The invention describes method for delivering and positioning radio-isotopes. The method uses encapsulating free flowing medicament into a leak proof vehicle and positioning the vehicle into the body. Also provided is a system for delivering and positioning radio-isotopes into the body, the system comprising fluid radio-isotope encapsulated in a leak proof material and/or absorbable material.

The present invention relates to therapeutic immunoconjugates comprising SN-38 attached to an antibody or antigen-binding antibody fragment. The antibody may bind to Trop-2 or CEACAM5 and the immunoconjugate may be administered at a dosage of between 4 mg/kg and 16 mg/kg, preferably 4, 6, 8, 9, 10, 12, or 16 mg/kg. When administered at specified dosages and schedules, the immunoconjugate can reduce solid tumors in size, reduce or eliminate metastases and is effective to treat cancers resistant to standard therapies, such as radiation therapy, chemotherapy or immunotherapy. Surprisingly, the immunoconjugate is effective to treat cancers that are refractory to or relapsed from irinotecan.

An infusion system may include a strontium-rubidium radioisotope generator that generates a radioactive eluate via elution, a beta detector, a gamma detector, and a controller. The beta detector and the gamma detector may be positioned to measure beta emissions and gamma emissions, respectively, emitted from the radioactive eluate. In some examples, the controller is configured to determine an activity of rubidium in the radioactive eluate based on the beta emissions measured by the beta detector and determine an activity of strontium in the radioactive eluate based on the gamma emissions measured by the gamma detector.

An engineered radioactive polymeric microsphere, and a preparation and application thereof. The preparation method includes: adding a styrene monomer and a disperser and/or a crosslinker into a medium, followed by feeding of nitrogen or helium and stirring to obtain a first reaction mixture; heating the first reaction mixture, and adding an initiator, followed by reaction under stirring at a constant temperature to obtain a second reaction mixture; subjecting the second reaction mixture to washing with ethanol and water, and vacuum drying to obtain a crude polymeric microsphere; subjecting the crude polymeric microsphere to radiation-induced graft polymerization with a functional monomer to obtain the functionalized polymeric microsphere; and exposing the functionalized polymeric microsphere to a radionuclide to prepare the engineered radioactive polymeric microsphere.

A multi-purpose balloon intra-cavity catheter includes a catheter having a proximal end portion, a central portion and a non-branching distal end portion, a plurality of lumens associated with the catheter extending from the proximal end portion, and a plurality of inflatable balloons positioned in the central portion and/or the non-branching distal end portion. Each of the plurality of inflatable balloons is communicatively associated with a corresponding one of the plurality of lumens, the plurality of inflatable balloons being selectively inflated or deflated to position and stabilize the catheter in a cavity for delivery of a medical treatment. The catheter can include an extraction opening associated with a lumen to remove fluids and materials from the cavity, and a connector associated with a corresponding lumen adapted to selectively receive one or more of a fluid medium or a radioactive isotope provided to a corresponding lumen for delivery of the medical treatment.

An administration device that includes a hermetic container closed by a cap, containing a radiopharmaceutical medicament, and provided with a protective shield made of a radiopaque material. The device includes a support provided with attachment structure. The container is removably attached to the support in a position allowing access to the cap. The support includes a baseplate provided with an opening allowing access to the cap. A cover and rods connect the baseplate and the cover.

A surgical tool has an elongate tubular housing having an annular clamping region formed around an opening in the tubular housing. A vacuum source is operably engaged with the elongate tubular housing for providing a vacuum within the elongate tubular housing for drawing the damaged or diseased portion of a luminal body, such as an intestine, into the tubular housing. An elongate rod is provided having an annular clamping element shaped so that the intestine may be firmly clamped between the annular clamping element and the annular clamping region of the elongate tubular housing, so that the damaged or diseased portion of the intestine is entirely within the elongate tubular housing.

A radiation dermatitis prevention apparatus includes: a pack (10), including: a pocket (12) including a face panel (16) and a back panel (18), wherein the panels (16, 18) are secured to each other along their respective peripheries in such a way as to define an opening (20), wherein the face panel (16) is constructed from a material suitable for contact with a patients skin and which readily permits fluid to flow through its thickness; and an insert (14) sized to fit in the opening (20) and made of a material which is suitable for holding and releasing a radiation cream in viscous fluid form.

A catheter apparatus (10) includes a tubular member (11); multiple fluid-flow pipe members (13), each having a proximal end (19) and a distal end (18), and being disposed along a first axial direction of the tubular member; multiple node members (15) disposed along a first axial direction of the tubular member, wherein two adjacent node members (15) form a segment (1a); and a periphery member (14), wherein the periphery member (14) wraps the multiple node members (15) to form a space (1b) with the segment (1a) formed between the two adjacent node members (15). The catheter apparatus (10) can irradiate the entire diffuse tumor during one brachytherapy process without repeated placement of the catheter. Meanwhile, it can be smoothly inserted into the patient's narrow body cavity because there are no external balloons. A brachytherapy system adopts the catheter apparatus (10).

A multi-purpose balloon intra-cavity catheter includes a catheter having a proximal end portion, a central portion and a non-branching distal end portion, a plurality of lumens associated with the catheter extending from the proximal end portion, and a plurality of inflatable balloons positioned in the central portion and/or the non-branching distal end portion. Each of the plurality of inflatable balloons is communicatively associated with a corresponding one of the plurality of lumens, the plurality of inflatable balloons being selectively inflated or deflated to position and stabilize the catheter in a cavity for delivery of a medical treatment. The catheter can include an extraction opening associated with a lumen to remove fluids and materials from the cavity, and a connector associated with a corresponding lumen adapted to selectively receive one or more of a fluid medium or a radioactive isotope provided to a corresponding lumen for delivery of the medical treatment.