An embodiment of the invention relates to a substrate. A further embodiment relates to a target plate.
The wetting of a surface of a solid such as e.g. a polymer material, silicon, a metal or an alloy by a liquid indicates an interaction between the surface of the solid and a molecule of liquid (adsorption of liquid to the surface of a solid), and a competitive phenomenon of adhesion between the solid and liquid and cohesion between molecules of the liquid. A larger cohesion than adhesion brings about a decrease in wettability, and less cohesion than adhesion brings about an increase in wettability.
Good wettability to liquid water refers to hydrophilic properties, and poor wettability refers to hydrophobic properties.
Such wettability can be quantitatively determined by measuring a contact angle of a solid surface. The hydrophobic properties mainly depend on chemical properties of the surface and of the micro- and nano-structures thereof.
Various methods have been reported (e.g. in US 2007/0013106A1) to construct hydrophobic surfaces by modifying structures of the surfaces. Conventionally, hydrophobic surfaces are fabricated with the help of chemical treatment for changing the surface energy of materials or for modifying the surface roughness, for example by polypropylene etching, plasma enhanced chemical vapor deposition (PECVD), plasma polymerization, plasma fluorination of polybutadiene, microwave anodic oxidation of aluminum, solidification of an alkylketene dimer, nanostructuring carbon film, polypropylene coating, carbon nanotube aligning, forming poly(vinyl) alcohol nanofibers, making the surface of polydimethylsiloxane porous, or oxygen plasma treatment. US 2007/0013106 A1 in particular disclose a UV-nanoimprint lithography technique to produce a hydrophobic structure in a polymer film based on replicating the structure of a hydrophobic leaf, e.g. lovegrass leaf.
In Life Science diagnostics in order to analyze e.g. proteins, the proteins are solved in a liquid, also referred to as crystallization matrix and afterwards a droplet of the combination of crystallization matrix and protein, also referred to as analyte is applied on a surface of a substrate. The crystallization matrix evaporates and the protein/matrix alloy crystallize on the surface of the substrate. The crystallized proteins are then analyzed via e.g. a mass spectrometric process.
Known crystallization matrices have compounds like e.g. 2,5-dihydroxy benzoic acid, 3,5-dimethoxy-4-hydroxycinnamic acid, 4-hydroxy-3-methoxycinnamic acid, α-cyano-4-hydroxycinnamic acid, picolinic acid or 3-hydroxy picolinic acid and their respective solvents and applications are depicted in
It is an object of the invention to provide a substrate and a target plate for improving the analytic process.
This object is solved by a substrate and a target plate according to claims 1 and 20.
Further details of the invention will become apparent from a consideration of the drawings and ensuing description.
The accompanying drawings are included to provide a further understanding of embodiments and are incorporated in and constitute a part of this specification. The drawings illustrate embodiments and together with the description serve to explain principles of embodiments. Other embodiments and many of the intended advantages of embodiments will be readily appreciated as they become better understood by reference to the following detailed description. The elements of the drawings are not necessarily to scale relative to each other. Like reference numerals designate corresponding similar parts.
a shows a substrate according to a first embodiment;
b shows a top view on a substrate according to the first embodiment;
c shows a side view of a substrate according to the first embodiment;
d shows a cross-section of a substrate according to the first embodiment along the intersection line A-A of
e shows an enlarged detail of the cross-section of
f shows a further enlarged detail of the cross-section of
g shows a perspective view on a surface of a substrate according to the first embodiment,
a shows a substrate according to a second embodiment;
b shows a top view on a substrate according to the second embodiment;
c shows a side view of a substrate according to the second embodiment;
d shows a cross-section of a substrate according to the second embodiment along the intersection line A-A of
e shows an enlarged detail of the cross-section in
f shows a further enlarged detail of the cross-section in
g shows a further enlarged detail of the cross-section in
h shows a perspective view on a surface of a substrate according to the second embodiment,
a shows a top view on a substrate according to a third embodiment;
b shows a side view of a substrate according to the third embodiment;
c shows an enlarged section of the top view in
d shows an further enlarged detail of the top view in
e shows a perspective view on a surface of a substrate according to the third embodiment,
a shows a top view on a substrate according to a fourth embodiment;
b shows a side view of a substrate according to the fourth embodiment;
c shows an enlarged detail of the top view in
d shows an enlarged detail of the side view in
e shows a perspective view on a surface of a substrate according to the fourth embodiment,
In the following, embodiments of the invention are described. It is important to note, that all described embodiments in the following may be combined in any way, i.e. there is no limitation that certain described embodiments may not be combined with others. Further, it should be noted that same reference signs throughout the figures denote same or similar elements.
It is to be understood that other embodiments may be utilized and structural or logical changes may be made without departing from the scope of the invention. The following detailed description, therefore, is not to be taken in a limiting sense, and the scope of the present invention is defined by the appended claims.
It is to be understood that the features of the various embodiments described herein may be combined with each other, unless specifically noted otherwise.
In
As depicted in the top view of the substrate 100 in
In the side view depicted in
In
g shows a perspective view of the structured surface 102 of the first embodiment. As it is depicted in
Further on, the structured surface 102 is configured to stimulate a smooth crystallization of microcrystals, when a droplet of an analyte is applied on the substrate 100.
The structured surface 102, also referred to as microstructure, is simultaneously boosting the hydrophobic property of the substrate 100.
The nature, dimensions and forms of the structured surface 102 have been determined by taking into account size, crystallization form and shape of microcrystals as well as properties of the crystallization matrix and hydrophobic properties.
The regular or uniform pattern results in a uniform or smooth crystallization. Otherwise, microcrystallization of different fluids and crystallization-matrices at almost perfect even and glossy surfaces follow the rules of self-organization and shape tight dendritic or other mostly self-similar crystal forms, for instance as crystal arrangements as a dense layer of single crystals or chain-like clusters. These arrangements have random dispersion at almost perfect and even surfaces, resulting in a non-uniform signal in analyzing apparatuses, since e.g. a laser used for evaporating the microcrystals evaporates different amounts of the microcrystals due to the irregular microcrystal pattern on the surface of the substrates.
The regular pattern 104 of elevated structures 106, 108 increase the contact angle or coating angle of droplets on the surface 102, thereby decreasing an expansion of the matrix-droplets and decreasing the contact surface between analyte and substrate, and offering cores for crystallization for the used matrix. This leads to smoother and more homogeneous crystallization. Also the crystallization time is reduced, thus, increasing the throughput of analyzing apparatuses.
The substrate might be used for analyzing proteins in Life Sciences or in e.g. environmental/chemical analytics and forensics and for other analytes like polymers, sugars, lipids, metabolites, etc.
An additional surface treatment or a further surface chemistry is not necessary.
The first embodiment of the invention depicted in
The cross-section of the first elevated structures 106 and the second elevated structures 108 are depicted as squares, but might also be realized as rectangles.
A improved smoothness of crystallization has been achieved when in the pattern a first distance d1 between the first elevated structure 106 and the second elevated structure 108 is different from a second distance d2 between the second elevated structure 108 and the next first elevated structure 106.
A further improved pattern is achieved when the first distance d1 and a first side 11 of the first cross-section are equal in length and wherein the second distance d2 and a first side 12 of the second cross-section are equal in length. In
A further improved pattern results when a height h1 of the first cross-section perpendicular to the nominal surface 110 is twice a height h2 of the second cross-section perpendicular to the nominal surface 110. In
In
The substrate 200 has a diameter D of 1.5 mm. The pattern of the surface structure includes a basic unit of a third elevated structure 206 and a fourth elevated structure 208, which elongates along a first direction x in parallel to the surface 202 as is shown e.g. in
The height h3 of the third elevated structure with respect to a nominal surface 210 is chosen as 0.001 mm and, thus, is twice the height h4 of the fourth elevated structure with respect to the nominal surface 210 which is 0.0005 mm. The width w1 of the third elevated structure is chosen as 0.001 mm and the width of the fourth elevated structure is chosen as 0.0005 mm.
In
The elevated structures 304 as a basic unit of the pattern have the form of a pyramid, each, with a square base area and the sidelines of the base areas of different pyramids are arranged in parallel, respectively. The sidelines e.g. might have a width of 0.001725 mm and are spaced apart from each other by a space width of 0.001584 mm. The height of the pyramids with respect to a nominal surface 310 might be chosen to 0.0011 mm.
In
The pattern used for the fourth embodiment includes a basic unit of a fifth elevated structure and a sixth elevated structure. The fifth and sixth elevated structures are formed as a first cube 404 and a second cube 406 with different volumes. Within the depicted fourth embodiment the sidelines of the first cube 404 are twice as large as the sidelines of the second cube 406 resulting in a volume of the first cube 404 which is eight times the volume of the second cube 406.
The length c1 of the sidelines of the first cube 404 has been chosen to 0.016032 mm and the length c2 of the sidelines of the second cube 406 has been chosen to 0.008016 mm. The pattern is formed from a regular pattern of the first cube 404 and the second cube 406, wherein the first and the second cube are alternately arranged in parallel to a nominal surface 410 surface in a first direction x and a second direction y, which are parallel to the nominal surface 410 and perpendicular to each other.
The sidelines of the first cube 404 and the second cube 406 are arranged in parallel to the first direction x and the second direction y, respectively.
It is also possible to use cuboids with different side lengths instead of or together with cubes in order to build a structured surface.
In
The substrates 502, 504 might each have the same structured surface or different structured surfaces.
With a plurality of substrates having the same structured surface it is possible to analyze quickly a plurality of different analytes.
With a plurality of different structured surfaces it is possible to analyze the effect of different structured surfaces on the analyzing process.
As is readily apparent for a person skilled at the art the provided dimensions of the elevated structures might be changed for other applications, e.g. other crystallization matrixes. For instance, it is possible to scale the dimensions by a same amount to achieve similar effects.
The embodiments shown include one structured surface, however, as readily apparent for a person skilled at the art it is also possible to use structured surfaces on both, a top and a bottom, surface of a substrate. In addition, also the region 506 between the substrates 502, 504 of the target plate might be structured by e.g. different structures than used on the substrates 502, 504.
In
With the proposed substrate and the proposed target plate microstructures are proposed that are stimulating smooth crystallization of microcrystals. The substrate and the target plate might also be used for boosting, enhancing, increasing or influencing hydrophobic property of the surface in comparison to an unstructured surface.
Although specific embodiments have been illustrated and described herein, it will be appreciated by those of ordinary skill in the art that a variety of ultra net and/or equivalent implementations may be substituted for the specific embodiments shown and described without departing from the scope of the described embodiments. This application is intended to cover any adaptations or variations of the specific embodiments discussed herein. Therefore, it is intended that this invention be limited only by the claims and the equivalents thereof.
Similar smooth crystallization effects might be achieved when the structure is inverted, i.e. when the structures are not elevated with respect to a nominal surface but are formed as trenches below the nominal surface with the respective cross-sections and dimensions. Thus, the inverted structures might be interpreted as negative images of the elevated structures.
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