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56 results about "Recipient site" patented technology

Particulate acellular tissue matrix

A method of processing an acellular tissue matrix to give a particulate acellular tissue matrix includes: cutting sheets of dry acellular tissue matrix into strips; cryofracturing the dry acellular tissue matrix strips at cryogenic temperatures; separating the resulting particles by size at cryogenic temperatures; and freeze drying the fraction of particles desired size to remove any moisture that may have been absorbed to give a dry particulate acellular tissue matrix. Rehydration of the dry particulate acellular tissue matrix may take place just prior to use. The particulate acellular tissue may be applied to a recipient site, by way of injection, spraying, layering, packing, in-casing or combinations thereof. The particulate acellular tissue may further include growth and stimulating agents selected from epidermal growth factor, fibroblast growth factor, nerve growth factor, keratinocyte growth factor, platelet derived growth factor, vasoactive intestinal peptide, stem cell factor, bone morphogetic proteins, chondrocyte growth factor and combinations thereof. Other pharmaceutically active compounds may be combined with the rehydrated particulate material including: analgesic drugs; hemostatic drugs; antibiotic drugs; local anesthetics and the like to enhance the acceptance of the implanted particulate material. The particulate material product may also be combined with stem cells selected from mesenchymal stem cells, epidermal stem cells, cartilage stem cells, hematopoietic stem cells and combinations thereof.
Owner:LIFECELL

Process for the integrity check of lots of individual package units

A process for integrity check of lots of individual package units which comprises combining at least one RFID tag and a container which contains a large number of individual package units wherein each of the individual package units is marked with a marking code, the information of these codes of all individual package units is combined, and a hash code is generated based on the combined information of all marking codes of all individual package units, which combined hash code is stored in an RFID tag which is affixed to the container, this combined hash code together with the individual hash codes for the individual package units being stored in the data base of the SENDER site where the container is packed and sealed, the individual hash codes then being transmitted to the RECIPIENT of the said container, the information collected from the RFID tag being compared to the combined hash code which is calculated at the RECIPIENT site from the information received by the SENDER of the said container including all individual hash codes of all package units in the said container, and to the combined hash code calculated from the markings on the individual package units or boxes scanned at the RECIPIENT site, and the application of the said process in the verification of the integrity of pharmaceutical goods, video information such as movies on DVD, audio information such as music on CD, computer files, or paper documents
Owner:ADALBERT GUBO

High-density sample support plate for automated sample aliquoting

A sample support plate (100) for a variety of possible applications, including MALDI mass spectrometry, is disclosed. A plurality of spatially separated sample recipient sites (101) are arranged on the surface of a substrate. The recipient sites are mutually separated by areas having a different wettability than the recipient sites. They are arranged in a plurality of rows consisting of a plurality of recipient sites whose centers are regularly spaced along a first direction with a predetermined periodicity (D1), the rows being regularly spaced along a second direction perpendicular to the first direction with a predetermined centerline distance (D2). Each recipient site has a maximum lateral dimension that is preferably smaller than the diameter of a beam spot (104) of a desorption laser beam (103). In order to enable unsupervised splitting of bulk liquid samples into droplets at the sample recipient sites, the periodicity along the first direction and the centerline distance along the second direction are chosen such that each recipient sites has a next neighbor at a distance that is less than or equal to three times the minimum lateral dimension of each recipient site. In preferred embodiments, the sample recipient sites are arranged in a checkerboard-type pattern or in rows that are inclined relative to the edges of the sample support plate.
Owner:ETH ZZURICH +1

Preparation method and application of injectable allogeneic adipose acellular matrix particles

The invention discloses a preparation method and application of injectable allogeneic adipose acellular matrix particles. The injectable allogeneic adipose acellular matrix particles are obtained in the modes that adipose tissue obtained through liposuction operation is subjected to mechanical chylosis treatment, centrifugal degreasing and a subsequent gentle acellular working procedure, and centrifuged for further degreasing. The adipose tissue comes from human-derived adipose particles discarded by traditional liposuction operation of obese patients. Adipose cell physical crushing and degreasing methods are adopted, a gentle acellular technology is applied, operation is easy and convenient, damage to adipose matrix structure and components is small, an obtained material is closer to thehuman body natural adipose tissue microenvironment, and the three-dimensional structure and active components of the tissue are preserved; and the injectable allogeneic adipose acellular matrix particles can be injected through a 27g of small needle, after injection, proliferation and differentiation of tissue cells in a recipient site are more facilitated, thus tissue repairing and regeneration are promoted, and the long-term filling and rejuvenation effects are achieved. The injectable allogeneic adipose acellular matrix particles are suitable for facial rejuvenation and soft tissue defect repairing.
Owner:易成刚

Fine particle tissue filling material for injection and preparation method thereof

ActiveCN101366978BGood biocompatibilityQuick and arbitrary shapingProsthesisWrinkle skinFiber
The invention discloses an injectable filling material of particle tissues, wherein particulate acellular bio-derived materials are mixed with drug-containing release microspheres, after the filling material is evenly mixed with a gel solution before use, the filling material is injected into a recipient site, an operator can arbitrarily model the particle tissue before gel is solidified according to the condition of the recipient site so as to achieve a satisfactory cosmetic effect. The particle tissue material which can be moulded rapidly is implanted in the body to fill defective soft tissues and promote wound healing. Compared with the prior art, the injectable filling material of the particle tissues has high biocompatibility, and is capable of rapid arbitrarily modeling and rapid filling the defect of tissue organs, and can promote fibroblast ingrowth, the formation of new capillary, generation of granulation tissue and wound healing. The injectable filling material of the particle tissues has the following clinical functions that the injectable filling material can be used as a filler of defective soft tissues which is used for repairing body depression deformity; for filling wrinkles or ruga of skins; and for demands of cosmetic surgeries, such as soft tissue arthroplasty and so on.
Owner:SHAANXI RUISHENG BIOTECH
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