Abstract: A needle-less injector suitable for injecting fluid through a skin surface of a patient includes a housing, a driver, an intruding gas chamber activating mechanism and a trigger. The housing containing the fluid and a sealed gas storage chamber containing a gas. The driver forces the fluid out of the housing at a sufficient speed to pierce the skin surface of the patient. The intruding gas chamber activating mechanism is mounted in the housing to intrude through the sealed gas chamber to release gas seal into the housing. The trigger is operatively coupled to the intruding gas chamber activating mechanism to release the gas from the gas chamber into the housing to activate the driver to force the fluid out of the housing. The trigger is activated by moving the trigger towards and orifice in the housing and/or upon application of a predetermined amount of pressure to the trigger that is opposed by a predetermined amount of resistance from the skin surface of the patient.

Abstract: The invention relates to methods and devices for delivering medicament by jet injection to an injection site in a patient. The method includes inserting a needle into an insertion point, wherein the needle has a length of less than 5mm and is operatively associated with an orifice in a nozzle assembly in fluid communication with an ampule chamber containing the medicament. The needle extends less than about 5 mm from the nozzle assembly orifice when the medicament is expelled. Next, a force generating mechanism is activated, and a pressure wall member that is operatively associated with the force generating member moves in response to the activation of the force generating mechanism at a speed sufficient to jet inject the medicament from the ampule chamber through the orifice and needle under a pressure of less than about 4000 psi to deliver a substantial portion of the medicament through the needle and past the insertion point to the injection site.

Abstract: The present invention provides a method of targeting transient gene expression and stable gene expression from the exogenous administration of a DNA sequence, which sequence is less than a complete genome, wherein said DNA sequence encodes RNA and protein, or RNA only, to differentiate tissue of living organisms wherein said DNA sequence through a jet injector technique, and said DNA sequence of less than a complete genome is expressed in a living organism. The present invention further provides a flexible multi-nozzle injector device with a wide surface area to allow molding of the injector nozzle to the surface contours of the tissue. Another aspect of the present invention provides an injection device having a long nozzle for injection of DNA deep into the host tissue. Also, in a further aspect the present invention provides an injector device modified to be used with and/or inject through an endoscopic device.

Abstract: The invention relates to an injector device for delivery of liquid from a high pressure source, and also to a method of performing such an injection. The device comprises a storage chamber 6, for the liquid or the liquid precursor components, comprising a storage barrel 16 with at least a section of substantially constant cross-section, defining a storage chamber axis, and a pressure chamber 4 comprising a pressure barrel 10 of substantially constant cross-section, defining a pressure chamber axis, for accommodation of at least one piston therein and having a front end opening 14 for ejection of the liquid. The pressure chamber being of sufficient strength to sustain the liquid pressure.

Abstract: A system and method for producing a high repetition pulsed microjet for use in medical applications. The device includes a stagnation chamber and a hydraulic pump for pumping a sterile fluid into the stagnation chamber. A flexible walled volume disposed in the stagnation chamber and filled with a hydraulic fluid. The hydraulic piston is cyclically displaced towards/away from the stagnation chamber thereby increasing/decreasing the pressure of the hydraulic fluid on the flexible walled volume. In turn, the flexible walled volume is compressed and the sterile fluid is expelled through an orifice in the flexible walled volume under pressure producing the pulsed microjet. This process may be repeated to produce repetitive pulsed microjets. In addition, the flow conduction of the hydraulic fluid between the hydraulic pump and stagnation chamber may be controlled by inserting a blocking device therebetween.

Abstract: A needleless syringe capable of accelerating particles comprising a therapeutic agent across skin or mucosal tissue of a vertebrate subject is provided. The syringe comprises a body having a lumen with a diaphragm located adjacent to a terminus thereof. Particles comprising a therapeutic agent are delivered from an external surface of the diaphragm by means of the motive force provided by the impact of a gaseous shock upon the internal surface of the diaphragm. A method for transdermally delivering particles comprising a therapeutic agent from the needleless syringe is also provided.

Abstract: A system for injecting DNA-based medications into humans is provided by the present invention. The system includes a needle-free injector with an injection orifice of approximately 0.004 inches for supplying DNA-based medication at an initial pressure of from 3900 to 4300 psi, and then immediately declining to a level of about 2800 to 3800 psi, and then immediately cutting off pressure to terminate the injection. The injector includes an annular adapter for spacing the injection orifice from the skin of the patient. The adapter includes an abutment against which the injector is disposed so that the orifice is spaced approximately 0.76-1.0 inch from the skin of the patient, the adapter having an inner diameter at the distal end of approximately 0.50-0.70 inches.

Abstract: A probe and nozzle assembly for reducing the pressure at which a needleless injector must deliver medicament for proper delivery are disclosed. In one embodiment of the probe, the probe is retractably located within an injector nozzle assembly. Upon activation of the energy source a portion of the probe extends past the nozzle assembly to deliver the medicament through a discharge channel. After activation the probe retracts back into the nozzle assembly. In another embodiment, the probe is fixed to the end of the nozzle assembly. In both embodiments the ratio of discharge channel length to diameter is greater than 6/1. The present invention also relates to nozzle assemblies with a discharge channel length to diameter ratio greater than 6/1.

Abstract: A method for delivering compounds through epithelial cell layers using impulse transients is described. The method involves applying a compound to, e.g., the stratum corneum, of a patient and then inducing impulse transients to create transient increases in the permeability of epithelial tissue, thereby facilitating delivery of the compound across the epithelial cell layer.

Abstract: A gas-powered, single-use, needle-less hypodermic jet injection device (10, 210, 410) includes a hand-held injector (12, 212, 412), and a drug injection cartridge (14, 114, 414) which provides a volume of liquid medication to be injected, an injection orifice, and an injection piston. Forceful movement of the injection piston causes an injection jet of medication to be expelled from the injection orifice. The injection device also includes a hermetically sealed gas pressure cartridge (82, 182, 482) which remains sealed until the moment of injection and powers the jet injection after opening of this cartridge.

Abstract: An improved particle bombardment device for transporting biological substances such as DNA into living cells. The device has a flexible barrel (40) that facilitates endoscopic particle bombardment of in vivo cells without a significant concomitant blast effect and without a need for a vacuum. The device also involves a unique tapered particle-carrying macroprojectile that can travel through convolutions of such a flexible barrel (40) with minimal friction.

Abstract: The present invention is a modified single use hand-operated injector device consisting of a plunger, a base, a snap means for resisting plunger movement and an injection means for injecting parenteral medication through a skin surface of a patient. The improvement comprises a check valve seated in a cannula and a widened receptacle area within a high pressure barrel through which the cannula passes. When the check-valve plug expels upon increase in pressure, into the widened receptacle area the parenteral medication efficiently flows around the plug and into the subcutaneous tissue of the patient.

Abstract: An ejection device 1 for the high-pressure ejection of a liquid or a liquid containing solid particles, comprising a pressure chamber 13 to accommodate the liquid therein, which opens into an ejection opening 11 and is delimited by a working piston 5. The working piston 5 is, upon application of an elastic impact on its end facing away from the pressure chamber 13, capable of transmitting a compression wave which may displace the pressure chamber-facing end of the working piston 5 by a predetermined displacement stroke into the pressure chamber 13 so that the volume thereof is reduced. The reduction in volume of the pressure chamber 13 is signicantly smaller than the volume of the pressure chamber 13.

Abstract: A needle-less injector suitable for injecting liquid medication through a skin surface of a patient include a housing, a driver, a pop valve and a trigger. The housing containing the liquid medication and a gas storage chamber containing a gas. The driver that forces the medication out of the housing at a sufficient speed to pierce the skin surface of the patient. The pop valve is mounted in the housing to seal the gas in the housing. The resistance sensitive trigger is coupled to the pop valve and is used to release the pop valve, such that it pops open into the gas storage chamber of the housing, to release the gas to activate the driver to force the liquid medication out of the housing. The resistance sensitive trigger is activated upon application of a predetermined amount of pressure to the resistance sensitive trigger that is opposed by a predetermined amount of resistance from the skin surface of the patient.

Abstract: This invention relates to a method for treating erectile dysfunctionality by injecting pharmacological agents into the corpora cavernosa of the penis. The present invention employs an improved method for injecting pharmacological agents into the corpora cavernosa of the penis which does not require a hypodermic needle and the attendant problems associated with the use of hypodermic needles to inject pharmacological agents into the penis and to provide a new treatment option to many patients with erectile dysfunctionality.

Abstract: A pump, comprising an inlet portion having an ingress channel, an outlet portion having an egress channel, a firing portion, and a manifold having a passage in fluid communication with the ingress channel, the egress channel, and the chamber. The firing portion includes a firing cylinder and a firing piston. The firing piston is capable of performing compression strokes and expansion strokes within the firing cylinder. The firing cylinder forms a chamber in which fluid is drawn during an expansion stroke. A high-pressure actuation device drives the firing piston during the compression stroke to expel a high-pressure jet of fluid from the egress channel. If an injector device is held proximate to flesh, the jet of fluid has sufficient pressure to hypodermically inject the fluid without a needle. The inlet portion, outlet portion, and firing portion of the pump can be rearranged on the manifold to conform to the design requirements for a variety of slap injectors.

Abstract: A capsule for storing a fluid, for example helium, under pressure comprises a hollow body from which extends a hollow neck. A stopper engages with the neck in a fluid tight manner. The stopper includes a main hollow portion and a stem extending outwardly from the main hollow portion. The root of the stem where it joins the main hollow portion forms a frangible section which, when broken, will allow fluid in the capsule to escape under pressure.

Abstract: A needleless syringe particle delivery system is provided. The needleless syringe comprises an elongate nozzle which is connected at its upstream end to an open ended capsule chamber. The capsule chamber is configured to house and intimately enclose a nonrigid capsule containing particles of a therapeutic agent. An opening means is provided at the upstream end of the capsule chamber, and is used to pierce the upstream end of a capsule in the chamber. After the capsule is opened, an energizing means connected to the upstream end of the capsule chamber applies a gaseous pressure sufficient to force the particles out of the capsule and the open downstream end of the capsule chamber and thus to create through the nozzle a supersonic gas flow in which the particles are entrained.

Abstract: A needleless syringe capable of accelerating particles comprising a therapeutic agent across skin or mucosal tissue of a vertebrate subject is provided. The syringe comprises an elongate tubular nozzle having a bend along its length and is connected to or capable of connection to a suitable energizing means for producing in the nozzle a supersonic condition sufficient to cause delivery of the particles to a target surface. A method for delivering particles comprising a therapeutic agent from the needleless syringe is also provided.

Abstract: A gas delivery system includes a capsule for storing a propellant fluid, e.g. helium under pressure, e.g. between about 60 and 80 bar. The capsule is provided with a stopper having a stem formed with a frangible section. In use, mechanical means is employed to rupture the stem about the frangible section to release the fluid under high pressure.

Abstract: An apparatus and method for applying a particulate hemostatic agent to living tissue are disclosed. The apparatus includes a particulate hemostatic agent source (22) and a continuous gas source (14). A continuous gas stream from the continuous gas source is turbulently combined with the particulate hemostatic agent within the hemostatic agent source from a finely dispersed fluid stream of the particulate hemostatic agent in the continuous gas stream. An outlet conduit (34) extends from where the gas and particulate hemostatic agent are combined through an outlet (36) of the conduit, whereby the fluid stream is conducted through the outlet conduit and is discharged from the outlet conduit onto proximate living tissue, thereby applying the particulate hemostatic agent o the living tissue.

Abstract: A needleless injection system and method for injecting a medical product comprises a needleless injection device having a nozzle assembly defining an ampule chamber for holding medication, an energy device for pushing medication out of the nozzle assembly, and an energy device actuating mechanism. These components are operatively contained in a housing configured for a hand held operation. The energy device is a self-contained gas spring operatively connected to a plunger operating within the ampule chamber. The gas spring is preferably stepped which can be used in many different applications, an air gun being one. The injection device can be provide with a coupling device for coupling a medication supply vial to the nozzle assembly. The nozzle assembly is removably situated in the housing with the plunger removable therewith.

Abstract: A needleless injector for injecting medication through the skin of a patient includes a vial which holds a volume of liquid medication. The vial includes a vial piston which moves to force the liquid medication out of the vial. A power mechanism applies force to the vial piston. The power mechanism includes a power piston which has a plurality of ratchets. A spring is positioned to apply force to the power piston. A trigger engages the ratchets on the power piston to hold the power piston in place against the force applied by the spring. The trigger selectively releases the power piston so that the power piston moves in response to the force applied by the spring. The power piston applies the force to the vial piston to cause the vial piston to force the liquid medication out of the vial. A cocking mechanism applies force to the power piston to move the power piston against the force of the spring to engage the ratchets.

Abstract: A needleless syringe having a membrane which is ruptured by gas pressure to generate a supersonic gas flow in which particles containing a therapeutic agent are injected.

Abstract: In a needle-less injector combining an actuator and a medicament cartridge, the actuator includes a housing with a forward portion to which the cartridge is connected. An impact member is mounted within the housing inward of the forward portion so as to be movable toward the forward portion, where it may strike components of the cartridge to effect expulsion of a dose of medicament. A chamber is provided within the housing and is pre-filled with a pressurized gas which is in communication with and exerts a constant force on the impact member, tending to urge it towards the forward portion.

Abstract: A pneumatic retractable syringe in which the needle is retracted into the barrel of the syringe following use by compressed gas that is released from a gas reservoir when the gas reservoir is ruptured by applying force to the plunger after injection is completed.

Abstract: A safety mechanism for aiding in the prevention of accidental or unintentional discharge of a needleless injection device having a power unit, a housing, a plunger disposed within the housing, a trigger assembly, and a nozzle. The safety mechanism includes a locking member which is disposed at least partially on the exterior of the housing. The locking member works in concert with the triggering assembly to the prevent movement thereof, thereby preventing activation of the power unit to eject fluids through the nozzle. The locking member also works in concert with an interlocking sleeve which prevents activation of the injector when the nozzle is removed therefrom. The safety mechanism also includes a feature for automatically returning the locking member to a locked position after activation.

Abstract: An improved medication delivery device is a pen sized instrument that is powered by compressed inert gas. The needle-less injector device contains pre-filled and pre-measured medication dosages. The injector device has a pre-filled and self-contained compressed gas for providing pressure to inject the medication into the skin surface without the use of a needle. The injector device has a pressure sensitive deployment mechanism which insures proper seating of the injector face against the skin surface before medication delivery is accomplished. The needle-less injector device assures safe use by inexperienced operators (including children) under adverse conditions.

Abstract: Disclosed are compositions suitable for use in embolizing blood vessels which compositions comprise an ethylene vinyl alcohol copolymer, a biocompatible solvent and a water insoluble contrasting agent selected from the group consisting of tantalum, tantalum oxide and barium sulfate. Also disclosed are methods for embolizing a blood vessel using the compositions described herein.

Abstract: A capsule for storing a propellant fluid, for example, helium under pressure comprises a hollow body which includes a frangible area. An anchor member attaches an arm to the frangible area such that when a force is applied to the arm, said force together with the helium under pressure will cause the frangible area to rupture outwardly of the hollow body thereby to release the helium.

Abstract: The present invention relates to a conversion kit for converting a machine designed for intravascular injection of solutions, such as parenteral solutions, using high-pressure syringes, to a machine that can be used for injection using smaller manual syringes. The conversion kit, includes at least one conversion vessel (13) for releasable but substantially non-rotary reception of a high-pressure syringe with a cylindrical guide (19) formed through a receiving head (14) of the conversion vessel (13) and a recess (17) formed in the upper surface of the receiving head (14). The recess (17) may also receive the radial end regions of wing extensions of a manual syringe of predetermined size. The conversion kit also includes at least one reducing sleeve (23) for reducing the effective inner diameter of the guide (19), the reducing sleeve (23) adapted to snugly receive the outer diameter of a manual syringe (12).

Abstract: An improved medication delivery device is a pen sized instrument that is powered by compressed inert gas. The needle-less injector device contains pre-filled and pre-measured medication dosages. The injector device has a pre-filled and self-contained compressed gas for providing pressure to inject the medication into the skin surface without the use of a needle. The injector device has a pressure sensitive deployment mechanism which insures proper seating of the injector face against the skin surface before medication delivery is accomplished. The needle-less injector device assures safe use by inexperienced operators (including children) under adverse conditions.

Abstract: A nozzle assembly adapted for a fluid injector having a ram, includes a plunger assembly having first and second driving members. The first and second driving members are apart according to a predetermined first distance. The second driving member is spaced apart from the ram according to a predetermined second distance. The first and second distances are resiliently maintained by a resilient spring member operatively disposed between the two driving members. One of the first and second distances is selected to be the smallest and thereby controls the maximum pressure at which fluid is expelled from the nozzle assembly.

Abstract: The present invention relates to a nozzle assembly adapted for use with an injector device having an energy generating source and a chamber adapted for holding a fluid and having first and second end portions with an orifice defined at the first end portion for passage of the fluid and being open at the second end portion. The device includes a first driving member movably positioned in the chamber; a second driving member movably positioned in the chamber and spaced apart from the first driving member according to a predetermined travel distance and including an end portion operative for expelling fluid out of or drawing fluid into the chamber via the orifice; and a spacing member disposed between the first and second driving members for maintaining said predetermined travel distance during displacement of the first and second driving members before the energy generating source is activated.

Abstract: Disclosed are compositions suitable for use in embolizing blood vessels which compositions comprise an ethylene vinyl alcohol copolymer, a biocompatible solvent and a water insoluble contrasting agent selected from the group consisting of tantalum, tantalum oxide and barium sulfate. Also disclosed are methods for embolizing a blood vessel using the compositions described herein.

Abstract: A novel device and method for the application of two or more components of a fibrin sealant using a gas is disclosed. The novel device and method involve the concentric arrangement of annular apertures for each of the components concentric with and radially outward of a center gas discharge aperture in the exit end of a spray head. Reservoirs for each component, for example syringe cartridges or cylinders, are in dextrete fluid communication with the spray head and preferably can be activated by a common means.

Abstract: The invention pertains to a delivery device for controlling the injection of discrete quantities of fluid injectable materials through a conduit such as a hypodermic needle or a catheter. The delivery device is coupled to a pressurized driving fluid source, and the control means provides controlled passage of pressurized driving fluid into a syringe body to act against a piston which forces the fluid injectable material out the needle or catheter.In addition to the delivery device, the invention includes a needle depth guide which is preferably used in combination with the delivery device for cosmetic applications when a hypodermic needle is used to deliver a fluid injectable material to the dermis.

Abstract: A needless injection device includes an initiator valve controlling flow of compressed gas into a reservoir. A poppet valve connecting to the reservoir has a gas pressure regulation end to regulate flow from the initiator valve into the reservoir. A clamp piston is driven forward by gas pressure from the reservoir and causes jaws to clamp onto a plunger extending into an ampule. The poppet valve opens when reservoir pressure reaches the cracking pressure of the poppet valve. Gas from the reservoir rushes through the popper valve into a drive chamber and forces a drive piston, containing the clamp piston and jaws, forward causing the plunger to slide into the ampule. A jet of injectant sprays out of the nozzle of the ampule and penetrates through the patient's skin.

Abstract: The present invention is directed to a syringe that includes a gas driven piston to force liquid medication from a syringe cartridge through a variety of injection nozzles. The syringe may be mechanically operated for loading or aspirating the syringe.

Abstract: An apparatus for injecting liquids into a body without using hypodermic needles, the liquid being ejected from a small orifice in a probe at a velocity which will penetrate the surface of a body against which the probe is placed. The apparatus ejects a specific small volume of the liquid under a very high initial velocity and pressure followed by the ejection of the main charge of liquid at a lower velocity so that the liquid flows into the channel caused by the initial penetration without penetrating to a greater depth. The probe is connected to a hand-held portion whose other end is attached via a flexible tube containing a suitable hydraulic fluid to two remote pressure intensifiers, one of which creates the required high initial pressure for a short period of time and the other of which provides the pressure necessary to eject the main charge of liquid at a lower velocity.

Abstract: A needleless injection device has a housing containing a pilot valve connectable to a compressed gas source. A main valve is operatively connected to the pilot valve. The pilot valve and main valve form a two-stage valve with the pilot valve activatable to open the main valve utilizing gas pressure. Compressed gas in a reservoir flows through the open main valve to driven a plunger into an ampule to inject an injectant through a patient's skin.

Abstract: A liquid-injection instrument without needle comprises an elongated body in two separable parts placed end to end. The first, so-called medical part, comprises at least one cavity receiving a liquid-tight cell which contains the injection liquid and has a movable base which, when displaced, forces liquid from the cell towards at least one variable-volume dosing chamber in the medical part. This communicates with a nozzle provided with an injector capable of forming a narrow jet of liquid following forcible expulsion of liquid from the dosing chamber. The second, so-called motor part, comprises a pneumatically controlled mobile assembly which effects alternating movements. The mobile assembly comprises a working piston (52-233-420) and a control and propulsion spring (62-241-444) which acts on the piston when gradually compressed by the movement of a plunger (52-276-445) caused by the pressure of the compressed air in a gas-tight chamber (51-287) in the body.

Abstract: A system is provided that is useful for hypodermic injection of medication without piercing the skin with a needle. The system includes a gas pressure actuated needleless hypodermic injection device for injecting medication through the skin. The injection device includes an injector assembly having an injector body with a chamber for a compressed gas container and an ampule assembly mounted on the injector body for containing the liquid medication. The system also includes an adaptor assembly for use on a medication vial for transferring medication to the ampule assembly.

Abstract: This invention relates to an apparatus for driving a syringe plunger into a barrel using manually created pneumatic pressure that is useful for inflating medical devices such as angioplaty balloons. The apparatus permits one handed, highly controlled application of pressure to a standard medical syringe.

Abstract: A device to introduce a liquid into the hypoderma, the device includes a reservoir which receives a gas under pressure, the gas is delivered via a valve to an interacting piston and cylinder. When the gas is delivered to the piston, the piston moves to eject a liquid from a capsule mounted within the device. The liquid contained in the capsule is then ejected through a nozzle located against the skin of the user.

Abstract: A hand-held and operated pneumatically powered device for injecting fluids, such as in medical applications, consisting of a housing that is sized and shaped to be hand held, and connected power and infusion assemblies contained within the housing. The power assembly includes a sealed vessel containing pressurized gas, a lever-needle vessel-puncturing mechanism, a gas flow path leading from the needle to the infusion assembly, and pressure regulator and pressure relief mechanism (which may include a pneumatic flow control orifice) interposed in the flow path.

Abstract: A pre-filled ampule and a powered, non-invasive injection device assembly wherein the device includes a housing having an ampule-receiving chamber, a gas charge, and means for delivering a predetermined amount of gas to an ampule-receiving chamber. The device includes an injection-counting ring which is received in a groove extending about the housing wherein the ring includes a counting mechanism thereon and is constructed to allow one-way only rotation thereof relative to the housing. The ampule includes an elongate ampule body having a medication holder located at one end thereof, a transfer area located adjacent the other end thereof and a bypass area located adjacent an end of the transfer area. A plunger is provided and has one end thereof received in and closing one end of the medication holder with the other end of the plunger being received in the ampule-receiving chamber of the injection device. A floating seal is received and encloses the other end of the medication holder.

Abstract: A needleless injector device includes an integral unit that is dimensioned and arranged to be grasped in the hand of a user, loaded with a selected dosage, and held proximate the skin in order to inject the selected dosage in a high pressure jet sufficient to pass the selected dosage through the skin for injection purposes, the unit having a barrel portion, a gas storage portion, and an intermediate portion. A trigger operates a release mechanism to release compressed gas from a storage compartment to act upon a piston and drive a plunger that ejects the selected dosage of medication through an aperture in the discharge end of the barrel portion, the piston face being larger than the plunger face to increase pressure.

Abstract: Loader-mixer device for endermic injectors which is suitable to cooperate with a portable endermic injector momentarily in loading, by aspiration through an injection-aspiration nozzle included in an injection head (17) of the portable endermic injector, the product to be injected, the device comprising in cooperation:at least one seating to lodge and position phials (12) together with two needles (13-14),a socket (31) to position the injection head (17), anda selector assembly (20) to connect a phial (12) to the injection head (17) as required.

Abstract: The present invention provides a pressure-operated hypodermic injection apparatus which is particularly suitable for needleless operation. The apparatus includes an elongate shell having an inwardly facing wall with a uniform configuration along a defined length thereof, with the shell further defining a discharge aperture adjacent one end thereof. It further includes a plunger which is slideably disposed within the defined length of the shell, and which is shiftable between a ready position and a spent position, with the spent position being closer to the aperture than the ready position. With the plunger in its ready position, the shell and plunger collectively define an ampule chamber which is capable of containing a dischargeable medication. A pressurized-gas cartridge is mounted to the plunger to shift therewith, and has gas-releasing means which faces away from the discharge aperture. A body is further included which is sealingly and releasably joined to the other end of the shell.