Abstract:In sexual assault cases, forensic samples are a mixture of sperm from the perpetrator and epithelial cells from the victim. To obtain an independent short tandem repeat (STR) profile of the perpetrator, sperm cells must be separated from the mixture of cells. However, the current method used in crime laboratories, namely, differential extraction, is a time-consuming and labor-intensive process. To achieve a rapid and automated sample pretreatment process, we fabricated a microdevice for hydrodynamic and size-b… Show more
“…One area where microfluidic devices have particularly excelled is the separation of sperm cells from samples with a low concentration of sperm cells relative to other material, including the separation of sperm from epithelial cells for forensic analysis, from white blood cells in contaminated semen, and from testicular cells after a testicular biopsy. Liu and coworkers developed a microfluidic system ( Figure 2 ) for the separation of sperm and epithelial cells for rapid forensic analysis ( 61 ). By designing a microchannel with functional structures, the hydrodynamic interaction between fluid flow and cells led to the separation of different sized cells.…”
Section: Microfluidics For Sperm Sortingmentioning
confidence: 99%
“… This figure depicts a microfluidic system designed for rapid separation of sperm from epithelial cells with application in forensics related to sexual assaults. (A) A picture of the actual device; (B) the cell mixture is aligned against the top wall in the pinched segment, and then the position difference of different sized cells is amplified in the expansion region; (C) sperm recovery rate is improved in the parallel capillary tubes ( 61 ). …”
Section: Microfluidics For Sperm Sortingmentioning
Microfluidics technology has emerged as an enabling technology for different fields of medicine and life sciences. One such field is male infertility where microfluidic technologies are enabling optimization of sperm sample preparation and analysis. In this chapter we review how microfluidic technology has been used for sperm quantification, sperm quality analysis, and sperm manipulation and isolation with subsequent use of the purified sperm population for treatment of male infertility. As we discuss demonstrations of microfluidic sperm sorting/manipulation/analysis, we highlight systems that have demonstrated feasibility towards clinical adoption or have reached commercialization in the male infertility market. We then review microfluidic-based systems that facilitate non-invasive identification and sorting of viable sperm for in vitro fertilization. Finally, we explore commercialization challenges associated with microfluidic sperm sorting systems and provide suggestions and future directions to best overcome them.
“…One area where microfluidic devices have particularly excelled is the separation of sperm cells from samples with a low concentration of sperm cells relative to other material, including the separation of sperm from epithelial cells for forensic analysis, from white blood cells in contaminated semen, and from testicular cells after a testicular biopsy. Liu and coworkers developed a microfluidic system ( Figure 2 ) for the separation of sperm and epithelial cells for rapid forensic analysis ( 61 ). By designing a microchannel with functional structures, the hydrodynamic interaction between fluid flow and cells led to the separation of different sized cells.…”
Section: Microfluidics For Sperm Sortingmentioning
confidence: 99%
“… This figure depicts a microfluidic system designed for rapid separation of sperm from epithelial cells with application in forensics related to sexual assaults. (A) A picture of the actual device; (B) the cell mixture is aligned against the top wall in the pinched segment, and then the position difference of different sized cells is amplified in the expansion region; (C) sperm recovery rate is improved in the parallel capillary tubes ( 61 ). …”
Section: Microfluidics For Sperm Sortingmentioning
Microfluidics technology has emerged as an enabling technology for different fields of medicine and life sciences. One such field is male infertility where microfluidic technologies are enabling optimization of sperm sample preparation and analysis. In this chapter we review how microfluidic technology has been used for sperm quantification, sperm quality analysis, and sperm manipulation and isolation with subsequent use of the purified sperm population for treatment of male infertility. As we discuss demonstrations of microfluidic sperm sorting/manipulation/analysis, we highlight systems that have demonstrated feasibility towards clinical adoption or have reached commercialization in the male infertility market. We then review microfluidic-based systems that facilitate non-invasive identification and sorting of viable sperm for in vitro fertilization. Finally, we explore commercialization challenges associated with microfluidic sperm sorting systems and provide suggestions and future directions to best overcome them.
“…Therefore, this method does not rely on sperm motility and can be used for selecting nonmotile sperms from other species. Liu et al used a modified version of PFF to separate a mixture of epithelial cells (with 40–60 µm diameter representing the victim's cells) from human sperm heads (with 4–6 µm diameter representing the perpetrator's cells) with the potential application in sexual assault and forensic medicine . However, numerical and experimental results conducted by Berendsen et al demonstrated that PFF alone could not be used to separate a mixture of sperms with flagellar (tails) from 11 µm microbeads.…”
Section: Continuous‐flow Microfluidics In Artmentioning
The fields of assisted reproductive technology (ART) and in vitro fertilization (IVF) have progressed rapidly, yet still need further improvements. Microfluidic technology can incorporate various ART procedures such as embryo/gamete (sperm/oocyte) analysis, sorting, manipulation, culture, and monitoring. The introduction of paper‐based and droplet‐based microfluidics further improves the commercialization potential of this technology. The progress in 3D printing technology allows for the integration of microfluidics with tissue engineering that may revolutionize current practices in biology and medicine. This review categorizes ART methods according to continuous‐flow microfluidics, paper‐based microfluidics, droplet‐based microfluidics, and organ‐on‐a‐chip. The advances are summarized and potential opportunities in infertility diagnosis, sperm selection, sperm guidance, oocyte selection, insemination, embryo culture, embryo monitoring, and cryopreservation are identified. While some advances of continuous‐flow microfluidics for ART have already been reviewed, other microfluidic techniques are still in their early stages. It is envisioned that advances in droplet‐based microfluidics, especially digital microfluidics, will allow for more progress in human IVF, particularly single embryo transfer. Droplet‐based microfluidics may also lead to fully integrated and high‐throughput platforms for animal IVF. Recent advances in organ‐on‐a‐chip including ovary/uterus/oviduct‐on‐chip platforms hold promise for the integration of the whole human reproductive system‐on‐a‐chip for clinical applications.
“…These issues can result in lack of reproducibility, inefficient cell separation, and delayed processing-which can contribute to lagging backlogs. Several rapid and/or automated methods for differential separation of sperm cells have been developed as faster alternatives, including the use of alkaline plate-based methods [12], laser microdissection [13,14], antibodybased cell capture [15,16] and microdevice-based methods [17][18][19]; unfortunately, these techniques have not been widely adopted as they are either too laborious and complex or are not yet commercially available.…”
Sexual assault evidence often contains sperm cells, which are typically separated from nonsperm cells using manual differential lysis procedures. The goal of this study was to evaluate the automated QIAGEN QIAcube for this purpose and to compare it to manual QIAGEN and manual organic differential methods using DNA yields and STR profile data for assessment. DNA yields were determined by qPCR, followed by multiplex STR amplification, CE analysis, and mixture interpretation. The automated method was capable of effective cell separation, producing DNA yields sufficient for STR amplification. Further, sperm fraction human:male DNA ratios from the QIAcube samples were consistently closer to the desired 1:1 and STR profiles were less likely to result in mixtures, with 6-8Â fewer female alleles detected (median 1.5 alleles). Ultimately, using the QIAcube for automated differential processing of semen-containing mixtures reduces the need for downstream mixture interpretation and improves STR profile quality with substantially less hands-on time.
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