2 days ago5 min read
5 days ago5 min read

Modern life-science research has a plastic problem. As the industry accelerates toward a projected $278 billion valuation by 2034, its environmental footprint is expanding just as fast. While single-use consumables ensure sterility, they have created a massive environmental footprint that often fades into the background of daily lab work. Nowhere is this more evident than in the "scratch assay"—a foundational technique where habit, rather than necessity, generates tons of preventable waste. CytCut is changing this narrative.
In the fast-paced world of cell biology, the scratch assay (or wound-healing assay) is a staple. It is simple, intuitive, and essential for studying cell migration, cancer metastasis, and tissue repair. However, the standard method for creating these wounds—dragging a disposable pipette tip across a cell monolayer—is a prime example of scientific inefficiency. By treating this plastic tool as a one-time-use mechanical blade, the global research community creates a hidden mountain of waste.
CytCut was created to challenge this assumption. By replacing disposable tips with a reusable, sterilizable device, this technology is not just refining a method; it is eliminating a massive waste stream at the source.
To the individual researcher, one pipette tip seems negligible. A standard 200 µL polypropylene tip weighs approximately 1.1 grams. However, when viewed through the lens of global laboratory activity, these numbers aggregate into a startling reality.
In a typical scratch assay workflow, researchers use a fresh pipette tip for every single well to ensure consistency and prevent cross-contamination. Aggregating publication data, laboratory activity patterns, and experimental redundancy, conservative estimates place the global usage of scratch assays at approximately 3 million assays per year*.
When we do the math on 3 million assays—assuming an average of 50 disposable tips per experiment—the environmental impact creates a stark picture:
~150 million pipette tips are used annually solely to create scratches.
~165 metric tons of plastic waste are generated per year from scratch tips alone.
It is important to note that these figures are intentionally conservative. They account only for the mass of the tips themselves, excluding the substantial plastic weight of tip racks, packaging, and the waste generated from failed experiments.
Sustainability in the laboratory is often addressed through recycling, but for biological research, this solution has severe limitations. As noted by MIT's Environmental Health and Safety programs, recycling initiatives typically accept only "clean" plastics like tip boxes and racks. The tips themselves—contaminated with biological material—are frequently rejected by waste vendors and sent straight to incineration or landfills.
CytCut solves this problem through elimination at the source.
Zero Contaminated Waste: Instead of consuming dozens of plastic tips to scratch a 96-well plate, a single CytCut device performs the same task repeatedly without generating disposable plastic waste.
Carbon Footprint Reduction: Research published in PubMed Central and PLOS Biology indicates that reusable laboratory items can reduce CO2 equivalent (CO2e) footprints by up to 11-fold compared to single-use plastics.
Manufacturing Impact: When a single CytCut device is reused across months of experiments, its manufacturing footprint is spread across thousands of assays. In contrast, the traditional method incurs a new "plastic cost" every time an experiment is run. If applied globally, shifting away from pipette-tip scratching would prevent over 160 metric tons of polypropylene from entering the waste stream annually.
The environmental argument for CytCut extends beyond the physical plastic of the pipette tip. One of the greatest sources of waste in science is the failed experiment.
Manual scratching with a pipette tip is inherently variable. Inconsistent wound widths often lead to uninterpretable data, forcing researchers to discard plates and repeat entire workflows. Every repeated experiment multiplies the waste generated—consuming not just pipette tips, but also culture plates, media, chemical reagents, and the energy required for incubation and imaging.
By providing a purpose-built mechanical solution, CytCut significantly improves the reproducibility of the wound-healing assay.
Consistent Scratches: Reduces the likelihood of outliers and failed wells.
Fewer Repeats: Higher data quality means fewer experiments are needed to achieve statistical significance.
Holistic Savings: Avoiding a single repeat saves far more resources than simply eliminating the tips.
In this context, reproducibility acts as a sustainability intervention. Better science leads directly to a smaller environmental footprint.
The scientific community is increasingly aware of its environmental responsibilities. Reports from Eppendorf and MIT Sustainability highlight that single-use plastics are a dominant waste stream in labs. For years, researchers believed that reducing this waste required compromising experimental rigor. CytCut demonstrates that this is a false dichotomy.
This technology does not ask researchers to lower their standards. It simply replaces a disposable workaround with a durable tool. It represents a shift in laboratory culture—a recognition that small, thoughtful changes in routine techniques can collectively drive a massive reduction in global plastic waste.
By eliminating disposable plastics from the scratch step and reducing experimental repeats, CytCut aligns everyday cell biology with the values of modern, responsible science. Sustainability is no longer just a future goal; with tools like CytCut, it is a practical reality available to laboratories today.
References
*Note: Because no centralized database tracks how often scratch (wound-healing) assays are performed globally, we estimated annual assay volume using a conservative bottom-up approach. Bibliometric searches of PubMed and Google Scholar indicate approximately 3,000–6,000 papers per year explicitly report scratch or wound-healing assays; a midpoint of ~5,000 publications/year was used. To avoid overestimation, we assumed only four scratch plates per published paper, yielding ~20,000 published plates annually. Recognizing that published experiments represent only a fraction of laboratory activity due to optimization runs, negative results, reviewer-requested repeats, and internal industry studies, we conservatively assumed publications account for ~10% of total scratch assays, establishing ~200,000 assays/year as a strict lower bound. An independent cross-check based on laboratory activity—assuming ~10,000 active scratch-assay labs worldwide performing 1–6 plates per week—yields a range of ~0.5–3 million assays per year. Based on this triangulation, we adopt ~3 million scratch assays per year globally as a moderate, assumption-based estimate, with all environmental impact calculations scaling linearly to alternative volume assumptions.


