U.S. patent number 3,757,780 [Application Number 05/195,571] was granted by the patent office on 1973-09-11 for needle assembly with longitudinally movable filter.
This patent grant is currently assigned to Kabushiki Kaisha Ishikawa Susakusho. Invention is credited to Soji Ishikawa.
United States Patent |
3,757,780 |
Ishikawa |
September 11, 1973 |
NEEDLE ASSEMBLY WITH LONGITUDINALLY MOVABLE FILTER
Abstract
A needle assembly for use with a medical injector such as a
syringe or drip set. The needle assembly is provided with a filter
element in a fluid passage formed therein for completely removing
dust particles which might exist in a dosage solution or in a blood
transfusion when injected or dripped into a human body.
Inventors: |
Ishikawa; Soji (Tokyo,
JA) |
Assignee: |
Kabushiki Kaisha Ishikawa
Susakusho (Tokyo, JA)
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Family
ID: |
27279183 |
Appl.
No.: |
05/195,571 |
Filed: |
November 4, 1971 |
Foreign Application Priority Data
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Feb 25, 1971 [JA] |
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46/10945 |
Feb 25, 1971 [JA] |
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46/10946 |
May 20, 1971 [JA] |
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46/40176 |
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Current U.S.
Class: |
604/190 |
Current CPC
Class: |
A61M
5/3145 (20130101); A61M 5/158 (20130101) |
Current International
Class: |
A61M
5/158 (20060101); A61M 5/31 (20060101); A61M
5/14 (20060101); A61m 005/32 () |
Field of
Search: |
;128/221,218N,214R,215,216,214C,2F,272,276,218R,220,218NV,218M,218D |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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1,233,412 |
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Oct 1960 |
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FR |
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6,399 |
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Jun 1906 |
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FR |
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1,490,616 |
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Aug 1967 |
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FR |
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Other References
Millipore Data Sheet SW-13, Swinnex-13, Millipore Filter Corp.,
1965..
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Primary Examiner: Gaudet; Richard A.
Assistant Examiner: McGowan; J. C.
Claims
What is claimed is:
1. A needle assembly for use in a medical injector, comprising a
substantially cylindrical needle holder having a tapered bore for
communication through its enlarged end with a chamber in said
injector and a passageway leading from a reduced end of said bore
and smaller in cross sectional diameter than the bore, a needle
connected to said needle holder and having a passageway aligned and
communicating at one end with said passageway in the needle holder,
said needle having an opening at the other end forming a piercing
point, a plurality of annularly spaced projections formed on an
inner peripheral surface of said needle holder defining said bore
and located in proximity to said reduced end of said bore, and a
substantially disc-shaped filter element movable between said
reduced end and said projections and having a thickness smaller
than a distance between said reduced end of said bore and said
projections, said filter having a diameter substantially smaller
than a diameter of said reduced end of said bore and larger than a
diameter of said passageway in said needle holder and a diameter of
a circle described by ends of said projections.
Description
The present invention generally relates to a needle assembly for
use with a medical injector such as a syringe or drip set and, more
specifically, to a needle assembly of the above type for completely
removing dust particles which might exist in a dosage solution or
in a blood transfusion when injected or dripped into the human
body.
Dosage solutions such as a usual injection blood-for-blood
transfusion or glucose solution are packed in an ampoule or in a
so-called Bayer bottle in a sterile condition for shipping. The
packing process is usually under a careful administration so as to
prevent an ingress of dust particles into the dosage solutions.
However, the admixture or existence of the dust particles in the
dosage solutions can not be completely avoided. For example, when
the head portion of an ampoule is cut away to extract a dosage
solution therefrom into a syringe for injection, fine fragments of
glass may drop in the ampoule and therefore may be aspirated into a
barrel of the syringe. When, moreover, a needle adaptor of a drip
set is inserted into a rubber tap sealing the Bayer bottle for
effecting dripping of a dosage solution, fine chips of rubber may
also enter the particular bottle. On the other hand, dust particles
floating in the air may chance to steal into such containers during
the above operations. It is extremely harmful and dangerous to
introduce the dosage solution, containing these dust particles,
into a human body.
Notwithstanding this fact, it has never been proposed to provide
any removing or filtering means in the conventional syringe or in
its needle, thus suffering the above serious danger. On the other
hand, a pouched filter made of synthetic fibers is provided in a
fluid passage, for example, in the drip chamber or plastic tubing
of the drip set. However, the filter has rough structure so that
satisfactory filtering effect can not be expected. Even if, in this
instance, the conventional pouched filter had such dense structure
as to afford sufficient filtering effect, some danger would still
exist due to the fact that it is located midway of the fluid
passage, with its downstream left unfiltered.
It is, therefore, an object of the present invention to provide an
improved needle assembly for use with a medical injector for
eliminating the above disadvantage.
Another object of the invention is to provide an improved needle
assembly having a filter element for completely removing the dust
particles which might exist in a dosage solution when it is
introduced into a human body.
According to one of the important features of the invention, the
filter element is of dense structure so that highly effective
filtering operation can be achieved.
According to another important feature of the invention, the filter
element is provided directly in a needle, namely, at the closest
position to a human body, thus minimizing the prospective steal of
the dust particles into the dosage solution.
Other features and advantages will be understood from the
description made with reference to the accompanying drawings, in
which:
FIG. 1 is a longitudinal section of a needle assembly according the
invention, in which a disc-shaped filter is longitudinally movably
provided in a needle holder;
FIG. 2 is a plan view of the needle assembly of FIG. 1 when it is
fitted for use to a syringe;
FIGS. 3A and 3B are partially cutaway explanatory views of the
needle assembly of FIG. 1, respectively showing the locations of
the filter when in aspiration and injection operations;
FIG. 4 is similar to FIG. 1 but shows another embodiment of the
invention, in which a disc-shaped filter is fitted in the needle
holder;
FIG. 5 is a plan view of the needle assembly of FIG. 4 when it is
fitted for use to a drip set;
FIG. 6 is also similar to FIG. 1 but shows a further embodiment of
the invention, in which a stick-shaped filter is tightly fitted in
the needle bore; and
FIG. 7 is a plan view of the needle assembly of FIG. 6 when it is
fitted for use to a syringe.
Referring now to FIGS. 1 and 2, a needle assembly of the present
invention is generally designated at numeral 10, which is composed
of a needle holder 11 and a pointed needle 12. A counter-tapered
portion 13 of the needle holder 11 is of generally cylindrical
shape and has a counter-tapered longitudinal bore 14 formed
therein. This bore 14 is shaped and sized to be securely fitted
over an externally tapered end 15 of a syringe barrel 16, as best
shown in FIG. 2. The fitting or locking of the needle assembly 10
and the tapered end 15 may be carried out with use of the so-called
Luer lock. The other reduced portion 17, which is integral with the
counter-tapered portion 13, has also a longitudinal bore 18 of
reduced diameter in alignment with the countertapered bore 14.
Thus, the merging inner end of the two portions 13 and 17 has a
stepped form, as indicated at 19 in FIG. 1. The needle 12 is
inserted into the reduced bore 18 and is embedded or anchored in
the wall of the reduced portion 17, as shown. The needle 12 is
pointed as customary by obliquely machining the open end 21
thereof. A longitudinal bore 22 is also formed in the needle 12,
thus providing a fluid passage leading from the counter-tapered
bore 14 to the needle bore 22 through the reduced bore 18.
According to the invention, a disc-shaped filter 23 is provided in
the particular fluid passage in a manner to be longitudinally
movable therein within a limited distance. More particularly, a
plurality of inwardly extending projections 24 are formed on an
annular inside periphery of the counter-tapered portion 13 at a
spacing from the stepped inner end 19 of the reduced portion 17.
This spacing is determined in accordance with the distance within
which the filter 23 is permitted to longitudinally move. For this
longitudinal movement, the diameter d' of the filter 23 is present
slightly smaller than the smallest diameter d of the
counter-tapered bore 14 but is larger than the diameters, not
named, of the reduced bore 18. In order to confine the filter 23
within the above spacing, the diameter d' of the filter 23 should
be larger than the inner diameter d" of the projections 24.
Operations of the needle assembly 10 will now be explained with
reference to FIGS. 2, 3A and 3B. When the needle 12 is dipped into
an ampoule 25 containing a suitable dosage solution 26, and when a
piston 27 telescopingly received by the syringe barrel 16 is pulled
in the direction of an arrow P, as shown in FIG. 2, then suction is
established in the fluid passage to thereby aspirate the dosage
solution 26 into the counter-tapered bore 14 through the needle
bore 22 and the reduced bore 18 in this sequence. At this
particular instant, the disc-shaped filter 23 is conveyed by the
suction flow of the dosage solution with the resultant abutment
against the inner surfaces of the projections 24, as shown in FIG.
3A. The flow of the dosage solution is then allowed to freely pass
around the filter 23 into the chamber 28 formed in the syringe
barrel 16.
When injection is to be administered, on the other hand, the filter
23 is pressed tightly onto the stepped inner end 19 of the reduced
portion 17 by the reverse flow of the dosage solution. In this
instance, this reverse flow is allowed to pass only through the
central portion of the filter 23, as shown in FIG. 3B. Thus, the
dust particles, which might have been sucked into the chamber 28
during the aspiration operation, can be completely removed from the
dosage solution after it has passed through the filter 23 for
injection into the human body, not shown. Consequently, the needle
assembly 10 hereinbefore described finds its best application to a
needle for an injection syringe.
The material which can be used for this filter 23 is not
restricted, if it is of medically harmless property and of highly
dense structure. For instance, the filter may preferably be made of
synthetic resins, such as nylon (R.T.M.) or highly dense
polyethylene, having a particle size of 10 - 20 microns. More
specifically, the filter is prepared by pressure-moulding the above
material into a disc shape of a desired diameter d. The moulded
filter may preferably be baked to sinter the material. If the
sintered filter has a resilient property, it can be filled between
the inner end of the reduced portion and the projections by
slightly warping or bending. If, on the contrary, the filter is
required to have a sufficient rigidity, the once moulded filter may
be baked after it has been inserted therebetween. The filter
obtained by the latter method is advantageous in that it has such a
dense structure as to remove more efficiently the prospective dust
particles.
Turning now to FIG. 4, a modified disc-shaped filter 23' is
securely mounted on the stepped inner wall 19 in this embodiment.
It should be noted here that like reference numerals appearing
hereinafter will indicate counterparts numbered in FIGS. 1 to 3B.
The filter 23' has a diameter slightly larger than the smallest
inside diameter, not shown, of the counter-tapered bore 14. In this
instance, after the filter 23' has been moulded (and baked, if
desired), it is tightly fitted in the bore 14 to be seated on the
stepped end 19 in frictional engagement with the surrounding
annular inside wall of the countertapered portion 13.
This type of filter 23' might slip out of the annular inside wall,
if it were used for the aspiration operation. Therefore, this
filter can be used only in combination with a drip set. However, if
the filter is adhered to the stepped wall 19 by the use of a
suitable adhesive, then the above slippage is eliminated so that it
can also be used in combination with an injection syringe.
The conventional drip set as generally designated at numeral 30 is
provided with the so-called Bayer bottle 31 having an air vent
conduit 32. The drip set 30 is further provided with a needle
adaptor 33, which is shown in condition for use in FIG. 5 as being
inserted into the inside of the Bayer bottle 31 through a rubber
tap 34. The dosage solution or blood 26 is delivered by the water
head into a drip chamber 35 and further to another adaptor 36
through a suitable tubing 37. The thus delivered dosage solution is
then introduced into the human body, not shown, through the needle
assembly 10, which is hermetically fitted over the end 38 of the
adaptor 36. In this manner, the dosage solution flows downward, in
other words, only in the one-way direction, so that the filter 23'
need not be provided longitudinally movably in the particular fluid
passage. This remarkably simplifies the preparation of the filter
and accordingly leads to considerable reduction in its production
cost.
Reference is now to be made to FIGS. 6 and 7, in which a
stick-shaped filter 23" is tightly fitted in the needle bore 22.
For improving the filtering efficiency, this filter 23" may
preferably occupy the total length of the needle bore 22.
This type of needle assembly 10 may be prepared by inserting into
the bore 22 the stick-shaped filter which has been moulded (and
baked, if desired). However, it is preferable that the preparation
is performed by the process including the steps of filling a
powdered material of synthetic resin into the needle bore and
baking the needle assembly as a whole to form a sintered
stick-shaped filter.
The needle assembly 10 of this embodiment can be used with the drip
set 30 in a similar manner to the previous embodiment shown in FIG.
4. However, this needle assembly 10 can also be used in combination
with an injection syringe, as shown in FIG. 7. In a proposed safe
use, the aspiration operation is performed with use of a first
needle assembly which has been connected to the tapered end of the
injection syringe. After removal of this first needle assembly, a
second needle assembly in connected to the syringe in place of the
first one. As a result, the injection operation can be accomplished
with use of the second non-contaminated assembly. Although this use
may cost more per an injection operation and may require the
tedious replace operation, it should be appreciated that a serious
danger concomitant with inclusion of the dust particles can be
completely avoided. As has been pointed out previously, this use
can also be effected by the needle assembly of FIG. 4, when the
filter 23' is adhered to the stepped end 19.
From the above description, the needle assembly according to the
present invention is of simple structure but can effectively remove
the prospective dust particles, thus insuring safety for injection.
Therefore, the needle assembly finds a wide variety of applications
such as intravenous, intramuscular and hypodermic injections.
* * * * *