The present disclosure provides bio-imaging devices including multiple, modular (e.g., interchangeable) channels for imaging biological specimens, and methods of using same to obtain mono- or multi-channel images of biological specimens.
Currently available multi-channel bio-imaging devices are known to suffer from “crosstalk” between adjacent channels, especially when the device scans two or more channels simultaneously. Without wishing to be bound by theory, it is presently believed that the crosstalk occurs when light (e.g., excitation light or emission light) from one channel is detected by the optical sensor of another channel, for example when the light scatters or diverges from its intended optical path due to interaction with mirrors, reflectors, glass surfaces, etc. One representation of this crosstalk is illustrated graphically in
One method of reducing or eliminating crosstalk is to scan each channel separately. However, this method is undesirable because it substantially increases the time required to capture a multi-channel bio-image. In addition, changes in the specimen between iterative mono-channel scans may lead to inaccurate results for later-captured channels.
Further, known bio-imaging devices do not permit the user to conveniently change the excitation light source without substantially dismantling the device, or purchasing a new device to add a new excitation source to a research setting. The high cost to purchase a new bio-imaging device to utilize a new excitation source may be prohibitive.
A need therefore continues to exist for improved multi-channel bio-image devices, systems, and methods of analyzing biological substrates. Devices and systems consistent with the present disclosure meet this need.
The present disclosure provides bio-imaging devices including multiple, modular (e.g., interchangeable) channels for imaging biological specimens, and methods of using same to obtain mono- or multi-channel images of biological specimens.
In some embodiments, the present disclosure provides a bio-imaging device comprising: a first optical module; a second optical module; a scan bed configured to support a biological substrate and enable light radiation to pass therethrough; and a scan head disposed below the scan bed and in optical communication with the first optical module and the second optical module, the scan head comprising: a first scan lens in optical communication with the first optical module, a second scan lens in optical communication with the second optical module, a mirror in optical communication with each of the plurality of scan lenses, a first dye limiting filter (e.g., dual bandpass filter) disposed between the first scan lens and the mirror, and a second dye limiting filter (e.g., dual bandpass filter) disposed between the second scan lens and the mirror.
In some embodiments, the present disclosure provides an optical module comprising: a housing including: an aperture configured to permit light radiation to pass therethrough, a locking feature configured to mate with a complementary locking feature of a bio-imaging device, and at least one positioning feature configured to mate with a complementary positioning feature of a bio-imaging device; an illumination source disposed within the housing and configured to generate light radiation; a dichroic splitter disposed in optical communication with the aperture and the illumination source; a reflector disposed in optical communication with the dichroic splitter and the optical sensor; an optical sensor disposed in optical communication with the reflector; and optionally a lens disposed in optical communication with the reflector and the optical sensor.
In some embodiments, the present disclosure provides a bio-imaging device comprising: a scan bed including a surface configured to support a biological specimen; a scan head disposed below the scan bed and including at least one mirror disposed at an acute angle relative to the surface of the scan bed; a first receiver configured to: secure a first optical module as disclosed herein, and optically align the first optical module with a mirror of the scan head; a second receiver configured to: secure a second, different optical module as disclosed herein, and optically align the second, different optical module with a mirror of the scan head.
In some embodiments, the present disclosure provides a kit comprising: a first optical module as disclosed herein; a second, different optical module as disclosed herein; a third, different optical module as disclosed herein; and a bio-imaging device as disclosed herein.
In some embodiments, the present disclosure provides a method of obtaining a bio-image of a biological specimen, the method comprising: mating a first optical module as disclosed herein with a first receiver of a bio-imaging device as disclosed herein; optionally mating a second optical module as disclosed herein with a second receiver of a bio-imaging device as disclosed herein; optionally mating a third optical module as disclosed herein with a third receiver of a bio-imaging device as disclosed herein; placing a biological specimen on the scan bed of the bio-imaging device; and obtaining a single-channel or a multi-channel bio-image of the biological specimen via the first optical module, the optional second optical module, and/or the optional third optical module.
In some embodiments, the present disclosure provides a bio-imaging device comprising: a first optical module receiver configured to mate with a first removable optical module configured to emit and/or detect light for FRET, NIR, red, blue, or green fluorescent imaging; a second optical module receiver configured to mate with a second removable optical module configured to emit light for blue or red fluorescent imaging; a third optical module receiver configured to mate with a third removable optical module configured to emit and/or detect light for NIR or green fluorescent imaging; a scan bed configured to support a biological sample; and a scan head disposed to enable relay of light radiation from the first, second, and third removable optical modules with a biological sample supported by the scan bed, wherein the scan head comprises: a first dye limiting filter disposed between a first lens and a mirror and having at least two working wavelength ranges, and a second dye limiting filter disposed between a second lens and a mirror and having at least two working wavelength ranges that do not overlap with the working wavelength ranges of the first dye limiting filter.
The figures depict various embodiments of this disclosure for purposes of illustration only. One skilled in the art will readily recognize from the following discussion that alternative embodiments of the structures and methods illustrated herein may be employed without departing from the principles of embodiments described herein.
Referring generally to
Bio-Imaging Devices
Bio-imaging devices 100 consistent with the present disclosure generally include a scan bed 1, a scan head 7, and one or more optical module receivers 17 configured to receive (e.g., temporarily secure) an optical module 4. Optionally, the bio-imaging device 100 further includes one or more reflectors 2/3/16 configured to redirect light radiation between the scan head 7 and one or more optical modules 4.
The scan bed 1 is configured to support a specimen S, such as an electrophoresis gel or blot. In some embodiments, the scan bed includes (e.g., consists essentially of or comprises) a plate glass, optionally including an antireflective coating on one or both surfaces to eliminate ghosts from the glass reflection.
The scan head 7 is disposed below the scan bed 1 (e.g., opposite the specimen S) and is configured to align light radiation between the specimen S or a portion thereof and the one or more optical modules 4. The scan head 7 may be configured to move, for example along one or more axes parallel or substantially parallel with the scan bed 1. In general, the scan head 7 includes at least one scan lens 10/11/12, and at least one mirror 6/9 in optical communication with each of the lenses 10/11/12. In some embodiments, the scan head 7 includes one lens 10/11/12 and one mirror 6/9 in optical communication with the lens 10/11/12.
In other embodiments, the scan head 7 includes two lenses 10/11/12, each in optical communication with a single mirror 6/9. In other embodiments, the scan head 7 includes a first lens 10 in optical communication with a first mirror 6, and a second lens 11/12 in optical communication with a second mirror 9.
In still other embodiments, the scan head 7 includes three lenses 10/11/12, each in optical communication with one or more mirrors 6/9. For example, the scan head 7 may include a first lens 10 in optical communication with one mirror 6, a second lens 11 in optical communication with a second mirror 9, and a third lens 12 in optical communication with the first mirror 6 or with the second mirror 9. In the embodiment specifically illustrated in
The at least one mirror 6/9 may include a first mirror 6 and a second, separate mirror 9 or, as shown representatively in the embodiment shown in
The length L1 of the first mirror 6 or first reflective surface 6 may be greater than, about equal to, or less than the length L2 of the second mirror 9 or the second reflective surface 9. In general, the mirrors 6/9 or reflective surfaces 6/9 having longer length Lx will enable reflection of more optical channels without crosstalk between channels.
The mirrors 6/9 or single mirror with multiple reflective surfaces 6/9 may be secured to the scan head 7 via a mirror carrier 8.
In some embodiments, a filter 13/14 (e.g., a dye-limiting filter or a dual bandpass filter) is disposed between the lens 10/11/12 and the mirror 6/9 or the reflective surfaces 6/9 of the mirror. In some embodiments, a first dual bandpass filter 13 having a first pair of working wavelength ranges is disposed between a third lens 12 and the mirror 6/9, and a second dual bandpass filter 14 having a second pair of working wavelength ranges is disposed between a second lens 11 and the mirror 6/9. In some such embodiments, the working wavelength ranges of the two dual bandpass filters do not overlap. For example and without limitation, the first dual bandpass filter 13 may have working wavelength ranges of 320-525 nm and 620-750 nm, while the second dual bandpass filter 14 may have working wavelength ranges of 530-620 nm and 760-900 nm.
In general, the working wavelength range(s) of the filter 13/14 corresponds to the wavelength of light emission from the optical module 4 in optical communication with the filter 13/14. For example and without limitation, when the first dual bandpass filter 13 has working wavelength ranges of 320-525 nm and 620-750 nm, the corresponding optical module may be configured to emit blue light (e.g., at about 488 nm) or to emit red light (e.g., at about 638 nm or at about 658 nm or at about 685 nm). As just one more example, when the second dual bandpass filter 14 has working wavelength ranges of 530-620 nm and 760-900 nm, the corresponding optical module 4 may be configured to emit green light (e.g., at about 532 nm) or to emit NIR light (e.g., at about 780 nm).
Disposing the filters 13/14 between the lens 11/12 and the mirror 6/9 results in reduced crosstalk between optical channels, especially when the working wavelengths of the filters 13/14 do not overlap. Referring now specifically to
The optical module receiver 17 may include one or more side walls 17w configured to abut one or more walls of an optical module 4. The optical module receiver 17w may include at least one positioning pin 19, for example disposed on an inner surface of one of the side walls 17w, to mate with (e.g., temporarily mate with) one or more positioning holes 21 of an optical module 4. The positioning pin(s) 19 may be arranged on one or more side walls 17w and/or on an inner surface of the bio-imaging device 100 to enable alignment of the optical components of the optical module 4 with the optical components of the scan head 7. For example and without limitation, the positioning pins 19 may be arranged in the optical module receiver 17 in an asymmetric pattern to prevent installation of an optical module 4 in an improper orientation.
In some embodiments, the optical module receiver 17 includes a locking feature 20, such as a locking screw nut. The locking feature 20 is configured to mate (e.g., temporarily mate) with a locking feature (e.g., a locking screw) of an optical module 4 to further secure the optical module 4 in the optical module receiver 17.
In some embodiments, the positioning pin(s) 19 are arranged in the optical module receiver 17 to enable only some optical modules 4 to be installed in specific optical module receivers 17 of a bio-imaging device 100. For example and without limitation, arrangement of positioning pins 19 in an optical module receiver 17 may enable installation of a blue light-emitting optical module 4 only in a position that aligns blue light radiation emitted from the optical module 4 with a compatible filter 13/14 disposed in the corresponding optical path 11/102/103, but prevents installation of an optical module 4 that emits radiation incompatible with the filter 13/14 of that optical path 101/102/103.
Optical module receivers 17 consistent with the present disclosure enable convenient alignment of the optical components of an optical module 4 with the optical components of the scan head 7. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 without the need to run alignment procedures. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.1 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.09 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.08 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.07 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.06 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.05 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.04 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.03 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.02 mm without further alignment. In some embodiments, the optical module receiver 17 enables alignment of the optical components of the optical module 4 with the optical components of the scan head 7 within 0.01 mm without further alignment.
The optical module receiver 17 also, in some embodiments, includes an electrical connector 17e configured to engage with the electrical connector 4e of an optical module 4. The electrical connector 17e, when present, is configured to engage with a cable or other data transmission feature (e.g., WiFi or Bluetooth protocol transceiver) to receive and transmit data from and to an engaged optical module 4 and/or with a power supply of the bio-imaging device 100 to provide power to the optical module 4.
In some embodiments, the bio-imaging device 100 further includes one or more reflectors 2/3/16 in optical communication between an optical module 4 and the scan head 7. The reflectors 2/3/16 may be disposed at an angle sufficient to reflect light radiation between the mirror 6/9 and the corresponding optical module 4.
In some embodiments, the present disclosure provides a bio-imaging device 100 comprising: a first optical module 4; a second optical module 4; a scan bed 1 configured to support a biological substrate S and enable light radiation to pass therethrough; and a scan head 7 disposed below the scan bed 1 and in optical communication with the first optical module 4 and the second optical module 4, the scan head 7 comprising: a first scan lens 10/11/12 in optical communication with the first optical module 4, a second scan lens 10/11/12 in optical communication with the second optical module 4, a mirror 6/9 in optical communication with each of the plurality of scan lenses 10/11/12, a first dye limiting filter 13/14 (e.g., dual bandpass filter) disposed between the first scan lens 10/11/12 and the mirror 6/9, and a second dye limiting filter 13/14 (e.g., dual bandpass filter) disposed between the second scan lens 10/11/12 and the mirror 6/9. In some embodiments, the bio-imaging device 100 comprises: a first optical module receiver 17; a first optical module 4 configured to reversibly mate with the first optical receiver 17; a second optical module receiver 17; and a second optical module 4 configured to reversibly mate with the second optical receiver 17. In some embodiments, the first optical module 4 comprises: a housing 4h including: an aperture 5 configured to permit light radiation to pass therethrough, a locking feature 22 configured to mate with a complementary locking feature 20 of the bio-imaging device, and at least one positioning feature 21 configured to mate with a complementary positioning feature 19 of the bio-imaging device 100; an illumination source 23 disposed within the housing 4h and configured to generate light radiation; a dichroic splitter 25 disposed in optical communication with the aperture 5 and the illumination source 23; a reflector 26 disposed in optical communication with the dichroic splitter 25 and the optical sensor 30/31; an optical sensor 30/31 disposed in optical communication with the reflector 26; and optionally a lens 27 disposed in optical communication with the reflector 25 and the optical sensor 30/31; and the second optical module 4 comprises: a second housing 4h including: a second aperture 5 configured to permit light radiation to pass therethrough, a second locking feature 22 configured to mate with a second complementary locking feature 20 of the bio-imaging device 100, and at least one second positioning feature 21 configured to mate with a complementary second positioning feature 19 of the bio-imaging device 100; a second illumination source 23 disposed within the second housing 4h and configured to generate light radiation; a second dichroic splitter 25 disposed in optical communication with the second aperture 5 and the second illumination source 23; a second reflector 26 disposed in optical communication with the second dichroic splitter 25 and the second optical sensor 30/31; a second optical sensor 30/31 disposed in optical communication with the second reflector 26; and optionally a second lens 27 disposed in optical communication with the second reflector 26 and the second optical sensor 30/31; a scan bed 1 configured to support a biological substrate S and enable light radiation to pass therethrough; and a scan head 7 disposed below the scan bed 1 and including: a plurality of scan lenses 10/11/12, and a mirror 6/9 in optical communication with each of the plurality of scan lenses 10/11/12. In some embodiments, the bio-imaging device 100 further comprises: a third optical module receiver 17; and a third optical module 4 configured to reversibly mate with the third optical receiver 17. In some embodiments, the third optical module 4 comprises: a third housing 4h including: a third aperture 5 configured to permit light radiation to pass therethrough, a third locking feature 22 configured to mate with a third complementary locking feature 20 of the bio-imaging device 100, and at least one third positioning feature 21 configured to mate with a complementary third positioning feature 19 of the bio-imaging device 100; a third illumination source 23 disposed within the third housing 4h and configured to generate light radiation; a third dichroic splitter 25 disposed in optical communication with the third aperture 5 and the third illumination source 23; a third reflector 26 disposed in optical communication with the third dichroic splitter 25 and the third optical sensor 30/31; a third optical sensor 30/31 disposed in optical communication with the third reflector 26; and optionally a third lens 27 disposed in optical communication with the second reflector 26 and the second optical sensor 30/31. In some embodiments, the mirror 6/9 includes at least two reflective faces 6, 9. In some embodiments, a first face 6 of the mirror is configured to place a first scan lens 10 in optical communication with the first optical module 4. In some embodiments, a second face 9 of the mirror is configured to place a second scan lens 11 in optical communication with the second optical module 4. In some embodiments, the first face 6 of the mirror or the second face 9 of the mirror is configured to place a third scan lens 12 in optical communication with the third optical module 4. In some embodiments, the scan head 7 is configured to move relative to the scan bed 1. In some embodiments, the scan head 7 is in optical communication with the third optical module 4 and further comprises a third scan lens 10/11/12 in optical communication with the third optical module 4. In some embodiments, the scan head 7 does not include a dye limiting filter 13/14 disposed between the third scan lens 10/11/12 and the mirror 6/9. In some embodiments, the first dye limiting filter 13/14 is a dual bandpass filter. In some embodiments, the dual bandpass filter has a first working wavelength range of 320-525 nm and a second working wavelength range of 620-750 nm. In some embodiments, the second dye limiting filter is a dual bandpass filter. In some embodiments, the second dual bandpass filter has a working wavelength range that does not overlap with a working wavelength range of the first dye limiting filter. In some embodiments, the second dual bandpass filter has a first working wavelength range of 530-620 nm and a second working wavelength range of 760-900 nm.
In some embodiments, the present disclosure provides a bio-imaging device 100 comprising: a first optical module receiver 17 configured to mate with a first removable optical module 4 configured to emit and/or detect light for FRET, NIR, red, blue, or green fluorescent imaging; a second optical module receiver 17 configured to mate with a second removable optical module 4 configured to emit and/or detect light for blue or red fluorescent imaging; a third optical module receiver 17 configured to mate with a third removable optical module 4 configured to emit and/or detect light for NIR or green fluorescent imaging; a scan bed 1 configured to support a biological sample S; and a scan head 7 disposed to enable relay of light radiation from the first, second, and third removable optical modules 4 with a biological sample S supported by the scan bed 1, wherein the scan head 7 comprises: a first dye limiting filter 13/14 disposed between a first lens 10/11/12 and a mirror 6/9 and having at least two working wavelength ranges, and a second dye limiting filter 13/14 disposed between a second lens 10/11/12 and a mirror 6/9 and having at least two working wavelength ranges that do not overlap with the working wavelength ranges of the first dye limiting filter 13/14. In some embodiments, the scan head 7 comprises: a first reflective surface 6 configured to redirect light emitted by the first removable optical module 4 to the biological sample S; and a second reflective surface 9 configured to redirect light emitted by the second removable optical module 4 and the third removable optical module 4 to the biological sample S. In some embodiments, the scan 7 head comprises: a first lens 10 disposed between the first reflective surface 6 and the scan bed 1 and configured to focus light emitted by the first removable optical module 4 to the scan bed 1; a second lens 11 disposed between the second reflective surface 9 and the scan bed 1 and configured to focus light emitted by the second removable optical module 4 to the scan bed 1; and a third lens 12 disposed between the second reflective surface 9 and the scan bed 1 and configured to focus light emitted by the third removable optical module 4 to the scan bed 1. In some embodiments, the bio-imaging device 100 further comprises: a first filter 13 disposed between the first reflective surface 6 and the first lens 10 and configured to enable passage of FRET, NIR, red, green, and blue light; a second filter 13 disposed between the second reflective surface 9 and the second lens 11 and configured to enable passage of blue and red light; and a third filter 14 disposed between the second reflective surface 9 and the third lens 12 and configured to enable passage of NIR and green light. In some embodiments, a working wavelength range of the second filter 13 does not overlap with a working wavelength range of the third filter 14. In some embodiments, the first filter 13 between the first lens 10 and the mirror 6 is not present. In some embodiments, the second filter 13 is a 320-525 nm/620-750 nm dual bandpass filter. In some embodiments, the third filter 14 is a 530-620 nm/760-900 nm dual bandpass filter. In some embodiments, the second optical module receiver 17 is configured to not mate with an optical module 4 configured to emit fluorescent, NIR, or green light. In some embodiments, the third optical module receiver 17 is configured not to mate with an optical module 4 configured to emit FRET, red, or blue light.
Optical Modules
Referring now to
The housing 4h may include a aperture 5 through which light radiation may enter and/or exit the housing 4h. In some embodiments, the aperture 5 is an aperture in the housing 4h.
The housing 4h also generally includes positioning features 21 configured to mate (e.g., temporarily mate) with positioning pins 19 of a corresponding optical module receiver 17. In some embodiments, the positioning features 21 are disposed to enable an optical module 17 to mate only with fewer than all optical module receivers 17 of a bio-imaging device 100. For example and without limitation, the positioning features 21 of an optical module 17 including a light emitter 23 that emits a near infrared (NIR) light may enable installation of the optical module 17 in an optical module receiver 17 of a bio-imaging device 100 aligned with a filter 13/14 that allows passage of NIR light but not with an optical module receiver 17 of the bio-imaging device 100 aligned with a filter 13/14 that does not enable passage of NIR light.
In some embodiments, the housing 4h includes an electrical connector 4e configured to mate with the electrical connector 17e of a corresponding optical module receiver 17. The electrical connector 4e may be configured, for example, to enable transmission of data and/or power to and/or from the bio-imaging device 100.
The housing 4h may also include a locking feature 22, such as a screw, configured to mate (e.g., temporarily mate) with the locking feature 20 of the optical module receiver 17. When engaged with the locking feature 20 of the optical module receiver, the locking feature 22 of the housing 4h may align (e.g., substantially align) the optical path 101/102/103 of the optical module 4 with the scan head 7, for example within 0.1 mm, within 0.09 mm, within 0.08 mm, within 0.07 mm, within 0.06 mm, within 0.05 mm, within 0.04 mm, within 0.03 mm, within 0.02 mm, or within 0.01 mm.
The housing 4h may support optical components including, for example, a light source 23. The light source 23 may emit light suitable for FRET, NIR, red, blue, or green fluorescent imaging. The light source 23 may be a laser.
The emitted light may optionally pass through an excitation filter 24 with optical properties corresponding to the wavelength of emitted light.
The emitted light may strike a dichroic splitter 25 configured to reflect the emitted light through the aperture 5. The light reflected through the aperture 5 may then be redirected by the mirror 6/9 or one of the reflective surfaces 6/9 of the mirror, optionally after being redirected by a reflector 2/3/16, if present.
In some embodiments, such as those generally consistent with the embodiment shown representatively in
In other embodiments, such as those generally consistent with the embodiment shown representatively in
The aperture 5 is configured to enable light emitted by or transmitted by the biological sample S on the scan bed 1 via the scan head 7 and optional reflector 2/3/16 to reenter the housing 4h. Upon reentry, the light passes through the dichroic splitter 25 to the sensor 30/31, via the optional internal reflector 26, the lens 27, the emission filter 28, and aperture 29.
In some embodiments, the present disclosure provides an optical module 4 comprising: a housing 4h including: an aperture 5 configured to permit light radiation to pass therethrough, a locking feature 22 configured to mate with a complementary locking feature 20 of a bio-imaging device 100, and at least one positioning feature 21 configured to mate with a complementary positioning feature 19 of a bio-imaging device 100; an illumination source 23 disposed within the housing 4h and configured to generate light radiation; a dichroic splitter 25 disposed in optical communication with the aperture 5 and the illumination source 23; a reflector 26 disposed in optical communication with the dichroic splitter 25 and the optical sensor 30/31; an optical sensor 30/31 disposed in optical communication with the reflector 26; and optionally a lens 27 disposed in optical communication with the reflector 26 and the optical sensor 30/31. In some embodiments, the optical module 4 further comprises an excitation filter 24 in optical communication with the illumination source 23 and the dichroic splitter 25. In some embodiments, the optical module 4 further comprises an emission filter 28 disposed in optical communication with the lens 27 and the optical sensor 30/31. In some embodiments, the optical module 4 further comprises a second aperture 29 disposed between the lens 27 and the optical sensor 30/31. In some embodiments, the optical sensor 30 is disposed within the housing. In some embodiments, the optical sensor 31 is disposed on an exterior surface of the housing 4h. In some embodiments, the illumination source 23 emits light radiation having a wavelength of 488 nm, 532 nm, 638 nm, 658 nm, 685 nm, or 780 nm. In some embodiments, the optical module 4 is configured to illuminate a specimen and/or receive light from a specimen for phosphor imaging, FRET imaging, NIR imaging, red fluorescent imaging, green fluorescent imaging, or blue fluorescent imaging. In some embodiments, the at least one positioning feature 21 is disposed to prevent the optical module 4 from being inserted into one or more optical module receivers 17 of a multi-receiver bio-imaging device 100. In some embodiments, the locking feature 21 is configured to mate with the complementary positioning feature 19 of a bio-imaging device 100 to align the optical sensor with a scan head of the bio-imaging device within 0.1 mm, within 0.08 mm, within 0.06 mm, within 0.04 mm, within 0.03 mm, within 0.02 mm, or within 0.01 mm.
Methods of Use
The present disclosure provides methods of obtaining a bio-image of a sample S, such as a multi-channel bio-image of the sample S. In some embodiments, the method results in capture of a multichannel bio-image with reduced (e.g., substantially reduced) crosstalk (e.g., interference) between the various channels.
Generally, a method of the present disclosure comprises installing one or more optical modules 4 corresponding to the desired illumination channel(s) in a bio-imaging device 100 including one or more optical module receivers 17; placing a biological sample S on a scan bed 1 of the bio-imaging device 100; illuminating the biological sample S with light emitted by the one or more installed optical module(s) 4; and collecting data captured by sensors 30/31 of the optical module(s) 4.
In operation, the filters 13/14 reduce or even eliminate (e.g., substantially eliminate) crosstalk between optical channels. Generally, the term “crosstalk” refers to signal observed by an optical sensor 30/31 of one channel of an imaging instrument that originates from a second, different channel of the imaging instrument. Reduction or elimination of crosstalk in multichannel imaging devices has been a persistent problem in the art.
In one embodiment, optical channel 101 includes an optical module 4 configured to emit blue light (e.g., having an excitation wavelength of about 488 nm). The working wavelength of the excitation beam filter 24 of the optical module 4 is about 488 nm, and the working wavelength of the fluorescence filter 28 of the optical module 4 is about 513 nm. Optical channel 102 includes a second optical module 4 configured to emit red light (e.g., having an excitation wavelength of about 685 nm). The working wavelength of the excitation beam filter 24 of the second optical module 4 is about 685 nm, and the working wavelength of the fluorescence filter 28 of the optical module 4 is about 720 nm. Optical channel 103 includes a third optical module 4 configured to emit green light (e.g., having an excitation wavelength of about 532 nm). The working wavelength of the excitation beam filter 24 of the third optical module 4 is about 532 nm, and the working wavelength of the fluorescence filter 28 of the third optical module 4 is about 572 nm.
In operation, the blue excitation light emitted by the first optical module 4 (e.g., optical channel 101) at about 488 nm passes through the excitation filter 24, and then is deflected out of the aperture 5 of the optical module 4 by the dichroic splitter 25. The excitation beam then impinges upon the reflector 16 and enters the scan head 7. In the scan head 7, the excitation beam is deflected by the scan mirror 6 and then passes through the scan lens 10, through the scan bed 1 and to the sample S. The fluorescence emission from the sample S is directed along a path substantially retracing the path 101 of the excitation beam through the scan lens 10, then to the mirror 6 and reflector 16 and back into the optical module 4 via the aperture 5. Once in the optical module 4, the fluorescence emission passes through the dichroic splitter 25, is reflected by a fluorescence reflector 26, then passes through the lens 27, the fluorescence filter 28, the aperture 29 and is finally detected by a photoelectric sensor 30/31.
Simultaneously or nearly simultaneously, red light emitted by the second optical module 4 (e.g., optical channel 102) at about 685 nm passes through the excitation filter 24, and then is deflected out of the aperture 5 of the second optical module 4 by the dichroic splitter 25. The red excitation beam then impinges upon the reflector 2 and enters the scan head 7. In the scan head 7, the excitation beam is deflected by the scan mirror 9 and then passes through the dual bandpass filter 14, through the scan lens 11, and through the scan bed 1 to the sample S. The fluorescence excited by the beam passes from the sample S through the scan lens 11 and the dual bandpass filter 14 before being reflected by the scan mirror 9 and the reflector 2 to the second optical module 4 via the aperture 5. Once in the second optical module 4, the fluorescence emission passes through the dichroic splitter 25, is reflected by a fluorescence reflector 26, then passes through the lens 27, the fluorescence filter 28, the aperture 29 and is finally detected by a photoelectric sensor 30/31.
Simultaneously or nearly simultaneously, green light emitted by the third optical module 4 (e.g., optical channel 103) at about 532 nm passes through the excitation filter 24, and then is deflected out of the aperture 5 of the third optical module 4 by the dichroic splitter 25. The green excitation beam then impinges upon the reflector 3 and enters the scan head 7. In the scan head 7, the excitation beam is deflected by the scan mirror 9 and then passes through the dual bandpass filter 13, through the scan lens 12, and through the scan bed 1 to the sample S. The fluorescence excited by the beam passes from the sample S through the scan lens 12 and the dual bandpass filter 13 before being reflected by the scan mirror 9 and the reflector 3 to the third optical module 4 via the aperture 5. Once in the third optical module 4, the fluorescence emission passes through the dichroic splitter 25, is reflected by a fluorescence reflector 26, then passes through the lens 27, the fluorescence filter 28, the aperture 29 and is finally detected by a photoelectric sensor 30/31.
Due at least in part to scattering from reflector 2, part of the excitation light from optical channel 102 is undesirably scattered and might enter the scan lens 12 in optical channel 103. However, the working wavelength of the dual bandpass filter 13 in channel 103 blocks all or substantially all of the scattered excitation beam from adjacent optical channel 102 from entering the scan lens 12 of optical channel 103, thus reducing or even eliminating crosstalk. Similarly, scattering from reflector 3 of optical channel 103 may ordinarily undesirably enter lens 11 of optical channel 102. However, the working wavelength of the dual bandpass filter 14 in optical channel 102 blocks all or substantially all of the scattered excitation beam from adjacent optical channel 103 from entering the scan lens 11 of optical channel 102, thus reducing or even eliminating crosstalk.
Crosstalk also may ordinarily result from scattering of excitation and/or emission light from the scan bed 1. However, disposing the dual bandpass filters 13, 14 between the lens 11, 12 and the mirror 6/9 reduces or eliminates undesirable crosstalk from light scattered by the scan bed 1.
The step of installing the optical module(s) 4 into the bio-imaging device 100 may include mating one or more positioning features 21 of the optical module 4 with positioning features 19 of the optical module receivers 17 of the bio-imaging device 100. The step of installing the optical module(s) 4 may also or alternatively include securing a locking feature 22 of the optical module 4 to a locking feature 20 of the optical module receiver 17.
In some embodiments, the step of installing the optical module 4 is sufficient to align (e.g., substantially align) the optical path 101/102/103 created by the optical module 4 with the scan head 7 of the bio-imaging device 100. In some embodiments, installing the optical module 4 in the optical module receiver 17 by mating the complementary positioning features 19, 21 and/or securing the complementary locking features 20, 22 aligns the optical path 101/102/103 created by the optical module 4 with the scan head 7 within 0.1 mm, within 0.09 mm, within 0.08 mm, within 0.07 mm, within mm, within 0.05 mm, within 0.04 mm, within 0.03 mm, within 0.02 mm, or within 0.01 mm.
In some embodiments, the method does not include a step of adjusting an alignment of the optical path 101/102/103 created by the optical module 4 with the scan head 7 after the step of mating the complementary positioning features 19, 21 and/or securing the complementary locking features 20, 22 is complete. In some embodiments, the method does not include a step of adjusting an alignment of the optical path 101/102/103 created by the optical module 4 with the scan head 7 before the step of mating the complementary positioning features 19, 21 and/or securing the complementary locking features 20, 22 has commenced.
This application claims priority to U.S. Provisional Patent Application Ser. No. 63/393,009, filed on Jul. 28, 2022, the entire contents of which are incorporated herein and relied upon.
Number | Date | Country | |
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63393009 | Jul 2022 | US |