Patent Application
20210101117
The present invention relates to a microfilter, which is characterized in that the microfilter is a microfilm that is made of non-epoxy-based materials and is perforated to create a patterned array of microholes.
The microfilter structure may be a solid membrane structured with microholes to make it a semi-permeable medium. The microfilter structure has been commonly applied to separate micro objects from complex samples.
A large variety of materials have been used to manufacture microfilters such as polymers, metals or composites depending on the field of application. For example, the epoxy based microfilms have been commonly used in biomolecules isolation. Steel based microfilters are common in inkjet nozzles. The epoxy based microfilters are easy to be processed using a lithography method. However, the epoxy based thin films are brittle and difficult to fabricate.
The microfilter structure has been employed in various fields of applications such as in electronic, chemical, food and biotechnology industries. Examples of the microfilter application include size classification of solid objects between micro and macromolecules using microsieves, micro particles isolation from liquids in biomedical filtration or refining processes, uniform distribution of liquid or gas inlet for micro spray generation in printing or drug delivery and an MEMS structure fabrication making use of a deposition mask.
The biomolecules such as bacteria, viruses, cells, vesicles, etc. possess structural flexibility. For a particular target, a precision microfilter is required to optimize the membrane pressure. A uniform array of cylindrical microholes may give the efficient filtration yield and smooth biomolecules isolation from various body fluids such as saliva, blood, urine, dialysis fluid etc.
Methods of manufacturing the microfilters such as track-etching, laser drilling, photolithography, etc. have been studied for microfilter fabrication. A track-etching method is commonly used to generate cylindrical holes in the microfilm but meets with limitation of non-uniformity and pattern repeatability of microholes. A lithography method is good for uniform microholes pattern generation but can only be applied to a limited number of materials. Comparatively, a laser drilling method is applicable to a large number of materials with great uniformity, however, the size range of the microholes is limited to the diameter of the laser spot.
The present invention discloses a non-epoxy based transparent microfilter patterned with microholes, a method of fabricating the microfilter, and a microfiltration unit, or a microfilter holder unit, to carry the filtration process.
First, the present invention provides a microfilter, comprising: a non-epoxy based microfilm, and a plurality of microholes provided on the surface of the non-epoxy based microfilm and penetrating therethrough via laser ablation, wherein the surface of the non-epoxy based microfilm is patterned into predetermined sections to locate isolated targets on the surface of the microfilm and enumerate the number of the isolated targets. In one embodiment, the laser is UV laser.
In one embodiment, the non-epoxy based microfilm is composed of a transparent polymer without an epoxide chain. In a preferred embodiment, the material of the non-epoxy based microfilm is a transparent plastic material. Example of the polymer material of the non-epoxy based microfilm may include any thermoplastic materials such as polycarbonate, polyethylene, polyethylene terephthalate, polyethylene naphthalate, polymethyl methacrylate and polystyrene, etc. In certain embodiments, the material of the non-epoxy based microfilm has non-fluorescent or low fluorescent characteristics in a UV region. The fluorescent characteristics of the microfilm can interfere analysis of isolated components when being studied by using fluorescence microscopy.
In certain embodiments, the non-epoxy based microfilm has a planer surface without any uneven part. In an alternative embodiment, the non-epoxy based microfilm is further coated with a thin film to facilitate the filtration process. In one embodiment, the top surface of the non-epoxy based microfilm has a thin film. In a preferred embodiment, the thin film is a metal film or a metal oxide film. In such an embodiment, the surface of microfilter alters the interaction between a target and the filter surface. For example, a thin film of metal or metal oxide may be coated to improve the hydrophilicity of the microfilter surface.
In one embodiment, the microholes are circular microholes. The diameter of the microholes depends on the size of the screening targets. In another embodiment, the mean diameter of each microhole is less than or equal to 10 μm. In a preferred embodiment, the microholes diameter ranges from 5 to 9 μm. In a more preferred embodiment, the microholes diameter ranges from 6 to 8 μm. In an alternative embodiment, the non-epoxy based microfilm is patterned with a plurality of the circular microholes having a diameter of approximately 7 μm.
In one embodiment, the microholes have cylindrical walls through the non-epoxy based microfilm, i.e., the top and bottom surfaces of the microholes have the same diameter. In an alternative embodiment, the microholes have the tapered walls through the non-epoxy based microfilm, i.e., the diameter of the top and bottom surfaces of the microholes is different from the diameter of the tapered walls. In an alternative embodiment, the shape of the microholes can be rectangular or hexagonal, depending on the screening target. In an alternative embodiment, the microholes are patterned in a uniform array in a straight, staggered or hexagonal geometry in the microfilm.
In certain embodiments, the thickness of the non-epoxy based microfilm is less than or equal to 25 μm. In a preferred embodiment, the thickness of the non-epoxy based microfilm ranges from 5 to 25 μm. The microfilter possesses good strength and flexibility to sustain the pressure during filtration. Another aspect of this invention is that the thickness of the non-epoxy based microfilm is selected to maintain the minimum aspect ratio for microholes. In certain embodiments, the thickness of the microfilm may be equal to the diameter of the microholes. In an alternative embodiment, the aspect ratio of the microfilm thickness and microholes diameter should not be more than 3 μm. The tapered angle of the microholes may increase with an increase of the microfilm thickness.
In certain embodiments, the number of the microholes is designed to optimize the filtration pressure and avoid membrane stress during filtration. The number of the microholes in the filtration area optimized for submicron objects is found to be at least 50,000. In an alternative embodiment, the number of the microholes may increase to reduce the filtration time. In certain embodiments, the gap between two adjacent microholes is optimized at about 20 μm. In an alternative embodiment, the gap between two adjacent microholes may depend on the screening target or the application field. In one embodiment, the gap between two adjacent microholes is 1-100 μm. In a preferred embodiment, the gap between two adjacent microholes is 2-50 μm. In a more preferred embodiment, the gap between two adjacent microholes is 5-25 μm.
The surface of the non-epoxy based microfilm can be patterned into different sections. The number of microholes is distributed into different sections. In certain embodiments, the surface of the non-epoxy based microfilm is patterned into predetermined sections, for example, 16 sections, to locate the isolated targets and quick enumerate the number of the isolated targets. In an alternative embodiment, the filtration area of the non-epoxy based microfilm can be divided into further sections to precisely locate the target. The number of the isolated targets can be precisely enumerated in different sections. In one embodiment, the surface of the non-epoxy based microfilm is divided into 1-50 sections. In a preferred embodiment, the surface of the non-epoxy based microfilm is divided into 5-30 sections. In a more preferred embodiment, the surface of the non-epoxy based microfilm is divided into 10-20 sections.
Another aspect of the present invention directs to the method of microfilter fabrication, comprising the following steps: using laser ablation in a non-epoxy based microfilm to form microholes in a predetermined pattern; and patterning the surface of the non-epoxy based microfilm into predetermined sections. In one embodiment, the laser is UV laser. In certain embodiments, a UV laser is used to fabricate the microholes through the non-epoxy based microfilm. The UV laser is short in wavelength and produces fine holes in the non-epoxy based microfilm. The excimer laser (UV laser) has the advantage of high precision for microholes formation in the non-epoxy based microfilm with low thermal buildup. The energy and pulse of the laser need to be optimized for the non-epoxy based microfilm which is formed by a specific polymer. In an alternative embodiment, different kinds of laser, such as CO2, Nd:YAG, etc. may be used for microholes generation.
In one embodiment, the non-epoxy based microfilm is composed of a transparent polymer without an epoxide chain. In a preferred embodiment, the material of the non-epoxy based microfilm is a transparent plastic material.
In certain embodiments, the excimer laser may have projected directly to the non-epoxy based microfilm using focus lenses. The use of the focus lenses allows the formation of the taper angle of microholes to be controlled. Using the precise movement of the non-epoxy based microfilm, microholes design is translated to the membrane for microfilter fabrication. In an alternative embodiment, a laser mask is used to project multiple laser beams to the non-epoxy based microfilm and generate multiple arrays of microholes. This method provides high throughput of microholes perforation in the non-epoxy based microfilm.
In certain embodiments, the microfilter may be used for filtering biomolecules from biofluids. In one embodiment, the biofluids sample may be blood, urine, dialysis fluid, saliva, etc. In some embodiments, the microfilter may be used to screen nucleated cells from the blood having bigger size than the microholes such as circulating tumor cells (CTCs), colony-forming cells (CFCs), neutrophils, etc. In one embodiment, the sample is biofluid, and the targets are biomolecules.
The surface of the non-epoxy based microfilm can be patterned into different sections. A number of microholes is distributed into different sections. In certain embodiments, the surface of the non-epoxy based microfilm is patterned into predetermined sections, for example, 16 sections, to locate the isolated targets and quickly enumerate the number of the isolated targets.
Another aspect of the present invention is directed to a microfilter holder unit, or a microfiltration unit. The microfiltration unit comprises an upper frame and a bottom frame. The two frames have cylindrical side walls. The upper frame is connected with a side module which allows the sample inlet orifice to be adjusted from a wider opening to a narrower opening. The two frames are connected with each other through a screw coupling. The microfilter is sandwiched between the upper frame and the bottom frame of the microfilter holder unit. The microfilter holder unit is designed in such a way that it provides a linear passage of sample at the top and the bottom of the microfilter. The molecules in a sample having a size bigger than the microholes stay at the top of the microfilter surface while the remaining smaller molecules are filtered out through the microfilter.
The present invention may be implemented in many different forms and should not be construed as limited to the examples set forth herein. The described examples are not limited to the scope of the present invention as described in the claims.
As shown in
There was a plurality of circular perforated microholes with a diameter of approximately 7 μm in the microfilm. In addition, the shape of the perforated microholes was rectangular or hexagonal, depending on the screening targets. The perforated microholes were patterned in a uniform array in a straight, staggered or hexagonal geometry in the microfilm. The perforated microholes in the microfilm had the cylindrical walls or the tapered walls.
The number of the perforated microholes was at least 50,000, and the gap between two adjacent perforated microholes was optimized at about 20 μm. A number of perforated microholes was distributed into different sections.
The microfiltration unit was operated by applying negative pressure at the bottom. The sample passed through a top inlet of the microfiltration unit to a bottom outlet of the microfiltration unit due to a pressure difference. There was a microfilter in the microfiltration unit, wherein the microfilter was a thin film with multiple perforated microholes. The molecules in a sample having larger size than the microholes in the microfilter were isolated at the surface of the microfilter while smaller molecules were filtered through the microholes to the outlet. The negative pressure was applied by using a controlled suction pump.
The microfilter fabricated using perforation of non-epoxy-based microfilm using different lasers such as UV, visible and Infrared lasers. The microholes were generated by using the above lasers, the shorter wavelength provided microholes with good quality and a submicron diameter. The excimer lasers such as Krf & XeBr, etc. provided a fine cylindrical microholes structure.
The microfilter was used in medical diagnosis and prognosis. It isolated larger nucleated cells from the blood. The enumeration and collection of nucleated cell indicated the disease state. The isolated cells were further utilized for downstream analysis such as culture, immunostaining, PCR (Polymer chain reaction), NGS (Next-Generation sequencing), etc.
The microfilter was used for non-invasive tumor metastasis diagnosis by identifying the circulating tumor cells (CTCs). The tumor cells were larger in size than normal cells. The tumor cells were isolated by passing the blood through the microfilter. The isolated CTCs at microfilter surface were identified and enumerated by immunofluorescent staining and observed under fluorescence microscope.
In another example of the present invention, the microfiltration unit was used for non-invasive prenatal diagnosis by collecting colony-forming cells (CFCs) from the maternal blood. The CFC cells are bigger than normal blood components. The isolated CFCs were analyzed for genetic analysis by using FISH, NGS, etc.
In another example of the present invention, the microfilter was used for separating micro aggregates from the blood. In particular, preserved blood may have micro aggregates during storage. The microfilter was used to clear the micro aggregates before blood transfusion to a patient.
Please refer to
In the microfiltration unit of the present invention, the side module 113 of the upper frame 11 allowed the sample inlet orifice to be adjusted from a wider opening to a narrower opening.
In the microfiltration unit of the present invention, the upper frame 11 further comprised an upper gasket 114 disposed at an inner peripheral wall thereof, the lower frame 12 further comprised a lower gasket 123 disposed at an inner peripheral wall thereof, and the microfilter was sandwiched between the two gaskets.
The microfiltration unit of the present invention further comprised two gaskets respectively placed below and above the microfilter to avoid sample leakage and to hold the microfilter in place, wherein the material of the gaskets was rubber.
In the microfiltration unit of the present invention, the upper frame and the side module; including the flexible stripe and the transforming inlet head, were integrated into one piece.
In one embodiment, the flexible stripe was removably engaged with the lower part of the upper side wall, or removably engaged with the transforming inlet head, wherein the engagement was performed via a male and a female pair connector (not shown), such as a magic tape or other engageable elements.
In the microfiltration unit of the present invention, the diameter of the microfilter was 13 mm and the diameter of a filtration area was 9 mm.
The microfiltration unit of the present invention further comprised a controlled suction pump (not shown) for applying a negative pressure to the outlet orifice such that the linear passage of the sample was directed by a pressure difference.
The present application claims priority to U.S. Provisional Appl. No. 62/909,239, filed Oct. 2, 2019 which is incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62909239 | Oct 2019 | US |
