumor in the resection margins. Herein, geographic orientation of the excised specimen relative to the pre-operative image and the patient is critical. Currently, excised tissue is marked with India ink or sutures.19 When microscopic evaluation of the tissue shows positive resection margins, the location of these markings provides a rough estimate of the location at which more tissue should be excised. Three-dimensional bracketing of a lesion with differently colored marker seeds can be used as an alternative macroscopic marking method. The three-dimensional nature could provide more accurate geographical navigation. We have shown that a color scheme can be used to differentiate between different geographic locations [Fig. 1 and Fig. 6]. It must be noted that accidental damage of the marker seeds could possibly contaminate sectioning tools with dyes and radioactivity. Moreover, their use cannot replace microscopic analysis; it can merely help guide a pathologist to the regions that require detailed analysis.

Marker Seeds as a Versatile Multimodal Container

We have demonstrated that marker seeds can be used as containers that incorporate multiple contrast generating media and have utilized a number of such media viz dual-emissive dyes, Tc99m, and lipids. However, the variations that can be achieved with such containers are endless and mostly depend on the desire of the user. For example, the incorporation of isotopes with a different energy window provides the possibility to detect seeds with different modalities, e.g., PET, or to distinguish individual seeds using dual-isotope SPECT [see Fig. 4(bI)]. The latter can be combined with the use of differently colored dyes, improving the assessment of specimen orientation even further. Other contrast agents can also be incorporated to help improve the visualization/differentiation in the different modalities, e.g., paramagnetic contrast for MRI or alternative dyes.

Clinical Translation

With the described phantom data, we demonstrated the potential use of multimodal marker seeds in tumor bracketing applications. We realize however, that the described seeds are not swiftly translatable to a clinical application. In our opinion, the main limiting effects herein are (1) seed material, (2) the seed contents (the fluorescent component), and (3) real-time intra-operative (multispectral) fluorescence detection.

For a more straightforward clinical translation, perhaps the material of the outer shell of the seed should be adapted. Where the epoxy resin sealed glass seeds provided a relatively easy to produce capsule for our proof-of-concept studies, other materials, e.g., polymer based are also a possibility. Desirable properties for such encapsulating seed materials are transparency and rigidity. The latter will prevent spillage.

A major benefit of the marker seed approach is that the seeds will be removed during the surgical intervention. In combination with the confinement of a closed marker seed, this can aid in the translation of new contrast-generating media that have not yet been approved for (intravenous) clinical exposure. This said, rapid approval for a clinical use is probably most easily obtained using already clinically applied contrast media. In our case, the dual-emissive inorganic dyes used are not clinically approved. We have previously shown, however, that the clinically applied dyes fluorescein and ICG give tissue penetration similar to the two emissions of our dual-emissive inorganic dye.18 Hence, a mixture of fluorescein and ICG can perhaps also be used in such an application.

Ideally, intra-operative visualization should be performed with fast data acquisition. This requires a good SBR and a high sensitivity for the surgical fluorescence cameras. At present, the fairly long acquisition time needed to detect the defect-emission with the IVIS system (120s) compared to the time needed to detect the exciton emission (30s) slows down the acquisition process. Dyes with stronger emission intensities are expected to improve the detection sensitivity. Acquisition, however, also depends highly on the sensitivity of the camera system. Preferably, dye-camera combinations are specifically tailored.

We have provided a proof of concept for using multimodal marker seeds in tumor bracketing and surgical guidance. Using the unique multimodal properties of the seeds, placement accuracy can be validated and resection margins can be predetermined. Moreover, multispectral imaging of the dual-emissive fluorescent content provides the opportunity for estimation of surgical safety margins. Last, the differently colored fluorescent particles provide geographical information to the pathologist regarding the original orientation of the lesion in the patient.

This research is supported, in part, by a KWF-translational research award (Grant No. PGF 2009-4344; FvL) and via FP7-HYPERImage (Grant No. 201651).

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Citation

Tessa Buckle ; Patrick T. K. Chin ; Nynke S. van den Berg ; Claudette E. Loo ; Wim Koops, et al.
"Tumor bracketing and safety margin estimation using multimodal marker seeds: a proof of concept", J. Biomed. Opt. 15(5), 056021 (October 27, 2010). ; http://dx.doi.org/10.1117/1.3503955


Figures

Graphic Jump LocationF1 :

Schematic representation of the combined pre-, intra-, and post-operative imaging paradigm that can be achieved with multimodal marker seeds. (a) Tumor diagnosing imaging procedure. (b) Image-guided placement of bracketing tumor marker seeds. (c) Pre-operative validation of the marker placement accuracy. (d) Optical intra-operative detection of the tumor markers. (e) Geographical (re)orientation of the excised tissue section at pathology.

Graphic Jump LocationF2 :

Dual-emissive InPZnSn particles and generation of multimodal marker seeds. (a) Schematic representation of dual-emissive InPZnS particles. (b) Normalized fluorescent emission spectra with λem=520nm (exciton green) and λem=660nm (defect; red). (c) Schematic generation of multimodal marker seeds that incorporate dual-emissive dyes and Tc99m lipids. (Color online only.)

Graphic Jump LocationF3 :

Imaging of multimodal marker seeds: (a) Schematic representation of the placement of the seed in a mouse prostate. (b) 3-D SPECT/CT image visualizes the seed localization (color-coding: fire) with respect to the mouse anatomy, followed by (c) 660nm emission (color-coding: glow), (d) 520nm emission (color-coding: rainbow) and (e) a visual fluorescent (orange) image of the exposed marker seed. (Color online only.)

Graphic Jump LocationF4 :

“Pre-operative” multimodal seed bracketing and placement delineation in a tumor phantom. (a) 3-D tumor bracketing with multimodal marker seeds. Phantom contains a surrogate tumor in a fresh piece of tenderloin. (b) Pre-operative assessment of the marker seed localization using (I) ultrasound—the marker seeds deflect the ultrasound signal enabling accurate detection; (II) T2-weighted MRI—the marker seeds can be accurately discriminated from the surrounding by the lack of signal from the seed and the white signal from its contents; (III) a planar x-ray image—the high attenuation of the seed material is easily detected; and (IV) SPECT/CT—dual-isotope SPECT enables differentiation between Tc99m-containing multimodal marker seeds (color-coding: green) and the I125 containing iodine seed (color-coding: fire). (Color online only.)

Graphic Jump LocationF5 :

Margin estimation based on multispectral imaging of dual-emissive seeds. (a) Schematic representation of the tissue penetration depth of the different optical emissions from the marker seeds; fluorescence excitation (λex=366nm; blue) and the emissions λmax=520nm (green) and λmax=660nm (red). (b) Detection of 660nm (color-coding: glow) and 520nm (color-coding; rainbow) emissions during the layer-by-layer exposure of the marker seeds. Fluorescent signal intensities are depicted as signal-to-background ratio (SBR). (Color online only.)

Graphic Jump LocationF6 :

3-D tumor bracketing for (re)orientation at pathology: (a) Differences in emission peaks of the different InPZnS particles. (b) Schematic representation of 3-D tumor bracketing with differently colored seeds (green/orange/red). (c) Proof of concept on a die allowing accurate visual identification and differentiation of the marker seeds. (Color online only.)

Tables

References

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