Throughout history, ensuring the protection of economically important agricultural species has involved the storage, assessment, and distribution of genetic resources. One preservation method for these resources involves placing them in a frozen state, a technique known as cryopreservation. Cryopreserved samples are commonly stored in collections or repositories [ [1] , [2] , [3] , [4] ]. However, scalable cryopreservation technologies and germplasm repositories are not in place for most aquatic species despite the urgent need to protect the genetic resources that provide the foundation for aquaculture, food security, biomedical research, conservation, and wild fisheries. The genetic resources that support billions of dollars [ 5 ] of capture fisheries and human livelihoods are not protected, and the risk and expense of maintaining live animals (rather than frozen samples) hinder the growth of numerous aquatic industries [ 6 ]. These risks and expenses can be minimized by developing proprietary or shared (open) hardware devices that are capable of accelerating repository development and aiding in management and processing operations for the protection of genetic resources [ 7 ].
The growing climate crisis has exacerbated costs, risks, and needs associated with safeguarding genetic resources of aquatic species around the world. A vast majority of aquatic species that are important for aquaculture, food security, biomedical research, conservation, and wild fisheries are native to low-to-middle income nations where genetic resource protection is not a long-term priority or where equipment and reliable resources are scarce. Policy and long-term agendas must be addressed at scales beyond the individual. With the rapid growth of open-additive manufacturing, sustainable capabilities and resources can become widely accessible, and can be developed, customized, and fabricated by anyone.
Reliable tools and devices are essential for safeguarding genetic resources because they enable critical processing and quality management (QM) steps from sample collection to final usage. A relevant example is Bangladesh which is home to >600 species of freshwater and marine fishes. These fishes provide a primary protein source to sustain a growing human population of 171 million. Land use changes, introduced species, overharvesting, and other anthropogenic effects have strained open-water fisheries, and the country now relies heavily on farmed fishes (i.e., aquaculture) [ 8 ] with a narrowing gene pool. Cryopreservation is essential for preserving quality genetics, sustaining livlihoods, and ensuring sustainable production and improvement of aquatic species in Bangladesh and abroad. There are ongoing efforts to develop germplasm repositories for aquatic species in Bangladesh [ 8 , 9 ], but access to reliable tools and supplies, especially for quality management, are major roadblocks to these efforts. These same urgent needs for protection of aquatic genetic resources exist throughout the world, including the United States.
Capability needs for cryopreservation are driven by processing steps such as germplasm collection (e.g., sperm, eggs, early life stages, cells), quality evaluation, cryopreservation, storage, thawing, and final usage. Sample quality is of critical importance as the samples frozen today may be stored for decades and processing of poor quality samples wastes time and resources today and in the future. Quality management is a major driving force behind the need to develop novel, customizable, and accessible microdevices (e.g., micromixers [ 10 ], microfluidic lab-on-a-chip systems [ 11 ], and micro-separators [ 12 ]) to assist in safeguarding aquatic genetic resources. Such microdevices need to be versatile and practical for activities centered around germplasm QM, including quality planning, quality assurance (QA, process oriented), quality control (QC, product oriented), quality evaluation, and quality improvement.
There are existing devices to accomplish these processes, but they are often fixed in design, not suitable for multiple species, and prohibitively expensive for global deployment. For example, the process of counting sperm to calculate concentration can be accomplished by use of commercial devices such as a hemocytometer (>US$100) or a Makler chamber (>US$750) with counting by eye (which requires experience and is prone to variation) or by use of a computer-assisted sperm analysis (CASA) system (highly repeatable but >US$25,000). Integration of open-hardware microfluidic and microdevice systems would play a pivotal role in ensuring the dependable quality of germplasm materials, facilitating the isolation and culture of gametes and embryos, and optimizing the efficiency of sperm sorting and separation [ 13 ].
The use of soft lithography to develop microdevice systems (e.g., the Microfabricated Enumeration Grid Chamber [MEGC, 14] or the Single-piece Sperm Counting Chamber [SSCC, 15]) began to address some of the issues with sperm counting devices but suffer from prohibitively expensive initial costs and a lack of efficient options for iterative customization. Soft lithography typically makes use of the material, polydimethylsiloxane (PDMS) which yields high-resolution parts with excellent surface finish and low cytotoxicity [ [14] , [15] , [16] , [17] , [18] ]. In traditional PDMS-based soft lithography, microdevice fabrication relies on a master mold created through intensive soft lithography processes (e.g., photolithography and etching) [ 19 ]. Microdevice creation entails pouring the PDMS onto the master mold, letting it cure, and peeling it off to replicate the mold pattern. Despite its effectiveness, this process is expensive, time-consuming, complex [ 20 ], and has a number of drawbacks that limit use, especially for rapid prototyping. Soft lithography is more than capable of fabricating high-resolution devices for germplasm samples that exist at the smallest size ranges of aquatic germplasm (e.g., sperm of zebrafish [0.002 mm head width] or swordtails [0.001 mm head width]). However, it is not reliable for creating devices with larger or varied heights and depths that are required for most other species, and is slow, costly, and restricted to specialized facilities. In this study, we did not directly compare PDMS and resin prints, although such evaluations have been conducted in the past [ [21] , [22] , [23] , [24] , [25] , [26] ]. Instead, our focus was on the evaluation of the potential for shifting to new fabrication techniques, including overall consideration of factors such as cost reduction, improved fabrication accessibility, and development of open-hardware communities based on the sharing of digital design files.
Three-dimensional (3-D) resin printing techniques such as stereolithography (SLA) and digital light projection (DLP) offer a promising and effective alternative to soft lithography and are gaining traction in the development and prototyping of microdevices. These rapidly advancing technologies can play a crucial role in addressing the creation of hardware devices with broad applications in genetic resource protection [ 14 , 15 , 27 , 28 ]. Three-dimensional resin printers surpass many of the constraints of soft lithography and other traditional methods through layer-by-layer transformation of computer-aided designs into tangible hardware, crafting accurate 3-D shapes. This process eliminates the need for photo masks, alignment processes, etching, and bonding which require specialized facilities and well-trained personnel, offering a more efficient and flexible manufacturing approach [ 29 ]. In addition, resin printers have access to thousands of resin types, including those developed for application in human medicine (e.g., dental-grade resins) and for use with germplasm [e.g., [ 30 ]].
Two major levels of resin printers are industrial-grade and consumer-grade. In general, consumer-grade printers have lower prices (US$400 – US$1,000) and lower-grade components, often limiting the resolution that can be achieved. Industrial-grade printers come with greater up-front costs (>US$10,000) but have higher-grade components, access to customizable resin materials, optimized resin polymerization, and system processing features for faster and more successful prints. Even the higher-priced machines, however, are much more widely available and less expensive than traditional soft lithography. Although some groups have taken the approach of pushing the capabilities of consumer-grade printers, a slow and resource-intensive process [ 31 ], there are few studies that evaluate the accuracy and precision available and resources required for device fabrication using these different techniques (resin printing and soft lithography) and printer types (industrial and consumer). This understanding is vital for aquaculture and aquatic research communities outside of traditional engineering departments. Consumer-grade products are beneficial because of their accessibility, but for technology developers, it may be more advantageous to prototype quickly with industrial-grade printers before pushing the boundaries of consumer-grade products to make devices widely available. By finding a balance among these factors, 3-D resin printing can offer new opportunities for rapid prototyping and production of micro-scale devices as an alternative to conventional soft lithographic methods.
Thus, the goal of this study was to evaluate the capabilities of 3-D resin printers and demonstrate the fabrication quality of microdevices using industrial and consumer 3-D resin printers and conventional soft lithography (photolithography) techniques. The specific objectives were to: 1) evaluate accuracy and precision in feature fabrication with opaque and clear resins; 2) assess the accuracy and precision between fabrication techniques (resin printing and photolithography), particularly for small features (<1 mm); 3) analyze the visual morphology of features produced by different methods, and 4) evaluate the utility, time, and cost requirements for overall comparison of microfabrication among the methods.