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Note: this service is for Research Use Only and Not intended for clinical use.
Mold is a microorganism that can grow almost anywhere, whether it's warm or cold. For whatever sort of manufacturer, there are mold contamination danger regions. The right mold identification is crucial. Making decisions is made easier and unnecessary concern is reduced.
Alfa Chemistry provides professional mold testing to customers for use in environmental research applications. Samples for mold testing include air and surface samples such as swabs, bulk (material, dust or liquid), tapes and contact plates for live or non-live bacteria analysis.
In general, the majority of mold testing is sampling the air or surface. In essence, our inspectors test the air or surface to identify the type of mold that is present and/or determine whether the mold is able to grow in the test area.
The most common method is to use a spore trap. A known volume of air is passed via a sticky surface as it goes through the spore catcher sample apparatus to accomplish this. Most airborne particles, including mold spores, will hit this sticky surface and attach to it, adhering to it and becoming trapped.
There are several methods we can analyze these mold samples once they have arrived at the mold testing laboratory. The most typical procedures involve placing the pertinent portion (or the entire sample) of the submitted mold on a glass microscope slide, applying a stain that the mold spores can absorb, and examining the sample for signs of mold growth.
This includes counting colony forming units (CFUs) and identifying the types or genera of mold. RCS, Andersen, LARO-100, or any other media suited for culture analysis may be used as samples. The report provides a list of recovered molds and their colony forming unit (CFU) concentration, a statistical comparison of potential samples, and information on recovered molds that is currently available.
Samples include Air-O-Cell, VersaTrap Cassette, VersaTrap Sampling Cassettes, SKC BioStage, SKC BioCassette, Micro 5, Cyclex D, LARO-100, PCM and other sample cassettes. The analysis involves spore counting and the identification of different classes of mycobacterial spores. It includes spore counts for each class of spores and total spore counts for all spores per cubic metre of air. Spore counts and spore classes are compared for all samples where possible.
Alfa Chemistry's mold testing service is provided by a team of highly trained microbiologists. Please contact us if you have any questions about the services offered.
Aerosol Sampler
An aerosol sampler is a device that uses physical or chemical methods to collect organic and inorganic particles (including mold) from the air and measures their count or weight. The aerosol sampler can collect particles such as dust, bacteria, viruses, fungi, and pollen from both indoor and outdoor air, and it can assess the quality and quantity of mold in indoor air.
Mold Culture Medium
Mold culture medium is a type of medium used for cultivating and screening molds in the air. Aerosol samples collected can be placed on the mold culture medium, and by cultivating, observing, and identifying the strains, basic information about the quantity and types of molds in the air can be obtained.
Fungal Rapid Detection Instrument
The fungal rapid detection instrument uses fluorescent quantitative PCR technology, which allows for the simultaneous detection of multiple target microorganisms in a single test sample. Mold is one of the targets in this detection. The instrument can quickly identify the types and quantities of molds in the air, with the advantages of fast detection speed and high accuracy.
Biological Aerosol Detector
A biological aerosol detector is an optical technology detection device that is small in size and easy to operate and carry. It can detect biological aerosol particles in the air in real-time and non-intrusively, including smog, fungi, bacteria, viruses, and more. It can rapidly isolate, capture, and identify biological species within aerosol particles.
Li, Pao, et al. Microchemical Journal 193 (2023): 109203.
Citrus fruits, essential in global agriculture and trade, are vulnerable to mold infections, which can occur during production, storage, and transport, leading to significant postharvest losses. Detecting these infections, particularly in their early stages, is challenging, as mold often manifests internally, without visible symptoms. Traditional methods fail to identify mold hidden beneath the citrus peel, especially before sporulation.
A promising solution involves portable Near Infrared Diffuse Reflectance Spectroscopy (NIRDRS) combined with chemometric techniques. This study investigates the penetrability of NIR light into the citrus peel and evaluates its potential for detecting hidden mold. The results reveal that short-wave near infrared (SWNIR) light penetrates more effectively than long-wave near infrared (LWNIR). Identification models based on LWNIR significantly outperformed those based on SWNIR, achieving 100% accuracy in mold detection using advanced pattern recognition methods like Soft Independent Pattern Classification (SIMCA), Support Vector Machine (SVM), and Partial Least Squares Discriminant Analysis (PLS-DA). These models were further validated with an external data set collected one month later, ensuring robust performance.
This rapid, non-destructive approach offers a reliable method for detecting mold infection in citrus, safeguarding consumer rights and enhancing postharvest quality control.
Farrugia, Jessica, et al. Current Research in Food Science 4 (2021): 18-27.
The detection of mould contamination in food products is crucial for ensuring food safety and quality. In recent years, non-destructive process analytical technologies, such as hyperspectral imaging, have garnered significant attention in the food science industry for their ability to detect contaminants without damaging the product. This study explores the use of hyperspectral imaging combined with Principal Component Analysis (PCA) to detect mould growth on milk agar and cheeselet samples.
The results demonstrated that PCA effectively localized and visualized mycelial growth on the surface of contaminated samples. The first three principal components (PCs) accounted for over 99% of the total variance, with the second PC being particularly useful in highlighting the presence of mould on cheeselets. By applying PCA loadings obtained from a set of training samples, it was possible to accurately detect contamination on new test samples, confirming the method's robustness.
This approach offers a rapid, non-contact solution for detecting mould contamination in food production, potentially improving quality control in cheese production and other food industries. The study also suggests that this methodology can be adapted to detect contaminants in a variety of solid and semi-solid food products, paving the way for its widespread use in food safety monitoring.
Ebrahimi, Parvaneh, et al. Food Control 55 (2015): 82-89.
Accurate quantification of mold growth is essential for microbiological studies, particularly in the context of biopreservation and predictive microbiology. However, traditional methods often fail to provide precise, non-destructive measurements of mold colony dynamics. This study introduces a new approach for quantifying mold growth, employing multispectral imaging combined with k-means clustering to assess the size and composition of mold colonies.
The method was successfully applied to measure the growth of "Penicillium" mold on different media, including transparent and opaque surfaces like milk and CDIM (complex defined industrial media). The approach demonstrated exceptional sensitivity, allowing for the quantification of small colony size differences that would otherwise go undetected by visual inspection. Notably, the k-means algorithm effectively distinguished between the white and green segments of the colonies, enabling precise quantification of mold growth.
This non-destructive technique proved particularly valuable for studying how environmental factors, such as pH and medium composition, influence mold growth. The method was also successful in tracking the inhibition effects of antifungal treatments, revealing differences in growth patterns that would be difficult to discern through visual inspection alone.
The PCluster algorithm offers a robust, objective, and less labor-intensive solution for monitoring mold growth, providing a valuable tool for both academic and industrial applications in mold control and food biopreservation.
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