The present invention is related to devices for collection of specimen and delivery of specimen for diagnostic testing, particularly collecting and delivering saliva for diagnostic tests. The device of the present invention is particularly useful for collecting and delivering a specimen to a sample collection matrix from which a DNA template for PCR can be isolated.
Various methods and devices have been used to collect and deliver specimen for diagnostic testing. One conventional method for collecting a saliva specimen is to use a cotton swab. The saliva sample can then be applied to a test device by contact with the swab or the sample can be rinsed from the swab.
Various devices comprising test tube like structures with sample absorbing means have been described for collecting biological samples for diagnostic testing. Examples of such devices are described in U.S. Pat. No. 4,123,224, U.S. Pat. No. 5,000,193, U.S. Pat. No. 5,022,409, U.S. Pat. No. 5,260,031, U.S. Pat. No. 5,268,148, U.S. Pat. No. 5,283,038, U.S. Pat. No. 5,339,829, U.S. Pat. No. 5,376,337, U.S. Pat. No. 5,380,492, U.S. Pat. No. 5,393,496, U.S. Pat. No. 5,479,937 and U.S. Pat. No. 5,494,646.
The present invention provides a simple device for collecting and delivering a specimen for diagnostic testing. In accord with the present invention, a specimen collecting device comprises an elongated foam member having a longitudinal axis and an uncompressed cross sectional area, the elongated foam member being circumscribed by a hollow tubular member along a portion of the longitudinal axis, the hollow tubular member has a cross sectional area less than the uncompressed cross sectional area of the foam member so that the foam member is compressed along the circumscribed portion.
The sample collection device of the present invention is particularly useful for collecting saliva specimen and delivering the sample to a DNA collection matrix from which DNA for PCR testing can be isolated. The collection device of the present invention provides a simple and inexpensive method for collecting and delivering the saliva sample. Further, in preferred embodiments, the foam member of the collection device provides more consistent and accurate samples.
The invention also provides a method for obtaining a DNA template for PCR. The method comprises: providing a sample collection device as described above; inserting one end of the sample collecting device into a patient's mouth to absorb saliva into the foam member; delivering a sample of the saliva to a collection matrix by contacting the end of the sample collecting device with the collection matrix; drying the sample on the collection matrix; and subsequently isolating DNA from the sample for PCR.
The sample collection devices of the present invention can be used to provide saliva samples for DNA testing for forensic and paternal identification, RNA testing, antibody testing, testing for particular drugs, and other similar diagnostic procedures.
The sample collection device in accord with the present invention will be described with reference to the drawings.
The foam member 15 can be made of a variety of absorbent foams. Preferably, the foam is formed and cut to the desired size to expose the cell structure rather than a molded foam part having a surface skin. Preferred materials for the foam member include, for example, polyurethane foam, polyethylene foam, polyvinylchloride foam, ethylvinylacetate foam, polyethylene/ethylvinylacetate foam, polyester foam and polyether foam. Absorbent Porex™, silicone and latex foams can also be used. A particularly useful foam for the collection of saliva is a polyurethane foam sold under the mark HYDRASORB® by Avitar, Inc., Canton, Mass.
The preferred polyurethane foam has a uniform cell count of about 60 or more cells per linear inch. More preferably, the uniform cell count is about 80 to 120 cells per linear inch.
The tube 12 circumscribing the foam can be made of any suitable material having sufficient strength to compress and hold the foam member and to be handled during collecting and delivery of the specimen. Typical materials used for conventional straws, for example, paper tubes and polyethylene, polypropylene, polyester, vinyl or other plastic tubes, are suitable for the tube. Such straws also are economical and an appropriate diameter for, manufacturing of the collection device, handling and use. A circular cross section for the tube is preferred for convenience. However, other shaped cross sections, such as square or triangular tubes, also can be used.
The particular dimensions of the sample collecting device of the invention can vary depending upon the volume of specimen desired and the manner of handling the device for sample collection and delivery. For manual use, it is preferred that the tube length of the device be about 1.0 inch to about 5.0 inches long and that the mean cross sectional diameter of the tube be from about 0.12 to about 0.5 inch. More preferably, the tube is about 1.5 inches to about 3.5 inches long and has a mean cross sectional diameter from about 0.18 to about 0.38 inch.
A particularly useful collection device 10 has a circular hollow tube 12 three (3.0) inches long and 0.22 inch in diameter. An elongated foam member 15 is precut having a length of 3.5 inches and a square cross section 0.25 inch per side. The foam member 15 is compressed and inserted into the tube 12 so that 0.25 inch of foam protrudes on each end. This device can be used to collect a sample using either end, or to collect two samples using both ends. The tube provides a convenient handle to hold the device during use. Saliva can be collected by wicking the saliva into the foam member in as little as 15 seconds. The saliva can be delivered for diagnostic testing by dabbing the foam member onto a slide or membrane, or other device. Pressure also can be exerted on the tube to compress the foam and provide pressure to facilitate delivery of the sample.
The sample collection device of the present invention is particularly useful for collecting samples of saliva and spotting the samples on a matrix collection matrix device 20 (
The collection device of the present invention can be used to provide samples for diagnostic analysis or identification of DNA, RNA, antibodies, drugs, and the like.
The invention has been described in detail with reference to preferred embodiments thereof. However, it will be appreciated that, upon consideration of the present specification and drawings, those skilled in the art may make modifications and improvements within the spirit and scope of this invention as defined by the claims.
Number | Name | Date | Kind |
---|---|---|---|
86453 | Robinson, Jr. et al. | Feb 1869 | A |
489152 | Legg | Jan 1893 | A |
668285 | Dayton | Feb 1901 | A |
1313566 | Trowbridge | Aug 1919 | A |
1687472 | Dorman et al. | Oct 1928 | A |
1903664 | Yutts | Apr 1933 | A |
2249912 | Oxley | Jul 1941 | A |
2355917 | Knight | Aug 1944 | A |
2712143 | Palma, Jr. et al. | Jul 1955 | A |
2847000 | Nieburgs | Aug 1958 | A |
RE24666 | Draghi | Jul 1959 | E |
2902041 | Bau | Sep 1959 | A |
3056998 | Ebner | Oct 1962 | A |
3152352 | Kosik, Jr. | Oct 1964 | A |
3457014 | Ward | Jul 1969 | A |
3491397 | Hesener | Jan 1970 | A |
3783469 | Siemund | Jan 1974 | A |
3831598 | Tice | Aug 1974 | A |
3871375 | Nennett | Mar 1975 | A |
3946457 | Robinson | Mar 1976 | A |
4079936 | Schachter | Mar 1978 | A |
4123224 | Givner et al. | Oct 1978 | A |
4157709 | Schuster et al. | Jun 1979 | A |
4283809 | Prost | Aug 1981 | A |
4332251 | Thompson | Jun 1982 | A |
4778457 | York | Oct 1988 | A |
4820259 | Stevens | Apr 1989 | A |
4828419 | Porter et al. | May 1989 | A |
4846802 | Sanders, III | Jul 1989 | A |
4925327 | Wirt | May 1990 | A |
4935001 | George | Jun 1990 | A |
5000193 | Heelis et al. | Mar 1991 | A |
5000202 | Stepan | Mar 1991 | A |
5022409 | Goldstein et al. | Jun 1991 | A |
5147288 | Schiavo | Sep 1992 | A |
5250412 | Giegel | Oct 1993 | A |
5260031 | Seymour | Nov 1993 | A |
5268148 | Seymour | Dec 1993 | A |
5283038 | Seymour | Feb 1994 | A |
5339829 | Thieme et al. | Aug 1994 | A |
5376337 | Seymour | Dec 1994 | A |
5380492 | Seymour | Jan 1995 | A |
5393496 | Seymour | Feb 1995 | A |
5479937 | Thieme et al. | Jan 1996 | A |
5490736 | Haber et al. | Feb 1996 | A |
5494646 | Seymour | Feb 1996 | A |
5531671 | Bennett | Jul 1996 | A |
5591507 | Jones | Jan 1997 | A |
5611687 | Wagner | Mar 1997 | A |
5675858 | Von Meyer | Oct 1997 | A |
5704906 | Fox | Jan 1998 | A |
5816270 | Nadel | Oct 1998 | A |
6200275 | Cesarczyk | Mar 2001 | B1 |