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The problems of determining the protective properties of barrier materials used for the production of body surface protection products of an isolative type are very actual. These garments are expected to have long-term resistance against permeation of toxic substances. The paper deals with the study of the effect of organic solvent vapours on the changes in protective properties of selected anti-gas protective garments commonly used by the North Atlantic Treaty Organization armed forces. Permeation measurements of selected gases with integral permeameter were performed to verify their barrier properties, surface changes after exposure to selected solvents by using a 3D optical profilometer, permeation measurements for vapours of these solvents with differential permeameter, and experimental simulating the possible influence of barrier properties of garments within permeation of air. It has been shown that in the case of gases, the permeability of the studied materials increases with decreasing kinetic diameter of the penetrant molecule used. In the case of acetonitrile and isooctane vapours, permeability increased with increasing vapour concentration due to interactions between polymeric materials and molecules of organic compounds. The permeation measurements of pure vapours and air/vapour mixtures indicate that the level of interactions between the molecules of the penetrant and the material of the protective garment is not strong enough to degrade the material of the garment in such a way as to allow a greater penetration of the pollutants through it. The results of permeation experiments for gases and organic vapours showed very good barrier properties of studied chemical isolated garments., Competing Interests: Declaration of competing interest The authors declare no conflict of interest., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Barrier materials have wide applicability in both professional (military, medical, industrial) and non-professional (leisure and sports) fields. This paper focuses on the preparation of real conductive polymer (CP) sensors, for the study of the permeation of volatile toxic compounds through barrier materials. Use of such a CP sensor can help improve the quality of barrier materials used in protective clothing. Several types of platforms have been manufactured or purchased for use as comb sensors with different electrode dimensions, and a suitable method of applying the detection layer of conductive polymers (polyaniline and poly-pyrrole) has been developed. Prepared sensors were obtained using various technologies and were assessed not only for response to exposure to vapors of volatile toxic substances, but also for the possibility of their incorporation into a permeation cell, in order to expand the possibilities of using existing permeation devices. The resulting conductivity of the surface film ranges from 50 to 10,000 μS/cm. When exposed to ethanol vapors, the conductivity of the sensors dropped significantly and returned to the original value after exposure ended. The conductivity of the B12 CP sensor was in the range of 10-100 mS/cm and is considered the most valuable tested sensor. CPs deposited on this substrate have very high sensitivity in units of ppm (in special cases, even ppb) within the detection of analytes (in this case toxic vapors of ethanol, acetic acid) and the ability to return to initial (zero) conductivity., (Copyright © 2019 Elsevier B.V. All rights reserved.)

According to general principles of good practice, adopted at the international level, quality control is a key function in management and not just a simple means of verification. In a clinic or hospital pharmacy, the chief pharmacist has the training and authority to take the control measures necessary to develop and implement an Internal Managerial Control System (IMCS). The present article analyzes and describes the case of the County Hospital of Oradea, Romania, and presents how the IMCS was adopted and integrated. Quality assessment in the health services takes place via an accreditation process and quality certification, as well as through an internal audit of the hospital pharmacy. The authors report a retrospective and descriptive study carried out from 2012 to 2017, analyzing how current legislative standards are applied. The IMCS in the hospital pharmacy is a dynamic process of continuous transformation, permanently adapted to hospital requirements, achieved under the direction of the chief pharmacist and involving all pharmacy employees, as well as through good coordination practices applied by hospital management. In this specific case, the IMCS features 11 annually updated compliance standards, classed under the headings of work procedures, risk register, job descriptions and staff training. The pharmacy's good practice model for IMCS development, was adopted by all of the hospital's sectors, services and departments., (Copyright © 2019 Elsevier B.V. All rights reserved.)