Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Annu Int Conf IEEE Eng Med Biol Soc ; 2020: 1907-1910, 2020 07.
Article in English | MEDLINE | ID: mdl-33018374

ABSTRACT

Two-photon microscopy (TPM) can provide a detailed microscopic information of cerebrovascular structures. Extracting anatomical vascular models from TPM angiograms remains a tedious task due to image degeneration associated with TPM acquisitions and the complexity of microvascular networks. Here, we propose a fully automated pipeline capable of providing useful anatomical models of vascular structures captured with TPM. In the proposed method, we segment blood vessels using a fully convolutional neural network and employ the resulting binary labels to create an initial geometric graph enclosed within vessels boundaries. The initial geometry is then decimated and refined to form graphed curve skeletons that can retain both the vascular shape and its topology. We validate the proposed method on 3D realistic TPM angiographies and compare our results with that obtained through manual annotations.


Subject(s)
Algorithms , Microvessels , Brain/diagnostic imaging , Microscopy , Microvessels/diagnostic imaging , Neural Networks, Computer
2.
Sci Rep ; 7: 43275, 2017 02 23.
Article in English | MEDLINE | ID: mdl-28230188

ABSTRACT

We present a 3D time-lapse imaging method for monitoring mitochondrial dynamics in living HeLa cells based on photothermal optical coherence microscopy and using novel surface functionalization of gold nanoparticles. The biocompatible protein-based biopolymer coating contains multiple functional groups which impart better cellular uptake and mitochondria targeting efficiency. The high stability of the gold nanoparticles allows continuous imaging over an extended time up to 3000 seconds without significant cell damage. By combining temporal autocorrelation analysis with a classical diffusion model, we quantify mitochondrial dynamics and cast these results into 3D maps showing the heterogeneity of diffusion parameters across the whole cell volume.


Subject(s)
Imaging, Three-Dimensional/methods , Microscopy/methods , Mitochondrial Dynamics , Time-Lapse Imaging/methods , HeLa Cells , Humans , Staining and Labeling/methods
SELECTION OF CITATIONS
SEARCH DETAIL
...