Approximately 99% of plastics are produced from chemicals which are connected to the refining and processing of fossil feedstocks extracted as oil or gas from land, or seabed. The estimates on the depletion year of fossil resources vary from 2050 to 2060, providing that the demand is further increasing and no new reserves will be found. Not only the depletion of fossil resources but also the high CO₂ emission when fossil fuels are burnt is a big concern. Although only ca. 4-6% of oil and gas, estimated for Europe, are used in the production of polymers, the interest in considering renewable resources as an alternative to fossil resources is significant.
The feedstock of renewable resources can be derived, for example from agricultural products, starch, cellulose, and chitin. Renewable resource-based polymers might have different properties in comparison to traditional fossil-based polymers.
For medical device applications with strict regulatory requirements, a change in material would require recommencement of the time-consuming and costly approval process. Hence, drop-in solutions like polypropylene derived from used cooking oil could be an ideal option.
Similar to fossil oil, used cooking oil is broken down into its components on a molecular level. Due to this, PP derived from used cooking oil provides the same mechanical properties and maintains the same regulatory compliance as its fossil-based sibling. In order to track the whole supply chain of sustainable feedstock, IMCD is ISCC Plus certified and thus can carry out the mass-balance approach.
Historically, medical devices were made of glass or metal and were made reusable by steam sterilisation. With the growth of the population, the higher demand for healthcare treatments and the increasing concerns regarding blood transmitted diseases – like hepatitis and HIV – the call for developing single-use devices (SUD) became inevitable. The development of more complex devices, minimally invasive procedures and the simultaneous discovery of new materials like plastics boosted the trend towards SUD.
During COVID-19, the demand for single use PPE (personal protective equipment) increased significantly in order to limit further infections. This resulted in a massive increase of several million tons of waste. Considering reducing single-use items by designing these for durability and reusability could be a viable solution for achieving more sustainability in certain medical and healthcare applications.
In order to be safely reusable, the medical device must be capable of being appropriately reprocessed to remove contamination of microorganisms. A reprocessing in the medical and healthcare context could be disinfection or sterilisation of the device. In our “Selecting materials for medical device sterilisation” article, we de-complexify the challenge of matching the device material with the different sterilisation techniques.
Although there are certain applications in which reusable medical devices are meaningful, there are many devices, especially those used in certain invasive procedures, which will likely stay disposable to maintain safety and hygiene as well as to comply with the strict regulatory controls. Other aspects to consider are costs and time as well as usage of resources like water, logistics, and electricity of reprocessing methods which also have an environmental impact.
The WHO World Health Organization has been addressing the subject of medical waste for several decades. Medical waste is generated not only in hospitals but also in laboratories, research centres, nursing homes for the elderly and at collection services. The type of waste and by-products are divided into the following categories by the WHO as quoted below:
Managing waste is a big challenge for the medical and healthcare industry. In addition to the aforementioned options of closing the loop by recycling as well as designing medical devices for reusability, the industry also investigates another aspect:
With the increase of vaccinations and the further developments of parenteral drugs, the usage of PFS (prefilled syringes) is becoming more popular. Traditionally, glass vials were the first choice for providing drug products, but these are usually overfilled to make sure the full dose will be administered to the patient. Prefilled syringes can be made of COC, are easier and faster to handle, reduced in risk and have improved dose control so that they help reduce drug product waste.
Disclaimer: The information contained herein is to the best of our knowledge and belief. No warranty or guarantee is expressed or implied regarding the accuracy of information.
1. Fletcher, Elaine Ruth (10/09/2019). Health care climate footprint is 4.4% of global emissions; larger than Japan or Brazil. Health Policy Watch.
2. Howarth, Jackson (02/12/2019). When will fossil fuels run out? Octopus Energy
3. Oil consumption. (21/05/2019). British Plastics Federation.