Field of the Invention
[0001] The present invention relates to medical devices and, more specifically, to a device
for transporting radio-pharmaceuticals used in positron emission tomography.
Description of the Prior Art
[0002] Positron emission tomography (PET) imaging is a diagnostic examination that involves
acquiring physiologic images based on the detection of positron radiation. Positrons
are particles emitted from radioactive substances. The radioactive substances used
are injected into a patient and positrons from the radioactive substance are detected
and imaged by a PET scanner. The resulting images are used to evaluate a variety of
diseases.
[0003] Pharmaceutical compositions used in PET scans are administered in liquid form by
injection into the patient. Radio-pharmacists typically calculate a unit dose based
on the amount of decay that a dose will undergo during transport to the hospital at
which the dose will be administered. In preparing the dose, the radio-pharmacist places
the dose into a syringe and then places the syringe into a "pig" that shields those
handling the dose from the radioactive contents of the syringe. The pig is then transported
to the hospital for administration to a patient.
[0004] With many types of radio-pharmaceuticals, a lead pig is sufficient to shield those
handling the dose. However, for radio-pharmaceuticals designed for PET scans, a typical
lead-shielded pig does not provide sufficient protection by itself. To compensate,
existing PET radio-pharmaceutical transport systems require an extra level of shielding.
This is accomplished by providing a secondary shielded case for the pig. Such a shielded
case includes lead shielding about a cylindrical opening into which the pig fits.
[0005] Existing PET radio-pharmaceutical pigs tend to need to be replaced on a regular basis.
This is because the shielding quality of lead breaks down in the presence of PET pharmaceutical
radiation. Thus, the cost is increased. Also, there is a danger of insufficient protection
if a radio-pharmacist continues to use a pig past its designed life span.
[0006] Because most pigs are roughly cylindrical in shape (see e.g.
US 4869299,
US 5828073, or
US 2005/0198800), rolling of such pigs is a problem. If a pig is allowed to roll, it could roll off
of the surface on which it is placed and fall, causing injury, destroying the dose
of the radio-pharmaceutical composition contained therein, or both. Some existing
pigs include a flat surface milled into the outer surface of the pig. The milling
is done by removing several exterior chords of the cylinder forming the pig, thereby
forming flat surfaces. Also, several small evenly-spaced bumps may be added to the
exterior surface of the pig. Both of these methods of preventing rolling may be satisfactory
for ordinary conditions, but they do not provide a sufficient anti-roll capability
in situations in which a pig is accidentally bumped with considerable force. Furthermore,
most pigs include two sections that must be separated when accessing the syringe inside.
However, many existing pigs usually include anti-roll texturing on only one section.
Thus, if the section without the anti-roll texturing is placed on a table, it may
roll off and cause injury.
[0007] Typical radio-pharmaceutical pigs have an inner chamber into which a filled syringe
is placed. A plastic liner is frequently employed to prevent spillage from the syringe
from accumulating inside the pig. Such a liner is typically made from rigid plastic
and used only once. Because the liner is rigid, it takes up a considerable amount
of space to store and to dispose of.
[0008] Typically, when administering a radio-pharmaceutical to a patient, the syringe is
removed from the pig and placed in a shielded holder that protects the physician's
hands from radiation while injecting the radio-pharmaceutical into an IV bag. The
transfer of the syringe causes a brief exposure to the user and increases the risk
that the syringe could fall and be harmed.
[0009] Therefore, it would be desirable for a radio-pharmaceutical pig to be capable of
providing a mechanism for administering a radio-pharmaceutical without having to transfer
it to a shielded holder.
SUMMARY OF THE INVENTION
[0010] The disadvantages of the prior art are overcome by the present invention which, in
one aspect, is a radio-pharmaceutical pig according to the subject-matter of claim
1.
BRIEF DESCRIPTION OF THE FIGURES OF THE DRAWINGS
[0011]
FIG. 1 is a top perspective view of an illustrative example.
FIG. 2A is an elevational view of an example.
FIG. 2B is a cross-sectional view of the example shown in FIG. 2A, taken along line 2B-2B.
FIG. 2C is an expanded cross-sectional view of the example shown in FIG. 2B.
FIG. 2D is a bottom plan view of the example shown in FIG. 2A.
FIG. 2E is a bottom plan view of an alternate example.
FIG. 2F is a cross sectional view of a detail of the example shown in FIG. 2B.
FIG. 3 is a plan view of a plastic insert.
FIG. 4A is a cross-sectional view of the insert shown in FIG. 3, taken along line 4-4.
FIG. 4B is a second cross-sectional view of the insert shown in FIG. 3, taken along line
4-4.
FIG. 5 is a cross-sectional view of an insert disposed within a pig.
FIG. 6 is a plan view of a plastic insert including stiffening ribs.
FIG. 7 is a side view of a roll of plastic inserts.
FIG. 8 is a plan view of a strip of plastic inserts.
FIG. 9 is a cross sectional view of a three section pig.
FIG. 10 is a cross sectional view of the center section of a three section pig as it is ready
for administration of a radio-pharmaceutical.
FIG. 11 is a plan view of the center section shown in FIG. 10 being employed.
DETAILED DESCRIPTION OF THE INVENTION
[0012] Referring to the drawings, like numbers indicate like parts throughout the views.
As used in the description herein and throughout the claims, the following terms take
the meanings explicitly associated herein, unless the context clearly dictates otherwise:
the meaning of "a," "an," and "the" includes plural reference, the meaning of "in"
includes "in" and "on."
[0013] As used herein, "plastic" means capable of being deformed without rupture and a "plastic
material" includes materials that are deformable. Plastic materials, as used herein,
include, but are not limited to, synthetic polymer materials, natural latex materials,
thin metal sheets and combinations thereof. It will be readily understood that many
other materials, not specifically listed herein, will meet the criteria for being
a plastic within the scope of the present invention.
[0014] As shown in FIG. 1, one illustrative example of a radio-pharmaceutical pig
100 includes a tungsten cylinder
110 having a first elongated member
112 and a second elongated member
114. The outer surface of the first elongated member
112 and the second elongated member
114 includes a rough textured portion
120 that facilitates gripping of the pig
100 by a user. Typically, the pig
100 is formed from titanium stock and formed on a metal lathe using conventional methods.
[0015] As shown in FIGS. 2A-2C, the first elongated member
112 terminates in a first engagement surface
150 and an opposite first distal end
118, the second elongated member
114 terminating in a second engagement surface
152 that is complimentary to the first engagement surface
150 and an opposite second distal end
116. The pig
100 defines an elongated cavity
113 therein that is substantially coaxial with the tungsten cylinder
110. The cavity
113 is of sufficient size to receive a syringe
10 therein. The tungsten cylinder
110 is thick enough to shield users from a PET radio-pharmaceutical without requiring
additional shielding. The actual thickness may be calculated easily by referring to
standard radiological shielding tables and depends on the type and amount of radio-pharmaceutical
being used.
[0016] A recess
160 may be milled into either the first engagement surface
150 or the second engagement surface
152 (or both) to receive the finger grip tabs of the syringe
10, thereby preventing the syringe
10 from rocking during transport. An O-ring
154 may be embedded in one of the engagement surfaces
150 or
152 to prevent leakage from the pig
100.
[0017] Returning to FIG. 1, a first anti-roll member
132 extends outwardly from the first distal end
118 and a second anti-roll member
130 extends outwardly from the second distal end
116. The first anti-roll member
132 and the second anti-roll member
130 each include at least three (and in the embodiment shown, four) flat surfaces
134 that inhibit rolling. Including an anti-roll member
132 and
130 on each of the first elongated member
112 and the second elongated member
114, ensures that neither member will roll if left unattended on a flat surface. This
may be a substantial advantage, given that each elongated member
112 and
114 will likely be quite heavy due to the thickness of the tungsten employed.
[0018] The second distal end
116 is supplied with a lifting ring
140 that facilitates lifting of the pig
100 out of any carrying container (not shown) used to transport the pig
100. The lifting ring may be affixed to the top surface
136 of the pig
100 with an attachment
146 and a spacing plug
142 may be affixed to the top surface
136 inside the ring
140 when the ring
140 is in the down position.
[0019] As shown in FIG. 2D, the anti-roll members
132 are blocks of titanium that could include four flat sides
134, or, as shown in FIG. 2E, only three flat sides
134, or even more than four flat sides
134, so long as the flat side
134 has dimensions sufficient to prevent rolling. The anti-roll members
132 may be formed from the same titanium stock as the rest of the pig
100.
[0020] As shown in FIG. 2F, a stainless steel sleeve
220 may disposed about a portion of the tungsten cylinder
110. The textured portion
222 may be cut into the stainless steel sleeve
220 and may include diamond patterned scoring.
[0021] As shown in FIGS. 3-5, a disposable plastic insert
300 is disposed within the cavity
113 to prevent leakage of radio-pharmaceutical materials into the cavity
113. Each insert
300 includes an elongated plastic envelope
310 made from a first plastic sheet
309 and an oppositely-disposed second plastic sheet
311 that are sealed together along a sealing surface
312 (through thermal sealing, for example) and that open to a top side
316, thereby defining passage therein
318. The passage is of sufficient size to allow a syringe
10 to fit therein. The disposable plastic insert
300 could be made of materials including polyethylene and polyvinyl chloride, but should
be thick enough to resist punctures from any exposed needles placed into the insert
300.
[0022] A first adhesive tab
320 is placed on the first sheet
309 adjacent the top side
316 and a second adhesive tab
320 is placed on the second sheet
311 adjacent the top side
316. The first adhesive tab
320 and the second adhesive tab
320 each include a peel-off cover that may be peeled off to allow exposure of the adhesive
tabs
320 so as to facilitate sealing the top side (as shown in FIG. 4B). This facilitates
easy sealing of the syringe
10 for disposal after use.
[0023] As shown in FIG. 6, the disposable plastic insert
300 may also include a plurality of elongated rib structures
610 embedded in one of the plastic sheets
310 and
311 to provide structural support to the plastic insert
300. The elongated ridge structures
610 could include wires embedded in one of the plastic sheets
310 and
311, or could be thickened plastic that is molded into the plastic sheets
310 and
311 using commony-known plastic sheet forming methods.
[0024] As shown in FIG. 7, because the inserts
300 are flexible, a plurality of inserts
300 may be formed continuously and stored in the form of a roll
700. This facilitates easy manufacturing and storage of the inserts. As shown in FIG.
8, when the inserts are formed as a continuous strip
800, a serration
810 may be cut in the sealed portion between each successive insert
300 in the strip
800 to facilitate separation of the inserts
300.
[0025] An embodiment of the present invention is shown in FIGS. 9-11. As shown in FIG. 9,
the radio-pharmaceutical pig
900 includes a first cylindrical member
910, a second cylindrical member
930 and a third cylindrical member
950. The first cylindrical member
910 includes a first tungsten body
912 defining a first cavity
916 that opens to a first end
922. A first anti-roll structure
918 extends outwardly from a second end
920. The first cylindrical member
910 also includes a first external stainless steel sleeve
914 that covers a portion of the first cylindrical member
910. Cut into the first external stainless steel sleeve
914 is a gripping surface
902, which could be a diamond pattern scored surface.
[0026] The second cylindrical member
930 includes a second tungsten body
932 that defines a second cavity
936 therethrough. The second cylindrical member
930 includes a proximal end
940 and an opposite distal end
942. The proximal end
940 is capable of engaging (such as with complimentary threading, etc.) the first end
922 of the first cylindrical member
910 so that the first cavity
916 is in substantial alignment with the second cavity
936. A second anti-roll structure
938 extends outwardly from a portion of the second cylindrical member
930. As demonstrated in FIG. 11, the second anti-roll structure
938 also prevents slippage of the second cylindrical member
930 when it is being used to shield the user during delivery of the radio-pharmaceutical.
Returning to FIG. 9, the second cylindrical member
930 also includes a second external stainless steel sleeve
934 that covers a portion of the second cylindrical member
930, with a gripping surface
902 cut into the second external stainless steel sleeve
934.
[0027] The third cylindrical member
950 includes a third tungsten body
952 that defines a third cavity
956 that opens to a primary end
960. The primary end
960 is capable of engaging the distal end
942 of the second cylindrical member
930 so that the third cavity
956 is in substantial alignment with the second cavity
936. A third anti-roll structure
958 extends outwardly from a secondary end
962 of the third cylindrical member
950. The third cylindrical member
950 also includes a third external stainless steel sleeve
954 that covers a portion of the third cylindrical member
950 with a gripping surface
902 cut into the third external stainless steel sleeve
954. The first cavity
916, the second cavity
936 and the third cavity
956are shaped so as to be complimentary in shape of the syringe
10.
[0028] As shown in FIG. 10, the second cylinder member
930 may be disengaged from the first cylinder member
910 and the third cylinder member
950. The second cylinder member
930 has dimensions that allow it to be used to shield the syringe
10 while the syringe
10 is being used to deliver the radio-pharmaceutical to a receptacle. This is shown
in FIG. 11, wherein the physician
14 grips the second cylinder member
930 with the syringe
10 disposed therein. The needle
12 extends from the second cylinder member
930 so that the physician
14 can inject the contents of the syringe
10 into a receptacle
16 (such as an injection port of an IV bag).
[0029] The above described embodiment, while including the preferred embodiment and the
best mode of the invention known to the inventor at the time of filing, is given as
illustrative example only. It will be readily appreciated that many deviations may
be made from the specific embodiments disclosed in this specification without departing
from the scope of the invention. Accordingly, the scope of the invention is to be
determined by the claims below rather than being limited to the specifically described
embodiment above.
1. Radiopharmazeutischer Behälter (900) zum Transportieren einer Spritze, die einen radiopharmazeutischen
Stoff enthält, mit:
a. einem ersten zylindrischen Element (910), das einen ersten Wolframkörper (912)
aufweist, der darin einen ersten Hohlraum (916) definiert, der zu einem ersten Ende
(922) geöffnet ist;
b. ein zweites zylindrisches Element (930), das einen zweiten Wolframkörper (932)
umfasst, der einen zweiten Hohlraum (936) dadurch definiert, und das ein proximales
Ende (940) und ein entgegengesetztes distales Ende (942) umfasst, wobei das proximale
Ende in der Lage ist, mit dem ersten Ende (922) des ersten zylindrischen Elementes
(910) so zusammenzuwirken, dass der erste Hohlraum (916) im Wesentlichen mit dem zweiten
Hohlraum (936) ausgerichtet ist, wobei das zweite zylindrische Element (930) auch
eine äußere Hülse (934) aus nicht rostenden Stahl, die einen Bereich des zweiten zylindrischen
Elementes mit einer Greiffläche (902) bedeckt, mit einer Greifoberfläche (902) umfasst,
die in die zweite äußere Hülse aus nicht rostenden Stahl geschnitten ist;
c. ein drittes zylindrisches Element (950), das einen dritten Wolframkörper (952)
umfasst, der einen dritten Hohlraum (956) definiert, der sich zu einem primären Ende
(960) öffnet, wobei das primäre Ende in der Lage ist mit dem distalen Ende (942) des
zweiten zylindrischen Elementes (930) zusammenzuwirken, so dass sich der dritte Hohlraum
(956) im Wesentlichen in Ausrichtung mit dem zweiten Hohlraum (936) befindet,
wobei der erste Hohlraum (916), der zweite Hohlraum (936) und der dritte Hohlraum
(956) so geformt sind, dass sie komplementär zur Form der Spritze (10) sind,
wobei sich ein erstes Anti-Roll-Element (918) auswärts von dem zweiten Ende (920)
des ersten zylindrischen Elementes (910) erstreckt sich ein zweites Anti-Roll-Element
(938) auswärts von einem Bereich des zweiten zylindrischen Elementes (930) erstreckt
und sich ein drittes Anti-Roll-Element (958) von dem zweiten Ende (962) des dritten
zylindrischen Elementes (950) erstreckt.
2. Radiopharmazeutischer Behälter (900) nach Anspruch 1, wobei:
das erste zylindrische Element (910) eine erste äußere Hülse (914) aus nicht rostenden
Stahl, die einen Bereich des ersten zylindrischen Elementes bedeckt, mit einer Greifoberfläche
(902) umfasst, die in die erste äußere Hülse aus nicht rostenden Stahl geschnitten
ist; und
das dritte zylindrische Element (950) eine dritte äußere Hülse (954) aus nicht rostendem
Stahl umfasst, die einen Bereich des dritten zylindrischen Elementes (950) mit einer
Greifoberfläche umfasst, die in die dritte äußere Hülse aus nicht rostendem Stahl
geschnitten ist.
3. Radiopharmazeutischer Behälter (900) nach Anspruch 1 oder 2, wobei das zweite zylindrische
Element (930) vom ersten zylindrischen Element (910) und vom dritten zylindrischen
Element (950) gelöst werden kann und wobei das zweite zylindrische Element Abmessungen
hat, die ermöglichen, dass das zweite zylindrische Element dazu verwendet werden kann,
die Spritze (10) abzuschirmen, während die Spritze dazu verwendet wird, den radiopharmazeutischen
Stoff in einen Behälter abzugeben.
4. Radiopharmazeutischer Behälter (900) nach Anspruch 1 oder 2, wobei die Greifoberfläche
(902) eine rautenförmig gemusterte aufgeraute Oberfläche aufweist.
5. Radiopharmazeutischer Behälter (900) nach Anspruch 1 oder 2, wobei das erste Anti-Roll-Element
(918) und das zweite Anti-Roll-Element (938) je einen Block aufweisen, der sich auswärts
von dem Wolframkörper erstreckt, wobei der Block zumindest drei im Wesentlichen flache
Seiten aufweist.
6. Radiopharmazeutischer Behälter (900) nach Anspruch 5, wobei der Block 4 im Wesentlichen
flache Seiten aufweist.