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Dive into the research topics where John A. Pickrell is active.

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Featured researches published by John A. Pickrell.


Cutaneous and Ocular Toxicology | 2009

Nanocrystalline titanium dioxide and magnesium oxide in vitro dermal absorption in human skin

Deon van der Merwe; Snehal Tawde; John A. Pickrell; Larry E. Erickson

The dermal absorption potential of a nanocrystalline magnesium oxide (MgO) and titanium dioxide (TiO2) mixture in dermatomed human skin was assessed in vitro using Bronaugh-type flow-through diffusion cells. Nanocrystalline material was applied to the skin surface at a dose rate of  50 mg/cm2 as a dry powder, as a water suspension, and as a water/surfactant (sodium lauryl sulfate) suspension, for 8 hours. Dermal absorption of nanocrystalline MgO and TiO2 through human skin with intact, functional stratum corneum was not detectable under the conditions of this experiment.


Human & Experimental Toxicology | 2005

Examining the risks and benefits of replacing traditional dose-response with hormesis.

John A. Pickrell; Frederick W. Oehme

In responding to Drs Calabrese and Baldwins question, ‘At what point, if ever, should hormesis be employed as the principal dose response default assumption in risk assessment?’, we examined the benefits of replacing traditional dose-response with hormesis. In general, hormesis provides more complete useful information for risk assessment than does traditional dose-response. A major limitation of using hormesis as a default assumption in risk estimation is the difficulty of differentiating complex low-level hormetic responses from the placebo effect. A second limitation is that hormesis merely further defines one response. Most toxicoses have many responses. The most complete information takes all responses and their connections into account.


Journal of Immunological Methods | 1994

Chamber for testing metered-dose propellant-driven aerosols of immunologically relevant proteins

Alan R. Brown; John A. Pickrell

A small aerosol chamber was developed for testing and delivery of aerosols of immunologically important proteins to the respiratory tracts of rodents. The chamber was designed to accommodate the small aerosol volumes produced by metered-dose propellant-driven aerosol canisters. Metered bursts of protein aerosols released into the chamber could be sampled for their particle sizes or used to expose the noses of up to six mice to the aerosols. The chamber consisted of a polyethylene tank with two removable plexiglass end plates. One end plate accommodated the propellant-driven, metered-dose, aerosol vial. The other end of the tank was fitted with a plate accepting aerosol sampling devices or a plate containing mouse restrainers. Uniform concentrations of aerosolized proteins were obtained at different positions in the chamber when sampled for particles of respirable size. Respirable-sized protein particles produced by propellant-driven aerosols ranged from 5 to 50% of total aerosolized protein. Propellant-driven aerosols of proteins released in the chamber produced aerosol particles equivalent to 15-26 micrograms of total protein exposure to the respiratory tract of each mouse. The chamber permitted aerosol releases without risk of operator exposure. This aerosol chamber will permit the testing of protein aerosols for their immunologic consequences to the respiratory tract. Potential proteins for testing in this device include immunizing vaccine antigens, immunomodulating cytokine proteins, and passive antibody aerosol therapies against respiratory infections.


Veterinary Toxicology (Second Edition) | 2012

Toxicity of nanomaterials

Deon van der Merwe; John A. Pickrell

Abstract Nanotoxicology includes the study of adverse effects of nanomaterials on organisms and ecosystems. It is a challenging field because of the unique physical–chemical properties of materials at the nanoscale. At this scale the biological impacts of materials tend to be dependent on the unit size and shape of the material. Engineered nanomaterials are increasingly produced and utilized in a wide variety of products, and the uncertainties regarding their potential adverse health effects, which are associated with their unique properties, makes risk assessment challenging. Evidence of adverse health effects have been demonstrated in in vitro studies, in vivo studies, and in epidemiological studies. In many cases, however, the interpretation of available data is complicated by the use of very high doses to elicit cell responses and adverse effects; a lack of data relevant to chronic, low-dose exposures; complexities associated with nanomaterial characterization; and the dynamic nature of nanomaterials in the environment and in biological systems. The rate at which new nanomaterials with unique properties are developed is increasing and often outpaces the ability to characterize the potential adverse health risks associated with these materials. The growth of the nanomaterials and nanotechnology industries promises many benefits, which should be balanced by effective risk assessment. Emerging areas of nanotoxicological investigation include the interactions of nanomaterials with other toxicants, either by enhancing, or reducing adverse health risks as well as the potential adverse environmental effects associated with nanomaterials pollution.


World Environmental and Water Resources Congress 2009: Great Rivers | 2009

Beyond Compliance and toward Sustainability: Advantages of Systems Environmental Engineering

Oral Saulters; Blase Leven; Larry E. Erickson; John A. Pickrell; Leslie Jamka; Ryan Green

New technologies are not only critical in supporting military and industrial success, but also play a significant role in advancing sustainable development. With the current global economic challenges, effective tools and partnerships which streamline the design and dissemination of these technologies are more important than ever. Accordingly, the systems environmental engineering approach utilized by the Urban Operations Laboratory (UOL), [comprised of M2 Technologies, Kansas State University, and CABEM Technologies], has facilitated innovative research, training, assessment, and product design for DoD and other stakeholders. Through strategic life-cycle environmental assessments (LCEA); programmatic environment, safety, and occupational health evaluations (PESHE); Health Hazard Assessments; and other proactive studies and reports, UOL has helped foster successful development and deployment of non-lethal technologies. More specifically, these efforts provide a framework for addressing complex environment, safety, and occupational health (ESOH) risks that affect personnel, infrastructure, property, and natural/cultural resources. Integrated analyses (comprehensive and transdisciplinary) involving flexible groups of subject matter experts, are employed in support of public and private collaborations with a focus on inputs, hazards, and constraints. This paper highlights the UOL process which can translate into advantages for a variety of projects (e.g., environmental, water, energy, infrastructure, etc.).


American Journal of Physiology-lung Cellular and Molecular Physiology | 1994

Perinatal hypocuprosis affects synthesis and composition of neonatal lung collagen, elastin, and surfactant.

A. B. Abdel-Mageed; R. Welti; Frederick W. Oehme; John A. Pickrell


Toxicology Letters | 1994

Advances in controlled clinical inhalation studies: Edited by U. Mohr, D.V. Bates, H. Fabel, M.J. Utell. Springer-Verlag, Heidelberg, Germany, 1993, 420 pp.

John A. Pickrell


Journal of Aerosol Medicine-deposition Clearance and Effects in The Lung | 1995

150.00

Alan R. Brown; John A. Pickrell


Journal of Veterinary Medical Education | 2002

Propellant-Driven Aerosols for Delivery of Proteins in the Respiratory Tract

John A. Pickrell; John Boyer; Frederick W. Oehme; Victoria L. Clegg; Nikki Sells


Biomedical and Environmental Sciences | 2003

Group learning improves case analysis in veterinary medicine.

Frederick W. Oehme; John A. Pickrell

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Blase Leven

Kansas State University

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Kiran Dhakal

Kansas State University

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Leslie Jamka

Kansas State University

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Ryan Green

Kansas State University

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