A microplate assembly with closure comprises a microplate base 101 having a geometric array of wells 103. vials 113 of borosilicate glass inserted into the wells comprise flanges on the top portion of the vials. closure 117 comprises an array of caps 119 having a complementary geometric pattern to the wells of the microplate base. The caps each comprises a septum and are connected by a thin membrane 121. Each cap comprises a sidewall 403 having a vial engagement ring which snaps over the flange 115 of the vials. septum openings 135 in the caps extend through the top of the caps and provide a means to fill and evacuate the vials with a penetration device passing through the septa of the caps of the closure.
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0. 12. A sample vial and cap assembly for insertion in a sample containable well of a microplate base, the sample vial and cap assembly comprising:
a glass vial of dimensions providing a predetermined fit in said sample containable well in the microplate base, the glass vial comprising a vial top opening, a vial top flange comprising a top sealing surface, and a closed vial bottom; and a snap cap insertable onto said glass vial, the snap cap comprising a top, a sidewall comprising a flange engagement element, and a septum comprising an upper resealable portion and a lower barrier portion, the septum disposed between the top and the flange engagement element; whereby the barrier portion seals the top sealing surface of the glass vial when the flange engagement element engages the vial flange.
0. 9. A microplate assembly with closure comprising:
a microplate base comprising a plurality of sample containable wells arranged in a geometric pattern; at least one glass vial of dimensions providing a predetermined fit in said plurality of sample containable wells in the microplate base, said at least one glass vial comprising a vial top opening, a vial top flange comprising a top sealing surface, and a closed vial bottom; and at least one snap cap insertable onto said at least one glass vial, said at least one snap cap comprising a top, a sidewall comprising a flange engagement element, and a septum comprising an upper resealable portion and a lower barrier portion, the septum disposed between the top and the flange engagement element; whereby the barrier portion seals the top sealing surface of the glass vial when the flange engagement element engages the vial flange.
4. A closure for a plurality of glass vials dimensioned for insertion into a plurality of sample containable wells of a microplate arranged in a geometrical pattern, the closure comprising:
a plurality of caps attached to a membrane, said plurality of caps arranged in the geometric pattern of said plurality of sample containable wells; each of said plurality of caps comprising a cylindrically shaped sidewall, the sidewall comprising a bottom cap opening and comprising a vial flange engagement ring on the protruding inside an inner diameter of the sidewall, the vial flange engagement ring comprising a ring inner diameter sufficient to fit over and engage an outer diameter of a flange of each of said plurality of glass vials, ; a top septum opening, and a septum between the bottom cap opening and the top septum opening.
1. A microplate assembly with closure comprising:
a microplate base comprising a plurality of sample containable wells arranged in a geometric pattern; a plurality of glass vials comprising dimensions providing a predetermined fit in said plurality of sample containable wells in the microplate base, each of said plurality of glass vials comprising a vial opening, a flange, and a closed vial bottom and; a closure comprising a plurality of caps attached to a membrane, said plurality of caps arranged in the geometric pattern of said plurality of sample containable wells in the microplate base, each of said plurality of caps comprising a bottom cap opening, a top septum opening, a sidewall engageable to an outside surface of said each of said plurality of glass vials, the sidewall of each of said plurality of caps comprising a vial flange engagement ring on an inside surface of said sidewall for engaging the flange of each of said plurality of glass vials, said flange engagement ring protruding inside of said sidewall, and a septum between the top septum opening and the bottom cap opening.
2. The microplate assembly with closure of
3. The microplate assembly with closure of
5. The closure of
6. The closure of
0. 10. The microplate assembly with closure of
0. 11. The microplate assembly with closure of
0. 13. The sample vial and cap assembly of
0. 14. The sample vial and cap assembly of
0. 15. The microplate assembly with closure of
0. 16. The microplate assembly with closure of
0. 17. The closure of
0. 18. The microplate assembly with closure of
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The present invention relates to sample handling and storing assemblies and, more particularly, to microplate assemblies.
The growth in medical and pharmaceutical research as well as diagnostic analysis and testing has created a need for equipment and procedures for low cost, efficient handing of samples. Automated equipment is available for filling and retrieval of samples from sample containers.
Microplates comprising a plurality of sample wells have provided a convenient means to store samples. Automated equipment is available to position microplates for sample filling, retrieving, and analysis. Despite improvements in sample handling equipment, many applications require manual labor when performing evolutions such as preparing sample containers or vials, or covering or uncovering the samples. This is especially the case when sample numbers are insufficient to justify design and building of custom automated equipment.
Normally the wells of microplates are used as the sample containers. One of the problems arising from this technique is cross contamination of samples due to the base of sample migration across the top surface of the microplate. Also, the use of adhesive web closures to cover multiple wells further increases cross contamination between wells. Due to the high cost of making microplates of glass, use of plastics has become common. These units suffer the additional problem of contamination of samples due to the fact that most plastics are less inert to sample solvents than glass.
Therefore and object of the present invention is to provide a microplate assembly with a closure which can be quickly and easily applied to a plurality of the sample containers of the microplate.
Another object of the present invention is to provide a microplate assembly with closure which reduces cross contamination of samples.
A further object of the present invention is to provide a microplate assembly with closure which improves chemical inertness as compared to using wells of plastic microplates.
Yet another object of the present invention is to provide a microplate assembly with closure which is low in cost, rugged and reliable.
The microplate assembly with closure of the present invention comprises a microplate base having a plurality of wells arranged in a geometric pattern. Glass vials having the quality of good chemical inertness are insertable into the wells of the microplate base. Caps, preferably integral with a flexible or semi-rigid membrane and in the geometric pattern of the microplate base wells, are placed over the vials. The caps comprise a sidewall. The inner diameter of the sidewall engages an outside surface of the glass vials. The caps have a septum opening and septum comprising a resealable portion and a barrier portion. The septum allows insertion of a probe such as a hypodermic needle for filling and retrieving samples while the caps are engaged on the vials. A vial seal of chemically inert material prevents contact of the sample and the septum seal.
In the preferred embodiment, a standard 96 well microplate base is utilized. Vials are made of borosilicate glass for inertness and long life. The vials have an outer diameter selected to make them insertable into the wells of the microplate base. The vials may be flanged, plain or serum finish. The closure comprises 96 caps arranged in the same geometric pattern as the wells of the microplate base. The caps are integrally formed with a membrane connecting the caps. The caps fit over the outer diameter of the vials and comprise a vial or flange engagement ring to retain the cap on the vial.
The microplate closure allows rapid capping or uncapping of a full complement of vials in the microplate simultaneously. In other embodiments, cap strips cover one or more rows or columns of vials. In yet another embodiment, single septum caps are utilized.
These and other features, aspects and advantages of the present invention will become better understood with regard to the following description, appended claims and accompanying drawings where:
The following is a description of the preferred embodiments of a microplate assembly with closure that provides for sealing and sampling a plurality of sample vials in the microplate.
Wells 103 act as receptors for vials 113. In the preferred embodiment, vials 113 are made of glass such as borosilicate glass and comprise a flange 115. Glass vials provide a vial material which is inert to most sample materials. In the preferred embodiment, the diameter of vials 113 provide a loose fit in wells 103, providing easy removal and replacement of vials 113. In other embodiments, the outer diameter of vials 113 provide a snug or slight interference fit with wells 103.
Closure 117 comprises a plurality of caps 119 attached to membrane 121. Caps 119 are arranged in a geometric pattern similar to the geometric pattern of wells 103. In the preferred embodiment, caps 119 form a rectangular array 8 caps wide by 12 caps in length. The similar geometric pattern of caps 119 and wells 103 provides alignment of caps 119 to vials 113 placed in wells 103. When respective corners 123A-D or edges 125A-D, of closure 117 are aligned to respective corners 129A-D and edges 131A-D of microplate 101, caps 119 are aligned with vials 113 placed in wells 103.
In the preferred embodiment, caps 119 fit over flanges 115 of vials 113. Pressing of closure 117 on vials 113 inserted in wells 103 engages caps 119 and respective vials 113, sealing vials 113. Hand or mechanical applicator pressure may be used to provide closure 117 engagement to vials 113. Septum openings 135 provide access for insertion of injection needles.
In the preferred embodiment, a barrier portion 503 disposed between septum resealable portion 409 and vial 113 provides a chemically resistant barrier seal for contents of vial 113. In the preferred embodiment, barrier portion 503 is made of polytetrafluoroethylene (PTFE). In other embodiments, other polymers or metallic seals may be used.
Flange engagement ring 707 of cap 721 engages ledge 720 when cap 721 is pressed onto vial 713. The inner diameter 723 of flange engagement ring 707 is less than the outer diameter 725 of flange 715. Use of a resilient material for sidewall 703 of cap 721 and flange engagement ring 707 provides an expansion and contraction means of flange engagement ring 707, allowing cap 721 to be pressed on vial 713. Once flange engagement ring 707 is advanced to crimp recess 719, flange engagement ring 707 expands inwardly and engages ledge 720 of flange 715. Removal of cap 721 requires pulling of the cap sufficiently to expand flange engagement ring over flange 715.
Cap strip 905 comprises 16 integral caps 907 on membrane 909, similar to those of
Accordingly the reader will see that the MICROPLATE ASSEMBLY AND CLOSURE provides fast closure and access to of a plurality of vials inserted into the wells of a microplate base. The device provides the following additional advantages:
The samples are housed in chemically inert vials;
Septa in the caps provide for filling and removal of samples while the caps are inserted on the vials;
Closure strips provide caps for selected rows or columns of vials; and
The device is simple and low in cost.
Although the description above contains many specifications, these should not be construed as limiting the scope of the invention but as merely providing illustrations of some of the presently preferred embodiments of this invention. Thus the scope of the invention should be determined by the appended claims and their legal equivalents, rather than by the examples given.
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