scholarly journals Modular microfluidics for point-of-care protein purifications

Lab on a Chip ◽  
2015 ◽  
Vol 15 (8) ◽  
pp. 1799-1811 ◽  
Author(s):  
L. J. Millet ◽  
J. D. Lucheon ◽  
R. F. Standaert ◽  
S. T. Retterer ◽  
M. J. Doktycz

Customizable 3-D fluidic bridges enable low-volume, leak-free connections between multiple masters for integrated point-of-care protein purification strategies in microfluidics.

Cancers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3730
Author(s):  
Parsa Charkhchi ◽  
Cezary Cybulski ◽  
Jacek Gronwald ◽  
Fabian Oliver Wong ◽  
Steven A. Narod ◽  
...  

Ovarian cancer is the second most lethal gynecological malignancy. The tumour biomarker CA125 has been used as the primary ovarian cancer marker for the past four decades. The focus on diagnosing ovarian cancer in stages I and II using CA125 as a diagnostic biomarker has not improved patients’ survival. Therefore, screening average-risk asymptomatic women with CA125 is not recommended by any professional society. The dualistic model of ovarian cancer carcinogenesis suggests that type II tumours are responsible for the majority of ovarian cancer mortality. However, type II tumours are rarely diagnosed in stages I and II. The recent shift of focus to the diagnosis of low volume type II ovarian cancer in its early stages of evolution provides a new and valuable target for screening. Type II ovarian cancers are usually diagnosed in advanced stages and have significantly higher CA125 levels than type I tumours. The detection of low volume type II carcinomas in stage IIIa/b is associated with a higher likelihood for optimal cytoreduction, the most robust prognostic indicator for ovarian cancer patients. The diagnosis of type II ovarian cancer in the early substages of stage III with CA125 may be possible using a higher cutoff point rather than the traditionally used 35 U/mL through the use of point-of-care CA125 assays in primary care facilities. Rapid point-of-care testing also has the potential for effective longitudinal screening and quick monitoring of ovarian cancer patients during and after treatment. This review covers the role of CA125 in the diagnosis and management of ovarian cancer and explores novel and more effective screening strategies with CA125.


2017 ◽  
Vol 17 (21) ◽  
pp. 7149-7156 ◽  
Author(s):  
Animesh Halder ◽  
Probir Kumar Sarkar ◽  
Poulomi Pal ◽  
Subhananda Chakrabarti ◽  
Prantar Chakrabarti ◽  
...  

2020 ◽  
Vol 24 (1) ◽  
pp. 30-33
Author(s):  
Isabelle Vasconcellos ◽  
Diana Mariani ◽  
Marcelo C.V.M. de Azevedo ◽  
Orlando C. Ferreira ◽  
Amilcar Tanuri

2006 ◽  
Vol 175 (4S) ◽  
pp. 154-154
Author(s):  
Michael Alschibaja ◽  
Joerg Massmann ◽  
Armin Funk ◽  
Heiner Van Randenborgh ◽  
Rudolf Hartung ◽  
...  

VASA ◽  
2011 ◽  
Vol 40 (6) ◽  
pp. 429-438 ◽  
Author(s):  
Berent ◽  
Sinzinger

Based upon various platelet function tests and the fact that patients experience vascular events despite taking acetylsalicylic acid (ASA or aspirin), it has been suggested that patients may become resistant to the action of this pharmacological compound. However, the term “aspirin resistance” was created almost two decades ago but is still not defined. Platelet function tests are not standardized, providing conflicting information and cut-off values are arbitrarily set. Intertest comparison reveals low agreement. Even point of care tests have been introduced before appropriate validation. Inflammation may activate platelets, co-medication(s) may interfere significantly with aspirin action on platelets. Platelet function and Cox-inhibition are only some of the effects of aspirin on haemostatic regulation. One single test is not reliable to identify an altered response. Therefore, it may be more appropriate to speak about “treatment failure” to aspirin therapy than using the term “aspirin resistance”. There is no evidence based justification from either the laboratory or the clinical point of view for platelet function testing in patients taking aspirin as well as from an economic standpoint. Until evidence based data from controlled studies will be available the term “aspirin resistance” should not be further used. A more robust monitoring of factors resulting in cardiovascular events such as inflammation is recommended.


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