Jack McPartland of Future Buro in Australia will work to turn the figure "0.7%" – which is the United Nations target for aid donations from the Gross Domestic Product (GDP) of developed countries – into a brand that can be communicated to tell the story about the proportionally small amount of financial resources needed to make an impact in the developing world. After branding is created, Future Buro will work to secure partnerships to facilitate donations of 0.7% of incomes, budgets, and media space to expand the reach of targeted communications about the positive impact of foreign aid.

Hideaki Tsutsui of the University of California, Riverside in the U.S. will develop a low-cost stamp to directly print biosensors on maize leaves for colorimetric detection of biotic stresses. The strategy is to develop an immunochromatographic assay using microneedle probes while printing an easily-read color-change detector.

Ian Matthews of Cardiff University in the United Kingdom proposes to develop a self-sampling micro-needle patch device for the collection of small volumes of blood. Micro-needles will be fabricated using Deep Reactive Ion Etching. The device will permit non-refrigerated transport of collected blood for subsequent assays for diagnosis of infectious disease.

Koen Dechering of TropIQ Health Sciences in the Netherlands is developing a high-throughput functional assay to identify new compounds that specifically block transmission of the malaria parasites to their vector hosts, which is a difficult stage to target, and to test candidate drugs. The assay incorporates luciferase- expressing parasites, which emit light as they develop in the mosquito midgut, along with barcoded chemical libraries. In Phase I, they tested several barcoding strategies and identified a bacterium that could be genetically modified to carry a unique barcode for identifying hit compounds selected in the screen. They also developed the luminescent reporter parasite to track transmission. In Phase II, they will further develop the assay for higher throughput, and screen compounds from the Tres Cantos Antimalarial Set and the MMV Validation, Malaria and Pathogen boxes. They will also use the assay to characterize the mechanisms of action of other candidate transmission-blocking compounds.