摘要:
A method of formulating a particle composition having a pre-selected cell internalization mode involves selecting a target cell having surface receptors and obtaining particles that have i) surface moieties, that have an affinity for or are capable of binding to the surface receptors of the cell and ii) a preselected shape, where a surface distribution of the surface moieties on the particles and the shape of the particles are effective for the pre-selected cell internalization mode.
摘要:
Opsonizable micro- or nanoparticles, that contain at least one active agent, such as an imaging or therapeutic agent; that have a positive surface charge and that do not contain on their surface targeting ligands, such as antibodies, peptides or aptamers, can be used to treating and/or monitoring a condition associated with an inflammation, such as a cytokine stimulated inflammation.
摘要:
A folding unit for producing sealed packages of pourable food products from respective packs, each having a main portion folded into a desired shape, and opposite end portions to be folded to form respective folded ends of a relative finished package. The unit has a first folding station, in turn having a first retaining mechanism for securing each pack by a relative first end portion, and a first folding mechanism for folding a relative second end portion of the pack. The unit also has a second folding station located downstream from the first folding station in the traveling direction of the packs, a second retaining mechanism for securing each pack by the relative folded second end portion, and a second folding mechanism for folding the relative first end portion.
摘要:
A folding unit for producing sealed packages of pourable food products from respective packs, each having a main portion folded into a desired shape, and opposite end portions to be folded to form respective folded ends of a relative finished package. The unit has a first folding station, in turn having a first retaining mechanism for securing each pack by a relative first end portion, and a first folding mechanism for folding a relative second end portion of the pack. The unit also has a second folding station located downstream from the first folding station in the traveling direction of the packs, a second retaining mechanism for securing each pack by the relative folded second end portion, and a second folding mechanism for folding the relative first end portion.
摘要:
Endocytosis of an active agent into a cell having surface receptors can be enhanced by using particles that have a radius no less than an endocytotic threshold determined based on a surface density of the receptors, a surface density of the moieties and interaction parameters that include at least one of a receptor-moiety spring constant and a non-specific interaction strength.
摘要:
A bifurcated vascular prosthesis implanted using a combined laparoscopic/open and endovascular technique for curing aneurysms of the abdominal aorta includes two stents on distal arms of the prosthesis. A delivery system and surgical kit for the release of the vascular prosthesis includes a pair of balloon release catheters, to be inserted within each corresponding stent and to remain adhering thereto throughout the time prior to release until reinflated with an inflating syringe, and a pair of balloon guide catheters, each including a dilator and a sheath. A method for implanting the prosthesis is also provided.
摘要:
Microfabricated, asymmetrical, reservoir-containing particles for use in the oral delivery of biopolymer therapeutic agents such as peptides, proteins and oligonucleotides are disclosed. The particles are encapsulated in enteric-coated capsules or tablets to provide passage through the stomach and release of a suspension of the particles in the intestinal lumen. The particles have a selected shape, and uniform dimensions preferably in the 100 &mgr;m to 1 mm range. The reservoirs open to the face of the particle and are filled with a therapeutic agent and selected excipients. The excipients are selected to delay the dissolution/release of the agent from the particle reservoirs for 5-60 minutes after the particle is released in the intestinal lumen. Alternatively, the pore is plugged with an erodable material. The face of the particle is grafted with a layer of muco-adhesive ligands designed to quickly bind the particle to the intestinal mucosa for several minutes to several hours after release of the particles from the enteric-coated carrier.
摘要:
Microfabricated filters utilizing a bulk substrate structure and a thin film structure and a method for constructing such filters. The pores of the filters are defined by spaces between the bulk substrate structure and the thin film structure and are of substantially uniform width, length and distribution. The width of the pores is defined by the thickness of a sacrificial layer and therefore may be smaller than the limit of resolution obtainable with photolithography. The filters provide enhanced mechanical strength, chemical inertness, biological compatibility, and throughput. The filters are constructed using relatively simple fabrication techniques. Also, microfabricated containment wells and capsules constructed with such filters for the immunological isolation of cell transplants and a method for constructing such containment wells and capsules. The pores of the wells and capsules are large enough to let a desired biologically-active molecular product through, while blocking the passage of all larger immunological molecules. The containment wells and capsules provide enhanced biological compatibility and useful life.
摘要:
The present invention provides a capsule made of a biologically compatible material with sufficient mechanical strength to form a very thin membrane shell having at least a region with approximately uniformly sized and spaced holes or pores that are large enough to let a desired biologically active molecular product through, while blocking the passage of all larger immunological molecules. The present invention thus provides an immunological isolation of cell transplants contained therein. The present invention also provides a free standing thin film structure that may be used as a component of such a capsule and method for the fabrication of such component and capsules.