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Biomedical subjects

L C Kenny

Publications and source records attributed to L C Kenny.

12 recordsLinked to original sources

An overview of endothelium-derived hyperpolarising factor (EDHF) in normal and compromised pregnancies.

Normal pregnancy is associated with decreased peripheral vascular resistance, although the mechanisms are poorly understood. Pre-eclampsia is characterised by increased vessel resistance and a decreased relaxant capacity, contributing to the associated hypertension, multi-organ damage and intra-uterine growth restriction. An endothelium-derived vasoactive substance-endothelium-derived hyperpolarising factor may be responsible for the physiological changes in the maternal vasculature. This is a review of the current understanding of the complexities of vessel behaviour. Evidence is reviewed to support the possible contribution of endothelium-derived hyperpolarising factor to the compromised vascular state in pre-eclampsia. This is an important area of research which may help to understand further the pathogenesis of this specific pregnancy related disease, that contributes greatly to maternal and fetal morbidity and mortality.

Animals↗

The international conventions for health-related sampling of aerosols--a review of current status and future evolution.

This review article discusses the status of international conventions for size-selective sampling of particles and the extent to which they have been implemented worldwide. Some of the problems that have arose in the implementation process are addressed and solutions proposed. The article concludes that it is too early to revise the sampling conventions at this time, although there may be a case to do so in the future.

Aerosols↗

Field testing of a personal size-selective bioaerosol sampler.

Existing samplers for the collection of bioaerosols have been designed with the aim of maintaining biological stability of the collected material, and in general do not select particles in accordance with international conventions for aerosol sampling. Many have uncharacterised sampling efficiencies and few are designed as personal samplers. If standard personal dust samplers are used for bioaerosols the viability of collected microorganisms may be compromised by dehydration. The objective of this study was to evaluate a novel personal bioaerosol sampler designed to collect the inhalable dust fraction and further subdivide the sample into thoracic and respirable fractions. The new sampler was tested to see whether it enhanced the survival of the collected microorganisms, and was assessed for ease of use in the field and in subsequent laboratory analyses. A number of occupation-related field sites were selected where large concentrations of bioaerosols were to be expected. The prototype sampler was found to be simple to use. Analysis could be carried out with similar efficiency either with all three fractions together for a total count, or separately for size selective data. The sampler performed at least as well as the standard IOM filter method but with the added advantage of size fractionation. The field trials showed that for sampling periods lasting several hours, microorganism survival within the sampler was adequate for culture and identification of the organisms present. This new sampler is now commercially available. In addition to bioaerosol sampling, the principle of size selective sampling using porous foams can be applied to other occupational hygiene problems, and also to indoor air monitoring of PM10 and PM2.5 concentrations.

Aerosols↗

The adaptation of existing personal inhalable aerosol samplers for bioaerosol sampling.

Health-related monitoring of bioaerosol exposures in the workplace should ideally be carried out using size-selective personal samplers that separate the aerosol into biologically relevant size fractions and allow both quantification and identification of the microorganisms present in each fraction. As a first stage in the development of personal bioaerosol samplers a number of collection substrates were assessed for their ability to maintain the viability of the collected microorganisms, so that subsequent culturing and species identification may be carried out. The substrates were tested with bioaerosols of varying robustness, consisting of Saccharomyces cerevisiae cells, Escherichia coli cells, and Penicillium expansum spores, aerosolized under controlled environmental conditions. The survival of microorganisms on each test substrate, assessed on the basis of the culturable fractions of cells recovered, was compared with that of microorganisms collected in a reference glass cyclone sampler. These bioefficiency tests identified the substrate combinations with the potential to fulfill personal sampler design criteria. The substrates were then subjected to further development to evaluate and optimize their particle size selection characteristics. The outcome of this work is two prototype personal bioaerosol samplers in which size-selective substrates are adapted for use in existing designs of personal inhalable sampler. This offers an effective and low-cost solution to personal monitoring of bioaerosol exposures in the workplace.

Aerosols↗

A collaborative European study of personal inhalable aerosol sampler performance.

Following the adoption of new international sampling conventions for inhalable, thoracic and respirable aerosol fractions, a working group of Comité Européen de Normalisation (CEN) drafted a standard for the performance of workplace aerosol sampling instruments. The present study was set up to verify the experimental, statistical and mathematical procedures recommended in the draft performance standard and to check that they could be applied to inhalable aerosol samplers. This was achieved by applying the tests to eight types of personal inhalable aerosol sampler commonly used for workplace monitoring throughout Europe. The study led to recommendations for revising the CEN draft standard, in order to simplify the tests and reduce their cost. However, some further work will be needed to develop simpler test facilities and methods. Several of the samplers tested were found to perform adequately with respect to the inhalable sampling convention, at least over a limited range of typical workplace conditions. In general the samplers were found to perform best in low external wind speeds, which are the test conditions thought to be closest to those normally found in indoor workplaces. The practical implementation of the CEN aerosol sampling conventions requires decisions on which sampling instruments to use, estimation of the likely impact that changing sampling methods could have on apparent exposures, and adjustment where necessary of exposure limit values. The sampler performance data obtained in this project were affected by large experimental errors, but are nevertheless a useful input to decisions on how to incorporate the CEN inhalable sampling convention into regulation, guidance and occupational hygiene practice.

Europe↗

Developments in workplace aerosol sampling. A review.

Sampling conventions for inhalable, thoracic and respirable aerosol fractions have now been agreed internationally and published as both European and International standards. Implementation of these sampling conventions will require discussion of the target fractions appropriate for various aerosol hazards, the sampling instruments to recommend for the three target fractions and estimation of the likely impact that any changes in sampling method could have on apparent exposures. This paper reviews the performance of both available and developing aerosol sampling technologies and discusses some of the wider issues involved in moving to improved sampling methods.

Aerosols↗

Comparison of measured respirable dust sampler penetration curves with sampling conventions.

Measured sampler penetration curves are presented for British personal cyclone samplers and the MRE 113A static horizontal elutriator in calm air. These curves are compared with previous results for these instruments, and with theoretical models of sampler behaviour. The sampling efficiency of the elutriator when facing a moderate wind is discussed. The penetration curves are assessed by comparison with standard sampling conventions for respirable dust.

Air Pollutants, Occupational↗

The application of performance standards to personal airborne dust samplers.

This paper summarizes current proposals for the specification and testing of personal sampler performance, and discusses their implications for the precision of dust concentration estimates. A method of specifying the performance of a sampling instrument in terms of the range of masses it would collect from various dust clouds is proposed. Some of the practical difficulties which are likely to arise in the process of testing real samplers with respect to performance standards are discussed.

Aerosols↗

Design and validation of a high-flow personal sampler for PM2.5.

A high-flow personal sampler (HFPS) for airborne particulate matter has been developed and fully characterised, and validation tests have been carried out. The sampler is a low-cost gravimetric instrument designed to collect particulate matter with a 50% cut point at 2.5 microm aerodynamic equivalent diameter (PM2.5), where size selection is achieved by the use of porous polyurethane foam. Development of a porous foam selector was chosen over a cyclone or impactor due to the lightweight, low-cost, and compact design that could be achieved. The sampler flow rate of 16 1/min is achieved using a portable, flow-controlled pump; this flow rate is far higher than that of conventional personal samplers and the HFPS can therefore be used for personal sampling in the ambient environment over short sampling periods of much less than 24 h. The HFPS is currently being used in a study of particle exposure of urban transport users (cyclists, car drivers, bus and Underground rail passengers) where personal sampling over short time periods representing typical commuter journey times is required. The HFPS was fully characterised in chamber studies with a TSI aerodynamic particle sizer (APS). The sampler was then validated against a co-located U.S. EPA Federal Reference PM2.5 Well Impactor Ninety Six (WINS) and a KTL cyclone, and parallel testing was performed. Initial testing showed some penetration of particles through the porous foam structure; applying an oil coating to the foam eliminated this problem. Chamber testing was carried out on a number of different selector prototypes, with the final design giving a 50% penetration diameter (i.e., d50) of 2.4 microm at 16 1/min. The new sampler exhibited good agreement in three sets of co-located tests with established samplers, and parallel testing showed excellent agreement between paired HFPS samplers.

Air Movements↗

Trophoblast invasion of spiral arteries: a novel in vitro model.

Extravillous trophoblasts invade the uterine wall (interstitial invasion) and the spiral arteries (endovascular invasion), replacing the cells of the vessel wall and creating a high-flow low-resistance vessel. We have developed a novel model to allow the interactions between the invading trophoblast cells and the cells of the spiral artery to be directly examined. Unmodified (non-placental bed) spiral arteries were obtained from uterine biopsies at caesarean section. Fluorescently labelled trophoblasts were seeded on top of artery segments embedded in fibrin gels (to study interstitial invasion) or perfused into the lumen of arteries mounted on a pressure myograph (to study endovascular invasion). Trophoblasts were incubated with the vessels for 3-5 days prior to cryo-sectioning. Both interstitial and endovascular interactions/invasion could clearly be detected and a comparison of the extravillous trophoblast cell line, SGHPL-4 and primary first trimester cytotrophoblasts showed both to be invasive in this model. This novel method will prove useful in an area where in vitro studies have been hampered by the lack of suitable models directly examining cellular interactions during invasion.

Adult↗