The largest database of trusted experimental protocols

Prusa i3 mk3

Manufactured by Prusa Research
Sourced in Czechia

The Prusa i3 MK3S is a desktop 3D printer designed and manufactured by Prusa Research. It features a self-leveling and self-calibrating print bed, a built-in power supply, and a silent stepper motor drivers. The printer has a build volume of 250 x 210 x 210 mm and supports a wide range of 3D printing filaments.

Automatically generated - may contain errors

27 protocols using prusa i3 mk3

1

FFF 3D Printing of Hardened Steel Rods

Check if the same lab product or an alternative is used in the 5 most similar protocols
For the printing of the rods a commercially available FFF printer Prusa i3 MK3 (Prusa Research, Prague, Czech Republic) was used. The nozzles were made of hardened steel with diameters of 0.25 mm, 0.4 mm, and 0.5 mm.
+ Open protocol
+ Expand
2

3D Printed Drug-Loaded Oral Dosage Forms

Check if the same lab product or an alternative is used in the 5 most similar protocols
The drug-loaded filaments were printed on a FDM 3D printer (Prusa i3 Mk3, Prusa Research, Prague, Czech Republic) to oral dosage forms in various geometries. The geometries were designed with Fusion 360® (Autodesk, San Rafael, CA, USA) and sliced in Simplify3D® (Simplify3D, Cincinnati, OH, USA) to obtain the desired G-code. The print temperature for the PVA-PDM filaments was set to 185 °C, the bed temperature to 60 °C and the printing speed was 20 mm/s. The printing temperature had to be increased for the EVA-LD formulation, as the filament was very flexible and could not be transported reliably through the nozzle by the conveying wheels in the print head at lower temperatures, as the filament would otherwise wrap around the wheels. To ensure a constant filament-flow through the nozzle, the temperature of the nozzle was set to 220 °C and the printing speed was reduced to 10 mm/s. For the PVA-PZQ formulation, a nozzle temperature of 185 °C could again be used, but the bed temperature had to be increased to 90 °C because the printed objects adhered poorly to the print bed and detached from the bed more often. Therefore, a printing speed of 10 mm/s was also selected here. To obtain high print accuracy, the layer height was set to 0.1 mm and the extrusion width to 0.4 mm using a nozzle with a diameter of 0.4 mm. The infill percentage of the concentric infill was set to 100%.
+ Open protocol
+ Expand
3

Fabrication of Soft Pneumatic Actuators

Check if the same lab product or an alternative is used in the 5 most similar protocols
The design and fabrication steps of the pneumatic actuator were adapted from the Soft Robotics Toolkit50 (link). The dimensions of the actuator were slightly changed: the actuator chambers had a length of 77 mm, a width of 15 mm wide, and a height of 12 mm. Detailed drawings of the actuators are provided in the supplementary material (Supplementary Fig. 13). We cast soft silicone (Dragon skin 30, Smooth-On) to 3D printed molds made out of polylactic acid (PLA, Prusa I3 MK3, Prusa Research). The actuator was molded in two parts: an upper part including the pneumatic chambers and a lower part including the strain-limiting layer (a glass fiber net). The parts were bonded together by spreading a thin layer of the same silicone between the parts. An air inlet was added to the actuator by first using a biopsy punch and then attaching a tube to the punched hole. The pneumatic strain gauge was glued to the bottom of the actuator with a thin layer of silicone.
+ Open protocol
+ Expand
4

3D Printed Bee-Inspired Joint Design

Check if the same lab product or an alternative is used in the 5 most similar protocols
Using the computer‐aided design software Rhinoceros 6, a 3D model of a bee‐inspired joint was designed and developed. The model consisted of two parts that represent hooks and membrane in the real coupling mechanism (Figure 5A and Video S1, Supporting Information). To examine the function of the joint in practice, the design was fabricated using 3D printing. For this purpose, the 3D printer Prusa i3 MK3 (Prusa Research, Prague, Czech Republic) and polylactic acid filament (Amolen Firefly filament, filament diameter: 1.75 mm, printing temperature: 200–220 °C, Prusa Research) were employed. The bee‐inspired joint was then used in the conceptual design of a cartridge razor (Figure 5C and Video S2, Supporting Information).
+ Open protocol
+ Expand
5

3D Printed Macroscopic Scaffold for Tissue Engineering

Check if the same lab product or an alternative is used in the 5 most similar protocols
Macroscopic scaffolds were printed with PCL filament (1.75 ​mm eMorph 3D filament Natural, esun, Shenzen Esun Industrial Co.Ltd) in a FDM 3D printer (Prusa i3 MK3 (Prusa Research a.s., Holešovice, Czech Republic) with a 0.4 ​mm nozzle) with heated bed. This external framework was designed with Prusa Slicer (version 2.1, Prusa Research a.s., Holešovice, Czech Republic) software to provide geometrical shape and support to the subsequent layer of electrospin fibers. Printer head was purged 3 times with PCL filament and cleaned with a wire brush. Printer plate was cleaned with water and 70% ethyl alcohol. The patch was printed at 180 ​°C, 20 ​mm/s speed and 0.1 ​mm layer thickness. The patch was designed using a four-layered grid pattern. The strand thickness was 400 ​μm and distance between strands was 2000 ​μm. The diameter of the patch was 34.8 ​mm. More details of the printing process are provided in Appendix A.
+ Open protocol
+ Expand
6

3D Printed Lactoprene® Scaffolds for Tissue Engineering

Check if the same lab product or an alternative is used in the 5 most similar protocols
Lactoprene® 100 M (Poly‐Med Inc) was used to fabricate the scaffold. Lactoprene® is a PLLA, 100% l‐lactide with a molecular weight of 165–170 kDa that is supplied as a 1.75 ± 0.05 mm diameter filament. Scaffold design was accomplished with design application software (Rhinoceros 5.0, Robert McNeel & Associates). The finished design included a fiber diameter of 150 μm and an osteogenic critical pore size of 450 µm. Multiple layers with these dimensions were stacked to obtain the desired overall size of the scaffold. Conversion of the standard tessellation language (STL) file to an applicable G code for the 3D print format was done with conversion software (PrusaSlicer 2.0, Prusa Research a.s., Praha, Czechia). Printing in these minute dimensions demanded a precise printer nozzle that could move without dragging the fiber from one point to another. G Code modifications controlled this issue and printed the scaffolds successfully. Scaffolds were fabricated with a fused deposition modeling printer (Prusa i3 MK3®, Prusa Research a.s.) equipped with an E3D v6 Nozzle (MatterHackers) with an inner diameter of 150 µm. The scaffolds were printed in the following configurations: 5 × 2 mm cylinders (n = 50); 5 × 10 mm cylinders (n = 10); 5 mm cubes (n = 6) and a 20 ×20 mm square sheet, one‐layer thick.
+ Open protocol
+ Expand
7

Additive Manufacturing of Filament Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
The basis for AM is a CAD data file generated in conventional CAD programs. These data are transferred as an STL file to the slicing program, where they are parameterized according to the print strategy and device-specific aspects. For slicing, the commercial software Simplify3D® Version 4.1.2 (Simplify3D®, Blue Ash, OH, USA) was used.
For AM of the samples, a standard printer Prusa i3 MK3S+ (Prusa Research, Prague, Czech Republic) with a standard brass nozzle was used. Manufacturing parameters after parameter adaption are presented in Table 1.
To demonstrate the system openness of the filament, print tests were performed on a Hage 140L (Hage 3D GmbH, Obdach, Austria), which has a direct belt drive and a direct driven Renkforce RF100 (Conrad Electronic SE, Hirschau, Germany). The results showed that the filament does not cause any problems when manufacturing parts with these commercially available standard machines.
+ Open protocol
+ Expand
8

3D-Printed Spectroscopy Sample Holder

Check if the same lab product or an alternative is used in the 5 most similar protocols
All parts were manufactured using a Prusa i3 MK3S (Prusa Research s.r.o., Prague, Czech Republic) with black (for one of the inlays) and white (for all other parts) coloured polylactic acid (PLA) filament (Prusa Research s.r.o., Prague, Czech Republic). Although PLA can be obtained in a very broad range of colours, we recommend using white PLA, to maximize reflection and avoiding an unwanted change of the colour of the reflected light. Prior to printing, the software Slic3r PE (Version 1.2, Prusa Research s.r.o., Prague, Czech Republic) was used to assemble parts into printing batches, and convert the 'stl.' files into '.gcode' files readable by the printer. We printed at an extruder temperature of 215 °C, and a bed temperature of 60 °C. The layer height was set to 0.2 mm and infill to 15%. Furthermore, we used “only on build plate” support structures to print the dome and the “spiral-vase” mode for the light-shielding ring. All other printing settings were left on default state of the PrusaSlicer for Generic PLA Filament but can be found in Supplementary Information 2. Print settings may vary between different printers (even of the same model) and filament types. Therefore, adjusting the parameters to your printer may be necessary.
+ Open protocol
+ Expand
9

Pancreas Tissue Slicing and Imaging

Check if the same lab product or an alternative is used in the 5 most similar protocols
A slicing matrix was designed with a section thickness of 2.8 mm, providing an optimal balance between reagent penetration and resolution/magnification to distinguish individual insulin-positive (INS+) objects for thresholding and quantification (Tinkercad, Autodesk, USA), using a 3D printer (Prusa i3 MK3S, Prusa Research, Czech Republic). Pancreata were mounted in 1.5% (w/v) low melting temperature agarose (Cat. No. 50100; Lonza, USA) at 37 °C in the custom-made 3D-printed matrix (Supplementary Fig. S1). Subsequently, whole pancreata were cut into 2.8 mm thick “slabs” and the agarose carefully removed. Tissue slabs wider than 2 cm (in the head region) were cut in two to ensure a good fit in the field of view when applying near infra-red optical projection tomography (NIR-OPT) microscopy (see below). Images were taken during the slicing process to document X, Y and Z coordinates for each slab (Supplementary Fig. S1). Tissue slabs were then stored in 100% methanol (MeOH; Cat. No. 67-89-4; Fisher Scientific, Sweden) at −20 °C until further processing.
+ Open protocol
+ Expand
10

Pressure Drop Rig with Real-Time Flow Validation

Check if the same lab product or an alternative is used in the 5 most similar protocols
The pressure drop rig can perform a real time check of the flow rate through the inlet (by using a flowmeter) and compare against the outlet flow rate (controlled using a mass flow controller) and thus enables real time verification that the leak in the test rig is minimal. Details of flow loop components are in Table I below.
We fabricated the 3D printed components on a PRUSA i3 MK3S (Prusa Research, Prague, Czechia) using MatterHackers (MatterHackers, Lake Forest, CA) silver MH Build series polylactic acid (PLA) filament (1.75 mm nominal diameter). The STL files were sliced in PrusaSlicer (Prusa Research, Prague, Czechia) and printed with a 0.25 mm brass nozzle, a layer height of 0.2 mm, a nozzle velocity of 25–60 mm/s, and an extrusion temperature of 210–215 °C.
The PX165 low range differential pressure transducers have a range of 0.25 to 2 inH2O, has an accuracy of ±1%, a stability of ≤±0.50% span/year, and a proof pressure of 7.25 psi. The ADS1115 is an analog to digital convertor (ADC) that has a 16-bit output resolution, up to 860 samples per second sampling rate, and an offset error and gain error of ±3 LSB and 0.01% respectively.
The pressure drop set up has a real time verification of flow and leakage built in to the set up that enables the measurement of the volumetric flow rate before and after the coupon, and thus ensures that there is no leak in the test rig.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!