Real-Time Label-Free Embolus Detection Using In Vivo Photoacoustic Flow Cytometry

Autor: Alexander V. Melerzanov, Dmitry A. Nedosekin, Tareq A. Juratli, Vladimir P. Zharov, James Y. Suen, Ekaterina I. Galanzha, Mustafa Sarimollaoglu, Yulian A. Menyaev, Eric R. Siegel, Mazen A. Juratli
Rok vydání: 2015
Předmět:
Melanomas
Pathology
Cardiovascular Procedures
medicine.medical_treatment
Embolism
Melanoma
Experimental

Cancer Treatment
lcsh:Medicine
030204 cardiovascular system & hematology
Embolectomy
01 natural sciences
Mice
0302 clinical medicine
Medicine and Health Sciences
lcsh:Science
Early Detection of Cancer
Multidisciplinary
medicine.diagnostic_test
Melanoma
Animal Models
Flow Cytometry
3. Good health
Molecular Imaging
Surgical Oncology
Oncology
Optical Equipment
Cauterization
cardiovascular system
Engineering and Technology
Radiology
Anatomy
Research Article
Clinical Oncology
medicine.medical_specialty
Mice
Nude

Equipment
Mouse Models
Surgical and Invasive Medical Procedures
Research and Analysis Methods
Extracorporeal
Flow cytometry
010309 optics
Photoacoustic Techniques
03 medical and health sciences
Model Organisms
Embolus
In vivo
0103 physical sciences
medicine
Animals
ddc:610
cardiovascular diseases
Surgical Excision
business.industry
Lasers
lcsh:R
Cancer
Cancers and Neoplasms
Biology and Life Sciences
medicine.disease
Transplantation
Disease Models
Animal

Ears
lcsh:Q
Clinical Medicine
business
Head
Zdroj: PLoS ONE
PLoS ONE, Vol 11, Iss 5, p e0156269 (2016)
ISSN: 1932-6203
Popis: Thromboembolic events are one of the world's leading causes of death among patients. Embolus or clot formations have several etiologies including paraneoplastic, post-surgery, cauterization, transplantation, or extracorporeal circuits. Despite its medical significance, little progress has been made in early embolus detection, screening and control. The aim of our study is to test the utility of the in vivo photoacoustic (PA) flow cytometry (PAFC) technique for non-invasive embolus detection in real-time. Using in vivo PAFC, emboli were non-invasively monitored in the bloodstream of two different mouse models. The tumor-free mouse model consisted of two groups, one in which the limbs were clamped to produce vessel stasis (7 procedures), and one where the mice underwent surgery (7 procedures). The melanoma-bearing mouse model also consisted of two groups, one in which the implanted tumor underwent compression (8 procedures), and one where a surgical excision of the implanted tumor was performed (8 procedures). We demonstrated that the PAFC can detect a single embolus, and has the ability to distinguish between erythrocyte-rich (red) and leukocyte/platelet-rich (white) emboli in small vessels. We show that, in tumor-bearing mice, the level of circulating emboli was increased compared to tumor-free mice (p = 0.0013). The number of circulating emboli temporarily increased in the tumor-free control mice during vessel stasis (p = 0.033) and after surgical excisions (signed-rank p = 0.031). Similar observations were noted during tumor compression (p = 0.013) and after tumor excisions (p = 0.012). For the first time, it was possible to detect unlabeled emboli in vivo non-invasively, and to confirm the presence of pigmented tumor cells within circulating emboli. The insight on embolus dynamics during cancer progression and medical procedures highlight the clinical potential of PAFC for early detection of cancer and surgery-induced emboli to prevent the fatal thromboembolic complications by well-timed therapy.
Databáze: OpenAIRE