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86results about How to "Promote cell adhesion" patented technology

Engineered Integrin Binding Peptides

Engineered peptides that bind with high affinity (low equilibrium dissociation constant (Kd)) to the cell surface receptors of fibronectin (α5β1) or vitronectin (αvβ3 and αvβ5 integrins) are disclosed. These peptides are based on a molecular scaffold into which a subsequence containing the RGD integrin-binding motif has been inserted. The subsequence (RGD mimic) comprises about 9-13 amino acids, and the RGD contained within the subsequence can be flanked by a variety of amino acids, the sequence of which was determined by sequential rounds of selection (in vitro evolution). The molecular scaffold is preferably based on a knottin, e.g., EETI (Trypsin inhibitor 2 (Trypsin inhibitor II) (EETI-II) [Ecballium elaterium (Jumping cucumber)], AgRP (Agouti-related protein), and Agatoxin IVB, which peptides have a rigidly defined three-dimensional conformation. It is demonstrated that EETI tolerates mutations in other loops and that the present peptides may be used as imaging agents.
Owner:THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIV

PVA-based polymer coating for cell culture

A UV-cross-linkable PVA-based polymer coating for cell culture that provides support for cell adhesion. The polymer coating may also contain bioaffecting molecules reversibly entrapped within the polymer coating that provides necessary nutrients to cell culture. Preferably, the UV-cross-linkable PVA-based polymer is PVA-SbQ.
Owner:BECTON DICKINSON & CO

Method for preparing nano-fiber-based guided bone regeneration membrane

The invention relates to the preparation of a hydroxyapatite-grafted polylactide / polylactic acid-copolymerized glycolic acid electrospun nano-fiber-based guided bone regeneration membrane. The membrane is prepared from a mixture of HA-g-PLLA (hydroxyapatite-grafted poly-L-lactic acid) nanoparticles and PLGA (poly(L-co-glycolic acid) by an electrospinning method, i.e., the novel biodegradable guided bone regeneration membrane is constructed. Compared with PLGA and HAP / PLA fiber membranes, the prepared HA-g-PLLA / PLGA composite fiber membrane has the advantages that high mechanical performance is achieved, the adhesion and ductility of osteoblasts on the surface of the membrane are superior to those of the other composite membranes, and the HA-g-PLLA / PLGA composite fiber membrane has a broad application prospect in the treatment of guided bone regeneration.
Owner:WUXI ZHONGKE GUANGYUAN BIOMATERIALS

Preparation method of DA-based gradient functional material

ActiveCN106267337AQuick combinationImprove rapid degradation behaviorTissue regenerationProsthesisPorosityCross-link
The invention provides a preparation method of a DA-based gradient functional material. DA serves as a functional group, and the chemical reactivity, oxidation auto-polymerization and adhesion of DA are utilized to prepare the functional material with a multistage pore channel and a gradient structure. The method includes the steps that firstly, Alg is subjected to graft modification with DA to prepare biologically-modified macromolecular Alg-DA with excellent adhesion performance; then, DA is subjected to oxidation auto-polymerization assembly in a slightly alkaline buffer solution to form PDA particles of a uniform particle size; then, Alg-DA of different concentrations and the PDA particles act on each other to form a first-stage cross-linked structure, and then the gradient functional material is prepared with a lamination freeze-drying method; then, the gradient functional material is cross-linked again with calcium ions, and the cross-linking degree and porosity of the material are further adjusted. The DA-based gradient functional material provides a new way for preparing composites with an ideal texture. The gradient functional material prepared through the method has high mechanical performance and excellent biocompatibility and biodegradability, can effectively improve the absorption separation performance and the regeneration performance of soft/hard tissue and has broad application prospects in the fields of multifunctional separation and absorption films and biomedicine.
Owner:JIANGNAN UNIV

Preparation method of intra-fibrous biomimetic mineralized collagen membrane capable of promoting osteogenic differentiation of cells

The invention discloses a preparation method of an intra-fibrous biomimetic mineralized collagen membrane capable of promoting osteogenic differentiation of cells. According to the invention, the preparation method comprises the following steps: preparing a collagen solution; pouring the collagen solution into a prefabricated mold, putting the mold into a closed container containing ammonia water,carrying out neutralizing, moving the neutralized solution out and then putting the solution into a constant-temperature box to carry out culturing continuously, and completing self-assembling and forming a gel mode; carrying out cross-linking on the gel to obtain pure collagen gel; and putting the pure collagen gel into a biomimetic mineralization solution and carrying out culturing for a plurality of days to obtain collagen gel with different biomimetic mineralization degrees; and cooling the collagen gel and carrying out freeze-drying on the cooled gel in a freeze dryer to obtain the finalintra-fibrous biomimetic mineralized collagen membrane. According to the invention, intra-fibrous mineralization of the collagen fiber can be formed by biomimetic mineralization; the fiber network structure of the collagen membrane is reserved and utilized while the mechanical property and the biological property of the hydroxyapatite crystal are utilized.
Owner:THE FIRST AFFILIATED HOSPITAL ZHEJIANG UNIV COLLEGE OF MEDICINE +1

Core-shell drug-loaded nano-fiber dressing and preparation method thereof

The invention belongs to the technical field of wound dressings, in particular to a core-shell drug-loaded nano-fiber dressing and a preparation method thereof. The invention provides the core-shell drug-loaded nano-fiber dressing, and the core-shell drug-loaded nano-fiber dressing is obtained through coaxial electrostatic spinning, and sustained release of drugs can be realized; a core layer is constituted by mel and polyvinyl alcohol, and a shell layer is constituted by epsilon-polylysine and polycaprolactone; due to a core-shell structure, the mel as a natural active substance can be effectively protected, an influence of an organic solvent on the active substance is avoided; through wrapping with polycaprolactone as a hydrophobic shell layer, the phenomenon that glutaraldehyde as a toxic and organic solvent is crosslinked with the polyvinyl alcohol can be avoided; the epsilon-polylysine is loaded on the shell layer, so that a good bacteria inhibition effect is achieved; and moreover, the epsilon-polylysine also can enhance interaction between cells and materials, is beneficial for adhesion and proliferation of the cells, and is high in biocompatibility.
Owner:GUANGDONG UNIV OF TECH

Dual-phase magnetic nano-composite scaffold material and preparation method thereof

The invention discloses a dual-phase magnetic nano-composite scaffold material. The dual-phase magnetic nano-composite scaffold material is prepared by compositing a cartilago phase with a bone phase,wherein the cartilago phase contains polylactic acid and a natural polymer compound; and the bone phase contains polylactic acid, nano-hydroxyapatite and magnetic nanoparticles. The invention furtherdiscloses a preparation method of the dual-phase magnetic nano-composite scaffold material. The three-dimensional dual-phase magnetic nano-composite scaffold material is prepared from polylactic acid, the natural polymer compound, nano-hydroxyapatite and the magnetic nano particles by virtue of a low-temperature rapid forming technique and is integrated with the advantages of the four materials,is capable of promoting the adhesion and proliferation of cells, reducing the toxicity of degradation products and improving the biomechanical properties based on good osteoconduction and biocompatibility and is relatively beneficial to the adhesion growth and vascularization of solid cells, and the speed and effect of the coalescence between artificial cartilages transplanted at bone defect partsof a joint cartilage and a subchondral bone and the bones are greatly increased and improved.
Owner:THE SECOND PEOPLES HOSPITAL OF SHENZHEN

EPS (Expandable Polystyrene) and mussel extract compounded skin barrier repairing dressing and preparation method thereof

The invention provides EPS (Expandable Polystyrene) and mussel extract compounded skin barrier repairing dressing and a preparation method thereof. The EPS and mussel extract compounded skin barrier repairing dressing comprises the following raw materials in percentage by weight: 0.05%-0.12% of hyaluronic acid, 0.5%-0.8% of sodium alginate, 0.06%-0.15% of tremella heteropolysaccharide, 6%-8% of glycerol, 0.3%-1% of dihydric alcohol, 1%-2% of trehalose, 1%-2% of mannose, 0.02%-0.05% of lactic acid bacteria exopolysaccharide, 0.03%-0.08% of a mussel extract, 1%-2% of betaine, 1.5%-2.3% of amino acid, 1.8%-2.5% of PCA (pyrrolidone carboxylate) sodium, 0.01%-0.03% of a preservative, and the balance of water. According to the preparation method of the EPS and mussel extract compounded skin barrier repairing dressing, the lactic acid bacteria exopolysaccharide and the mussel extract are compounded, the tremella heteropolysaccharide, the trehalose, the mannose and the dihydric alcohol are combined, the betaine, the PCA sodium and the like are matched, and optimized proportion is adopted, so that the prepared dressing has good anti-inflammatory activity and high skin wound healing rate; and thus, the dressing can better and quickly repair damaged skin, has higher skin barrier repairing capacity, and is ensured with good tolerance.
Owner:绽妍生物科技有限公司
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