RESUMEN
Single-photon emission computed tomography images of murine tumors are interpreted as the values of functions on a three-dimensional domain. Motivated by Morse theory, the local maxima of the tumor image functions are analyzed. This analysis captures tumor heterogeneity that cannot be identified with standard measures. Utilizing decreasing sequences of uptake values to filter the images, a modified form of the standard persistence diagrams for 0-dimensional persistent homology as well as novel childhood diagrams are constructed. Applying statistical methods to time series of persistence and childhood diagrams detects heterogeneous uptake of radioactive antibody within tumors over time and distinguishes uptake in two groups of mice injected with different labeled antibodies.
Asunto(s)
Radioisótopos de Indio/farmacocinética , Neoplasias Experimentales/diagnóstico por imagen , Neoplasias Experimentales/metabolismo , Radiofármacos/farmacocinética , Tomografía Computarizada de Emisión de Fotón Único/estadística & datos numéricos , Animales , Transporte Biológico Activo , Línea Celular Tumoral , Biología Computacional , Conceptos Matemáticos , Ratones , Modelos Biológicos , Modelos Estadísticos , Tomografía Computarizada por Tomografía Computarizada de Emisión de Fotón Único/estadística & datos numéricosRESUMEN
BACKGROUND: Though Maytenus senegalensis is one of the medicinal plants widely used in traditional medicine to treat infectious and inflammatory diseases in Africa, there is a lack of safety data regarding its use. Therefore, the study aimed to asselss the safety and tolerability of the antimalarial herbal remedy M. senegalensis. MATERIAL AND METHODS: The study design was an open-label, single-arm, dose-escalation. Twelve eligible male healthy Tanzanians aged 18 to 45 years were enrolled in four study dose groups. Volunteers' safety and tolerability post-investigational-product administration were monitored on days 0 to 7,14, and 56. RESULTS: There were no deaths or serious adverse events in any of the study groups, nor any adverse events that resulted in premature discontinuation. The significant mean changes observed in WBC (p = 0.003), Neutrophils (p = 0.02), Lymphocytes (p = 0.001), Eosinophils (p = 0.009), Alanine aminotransferase (p = 0.002), Creatinine (p = 0.03) and Total bilirubin (p = 0.004) laboratory parameters were not associated with any signs of toxicity or clinical symptoms. CONCLUSIONS: M. senegalensis was demonstrated to be safe and tolerable when administered at a dose of 800 mg every eight hours a day for four days. This study design may be adapted to evaluate other herbal remedies.
RESUMEN
The ability to accurately and noninvasively analyze illicit drugs is important for criminal investigations and prosecution. Current methods involve significant sample pretreatment and most are destructive. The goal of this work is to develop a method based on Raman spectroscopy to classify simulated street drug mixtures composed of one drug component and up to three cutting agents including those routinely found in confiscated illicit street drug mixtures. Spectra were collected on both a homebuilt instrument using a HeNe laser and on a handheld commercial instrument with a 785 nm light source. Mixtures were prepared with drug concentrations ranging from 10 to 100 percent. Optimal preprocessing for the data set included truncating, Savitzky-Golay smoothing, normalization, differentiating, and mean centering. Using principal component analysis (PCA), it was possible to resolve the spectral differences between benzocaine, lidocaine, isoxsuprine, and norephedrine and correctly classify them 100 percent of the time.