Transport Medium Research Articles

Modified transport medium for improving influenza virus detection.

Accurate detection of influenza virus in clinical samples requires correct execution of all aspects of the detection test. If the viral load in a sample is below the detection limit, a false negative result may be obtained. To overcome this issue, we developed a modified transport medium (MTM) for clinical sample transportation to increase viral detection sensitivity. We first validated the MTM using laboratory-stocked influenza A viruses (IAVs: H1N1, H3N2, H7N3, H9N2) and influenza B viruses (IBVs: Yamagata, Victoria). We also tested clinical samples. A total of 110 patients were enrolled and a pair of samples were collected to determine the sensitivity of real-time polymerase chain reaction (RT-PCR) following MTM treatment. After 24 h culturing in MTM, the viral loads were increased, represented by a 10-fold increase in detection sensitivity for H1N1, H9N2, and IBVs, a 100-fold increase for H3N2, and a 1,000-fold increase for H7N3. We further tested the effects of MTM on 19 IAV and 11 IBV stored clinical samples. The RT-PCR results showed that the positive detection rate of IAV samples increased from 63.16% (12/19) without MTM culturing to 78.95% (15/19) after 48 h culturing, and finally 89.47% (17/19) after 72 h culturing. MTM treatment of IBV clinical samples also increased the positive detection rate from 36.36% (4/11, 0 h) to 63.64% (7/11, 48 h) to 72.73% (8/11, 72 h). For clinical samples detected by RT-PCR, MTM outperformed other transport mediums in terms of viral detection rate (11.81% increase, P=0.007). Our results demonstrated that the use of MTM for clinical applications can increase detection sensitivity, thus facilitating the accurate diagnosis of influenza infection.

SERS detection of surface-adsorbent toxic substances of microplastics based on gold nanoparticles and surface acoustic waves.

Microplastics adsorb toxic substances and act as a transport medium. When microplastics adsorbed with toxic substances accumulate in the body, the microplastics and the adsorbed toxic substances can cause serious diseases, such as cancer. This work aimed to develop a surface-enhanced Raman spectroscopy (SERS) detection method for surface-adsorbent toxic substances by forming gold nanogaps on microplastics using surface acoustic waves (SAWs). Polystyrene microparticles (PSMPs; 1 μm) and polycyclic aromatic hydrocarbons (PAHs), including pyrene, anthracene, and fluorene, were selected as microplastics and toxic substances, respectively. Gold nanoparticles (AuNPs; 50 nm) were used as a SERS agent. The Raman characteristic peaks of the PAHs adsorbed on the surface of PSMPs were detected, and the SERS intensity and logarithm of the concentrations of pyrene, anthracene, and fluorene showed a linear relationship (R2 = 0.98), and the limits of detection were 95, 168, and 195 nM, respectively. Each PAH was detected on the surface of PSMPs, which were adsorbed with toxic substances in a mixture of three PAHs, indicating that the technique can be used to elucidate mixtures of toxic substances. The proposed SERS detection method based on SAWs could sense toxic substances that were surface-adsorbed on microplastics and can be utilized to monitor or track pollutants in aquatic environments.

Efficacy of sample collection without virus transport medium in suspected enteroviral infections for molecular diagnosis.

Clinical swabs with suspected viral infection are usually transported in virus transport medium (VMT). During epidemics/pandemics, tampons without VTM would be more suitable for saving space and cost. This study was conducted to verify the applicability of throat swabs without VTM in the diagnosis/screening of enteroviral infections by polymerase chain reaction (PCR) in avolunteer study group. Three different swab types were used in 40 volunteers: swabs with two different tips (cotton- or synthetic-tipped) without VTM and standard synthetic tips with VTM. The swabs were processed immediately or after 12 days of storage at either -80°C or +4°C. The molecular analysis included viral RNA extraction, and combination of reverse transcriptase PCR and nested PCR. Enteroviral RNA was detected in 15% (6/40) of the studied volunteers. When processed immediately, the results for all three swab types were compatible. Swabs without VTM may be used for collection of clinical samples in the diagnosis of suspected enteroviral infections or as potential screening tools for enteroviruses (Tab. 2, Ref. 15). Keywords: enterovirus infection, swab, transport medium, PCR, molecular diagnostics.

Collective motion of Nafion-based micromotors in water.

Ion exchange is one of the most interesting processes occurring at the interface between aqueous solutions and polymers, such as the well-known Nafion. If the exchanged ions have different diffusion coefficients, this interchange generates local electric fields which can be harnessed to drive fluid motion. In this work, we show how it is possible to design and fabricate self-propelling microswimmers based on Nafion, driven by ion-exchange, and fueled by innocuous salts. These Nafion micromotors are made using colloidal lithography by micro/nanostructuring Nafion in the form of asymmetric rods. These microswimmers exhibit fascinating collective motion in water driven by the interplay of their self-generated chemical/electric fields and their capability to pump matter nearby towards the collective motile structure. The pumping activity of the microswimmers induces the formation of growing mobile clusters, whose velocity increases with size. Such dynamic structures are able to trap nearby micro/nano-objects while purifying the liquid, which acts both as the transport media and as fuel. Such phenomenology opens the door to potential applications in water remediation that are currently under development.

Advances in metal-organic frameworks for efficient hydrogen storage

This article addresses environmental and energy issues by proposing the use of hydrogen as an alternative energy source. However, metal-organic frameworks (MOFs) were chosen as a medium for hydrogen storage and transport because of their large capacity, favourable reversibility, suitable reaction conditions, and relatively low density. The study also introduces the hydrogen storage mechanism of MOFs, and factors affecting their hydrogen storage capacity, and discusses some ways to improve the storage. also introduces the hydrogen storage mechanism of MOFs, factors affecting its hydrogen storage capacity, and discusses some ways to improve the storage The study also introduces the hydrogen storage mechanism of MOFs, factors affecting its hydrogen storage capacity, and discusses some ways to improve the storage features of MOFs. Furthermore, a few of the newest technologies that aid in the creation of MOFs are discussed. This makes it possible to find potential MOFs fast, which·h saves money and effort.1 Introduction.

LEGAL FRAMEWORKS FOR AİR TRANSPORT SAFETY

This comprehensive examination explores the critical role of legal frameworks in ensuring safety within the aviation industry across various facets of air transport. It delves into the international agreements and standards established by the International Civil Aviation Organization (ICAO) and the meticulous supervision provided by National Aviation Authorities. The article navigates through the intricate network of regulations governing airworthiness, crew training, air traffic management, and emergency response. By scrutinizing the nuanced details of each segment, the discussion highlights how these legal frameworks serve as imperceptible architects, cultivating a global environment where safety is prioritized, emergencies are adeptly managed, and the skies remain a secure medium for transportation.

NMR contributions to the study of water transfer in proton exchange membranes for fuel cells

As programs to support efficient and sustainable energy sources are expanding, research into the potential applications of the hydrogen vector is accelerating. Proton exchange membrane fuel cells are electrochemical converters that transform the chemical energy of hydrogen into electrical energy. These devices are used today for low- and medium-power stationary applications and for mobility, in trains, cars, bicycles, etc. Proton exchange membrane fuel cells use a polymer membrane as the electrolyte. The role of the membrane is multiple: it must separate gases, be an electronic insulator and a very good ionic conductor. In addition, it must resist free-radical chemical attack and have good mechanical strength. Nafion-type perfluorinated membranes have all these properties: the fluorinated backbone is naturally hydrophobic, but the hydrophilic ionic groups give the material excellent water sorption properties. The water adsorbed in the structure is extremely mobile, acting as a transport medium for the protons generated at the anode. Although it has been studied for a long time and has been the subject of a large number of papers perfluorinated membranes are still the reference membranes today. This article reviews some contributions of Nuclear Magnetic Resonance methods in liquid state to the study of water properties in the structure of Nafion-type perfluorinated membranes.

Household Transmission of SARS-CoV-2 in the Third Wave of the Pandemic with Special Reference to Clinico-epidemiological Characteristics.

Coronavirus disease 2019 (COVID-19) pandemic began in India in 2020. Despite successful vaccination, cases again started increasing from mid-December 2021. Therefore, this study was undertaken to find out the clinico-epidemiological characteristics and effectiveness of vaccination in the household transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in and around Pune. All samples received from December 15, 2021, till February 15, 2022, were included in the study. Samples received in viral transport medium (VTM) were extracted by the MagMAX RNA Extraction Kit, and reverse transcriptase-polymerase chain reaction (RT-PCR) was performed by the CoviPath Kit as per kit guidelines. Values of nucleocapsid (N) gene and open reading frame (ORF) less than 37 were considered positive. Clinico-epidemiological data were analyzed from the sample referral form (SRF). A total of 712 of 1032 household contacts of 271 families were positive. When geographical areas were compared, it was found that rural areas were affected more (63.76%) as compared to urban areas (36.24%). Males were more affected than females. The most commonly affected age group was 41-50 years (26.54%). Small families were found to have more household transmission. Mild symptoms were present in 97.89%. Among 271 infected individuals, seven were admitted to hospital, of which one patient died due to pneumonia. Two doses of vaccination were completed in 93.95%, and 3.79% had taken booster dose. Data from this study showed that a high rate of transmission was observed in household contact despite two doses of vaccination. However, these vaccinated individuals had mild symptoms, maybe due to the effect of vaccination and infecting variant omicron.

Effect of CeO2 support structure on the catalytic performance of ammonia synthesis in an electric field at low temperatures.

Ammonia is an extremely important storage and transport medium for renewable energy, and technology is expected to produce it on demand and onsite using renewable energy. Applying a DC (direct current) to a solid catalyst layer with semiconducting properties makes ammonia synthesis highly efficient, even at low temperatures (approximately 400 K). In this process, oxide supports with semiconducting properties play important roles as metal supports and conduction fields for electrons and protons. The influence of the degree of particle aggregation on the support properties and ammonia synthesis using an electric field was evaluated for CeO2, which is the best material for this purpose because of its semiconducting properties. The results showed that controlling the aggregation structure of the crystalline particles could significantly influence the surface conductivity of protons and electrons; thus, the activity could be largely controlled. The Ru-CeO2 interaction could also be controlled by changing the crystallinity, which suppressed the aggregation of the supported Ru and significantly improved the ammonia synthesis activity using an electric field at low temperatures.

Monkeypox Diagnosis in Clinical Settings: A Comprehensive Review of Best Laboratory Practices.

An outbreak of monkeypox (Mpox) was reported in more than 40 countries in early 2022. Accurate diagnosis of Mpox can be challenging, but history, clinical findings, and laboratory diagnosis can establish the diagnosis. The pre-analytic phase of testing includes collecting, storing, and transporting specimens. It is advised to swab the lesion site with virus transport medium (VTM) containing Dacron or polyester flock swabs from two different sites. Blood, urine, and semen samples may also be used. Timely sampling is necessary to obtain a sufficient amount of virus or antibodies. The analytical phase of infectious disease control involves diagnostic tools to determine the presence of the virus. While polymerase chain reaction (PCR) is the gold standard for detecting Mpox, genome sequencing is for identifying new or modified viruses. As a complement to these methods, isothermal amplification methods have been designed. ELISA assays are also available for the determination of antibodies. Electron microscopy is another effective diagnostic method for tissue identification of the virus. Wastewater fingerprinting provides some of the most effective diagnostic methods for virus identification at the community level. The advantages and disadvantages of these methods are further discussed. Post-analytic phase requires proper interpretation of test results and the preparation of accurate patient reports that include relevant medical history, clinical guidelines, and recommendations for follow-up testing or treatment.

Detection of Human Adenovirus from Clinical Samples of Conjunctivitis by Real-time PCR: A Cross-sectional Descriptive Study

Introduction: Human Adenoviruses (HAdV) have been implicated in a variety of infections, including conjunctivitis, respiratory tract infections, genitourinary infections and gastroenteritis. Epidemic Keratoconjunctivitis (EKC) is a severe ocular surface infection strongly associated with HAdV, known to occur in widespread outbreaks. HAdV species B, D and E are associated with ocular manifestations ranging from simple follicular conjunctivitis (types 3, 4, 7) and pharyngoconjunctival fever (types 3, 7, 14) to the more severe EKC (types 8, 19, 37, 53, 54, 56 and 64). Viral cell cultures of conjunctival specimens help confirm adenovirus infection through the characteristic Cytopathic Effect (CPE) and Polymerase Chain Reaction (PCR) is the best standard method to diagnose viral conjunctivitis due to its sensitivity, accuracy and rapidity. Aim: To diagnose HAdV in clinically suspected cases of viral conjunctivitis using real-time PCR. To isolate HAdV in viral cell culture and confirm it by observing its characteristic CPE and performing adenoviral real-time PCR. Materials and Methods: A cross-sectional descriptive study was conducted from July 2023 to September 2023 at the state-level Virus Research and Diagnostic Laboratory (VRDL) at Bangalore Medical College and Research Institute (BMCRI), Bengaluru, Karnataka, India. A total of 45 conjunctival swab samples from patients with suspected viral conjunctivitis, who attended the Ophthalmology Outpatient Department (OPD) or were admitted to the wards, were included in the study. Conjunctival swab samples collected in Viral Transport Medium (VTM) were centrifuged at 3000 rpm for five minutes at 4°C. Real-time PCR was performed and samples positive for HAdV by real-time PCR were taken up for viral cell culture. Confirmatory PCR was conducted for samples showing CPEs in the cell line. The data collected were analysed using descriptive statistics. Results: The majority of patients in the present study were in the age group of 18-45 years, comprising 25 (56%) of the total patients. Out of 45 conjunctival samples tested, 8 samples were positive in adenovirus real-time PCR. All eight PCR-positive samples showed a CPE in viral cell culture on the A549 cell line. The study found PCR positivity in 8 samples (17.7%), while adenoviral recovery from cell culture was observed in 6 samples (13.3%). Conclusion: Real-time PCR has become the standard diagnostic procedure for detecting adenovirus conjunctivitis. Rapid and accurate diagnosis is key to interrupting the contagious spread of adenoviral conjunctivitis, along with timely treatment.

Isolation and investigation of external reproduction tract mycoflora in healthy male cats.

Various infectious agents can infect the male reproductive system. The aims of this study were to provide current data on fungal and yeast flora of the external organs of reproductive system of male short hair cats including penis and prepuce. In total 28 samples were taken from external genital system of male stray cats using sterilised cotton swabs. Samples were taken based on the absence of any reproductive complications using physical examinations. The samples were transferred to sterilised Stuart transport media and were then incubated in the Sabouraud dextrose agar with chloramphenicol at 32°C for 48h. The identification of fungi and yeasts was confirmed by germ tube formation test, CHROM agar, urease testing and Corn meal agar medium with Tween 80. Fungal agents were isolated from 7 (25%) out of 28 male stray cats. Fungal isolates were obtained from the penis and prepuce of 4 (36%) and 7 (100%) male cats, respectively. The most commonly recovered species samples were Candida krusei (3.75%) and Penicillum spp. (6.86%) from the penis and prepuce of the cats, respectively. The external organs of male reproduction of cats were infected with 2-4 different fungal agents. Only 5 (45%) cats were infected with one fungus; however, in 6 (55%) cats, mixed fungal infections were isolated. Cats 3-4 years old had the highest fungal contamination in the prepuce region (4/7), while the penis at this age had the least contamination (1/4). It is concluded that the external reproduction organs of male cats could be infected by different fungal agents.

A Retrospective Observational Study to Assess the Quality Management System in a Molecular Diagnostic Laboratory of a COVID-19 Dedicated Hospital in Delhi, India

Introduction: A molecular diagnostic laboratory is the cornerstone of Coronavirus Disease-2019 (COVID-19) disease diagnosis, as the patient’s treatment and management protocol depend on molecular results. Therefore, the laboratory conducting these tests must adhere to quality management process to increase the accuracy and validity of the generated reports. Rajiv Gandhi Super Speciality Hospital established its molecular diagnostic set-up at the beginning of the pandemic. Hence, this study aims to generate quality management data to help improve weak points. Aim: To assess the quality management system for COVID-19 diagnosis. Materials and Methods: This retrospective observational study was conducted at Rajiv Gandhi Super Speciality Hospital in Delhi, India. A total of 14,561 samples were collected over six months, from February 2021 to July 2021. Data from all samples received during this period for COVID-19 ReverseTranscriptase Polymerase Chain Reaction (RT-PCR) testing were included. Data were retrospectively collected from the electronic Laboratory Information Management System (LIMS). Quality variables were analysed over six months from July to December 2021 and classified into preanalytical, analytical, and postanalytical variables. Quality Indicators (QIs) were selected from a common model of QIs set by the International Federation of Clinical Chemistry and Laboratory Medicine. The results were presented in percentages, and descriptive statistics were analysed using Statistical Package for Social Sciences (SPSS) software. Results: During the six-month study period, the molecular laboratory received 14,561 samples. Among the preanalytical variables, sample leakage was the most common cause of sample rejection (134 samples, 0.92%), followed by the non generation of Specimen Referral Form (SRF) identification (76 samples, 0.52%), and non compliance with triple packaging (44 samples, 0.3%). Other preanalytical aspects assessed included incomplete patient identification (17 samples, 0.11%), insufficient sample quantity (12 samples, 0.08%), missing forms/samples (7 samples, 0.04%), samples in the wrong vials/ empty Viral Transport Media (VTM) tubes (5 samples, 0.03%), and incomplete LIMS entry (2 samples, 0.01%). Internal Quality Control (QC) was not obtained in 55 samples (0.37%), and two incidents of cross-contamination resulted in false-positive results. Among the postanalytical factors, 11 samples (0.07%) could not be dispatched within the stipulated time frame. Conclusion: The assessment of the quality management system revealed some areas for improvement, emphasising the importance of adhering to QC processes for the smooth operation of diagnostic laboratories, especially those involved in critical reporting. The assessment of QIs helped monitor laboratory parameters effectively.

Implementing L-DNA analogs as mirrors of PCR reactant hybridization state: theoretical and practical guidelines for PCR cycle control.

In previous reports, we described a PCR cycle control approach in which the hybridization state of optically labeled L-DNA enantiomers of the D-DNA primers and targets determined when the thermal cycle was switched from cooling to heating and heating to cooling. A consequence of this approach is that it also "adapts" the cycling conditions to compensate for factors that affect the hybridization kinetics of primers and targets. It assumes, however, that the hybridization state of the labeled L-DNA analogs accurately reflects the hybridization state of the D-DNA primers and targets. In this report, the Van't Hoff equation is applied to determine the L-DNA concentration and ratio of L-DNA strands required by this assumption. Simultaneous fluorescence and temperature measurements were taken during L-DNA controlled cycling, and the optical and thermal switch points compared as a function of both total L-DNA concentration and ratio of strands. Based on the Van't Hoff relationship and these experimental results, L-DNA best mirrors the hybridization of PCR primers and targets when total L-DNA concentration is set equal to the initial concentration of the D-DNA primer of interest. In terms of strand ratios, L-DNA hybridization behavior most closely matches the behavior of their D-DNA counterparts throughout the reaction when one of the L-DNA strands is far in excess of the other. The L-DNA control algorithm was then applied to the practical case of the SARS-CoV-2 N2 reaction, which has been shown to fail or have a delayed Cq when PCR was performed without nucleic acid extraction. PCR Cq values for simulated "unextracted" PCR samples in a nasopharyngeal background and in an NaCl concentration similar to that of viral transport media were determined using either the L-DNA control algorithm (N = 6) or preset cycling conditions (N = 3) and compared to water background controls run in parallel. For preset cycling conditions, the presence of nasopharyngeal background or a high salt background concentration significantly increased Cq, but the L-DNA control algorithm had no significant delay. This suggests that a carefully designed L-DNA-based control algorithm "adapts" the cycling conditions to compensate for hybridization errors of the PCR D-DNA reactants that produce false negatives.

Compatibility of Caco-2 cells with Simulated Intestinal Fluid-Predicting Permeability

The Caco-2 cell model is considered the gold standard when analysing drug permeability and risk-assessing bioavailability. The use of Simulated Intestinal Fluid (SIF) as a tool in the Caco-2 models is beneficial as this generates a more physiologically relevant model.  Existing work using biorelevant media in Caco-2 cells has not fully captured the large-scale variability that can exist within the GI fluids. Furthermore, there is some evidence that the composition of biorelevant fluids can disrupt the Caco-2 monolayer, particularly when high levels of bile and cholesterol are present in these media. Therefore, understanding the compatibility of the simulated intestinal media with the Caco-2 cells is essential to determine its use as transport media in a Caco-2 assay.

Texture and major element geochemistry of channel sediments in the Orsang and Hiren River Basins, Gujarat, India: Implications for provenance and weathering

Size, shape, degree of sorting, and composition of sediments in the river channels are controlled by climate, lithology, weathering, sorting, and medium of transportation. The present investigation is focused on the grain-size and geochemical analysis of the channel sediments of the Orsang and Hiren river basins. Major outcrops in the study area are Archaean granites, granitic gneisses, Upper Cretaceous to lower Eocene Deccan Volcanic Basalts (DVB), Quaternary sediments and minor proportion of Proterozoic low grade metamorphic rocks. The sediments are poorly to moderately sorted, very finely skewed, suggesting its derivation from heterogenous sources, while the kurtosis value indicates a high-energy depositional environment. The sediments are with gravelly sand texture and the mean grain size is varying from 581.9µm to 1284.2µm. The DVB provenance of the Hiren river basin and granitic provenance of the Orsang river basin is clearly reflected in the texture and geochemical composition of sediments. The TiO2 and Fe2O3 contents of sediments from the Hiren river basin are distinctly higher and are comparable to the basalts of the Saurashtra region of the Deccan Province. Sediments collected after Orsang and Hiren rivers confluence and from Narmada river show higher concentration of felsic sources, indicating that Orsang river's sediment supply significantly outweighs Hiren rivers. The arkosic-litharenite nature points towards less transportation and moderate chemical weathering for the Orsang river sediments. The low Chemical Index of Alteration (CIA) values (Avg. 48.45 and 56.99 for Orsang and Hiren rivers, respectively) and A-CN-K plot also suggest the supply of sediments from minimally weathered detritus under a semi-arid condition.

Assessment of Periodontal Ligament Fibroblast Viability in Dymatize® Elite Casein as a Transport Medium for Avulsed Teeth at Different Time Intervals (An in - vitro study)

Abstract
 Aim: To evaluate the effectiveness of a sports dietary supplement, which is Dymatize® Elite Casein (micellar casein), as a storage medium for avulsed teeth compared to Hank’s balanced salt solution at three-time intervals.
 Methods: One hundred teeth freshly extracted for orthodontic treatment. Were divided into Hank’s balanced salt solution, Dymatize® Elite Casein, a Dry group, and a control that tested directly after extraction. Experimental groups' teeth were immediately immersed in the media and subdivided into three groups at time intervals (1 hr, 4 hrs, and 8 hrs). Cells of PDL were examined after being scraped, and labeled with trypan blue using a light microscope and a hemocytometer. The data were statistically analyzed, using one-way ANOVA with Graph Pad Prism 7. And, Post Hoc Tukey's test performed inferential to compare each test group to all other groups.
 Results: All groups showed highly significant changes, except for Dymatize® and control at one hour, which showed non-significant differences. All experimental groups had highly significant differences after 4 and 8 hours.
 Conclusion: The Dymatize® Elite Casein could serve effectively as a transport medium and preserve fibroblast viability over time ensuring replantation success. It is a good substitute with its superior properties.

CellShip: An Ambient Temperature Transport and Short-Term Storage Medium for Mammalian Cell Cultures.

Cell culture is a critical platform for numerous research and industrial processes. However, methods for transporting cells are largely limited to cryopreservation, which is logistically challenging, requires the use of potentially cytotoxic cryopreservatives, and can result in poor cell recovery. Development of a transport media that can be used at ambient temperatures would alleviate these issues. In this study, we describe a novel transportation medium for mammalian cells. Five commonly used cell lines, (HEK293, CHO, HepG2, K562, and Jurkat) were successfully shipped and stored for a minimum of 72 hours and up to 96 hours at ambient temperature, after which, cells were recovered into standard culture conditions. Viability (%) and cell numbers, were examined, before, following the transport/storage period and following the recovery period. In all experiments, cell numbers returned to pretransport/storage concentration within 24-48 hours recovery. Imaging data indicated that HepG2 cells were fully adherent and had established typical growth morphology following 48 hours recovery, which was not seen in cells recovered from cryopreservation. Following recovery, Jurkat cells that had been subjected to a 96 hours transport/storage period, demonstrated a 1.93-fold increase compared with the starting cell number with >95% cell viability. We conclude that CellShip® may represent a viable method for the transportation of mammalian cells for multiple downstream applications in the Life Sciences research sector.

Hydrate Control in Subsea Natural Gas Production

One of the most significant technological challenges that this industry faces today is securing the production flow in deep water exploration. Intense conditions of high pressure and low temperatures will favor the formation of the hydrates which could restrict or block the pathway to the extent that there can be a humungous financial loss.
 This research was devoted to hydrate control in subsea natural gas production using results from water concentration estimation for reservoir, wellhead and onshore receiving terminal conditions. For illustration, a natural gas stream from the Niger Delta was selected where the transportation medium is a pipeline. Further implementation as part of the hydrate formation assessment input was done on the temperature and pressure profile along this pipeline.
 A hydrate inhibition strategy based on monoethylene glycol (MEG) is under consideration. It is revealed that in the case if a temperature falls below 20°C and pressure will increase above 100 bar, then it would be met with a flow configuration in a region where hydrates are formed. Estimation of water concentration thus suffices to give useful information as possible prevention methods to hydrate formation while the gas flow is going on in the pipeline. The actual thermodynamic conditions required for the hydrate formation can also be deduced from the temperature and pressure data.

Pre-analytical properties of different respiratory viruses for PCR-based detection: Comparative analysis of sampling devices and sample stabilization solutions

After the decline of the COVID-19 pandemic, health systems were challenged by the simultaneous prevalence of different respiratory viruses causing a wide overlap in symptoms. This increased the demand for multi-virus diagnostic tests which require suitable pre-analytical workflow solutions in order to receive valid diagnostic results. In this context, the effects of specimen storage duration and temperature on the RNA/DNA copy number stability of influenza A/B, RSV A/B, SARS-CoV-2 and adenovirus were examined for four commercially available transport swab systems and saliva collection devices. The respiratory viruses were more stable in the saliva collection devices than in the transport swab systems when stored at RT or 37 °C for up to 96 h. Moreover, no differences between viral nucleic acid stability of enveloped and non-enveloped viruses were observed. The infectivity of all enveloped viruses could be inactivated by the saliva collection device from PreAnalytiX. The Norgen saliva device completely inactivated influenza A/B, while RSV A/B were partially inactivated. The non-enveloped adenovirus was inactivated by a reduction factor of 10E+ 4 in both saliva collection devices. All respiratory viruses remained infectious in the transport swab systems. Two possible transport medium additives were tested which inactivated or strongly reduced viral replication of tested enveloped viruses but had no effect on the non-enveloped adenovirus. Finally the implementation of multi-target detection procedures involving a direct amplification approach was successfully tested by spike-in of all enveloped viruses simultaneously into transport swab systems. This fast and reproducible setup presents a valuable solution for future implementations in multi-virus testing strategies.