From the Bench to the Field in Low-Cost Diagnostics: Two Case Studies

被引:124
作者
Kumar, Ashok A. [1 ]
Hennek, Jonathan W. [1 ]
Smith, Barbara S. [1 ]
Kumar, Shailendra [2 ]
Beattie, Patrick [2 ]
Jain, Sidhartha [2 ]
Rolland, Jason P. [2 ]
Stossel, Thomas P. [3 ,4 ]
Chunda-Liyoka, Catherine [5 ]
Whitesides, George M. [1 ,6 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Diagnost All, Cambridge, MA 02139 USA
[3] Brigham & Womens Hosp, Div Hematol, Boston, MA USA
[4] Brigham & Womens Hosp, Ctr Biomed Innovat, Boston, MA USA
[5] Univ Teaching Hosp, Dept Paediat, Lusaka, Zambia
[6] Harvard Univ, Wyss Inst Biol Inspired Engn, Cambridge, MA 02138 USA
基金
美国国家科学基金会;
关键词
field trials; liver injury; point-of-care diagnostics; sickle cell disease; technology-translation; SICKLE-CELL-ANEMIA; MICROFLUIDIC DEVICES; MULTIPHASE SYSTEMS; DENSE CELLS; PAPER; BLOOD;
D O I
10.1002/anie.201411741
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the growth of research in universities on point-of-care (POC) diagnostics for global health, most devices never leave the laboratory. The processes that move diagnostic technology from the laboratory to the field-the processes intended to evaluate operation and performance under realistic conditions-are more complicated than they might seem. Two case studies illustrate this process: the development of a paper-based device to measure liver function, and the development of a device to identify sickle cell disease based on aqueous multiphase systems (AMPS) and differences in the densities of normal and sickled cells. Details of developing these devices provide strategies for forming partnerships, prototyping devices, designing studies, and evaluating POC diagnostics. Technical and procedural lessons drawn from these experiences may be useful to those designing diagnostic tests for developing countries, and more generally, technologies for use in resource-limited environments.
引用
收藏
页码:5835 / 5852
页数:18
相关论文
共 54 条
[1]  
[Anonymous], 2011, POLITICAL DECLARATIO
[2]   Measuring agreement in method comparison studies [J].
Bland, JM ;
Altman, DG .
STATISTICAL METHODS IN MEDICAL RESEARCH, 1999, 8 (02) :135-160
[3]   Sickle cell disease: From membrane pathophysiology to novel therapies for prevention of erythrocyte dehydration [J].
Brugnara, C .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2003, 25 (12) :927-933
[4]  
BRUGNARA C, 1989, BLOOD, V74, P487
[5]   Power failure: why small sample size undermines the reliability of neuroscience [J].
Button, Katherine S. ;
Ioannidis, John P. A. ;
Mokrysz, Claire ;
Nosek, Brian A. ;
Flint, Jonathan ;
Robinson, Emma S. J. ;
Munafo, Marcus R. .
NATURE REVIEWS NEUROSCIENCE, 2013, 14 (05) :365-376
[6]   Global Health Technology 2.0 [J].
Caldwell, Aya ;
Young, Anna ;
Gomez-Marquez, Jose ;
Olson, Kristian R. .
IEEE PULSE, 2011, 2 (04) :63-67
[7]   Lab-on-a-chip devices for global health: Past studies and future opportunities [J].
Chin, Curtis D. ;
Linder, Vincent ;
Sia, Samuel K. .
LAB ON A CHIP, 2007, 7 (01) :41-57
[8]   Commercialization of microfluidic point-of-care diagnostic devices [J].
Chin, Curtis D. ;
Linder, Vincent ;
Sia, Samuel K. .
LAB ON A CHIP, 2012, 12 (12) :2118-2134
[9]   Microfluidics-based diagnostics of infectious diseases in the developing world [J].
Chin, Curtis D. ;
Laksanasopin, Tassaneewan ;
Cheung, Yuk Kee ;
Steinmiller, David ;
Linder, Vincent ;
Parsa, Hesam ;
Wang, Jennifer ;
Moore, Hannah ;
Rouse, Robert ;
Umviligihozo, Gisele ;
Karita, Etienne ;
Mwambarangwe, Lambert ;
Braunstein, Sarah L. ;
van de Wijgert, Janneke ;
Sahabo, Ruben ;
Justman, Jessica E. ;
El-Sadr, Wafaa ;
Sia, Samuel K. .
NATURE MEDICINE, 2011, 17 (08) :1015-U138
[10]   How do university inventions get into practice? [J].
Colyvas, J ;
Crow, M ;
Gelijns, A ;
Mazzoleni, R ;
Nelson, RR ;
Rosenberg, N ;
Sampat, BN .
MANAGEMENT SCIENCE, 2002, 48 (01) :61-72