CROSS REFERENCE TO RELATED APPLICATION

[001] This application claims priority to U.S. Application 15017959 filed on 2 ^nd February 2016 which is pending. The said U.S. application 15017959 is hereby incorporated by reference in its entireties for all its teachings.

FIELD OF INVENTION

[002] The present invention is generally directed to microtube cap for more accurate reading of the results of polymerized chain reaction products and others.

BACKGROUND

[003] Research and diagnostics testing process of real-time polymerized chain reaction (PCR) products the analyzer instrument uses a light source to gather data during the PCR amplification process. This process uses products such as single tubes and caps, strips tubes and caps (typically 8 or 12 inline format) and grid format plates (8 x 12, 16 x 24 etc.). Prior to the actual testing process the sample have to be prepared. The sample preparation involves filling the tubes with an assay reagents and sealing the tubes to prevent evaporation during the thermal cycling. With the current designs of products available in the market for real-time PCR the lens of the sealing caps, strips and films come directly in contact with hands, thumbs, fingers or automated sealing devices and adversely effects the surface of the lens for optical clarity. Direct contact of this type is not desirable.

[004] For manual application of real-time PCR microtube caps a researcher will typically align the caps, strips or films and body of the PCR tubes and apply 1 to 3 KG of pressure on top of caps with their hands, thumbs and finger or other device. This also changes the shape of the top surface that would be subsequently used for optical measurement.

[005] In automated capping and sealing film machines the sealing platform applies direct pressure and or heat to the lens area of the PCR caps strips and films directly contacting the lens area. This direct contact to the lens area through which light will pass and be used to gather the PCR reaction data is not desirable for the many reasons. There is a need for producing a more optically conducive microtube cap. SUMMARY

[006] The present invention is an improvement on the existing microtube cap. In one embodiment, the product as a microtube has a closed distal end and an open proximal end. The proximal end is attached to a hinge that connects the proximal end and the cap. In another embodiment, the cap is a spherical shaped lid for the proximal open end of the tube. It has various indentations as concentric circles. The outer ring is wider than the inner first ring and extends over the opening of the proximal end of the tube. The inner first ring encloses the opening of the proximal end of the tube. The inner second ring is lower than the inner first ring. The inner second ring is concave in shape.

[007] In one embodiment, the surface of the inner second ring is made up of a transparent material of different thickness. The outer first ring has an inward protrusion called a plug that extends downwards and snugly closes the inner walls of the proximal end.

[008] The product (microtube) can hold between O.Olul to 1.00 ml content. The product may be made of polypropylene, polycarbonate, cyclic olefin copolymer material.

[009] The instant product may be used for regular PCR or real-time PCR. In another embodiment, clear inner second circle that is recessed is used for accurate optical reading. In another embodiment, recessed inner second circle to prevent glove or hand touch smudges that interfere with optical reading, avoids scratched due to close packing, PCR plate depression due to heat, avoids contact while processing.

[010] The configuration of the microtube may be in the format of individual tube, eight tube strip, 96 well format tube, 8 strip cap, 8 x 12 grid microtube or plate cap with the lowered feature and a flat sealing film with 96 lowered cap to fit a 96 well plate.

[011] The product and method of using the product disclosed herein may be implemented in any means for achieving various aspects. Other features will be apparent from the

accompanying drawings and from the detailed description that follows.

BRIEF DESCRIPTION OF THE DRAWINGS

[012] Example embodiments are illustrated by way of example and not limitation in the figures of the accompanying drawings, in which like references indicate similar elements and in which:

[013] Fig. 1 is a front view of the microtube 100. [014] Fig. 2 is a bottom back view 200 of the microtube 100.

[015] Fig. 3 is a top view 300 of the microtube 100.

[016] Fig. 4 is the close up bottom view 400 of the cap for the microtube 100.

[017] Fig. 5 is the close up top view 500 of the cap for the microtube 100.

[018] Fig. 6 shows a plate cap 600.

[019] Fig. 7 shows a single 8 microtube cap strip 700 for microtube 100.

[020] Fig. 8 shows a single 8 microtube cap strip 800 for a plate or microtube 100.

[021] Other features of the present embodiments will be apparent from accompanying the detailed description that follows.

DETAILED DESCRIPTION

[022] The present invention is directed to a microtube product that has a special structural change at the cap. This cap design may be applied to other formats such as strip or grid formats. More specifically the change in the design of the cap enables the optical reading to be more accurate. In one embodiment, the microtube has a distal end and a proximal end. Fig. 1 shows the front view of the microtube 100. The microtube 100 has a distal end 102 and a proximal end 104. The distal end 102 is conical at the bottom which is closed and wider on the top that is open. The proximal end 104 has an opening 114 to house the inward protrusion called plug 112 to seal the microtube. The proximal end has a ridge like structure 116 that strengthens the opening structure and allows the microtube to withstand the process depended effects such as heating, cooling, boiling, centrifugation and storing.

[023] During the manufacture transit and use, the PCR caps and films are packaged hundreds or sometimes thousands in a plastic bag allowing them to rub and chafe causing the lens area to have possible blemishes. In the new designs, the lowered and better protected lens area is more likely to be protected against surface imperfections resulting is more consistent testing data.

[024] The new and improved cap, strip and film lens design is recessed into the caps avoiding the direct contact during the cap application in both manual and semi and automated processes. This key feature has many advantages as follows.

• Avoid direct contact with lens during cap application as the lens area is lower than cap that will take the pressure to apply it to the tubes.

• Optimal optical reading due to lack of smudge, scratch or stains. [025] The product also has consistent wall thickness that enables uniform heating and cooling for accurate results. The polished inner surface and distal conical bottom allows maximum sample recovery. A hinge 106 like structure connects the opening of the proximal end and the cap 110. The hinge 106 has a flexible structure 108 that allows the hinge to be folded to allow the cap to close the opening of the proximal end of the microtube. The cap has an overextended radiused and blended structure 110 that helps close the cap and also open the cap without touching the inner second ring with finger.

[026] Fig. 2 shows bottom back view 200 of the microtube 100. The conical end 202 for the distal end is clearly visible in this angle and shows that it is directly in line with the opening of the proximal end. The inner second ring 204 of the cap is shown as a recessed section in this view. It may be concave, flat or rounded and is lower than the inner second ring. The recessed second ring 204 of the cap depressed and prevents the user from touching it while performing experiments. It is also made up clear materials that are biologically inactive but optically provides a clear path for passing through to read the samples in the conical end 202. The conical end 202 accommodates very small amount of samples and helps perform experiments in smaller quantities. The concave recessed part is transparent to allow maximum optical clarity for measuring the concentration of a sample after a real-time polymerase chain reaction. The concave recessed part 204 is at least 20-80% of the cap surface and has a thickness from .025mm to 1.0mm.

[027] Fig. 3 shows top view 300 of the microtube 100. The conical end is shown as a narrow bottom 302. It also depicts how centrally it is situated and is covered very well by 204. The outer ridge shown as 304 is wider than the proximal end 104 and covers the entire open end of the proximal end. The inner ring of the ridge of the proximal open end 306 is shown to be made up of a stronger material. This allows the tube (used interchangeably with microtube) from getting destroyed while regular lab use such as boiling, heating and cooling.

[028] Fig. 4 shows the close up bottom view 400 of the cap for the microtube 100. A plug 112 is used to be housed in the opening of the proximal end to secure the content of the microtube. It has two flanges. The wider end of the flange 404 is equal to the circumference of the proximal part of the microtube and top end of the flange 402 has the same circumference to fit the opening of the top of the proximal end. This is a novel approach to make sure there is minimal loss of material and no evaporation of samples while in use. The tip of the cap 404 may be used for opening and closing the tube as well.

[029] Fig. 5 is the close up top view 500 of the cap for the microtube 100. It shows in detail the upper portion of the inner second ring 204 recessed cap. The ridge that surrounds and connects the recessed part to the inner first ring 502 is shown to have a shape. It could flat, concave or smooth. This provides the means for lowering the inner second ring 204 to be lower than inner first ring.

[030] Fig. 6 shows a plate cap 600. The plate cap may be in form of films, strips or individual caps. The figure shows a composition of 8x 4 strips that may be used on a limited number of microtubes or a partial PCR plate. The novel feature inner second ring 204 is present in the shown embodiment. The extra extension 602 allows the user to hold the strip before loading in on to the microtube or plate.

[031] Fig. 7 shows a single 8 microtube cap strip 700 for microtube 100. The strip of tubes may be secured using this embodiment. The novel feature inner second ring 204 is shown to exist in this configuration and helps secure and stop cross contamination of the samples as well.

[032] Fig. 8 shows a single 8 microtube cap strip 800 for a plate or microtube 100. This embodiment may also be used as a film. The hinge 106 may be made so that they can be broken off and each cap may be used individually.

[033] In addition, it will be appreciated that the various embodiments, materials, and compositions can be interchangeable used in the current embodiments and various combinations of the article of use. Accordingly, the specification and drawings are to be regarded in an illustrative rather than a restrictive sense.