Janine Anne Flood
Procter & Gamble
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Janine Anne Flood.
Toxicology | 2009
Katherine Sarlo; Karen Blackburn; Edwin D. Clark; Jeff T. Grothaus; Joel G. Chaney; Suzanne Neu; Janine Anne Flood; Dana Abbott; Clarence Bohne; Keith Casey; Charles Fryer; Mike Kuhn
Understanding tissue distribution and clearance of nanomaterials following different routes of exposure is needed for risk assessment. F344 female rats received single or multiple exposures to 20 nm, 100 nm or 1000 nm latex fluorospheres by intravenous (i.v.) injection or oral pharyngeal aspiration into the airways. The presence of fluorospheres in tissues was assessed up to 90-120 days after the final dose. Blood, perfusion fluid, bone marrow, brain, eyes, feces, gut, heart, kidney, liver, lung, muscle, skin, spleen, thymus, tongue, urine and uterus plus ovaries were collected for analysis. Liver, spleen and lung were the greatest tissue depots for all particles following i.v. injection. The proportion of 100 nm and 1000 nm but not 20 nm spheres significantly increased in the spleen over time. Lung was the greatest tissue depot for all particles following single or repeat airway exposure. Greater than 95% of 1000 nm spheres that were recovered were in the lung in contrast to 70-80% of 20 nm spheres or 89-95% of 100 nm spheres. All 3 sizes were found in gut or gut+feces 1-7 days after lung exposure. The thymus was the largest extra-pulmonary depot for the particles; up to 25% of recovered 20 nm particles were in the thymus up to 4 months after exposure compared to 6% of 100 nm particles and 1-3% of 1000 nm particles. A small proportion of 20 nm particles were detected in kidney following both acute and repeat airway exposure. Low numbers of particles were found in the circulation (blood, perfusion), bone marrow, brain, heart, liver and spleen but not in eye, muscle, skin, tongue, ovaries, uterus or urine. These data show that the tissue targets of nano- and micron-sized spheres are very similar whether exposure occurs systemically or via the airways while the proportion of particles in some tissues and tissue clearance varies based on particle size.
Archive | 2009
Marco Caggioni; Rafael Ortiz; Freddy Arthur Barnabas; Raul Victorino Nunes; Janine Anne Flood; Francesc Corominas
Archive | 2010
Rajan Keshav Panandiker; Kerry Andrew Vetter; Bernard William Kluesener; Iskender Yilgor; Christian Herzig; Richard Becker; Rafael Trujillo Rosaldo; Leslie Dawn Waits; Janine Anne Flood; Keith Homer Baker; Jennifer Beth Ponder; Mark Gregory Solinsky; Matthew Scott Wagner; Pradipta Sarkar; Emily Suzanne Klinker; Julie Ann O'neil
Archive | 2010
Matthew Scott Wagner; Leslie Dawn Waits; Janine Anne Flood; Mark Gregory Solinsky
Archive | 2016
Fernando Ray Tollens; David John Hoying; Janine Anne Flood; Brian Lee Keith; Jessica Lea Ellis
International Journal of Cosmetic Science | 2008
Jennifer Mary Marsh; Janine Anne Flood; Dirk Wilhelm Domaschko; Niranjan Ramji
Archive | 2016
Matthew Lawrence Lynch; Joanne Roberta Willman; Brandon Philip Illie; Kevin Graham Blyth; Carola Barrera; Philip Andrew Sawin; Robert Wayne Glenn; Yousef Georges Aouad; Janine Anne Flood; Benjamin John Kutay
Archive | 2016
Matthew Lawrence Lynch; Joanne Roberta Willman; Brandon Philip Illie; Kevin Graham Blyth; Carola Barrera; Philip Andrew Sawin; Robert Wayne Glenn; Yousef Georges Aouad; Janine Anne Flood; Benjamin John Kutay
Archive | 2016
Matthew Lawrence Lynch; Joanne Roberta Willman; Brandon Philip Illie; Kevin Graham Blyth; Carola Barrera; Philip Andrew Sawin; Robert Wayne Glenn; Yousef Georges Aouad; Janine Anne Flood; Benjamin John Kutay
Archive | 2016
Matthew Lawrence Lynch; Joanne Roberta Willman; Brandon Philip Illie; Kevin Graham Blyth; Carola Barrera; Philip Andrew Sawin; Robert Wayne Glenn; Yousef Georges Aouad; Janine Anne Flood; Benjamin John Kutay