Does bubble formation in IVF media during transport influence its quality?

Aug 2025 | Tips & Tricks

Bubbles seen in IVF media after transport do not generally affect the quality. They are often a result from the presence of human serum albumin (hSA)- a common additive in culture media, like in PureSperm Wash. HSA contains both hydrophilic and hydrophobic regions. These properties are like those of soap molecules, which form bubbles due to their ability to stabilize air-liquid interfaces. During transport, agitation may introduce air into the media. Human serum albumin (hSA) stabilizes these air pockets, resulting in visible bubbles that persist longer in the solution. The hSA-stabilized bubbles are reversible and will dissipate once the media has settled.

In unopened media, the air trapped within bubbles is the same as the air present in the bottle. As a result, it does not influence the pH level.

HSA acts as a carrier, providing cells with nutrients that support cellular metabolism. It binds crucial metal ions essential for development and growth of cells. In PureSperm Wash, hSA is also included to prevent sperm from sticking to the culture dishes and pipettes during the handling. HSA has antioxidant interactions that are relevant for the extracellular environment as well as the intracellular compartment of the cells, further contributing to a stable and supportive culture system. When comparing PureSperm Wash containing hSA to PureSperm Wash with no hSA, it is clear that hSA supports the sperm motility after density gradient separation and it supports sperm survival.

 

Other Tips & Tricks

Two types of high quality sperm separations

Two types of high quality sperm separations Nidacons product SpeediKit and a regular density gradient both serve the purpose of creating high quality sperm separations however, there are some distinct advantages to SpeediKit over a traditional density gradient. Key...

Precision Matters: How Gradient Preparation Determines Your Results

All solutions at room temperature Prepare the gradient using 2 ml layers. Prepare the gradient no more than 30 minutes before use to prevent the layers from mixing. Avoid overloading—do not exceed the recommended 1.5 ml of sample Follow the recommended centrifugation...

Adapt the freezing method to your workflow

Refrigerated Incubation (10–60 minutes): Incubating sperm in the refrigerator prior to time on liquid nitrogen for 10 to 60 minutes improves survival rates. While the difference between 10 and 60 minutes is slight, there is a significant increase in survival when...

Nidoil – Improved Quality Assurance

Additional information regarding Mouse Embryo Assay (MEA) results on day 6 will be provided on the Quality Assurance certificates for Nidoil. The Day 6 (eMEA) results offer an extra layer of safety assessment, enhancing our ability to detect potential toxicity and...

Optimize your sperm preparation

Semen osmolality increases during and after liquefaction due to enzymatic degradation of molecules in semen. The increased osmolality in the ejaculate can negatively impact the outcome of sperm preparation. To minimize this risk, early dilution of the ejaculate is...

Optimize your results

Can a washing solution help you to optimize your result? When comparing PureSpermWash to other washing buffers, it has been shown that PSW • maintains the correct ROS production better (1) • achieves the highest percentage of capacitated sperm (1) • produces higher...

Enhance your sperm preparation skills

Would you like to elevate your expertise in handling sperm samples? Our comprehensive semen workshop covers everything you need to know about sperm preparation, including optimizing the process and mastering sperm freezing techniques. While we haven't finalized the...

Is transportation without cold chain safe?

Concerns may arise regarding the effect of extreme weather conditions on product performance. To address these concerns, all Nidacon products undergo rigorous testing for elevated temperatures up to 50°C and down to -18°C over a span of 5 days. The results of these...

DNA fragmentation due to storage

Sperm are highly sensitive to temperature fluctuations during storage, it can have a negative effect on both semen motility and DNA integrity. The best way to store the sample is at room temperature (RT). Compared to storage at 37°C, maintaining samples at RT...