Early and accurate diagnosis of disease is of paramount importance for positive prognosis. Point-of-care testing, defined as testing at or near the site of patient care, is an attractive alternative to laboratory-based testing. By providing results immediately, point-of-care diagnostic devices increase the expediency with which patients can proceed along the proper course of treatment. The goal of this project is to develop a low-cost point-of-care device to be used for the diagnosis of infectious diseases. The development of such a device that is also both sensitive and selective is desirable, yet challenging. We will employ paper-based diagnostics for the direct detection of pathogen-derived enzymes. Specifically, we aim to use fluorogenic peptidic substrates of bacterial/viral proteases (enzymes that catalyze the hydrolysis of peptide bonds) to detect infection by these agents. En route to this device, we envision a multistep process in which issues of sensitivity, selectivity, and reliability will be encountered and addressed systematically. This method of diagnosis should be applicable to any disease in which an enzyme is either misregulated (neoplastic and autoimmune diseases) or merely present (infection). We will focus our initial efforts on the creation of a diagnostic device for the detection of human immunodeficiency virus (HIV) infection. Twenty-five years ago it was discovered that acquired immunodeficiency syndrome (AIDS) is caused by HIV. Despite that knowledge, no cure has yet been developed. As a result, considerable time and effort has been spent developing tools to diagnosis HIV infection. Several immunoassay-based tests have been approved by the FDA, each with their own strengths and weaknesses. In low-resource settings, where HIV is highly prevalent, most of these tests remain restrictively expensive. Thus, the development of a rapid, low-cost test for HIV infection remains an important goal. .

Public Health Relevance

Early and accurate diagnosis of disease leads to improved treatment and faster recovery. This application describes a general method for the design of low-cost paper- based point-of-care diagnostic devices. The method should be applicable to the rapid diagnosis of numerous diseases and will first be applied to human immunodeficiency virus (HIV) infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32AI089698-01
Application #
7911107
Study Section
Special Emphasis Panel (ZRG1-AARR-H (22))
Program Officer
Petrakova, Eva
Project Start
2010-05-18
Project End
2013-05-17
Budget Start
2010-05-18
Budget End
2011-05-17
Support Year
1
Fiscal Year
2010
Total Cost
$45,590
Indirect Cost
Name
Harvard University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
082359691
City
Cambridge
State
MA
Country
United States
Zip Code
02138
Shapiro, Nathan D; Soh, Siowling; Mirica, Katherine A et al. (2012) Magnetic levitation as a platform for competitive protein-ligand binding assays. Anal Chem 84:6166-72
Yoon, Hyo Jae; Shapiro, Nathan D; Park, Kyeng Min et al. (2012) The rate of charge tunneling through self-assembled monolayers is insensitive to many functional group substitutions. Angew Chem Int Ed Engl 51:4658-61
Mace, Charles R; Akbulut, Ozge; Kumar, Ashok A et al. (2012) Aqueous multiphase systems of polymers and surfactants provide self-assembling step-gradients in density. J Am Chem Soc 134:9094-7
Shapiro, Nathan D; Mirica, Katherine A; Soh, Siowling et al. (2012) Measuring binding of protein to gel-bound ligands using magnetic levitation. J Am Chem Soc 134:5637-46