Broadly the present invention describes the fabrication of spatially controlled polymeric structures using a radiation or particle beam. The resulting structures find use in a variety of electrophoretic and sensor applications, including clinical assays, high throughput screening for genomics, proteomics and pharmaceutical applications, point-of-care in vitro diagnostics, molecular genetic analysis and nucleic acid diagnostics, cell separations, and bioresearch generally, high throughput screening of materials for separation and catalysis.
Microarray fabrication technology has been developed recently, based on the deposition of a discrete amount of materials using a robotic handling device. In this approach an array of liquid pre-polymerisation mixture comprising of liquid monomer that may be combined with other monomer(s), solvent, initiator, chemical and biochemical compound(s), dissolved polymer is first deposited on a substrate and then polymerised in situ by presenting the array to initiating conditions. This approach suffers from the difficulty of maintaining integrity of the materials deposited before exposure to initiating conditions, which has large consequences on the quality of the resulting polymeric structures. Evaporation, effect of presence of oxygen, surface properties of the substrate, quantity that can be deposited and shapes of structures that can be fabricated all affect the quality and quantity of deposited material making it very difficult to control.
Polymer arrays can be formed using photomasks (EP1331516). This method is similar to manufacturing integrated circuits. Light is applied through a mask that has a predefined image pattern which leads to initiation at polymerisation in certain regions of a substrate but not in others. The substrate can include solids, such as silicon, glass, quartz, and polymers. The fabrication of a multicomponent array in general requires the use of multiple varieties of masks, which is not always convenient. In addition this approach suffers from the limitations highlighted above.
According to another approach, direct optical photolithography can be performed with an optical beam without the use of photomasks (U.S. Pat. No. 6,480,324). The light patterns are generated by a spatial light modulator controlled by a computer, rather than being defined by a pattern on a photomask. Here each pixel is illuminated with an optical beam of suitable intensity and the imaging (printing) of an individual feature on a substrate is determined dynamically by computer control. This invention employs a programmable micro-mirror array, which plays an essentially similar role to photomask. It is centered around the development of nucleic acid arrays and also involves photochemistry. Many of the compounds that are potentially useful for manufacturing polymer arrays are photosensitive and can decompose upon illumination.
A preferred embodiment of the invention can provide a fabrication method that avoids or reduces the limitations mentioned above in order to produce patterned polymeric structures. Thus the invention provides a method of fabricating a structure or pattern comprising a polymeric material on a substrate, comprising (a) providing a substrate; (b) providing a liquid phase comprising a polymerisable material in contact with a surface of said substrate; (c) directing a radiation beam to impinge on said surface at the substrate/liquid phase interface so as to initiate polymerisation adjacent the irradiated site; and (d) causing the beam to scan in a predetermined pattern, thereby initiating polymerisation in a corresponding pattern. NB The reference to causing the beam to “scan” means that it is caused to move across the surface in a controlled way corresponding to a desired pattern which can be continuous or discontinuous (or both in different regions).
The beam is preferably a laser beam, especially an IR laser beam.
Spatially controlled polymeric structures are fabricated by using a laser beam, preferably an IR heat generating CO2 laser, which initiates polymerisation on the pre-determined areas of surface. The polymer structures are created on a substrate surface by directing the laser beam according to a pre-determined pattern. Accordingly the invention provides a means to grow, rather than deposit, polymers of desired shapes from a pre-polymerisation mixture in the liquid phase on a substrate as predetermined by a user. The subject devices find use in a variety of electrophoretic and sensor applications, including clinical assays, high throughput screening for genomics, proteomics and pharmaceutical applications, point-of-care in vitro diagnostics, molecular genetic analysis and nucleic acid diagnostics, cell separations, and bioresearch generally, high throughput screening of materials for separation and catalysis.
A preferred embodiment of the invention will now be described with reference to the accompanying drawings.
The first embodiment of the present invention describes performing of the polymer deposition using IR laser with electromechanical laser galvanometer scanning system. The set-up consists of a reservoir 2 containing a solution 3 comprising a mixture of monomer(s) with initiator dissolved in an appropriate solvent. The monomer mixture is in contact with a thin sheet 1 of a substrate. Typically the substrate covers the reservoir, and a laser beam 4 is applied from above (4).
The laser beam is generated by a CO2 infrared laser 10 and passes to a movable mirror 12, moved by a motor 14 controlled by a computer 16. The diagram is highly schematic; in practice we used a commercial product, a FENIX laser marker (SYNRAD, Inc, Wisconsin, USA), with a 30 W CO2 laser and an X-scanning mirror. Laser beam 4 is directed to pass through the substrate (1) following a user-designed pattern. It heats locally zones of the substrate. The initiator in close proximity to these zones at the lower surface of the substrate decomposes, initiating polymerisation. The growth of polymer structures 5 is dependent on factors such as beam intensity, time of exposure, and properties of the substrate and its surface.
In some embodiments of the present invention the properties of the substrate and/or the wavelength and/or intensity of the laser beam are adapted using methods well established in the art, to allow higher control over the polymer adhesion, morphology and polymerisation time. Thus the surface of the substrate can be optionally modified with polymerisable compound or with immobilised initiator molecules to promote polymer growth and adhesion.
In some embodiments, initiator is not present in the solution and is used only in immobilised form.
The pre-polymerisation mixture may contain one or several monomers and be combined with solvents, polymerisation initiators, dissolved polymers, natural or synthetic biochemical and chemical compounds.
A reservoir for holding the mixture can be made of silicon, glass, metal, plastic, ceramic or a combination of these. The cavity containing pre-polymerisation mixture may be emptied and re-filled with pre-polymerisation mixture of varying compositions to allow for the fabrication of an array of structures of varying nature, composition and properties. This also offers the possibility to fabricate layered polymeric structures by successively growing polymer layers of different nature on top of each other.
In other embodiments of the invention the energy will be applied to initiate polymerisation in different ways, including using light (e.g. an excimer laser), focused ionic, particle, X-ray and electron beams. The pattern can be changed by re-focusing and re-directing the applied energy.
In some embodiments of the invention, the monomer mixture contains template molecules which will be extracted from the formed polymer structures creating imprinted cavities capable of selective recognition, signalling or catalysis. Development of these materials (molecularly imprinted polymers) is a well established process. Depending on the application, functional monomer(s) and/or template can contain fluorescent tags (reporters) which will allow detection of target compounds. The application of fluorescent tags and environmental sensitive probes is well known in the art.
The invention is also concerned with the application of the fabricated spatially controlled polymeric structures. These devices may be used in a variety of applications, including, e.g., high throughput screening assays in drug discovery, immunoassays, diagnostics, genetic analysis, and the like. In another aspect the structures (arrays) will be used as sensor components, lab-on-a-chip for performing chemical and/or biological experiments and as research platform for studying and optimising separation, molecular recognition and catalytic processes.
While advantageous embodiments have been chosen to illustrate the invention, it will be understood by those skilled in the art that various changes and modifications can be made therein without departing from the scope of the invention as defined in the corresponding embodiments.
The present invention will now be further particularly described with reference to the following, non-limiting examples.
Number | Date | Country | Kind |
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0411348.6 | May 2004 | GB | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/GB2005/002024 | 5/23/2005 | WO | 00 | 3/3/2008 |