The present invention relates to a syringe, and more particularly, to an apparatus obtained by improving a conventional syringe formed with an injection flow passage including an injection needle, so as to share a portion of the injection flow passage except the injection needle or to form a suction flow passage completely independent of the injection flow passage, thereby further smoothing suction of a liquid medicine. The syringe is configured such that the separate suction flow passage bypassing the injection needle is formed in the conventional syringe to more smoothly perform suction of the liquid medicine, thereby maximizing user's convenience and marketability of the conventional syringe, and further configured to forcibly close the suction flow passage upon injection of the liquid medicine.

An apparatus for vaccine generation includes a syringe with a cavity that includes a solution with photosensitizers. Microbial particles are added to the solution. A light source is capable of emitting one or more wavebands of light that are effectively absorbed by the one photosensitizers to generate singlet oxygen in the solution and other radical species that rapidly react with and damage lipids, proteins, DNA, and RNA of the microbial particles. This damage produces immunogens that can be applied as a vaccine to viruses and other infectious microbial particles. A plunger that fits within a proximal opening in the syringe is used for forcing the solution including the immunogens through the filter and out of the syringe while the photosensitizers, debris and unwanted microbial particles are trapped within the filter.

The present relates to a filter needle coupled between a fixation member having a needle for injecting a medical fluid after filtering foreign substances contained in the medical fluid and a disposable syringe, the filter needle includes an outer housing having a front end portion to which the fixation member is coupled and a rear end portion to which the disposable syringe is coupled and a filtering unit which is disposed inside the outer housing, and in which a medical fluid supplied from the fixation member to the disposable syringe is passed through as is, while a medical fluid supplied from the disposable syringe to the fixation member is filtered.

A fluid withdrawing, expelling and filtering apparatus includes a fluid container including a first chamber, a second chamber, and, a first through hole and a second through hole respectively disposed in communication between the first chamber and the second chamber, a filter device movable between a first position and a second position to open or close the second through hole of the fluid container and including a filter element mating with the first through hole, and a fluid withdrawing and expelling operator operable to withdraw and expel a fluid through the first chamber of the fluid container.

An autoinjector is described that includes an outer body, a first trigger, an output needle, and a first compartment. The first compartment is positioned within the outer body and includes (i) a main body, (ii) a first biasing member coupled to the first trigger, and (iii) a protrusion positioned at a distal end of the main body. The autoinjector further includes a second compartment positioned in the outer body and in fluid communication with the first compartment and the output needle. The autoinjector also includes a second biasing member coupled to a second trigger. The first biasing member is configured to, upon application of force to the first trigger, automatically move an ampule in a distal direction relative to the main body to force the ampule against the protrusion, so as to break the ampule and allow a medicament to flow from the ampule to the second compartment.

A telescoping syringe suitable for use with medications and other ejectable or injectable fluids is presented. The syringe includes a plunger, a barrel, and a valve. The plunger is extendible from and retractable into the barrel. The plunger defines a first reservoir. The barrel defines a second reservoir as the plunger is extended from the barrel. The valve is disposed at one end of the plunger adjacent to a nipple extending from the barrel. A first sealing interface is formed by the valve and a distal wall along the barrel adjacent to the nipple. A second sealing interface is formed by an annular flange along the one-way valve and an annular groove along the plunger. A third sealing interface is formed by the valve and a circumferential end along the plunger. The sealing interfaces are closed prior to extension of the plunger from the barrel thereby preventing a gas from entering and a fluid from existing the first reservoir. The sealing interfaces are open when the plunger is extended from the barrel so that the gas enters the first reservoir via an inlet(s) along the annular groove and fluid is communicated into the second reservoir via an outlet(s) along the valve. The second and third sealing interfaces are closed when the plunger is retracted into the barrel thereby allowing fluid to exit the second reservoir via the nipple.

Liquid drug cartridges and an associated inhaler are used to deliver one more separate doses of an aerosolized liquid drug. A cartridge includes a container for storing the liquid drug, an end cap having an ejection opening, a filter element, and a piston that is repositionable relative to the container to selectively eject a volume of liquid drug from the ejection opening. The filter element filters the liquid drug prior to ejection from the ejection opening. The liquid drug cartridge can be coupled with an inhaler that includes an aerosol generator. The aerosol generator includes a vibratable membrane onto which the liquid drug is ejected. The liquid drug is aerosolized by the vibration of the membrane for inhalation by a user.

A syringe with a filter is disclosed. When liquid medicine for treatment such as an analgesic is suctioned into the syringe by using a syringe needle and then injected into a human body through the syringe needle, foreign substances generated in an ampule and the like are filtered in the syringe prior to the liquid medicine being injected into the human body as the foreign substances are suctioned into the syringe through the syringe needle. In addition, the filter is configured so that the filter can be installed into the syringe with ease.

Various embodiments relate to a syringe for separating nucleic acids from a blood sample and systems that include the syringe and a portable PGR device. The syringe may include a shell defining a central aperture extending through a longitudinal axis of the syringe, a plunger disposed within the central aperture of the shell, and a core rotatably disposed within the central aperture. The syringe may further include a needle fluidically connectable to the inlet of the shell. Various embodiments relate to a method for separating nucleic acids from a blood sample, the method comprising drawing the blood sample from a patient using the syringe according to any of the embodiments described herein.

The present invention relates to a filtering syringe, and more particularly, to an apparatus obtained by improving a syringe provided with a filter means for filtering foreign substances such as glass fragments of an ampoule, so as to prevent the foreign substances from being injected together with a liquid medicine while allowing the liquid medicine to be smoothly sucked and injected with a small force, especially even though a filter means having micro-pores is employed. The filtering syringe is configured such that the filter means is provided in the injection flow passage to prevent the foreign substances from being injected together with the liquid medicine while enabling the liquid medicine to be more smoothly sucked and injected despite employing the filter means having the micro-pores, thereby maximizing user's convenience and marketability of the syringe.