Neurochemical variability among individual Drosophila heads has been examined with the sensitivity of electro-chemical detection and the selectivity of micellar electro-kinetic capillary chromatography. Homogenization of single Drosophila heads in volumes as small as 100 nL has been accomplished. Here we demonstrate reproducible separations for single fly heads in 250-nL volumes providing a 4-fold increase in sensitivity without overloading the electrochemical detector. This increase in sensitivity allows detection of previously undetected analytes, such as Nacetyltyramine (naTA) and octopamine (OA). Analytes including L-3,4-dihydroxyphenylalanine, Nacetyloctopamine, N-acetyldopamine, naTA, N-acetylserotonin, OA, dopamine, tyramine, and serotonin also have been consistently identified in single-head homogenates and observed with homogenates representing populations of Drosophila. Neurochemical variation between individual flies as well as the consistency within a population indicates varying amounts of neurotransmitter turnover. The inception, design, and fabrication of a miniature tissue homogenizer has enabled the separation of biogenic amines and metabolites from these severely volume-limited single Drosophila head homogenates.As an organism develops from a single cell to a complex, multicellular being, many changes occur at the cellular and physiological levels. All individuals in a population share similar neurochemical foundations that control diverse neural processes ranging from simple reflexive behaviors to higher order brain functions. Monoamine systems in the central nervous system, in particular, are crucial for motor control, emotion, and cognition. Anomalies in these systems underlie pathogenesis of various neurological and psychiatric disorders including Parkinson's disease, schizophrenia, and depression. 1-4 In normal individuals, subtle differences in monoamine levels and functions are postulated to affect traits and vulnerability to cognitive, addictive, and affective disorders. To facilitate the task of identifying the neurochemical and neurobiological basis of individual traits, it is critical to monitor the availability and turnover of each monoamine from one individual to another.Analytically, great strides have been made to improve methodologies for the analysis of biological microenvironments, which could provide insight into the functional significance of biogenic amines present. Advances in miniaturizing analytical instrumentation have led to an increase in chemical, temporal, and spatial information from a variety of samples. The difficulty