TY - JOUR
T1 - Simultaneous multiple-level magnification selective plane illumination microscopy (sMx-SPIM) imaging system
AU - S R, Rinsa
AU - Chitre, Kripa
AU - Kurup, Aditya
AU - Nongthomba, Upendra
AU - Murty Srinivasula, Srinivasa
AU - Suheshkumar Singh, Mayanglambam
N1 - Publisher Copyright:
© 2022 IOP Publishing Ltd.
PY - 2022/2
Y1 - 2022/2
N2 - We report an optical-based microscopy imaging technology-simultaneous multiple-level magnification selective plane illumination microscopy (sMx-SPIM) imaging system-that addresses a longstanding technological challenge of obtaining images, specifically of biological specimen non-destructively, at different field of views (FOVs) and spatial resolutions (or magnification powers) simultaneously in real-time. This imaging system provides not only 3D images but also time-resolved sequential images with temporal resolution ∼ msec. Magnification powers (or FOVs) of the individual images can be controlled independently that is achieved by housing two separate detection arms, in SPIM imaging system, fitted with objective lenses of different magnification powers. This unique feature holds promises to observe and study: (a) sub-microscopic details and entire structure of biological specimen side-by-side simultaneously and (b) spatio-temporal dynamics of functional activities of biological specimen. For validation study of robustness of the proposed sMx-SPIM imaging system, experiments are conducted in various biological samples including Danio rerio (zebrafish) embryo, Drosophila melanogaster, Allium cepa root, and A549 cell line. Experimental results demonstrate that the study is of significant impacts from two aspects, viz., technological implication and biological applications.
AB - We report an optical-based microscopy imaging technology-simultaneous multiple-level magnification selective plane illumination microscopy (sMx-SPIM) imaging system-that addresses a longstanding technological challenge of obtaining images, specifically of biological specimen non-destructively, at different field of views (FOVs) and spatial resolutions (or magnification powers) simultaneously in real-time. This imaging system provides not only 3D images but also time-resolved sequential images with temporal resolution ∼ msec. Magnification powers (or FOVs) of the individual images can be controlled independently that is achieved by housing two separate detection arms, in SPIM imaging system, fitted with objective lenses of different magnification powers. This unique feature holds promises to observe and study: (a) sub-microscopic details and entire structure of biological specimen side-by-side simultaneously and (b) spatio-temporal dynamics of functional activities of biological specimen. For validation study of robustness of the proposed sMx-SPIM imaging system, experiments are conducted in various biological samples including Danio rerio (zebrafish) embryo, Drosophila melanogaster, Allium cepa root, and A549 cell line. Experimental results demonstrate that the study is of significant impacts from two aspects, viz., technological implication and biological applications.
KW - 3D biological imaging
KW - imaging
KW - light sheet microscopy or selective plane illumination microscopy
KW - multiple field of views
KW - multiple level magnifications
KW - non-destructive biological imaging
KW - optical microscope
UR - http://www.scopus.com/inward/record.url?scp=85124241244&partnerID=8YFLogxK
U2 - 10.1088/2040-8986/ac4670
DO - 10.1088/2040-8986/ac4670
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:85124241244
SN - 2040-8978
VL - 24
JO - Journal of Optics (United Kingdom)
JF - Journal of Optics (United Kingdom)
IS - 2
M1 - 024010
ER -