Long-term dry storage of an enzyme-based reagent system for ELISA in point-of-care devices.

Lateral flow devices are commonly used for many point-of-care (POC) applications in low-resource settings. However, they lack the sensitivity needed for many analytes relevant in the diagnosis of diseases. One approach to achieve higher sensitivity is signal amplification, which is commonly used in laboratory assays, but uses reagents that require refrigeration and inherently requires multiple assay steps not normally compatible with POC settings. Enzyme-based signal amplification, such as the one used in ELISA, could greatly improve the limit of detection if it were translated to a format compatible with POC requirements. A signal-amplified POC device not only requires the reagents to be stored in a stable form, but also requires automation of the multiple sequential steps of signal amplification protocols. Here, we describe a method for the long-term dry storage of ELISA reagents: horseradish peroxidase (HRP) conjugated antibody label and its colorimetric substrate diaminobenzidine (DAB). The HRP conjugate retained ∼80% enzymatic activity after dry storage at 45 °C for over 5 months. The DAB substrate was also stable at 45 °C and exhibited no detectable loss of activity over 3 months. These reagents were incorporated into a two-dimensional paper network (2DPN) device that automated the steps of ELISA for the detection of a malarial biomarker. These results demonstrate the potential of enzyme-based signal amplification for enhanced sensitivity in POC devices for low resource settings.

[1]  E. Rock,et al.  Comparative analysis of the Plasmodium falciparum histidine-rich proteins HRP-I, HRP-II and HRP-III in malaria parasites of diverse origin , 1987, Parasitology.

[2]  J. Carpenter,et al.  Stabilization of phosphofructokinase with sugars during freeze-drying: characterization of enhanced protection in the presence of divalent cations. , 1987, Biochimica et biophysica acta.

[3]  J. Carpenter,et al.  Stabilization of phosphofructokinase during air-drying with sugars and sugar/transition metal mixtures. , 1987, Cryobiology.

[4]  J. Carpenter,et al.  Modes of stabilization of a protein by organic solutes during desiccation , 1988 .

[5]  J. Woodward,et al.  Stabilization of analytical enzymes using a novel polymer–carbohydrate system and the production of a stabilized, single reagent for alcohol analysis , 1992 .

[6]  T. Gibson,et al.  Extended shelf life of enzyme-based biosensors using a novel stabilization system☆ , 1992 .

[7]  J. Woodward,et al.  Preservation of shelf life of enzyme based analytical systems using a combination of sugars, sugar alcohols and cationic polymers or zinc ions , 1993 .

[8]  S. Hoffman,et al.  Diagnosis of malaria by detection of Plasmodium falciparum HRP-2 antigen with a rapid dipstick antigen-capture assay , 1994, The Lancet.

[9]  K. Nielsen Stability of freeze dried horseradish peroxidase conjugated monoclonal antibodies used in diagnostic serology. , 1995, Journal of immunoassay.

[10]  D S Reid,et al.  Is trehalose special for preserving dry biomaterials? , 1996, Biophysical journal.

[11]  J. Chirife,et al.  Protective Role of Trehalose on Thermal Stability of Lactase in Relation to its Glass and Crystal Forming Properties and Effect of Delaying Crystallization , 1997 .

[12]  M. Elias,et al.  Trehalose + water fragile system: properties and glass transition , 1999 .

[13]  M. A. Hemminga,et al.  High critical temperature above T(g) may contribute to the stability of biological systems. , 2000, Biophysical journal.

[14]  W. Wang,et al.  Lyophilization and development of solid protein pharmaceuticals. , 2000, International journal of pharmaceutics.

[15]  J. Cabral,et al.  Horseradish peroxidase immobilized through its carboxylic groups onto a polyacrylonitrile membrane , 2003, Applied biochemistry and biotechnology.

[16]  J. D. de Pablo,et al.  Stabilization of Lactate Dehydrogenase Following Freeze-Thawing and Vacuum-Drying in the Presence of Trehalose and Borate , 1998, Pharmaceutical Research.

[17]  S. Yoshioka,et al.  Physical Stability and Protein Stability of Freeze-Dried Cakes During Storage at Elevated Temperatures , 1994, Pharmaceutical Research.

[18]  Il-Hoon Cho,et al.  An enzyme immunoanalytical system based on sequential cross-flow chromatography. , 2005, Analytical chemistry.

[19]  Il-Hoon Cho,et al.  Plastic ELISA-on-a-chip based on sequential cross-flow chromatography. , 2006, Analytical chemistry.

[20]  Yan Zhang,et al.  Development of multianalyte flow-through and lateral-flow assays using gold particles and horseradish peroxidase as tracers for the rapid determination of carbaryl and endosulfan in agricultural products. , 2006, Journal of agricultural and food chemistry.

[21]  You-Lin Wu,et al.  Novel Dry-Type Glucose Sensor Based on a Metal–Oxide–Semiconductor Capacitor Structure with Horseradish Peroxidase + Glucose Oxidase Catalyzing Layer , 2007 .

[22]  R. Peeling,et al.  A guide for diagnostic evaluations , 2006, Nature Reviews Microbiology.

[23]  V. A. Stewart,et al.  Enzyme-Linked Immunosorbent Assay for Detection of Plasmodium falciparum Histidine-Rich Protein 2 in Blood, Plasma, and Serum , 2008, Clinical and Vaccine Immunology.

[24]  P. Yager,et al.  Point-of-care diagnostics for global health. , 2008, Annual review of biomedical engineering.

[25]  Jennifer L. Osborn,et al.  Enabling a microfluidic immunoassay for the developing world by integration of on-card dry reagent storage. , 2008, Lab on a chip.

[26]  Christian Drosten,et al.  Poor Clinical Sensitivity of Rapid Antigen Test for Influenza A Pandemic (H1N1) 2009 Virus , 2009, Emerging infectious diseases.

[27]  Tuomas Näreoja,et al.  Study on nonspecificity of an immuoassay using Eu-doped polystyrene nanoparticle labels. , 2009, Journal of immunological methods.

[28]  Xilin Zhao,et al.  Lateral flow immunoassay using europium chelate-loaded silica nanoparticles as labels. , 2009, Clinical chemistry.

[29]  S. Skidmore Poorly performing point-of-care tests for chlamydia: what can be done? , 2010, Sexually Transmitted Infections.

[30]  Il-Hoon Cho,et al.  Immunogold-silver staining-on-a-chip biosensor based on cross-flow chromatography. , 2010, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[31]  Moses Laman,et al.  Plasma Plasmodium falciparum histidine-rich protein-2 concentrations do not reflect severity of malaria in Papua new guinean children. , 2011, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[32]  Satoshi Ohtake,et al.  Trehalose: current use and future applications. , 2011, Journal of pharmaceutical sciences.

[33]  P. Walde,et al.  Immobilization of peroxidase on SiO2 surfaces with the help of a dendronized polymer and the avidin-biotin system. , 2011, Macromolecular bioscience.

[34]  Paul Yager,et al.  Enhanced sensitivity of lateral flow tests using a two-dimensional paper network format. , 2011, Analytical chemistry.

[35]  Jens Michaelis,et al.  Enhancement of the detection limit for lateral flow immunoassays: evaluation and comparison of bioconjugates. , 2012, Journal of immunological methods.

[36]  G. Whitesides,et al.  Measuring markers of liver function using a micropatterned paper device designed for blood from a fingerstick. , 2012, Analytical chemistry.

[37]  Paul Yager,et al.  Two-dimensional paper network format that enables simple multistep assays for use in low-resource settings in the context of malaria antigen detection. , 2012, Analytical chemistry.

[38]  Lisa Lafleur,et al.  Progress toward multiplexed sample-to-result detection in low resource settings using microfluidic immunoassay cards. , 2012, Lab on a chip.

[39]  Paul Yager,et al.  CO2 laser cutting and ablative etching for the fabrication of paper-based devices , 2013 .

[40]  Paul Yager,et al.  Programming paper networks for point of care diagnostics , 2013, Photonics West - Micro and Nano Fabricated Electromechanical and Optical Components.