Engineering the right final package for any application means ensuring the end result has the required properties to keep the product fresh and safe, extending it's shelf life and meeting consumer expectations whilst at the same time being as cost efficient and environmentally-friendly as possible.
Partner with PerkinElmer to benefit from expert support and analytical testing instrumentation for the development, design and manufacture of your packaging materials; from food contact materials testing to pharmaceutical packaging. We can provide you with trusted analytical solutions at every stage and across international standards to ensure compliance with essential regulations.
We have experience providing solutions for customers testing products and brands for food, drink, healthcare and cosmetics as well as electronic & consumer goods. Our comprehensive product portfolio supports the ever-changing requirements of labs worldwide.
Employ cutting-edge solutions for the identification and characterization of your materials. It's critical to understand physical properties to reach the packaging performance you need to keep the product within safe and fresh.
A common QC test in plastic production is the analysis of residual monomers in the final polymer material. This analysis is well suited for headspace sampling because headspace eliminates the sample preparation. The sample is analyzed directly with no need to dissolve the polymer. Multiple headspace extraction (MHE) is a technique to exhaustively extract a sample and calculate the amount of analyte by comparison to an external standard. This application note will discuss the testing of polymers for residual monomers by MHE-GC/MS. The polymers tested in this application are used for the manufacturing of corrective eyeglass lenses. This material is monitored for acrylic acids, such as methylmethacrylic acid methyl ester (MMA).
Dynamic Mechanical Analysis (DMA) is a technique used to investigate the stiffness of materials as a function of temperature, humidity, dissolution media or frequency. A mechanical stress is applied to a film sample or coated polymer or other material sample and the resultant strain is measured by the instrument. These parameters are used to evaluate glass transitions, degree of crystallinity and stiffness behaviour of the sample.
Detecting and monitoring the presence of impurities within the packaging material is vital for a safe and compliant route to market. Perform in-depth analysis on additives and emissions, get to the root of packaging failures and detect the presence of contaminants.
Polymer laminates are materials consisting of multiple layers of different polymers. These materials are ubiquitous in modern day life with a substantial amount of food and pharmaceutical packaging containing laminates. A common requirement of food packaging is that the internal layer must be appropriate to be in contact with food and the external layer must be suitable for printing product information. This application note describes how the PerkinElmer Spotlight™ 400 Imaging System with the ATR imaging allows layers with thicknesses down to 2-3 µm to be investigated.
The solvents in the inks used to print flexible packaging may represent a possible source of food contamination and therefore must be controlled for quality and consumer safety. For the determination of residual solvents from printed materials, it is highly recommended that an analytical method such as the official UNI EN 13628-2:20041 is followed. This Application Note describes how GC (Gas Chromatography) analytical techniques can be used to determine the presence and quantity of residual solvents using the Clarus 580 GC / TurboMatrix Headspace system for swift and simple sample preparation and accurate analytical results.
Meet comprehensive food-contact testing requirements to international regulatory frameworks. By providing you with a comprehensive solution, combining the right instrumentation, consumables accessories and reagents, we ensure QA/QC laboratories can meet stringent food and pharmaceutical regulations for the quality of primary packaging from plastic materials;
Packaging is defined as a means of providing protection, identification, and containment of a product during storage and transport until it is consumed. The pharmaceutical packaging industry has an estimated value of $68.7 billion, and when it comes to their packaging quality, it is essential that suitable physical, chemicals and biological properties are upheld to ensure integrity of the product and to meet relevant standards. The PerkinElmer Spectrum Two FT-IR Spectrometer with UATR accessory provides a fast and robust method for determination of pharmaceutical packaging material. Furthermore, when used in conjunction with the Spectrum 10TM Enhanced Security, packaging can be easily analyzed while fulfilling requirements of 21 CFR part 11 compliance.
Extractables and leachables studies are critical for maintaining the quality of your drug product and complying with GMP regulations during drug development and final batch release. Exposure to extractables and leachables could have a detrimental impact on the safety and efficacy of a final drug product. Testing for these contaminants is critical in every part of pharmaceutical packaging including the packaging system used to store drug products.
All medicinal products need to be protected and packaged in containers which conform to prescribed standards. The quality of pharmaceutical packaging can have a significant impact on the performance of pharmaceutical products and can reduce shelf-life if the improper packaging is used. The USP chapter, <671>, “Containers – Performance Testing” provides standards for the functional properties of packaging systems used for solid and liquid oral dosage forms for pharmaceuticals and dietary supplements. This application note demonstrates the determination of spectral transmission of plastic pharmaceutical containers using the PerkinElmer LAMBDA™ 1050+ UV/Vis/NIR spectrophotometer, in accordance with USP <671>.
Applications of Infrared Spectroscopy in the Analysis of Herbal Drug Quality and Packaging Materials