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37 results about "Biphosphonate" patented technology

A drug or substance used to treat hypercalcemia (abnormally high blood calcium) and bone pain caused by some types of cancer. Forms of bisphosphonates are also used to treat osteoporosis and for bone imaging. Bisphosphonates inhibit a type of bone cell that breaks down bone.

Method for preparing monophosphonate and biphosphonate mixed fire retardant

The invention discloses a method for preparing a monophosphonate and biphosphonate mixed fire retardant, which comprises the following steps of: (1) heating tris phosphite and dihalide in the presence of a catalyst: (2) refluxing the mixture after the temperature rises to 110 to130 DEG C and continuously heating the refluxed mixture, wherein the optimal refluxing temperature of 120 DEG C; (3) allowing the refluxing speed to reduce obviously when the temperature is 160 and 180 DEG C, wherein the optimal temperature is 170 DEG C; (4) continuing a reaction, keeping the temperature between 170 and 200 DEG C to perform a reaction for 1 hour when the reflux phenomenon basically disappears, wherein the reaction is performed at 180 to190 DEG C optimally; (5) distilling the reacting product under normal pressure and filtering the distilled product to obtain a colorless transparent product. The total product yield of the monophosphonate and biphosphonate mixed fire retardant is over 90 percent; and the reaction time is shortened, the product has good color and luster, the acid value is low, the viscosity is low and no additional de-coloration treatment is required. Serving as the additive-type phosphine fire retardant, the monophosphonate and biphosphonate mixed fire retardant has higher performance. The monophosphonate and biphosphonate mixed fire retardant has the advantages of high economy, high product utilization efficiency, zero emission in a production process and environmental protection.
Owner:NANJING NORMAL UNIVERSITY +1

Biphosphonate conjugates and methods of making and using the same

The present invention is directed to particular bisphosphonate compounds, and in particular, to bisphosphonate conjugates that are useful in the treatment of soft tissues surrounding bone and bone-related diseases, such as bone cancer and osteoporosis.
Owner:MBC PHARMA

Self-Assembling Nanoparticles for the Release of Bisphosphonates in the Treatment of Human Cancers

The present invention describe nanocomplexes also called auto-assembling nanoparticles comprising biphosphonates, lipid nanovectors and inorganic nanovectors.In particular the invention describes zoledronic acid complexed with calcium phosphate base nanoparticles; said particles in their turn mixed with lipidic particles e.g. liposomes.Said nanocomplexes are useful, and showed to be efficient in vivo, as pharmaceutical formulations of biphosphonates for the treatment or prevention of tumor growth and / or metastasis. Tumors can be solids and / or haematological such as prostate, lung, head / neck, colon, liver, breast, pancreas, kidneys, bladder, male and female urogenital tract, bones, multiple myeloma, primitive and secondary tumours of the central nervous system and lymphomas.
Owner:IST FISIOTERAPICI OSPITALERI +4

Detection method of contents of monophosphate, biphosphonate and fatty alcohol-polyoxyethylene ether in phosphate

The invention discloses a detection method of contents of monophosphate, biphosphonate and fatty alcohol-polyoxyethylene ether in phosphate. The method is as below: preparing a mobile phase by using an aqueous solution of ammonium acetate and methanol; preparing a sample solvent by using 50 mMol / L aqueous solution of ammonium acetate and methanol; then dissolving a phosphate sample by the sample solvent to prepare a phosphate sample solution; then taking an appropriate amount of the phosphate sample solution, injecting the phosphate sample solution into a column of reversed-phase high-performance liquid chromatography, eluting with a mobile phase, sending an eluent into an evaporative light scattering detector, and detecting the eluent by using the evaporative light scattering detector; and according to the areas of the characteristic response peaks of monophosphate, fatty alcohol-polyoxyethylene ether and biphosphonate in the spectrum of the evaporative light scattering detector, using an area normalization method for quantitative calculation of the contents of monophosphate, fatty alcohol-polyoxyethylene ether and biphosphate.
Owner:QUAKER CHEM CHINA

Process for making 1-hydroxyalkylidene-1,1-biphosphonic acids

InactiveUS20100010258A1Simple processHigh commercial scalePhosphorus organic compoundsHydrogenAlkoxy group
Synthesis of biphosphonate compounds can be advantageously carried out in a solvent / diluent comprising a compound of formula (3)wherein R is hydrogen or a C1-C6 alkyl group; each of R1 is a C1-C6 alkyl group or both R1 groups are linked to form a C1-C3 alkylene group; and R2 is hydrogen, a C1-C6 alkyl group, a C1-C6 alkoxy group, or is linked together with R to form a C3-C7 carbon ring.
Owner:SYNTHON BV

Enteric solid oral dosage form of bisphosphonate containing a chelating agent

Oral dosage forms of a bisphosphonate comprised of a safe and effective amount of a pharmaceutical composition comprising a bisphosphonate, a chelating agent, and, means for effecting delayed release of the bisphosphonate and the chelating agent in the lower gastrointestinal tract provide delivery of the pharmaceutical composition to the lower gastrointestinal tract of the mammal subject and pharmaceutically effective absorption of the bisphosphonate with or without food or beverages. The present invention substantially alleviates the interaction between bisphosphonates and food or beverages, which interaction results in the bisphosphonate active ingredient not being available for absorption. The resulting oral dosage form may thus be taken with or without food. Further, the present invention effects delivery of the bisphosphonate and the chelating agent to the lower GI tract, substantially alleviating the upper GI irritation associated with bisphosphonate therapies. These benefits simplify previously complex treatment regimens and can lead to increased patient compliance with bisphosphonate therapies.
Owner:THE PROCTER & GAMBLE COMPANY

Expanding T cell populations using biphosphonates, anti CD 3 antibody and IL-2

The present invention provides methods for expanding populations of T cells, including gamma delta T cells, by incubating peripheral blood mononuclear cells with biphosphonates and then with anti CD3 antibody and IL-2. Pharmaceutical compositions comprising the expanded T cells for treating infectious, autoimmune and malignant diseases are also provided.
Owner:TEL HASHOMER MEDICAL RES INFRASTRUCTURE & SERVICES

Non-crosslinked polypropylene material and cable

The invention discloses a non-crosslinked polypropylene material and a cable, and belongs to the technical field of cables, and the non-crosslinked polypropylene material comprises the following raw materials by weight: 20-30 parts of isotactic polypropylene, 40-50 parts of syndiotactic polypropylene, 5-10 parts of low density polyethylene, 1-5 parts of talcum powder, 3-6 parts of nanoparticles, 0.5-1 part of tetra (2, 4-di-tert-butylphenyl-4, 4-biphenyl) bisphosphonate, 0.5-1 part of tris- (3, 5-di-tert-butyl-4-hydroxyphenyl) isocyanurate and 0.5-2 parts of 2, 2-oxamido bis-[ethyl-3-(3, 5-di-tert-butyl-4-hydroxyphenyl) ] propionate. The cable material still has ultrahigh flexibility and toughness at the temperature of -30 DEG C and lower, therefore, the cold resistance, weather resistance and low-temperature impact resistance of the cable material are improved, the application range is wide, the practicability is high, and the oxidation resistance of the cable material is improved by using multiple antioxidants.
Owner:杭州龙源电力有限公司 +2

Use of derivatives with C-O-P bonds in patients with renal failure

The invention relates to the use of a derivative with C-O-P bonds in the form of controlled release for the treatment of patients with renal failure. The invention also relates to the use of said derived compounds together with other active substances, that can particularly be selected from the list comprising a calcimimetic, a vitamin, a phosphorus chelator, thiosulfate, biphosphonate, pyrophosphate, citrate, a diuretic, an antihypertensive and an anticholesterolemic agent.
Owner:SANIFIT THERAPEUTICS SA

Aromatic nitrogen-contg. bis-phosphonic acid derivs., process for preparing same and use thereof

A nitrogen-containing aromatic biphosphonate derivative used for preventing and treating osteoporosis, hypercalcemia, Paget's disease, etc is prepared from aromatic amine, triethyl orthoformate and dimethyl phosphonite in mole ratio of 1:(1-1.5):(3-5) through thermal reaction at 100-160 deg.C for 1-3 hr.
Owner:SHANGHAI INST OF MATERIA MEDICA CHINESE ACAD OF SCI

Production method of flame-retardant polyester fabric

The invention discloses a production method of flame-retardant polyester fabric. The production method comprises the following steps: adding carbon tetrachloride, phosphorus trichloride and pentaerythritol in a four-hole boiling flask in sequence and stirring, dripping bromine water in the four-hole boiling flask at a low temperature, meanwhile, exhausting the generated hydrogen chloride gas, reacting for a certain time, and postprocessing to obtain a chloro-biphosphonate flame retardant; jetting the solid chloro-biphosphonate flame retardant on the polyester fabric for 20 to 30 minutes through a vacuum magnetron sputtering instrument, and drying the polyester fabric at a low temperature to obtain the flame-retardant polyester fabric. Through the manner, the production method of the flame-retardant polyester fabric, which is provided by the invention, is simple to operate, has a low requirement on the operation proficiency of personnel and saves the labor cost; and the flame-retardant polyester fabric takes a self-extinguishing effect, is green and environment-friendly, and less in environmental pollution, does not generate melted drippings at a high temperature but is charred, and does not cause secondary damage.
Owner:重庆市纺织工业研究所有限责任公司

Preparation method of 2,7-dimethyl-2,4,6-octa-triene-1,8-diethylester biphosphonate

The invention provides a preparation method of 2,7-dimethyl-2,4,6-octa-triene-1,8-diethylester biphosphonate, which comprises the following steps of: preparing 2,7-dimethyl-2,4,6-octa-triene-1,8-diol by using 2,7-dimethyl-2,4,6-octa-triene-1,8-dialdehyde as an initiative raw material, adopting methanol, ethanol, dimethyl-tetrahydrofuran or isopropanol as a solvent, and using aluminum isopropoxide, potassium borohydride or sodium borohydride as a reducing agent for reduction; preparing 2,7-dimethyl-2,4,6-octa-triene-1,8-dihalide by using phosphorus tri-halide or thionyl chloride for halogenation; and finally, heating the 2,7-dimethyl-2,4,6-octa-triene-1,8-dihalide together with triethyl phosphate to remove chloroethane or bromoethane to obtain the target compound. While achieving the aims of facilitating industrial application and making reaction easily controlled, the preparation method provided by the invention ensures that the yield of the reaction of each step exceeds 60 percent.
Owner:ZHEJIANG MEDICINE CO LTD XINCHANG PHAMACEUTICAL FACTORY

Preparation method of 2,7-dimethyl-2,4,6-octa-triene-1,8-diethylester biphosphonate

The invention provides a preparation method of 2,7-dimethyl-2,4,6-octa-triene-1,8-diethylester biphosphonate, which comprises the following steps of: preparing 2,7-dimethyl-2,4,6-octa-triene-1,8-diol by using 2,7-dimethyl-2,4,6-octa-triene-1,8-dialdehyde as an initiative raw material, adopting methanol, ethanol, dimethyl-tetrahydrofuran or isopropanol as a solvent, and using aluminum isopropoxide, potassium borohydride or sodium borohydride as a reducing agent for reduction; preparing 2,7-dimethyl-2,4,6-octa-triene-1,8-dihalide by using phosphorus tri-halide or thionyl chloride for halogenation; and finally, heating the 2,7-dimethyl-2,4,6-octa-triene-1,8-dihalide together with triethyl phosphate to remove chloroethane or bromoethane to obtain the target compound. While achieving the aims of facilitating industrial application and making reaction easily controlled, the preparation method provided by the invention ensures that the yield of the reaction of each step exceeds 60 percent.
Owner:ZHEJIANG MEDICINE CO LTD XINCHANG PHAMACEUTICAL FACTORY

Method for preparing monophosphonate and biphosphonate mixed fire retardant

The invention discloses a method for preparing a monophosphonate and biphosphonate mixed fire retardant, which comprises the following steps of: (1) heating tris phosphite and dihalide in the presence of a catalyst: (2) refluxing the mixture after the temperature rises to 110 to130 DEG C and continuously heating the refluxed mixture, wherein the optimal refluxing temperature of 120 DEG C; (3) allowing the refluxing speed to reduce obviously when the temperature is 160 and 180 DEG C, wherein the optimal temperature is 170 DEG C; (4) continuing a reaction, keeping the temperature between 170 and 200 DEG C to perform a reaction for 1 hour when the reflux phenomenon basically disappears, wherein the reaction is performed at 180 to190 DEG C optimally; (5) distilling the reacting product under normal pressure and filtering the distilled product to obtain a colorless transparent product. The total product yield of the monophosphonate and biphosphonate mixed fire retardant is over 90 percent; and the reaction time is shortened, the product has good color and luster, the acid value is low, the viscosity is low and no additional de-coloration treatment is required. Serving as the additive-type phosphine fire retardant, the monophosphonate and biphosphonate mixed fire retardant has higher performance. The monophosphonate and biphosphonate mixed fire retardant has the advantages of high economy, high product utilization efficiency, zero emission in a production process and environmental protection.
Owner:NANJING NORMAL UNIVERSITY +1

Pharmaceutical composition for the prevention and treatment of bone tissue resorption of various etiology

The invention relates to medicine and pharmacology, and represents a pharmaceutical composition for the treatment of bone resorption of various etiology comprising, as the biologically active ingredient, liposomes with biphosphonates in gel dosage form suitable for transdermal delivery of biphosphonates and effective local therapy. Using this composition, methods for the prevention and treatment of osteoporosis, Paget's disease, patoplogical fractures associated with oncological diseases, and some other pathological processes associated with bone resorption and reparation are proposed.
Owner:LUGS INT

Method of delivering a biphosphonate and/or strontium ranelate below the surface of a bone

A method for delivering a bisphosphonate and / or strontium ranelate below the surface of a bone using a mechanical force. The method includes the steps of combining a bisphosphonate and / or strontium ranelate with a carrier to form a delivery composition and delivering an effective amount of the delivery composition below the surface of the bone with a mechanical force. Also provided is a method for strengthening a portion of a bone. This method includes the step of delivering an effective amount of a bisphosphonate and / or strontium ranelate below the surface of a portion of a bone with a mechanical force.
Owner:STRYKER EURO OPERATIONS HLDG LLC

18f-labeled bisphosphonates for pet imaging

A novel method for rapidly and efficiently introducing fluorine into the P-C-P backbone of bisphosphonates starting from readily accessible diazomethylenebisphosphonate esters is provided. The method is applied successfully to create novel [18F]-labeled bisphosphonates for positron emission tomography imaging. Some versions of the method include reacting a diazomethylenebisphosphonate tetraalkyl ester with a fluorinating agent in the presence of an acidic HF / base complex and a t-butyl hypohalite to produce a halofluoromethylenebisphosphonate tetraalkyl ester, and dealkylating the halofluoromethylenebisphosphonate alkyl ester to produce a halofluoromethylenebis(phosphonic acid). Methods of replacing the halogen group with hydrogen are further provided. 18F-labeled bisphosphonates prepared by the methods, and methods of using such compounds for positron emission tomography imaging in patients and animal models, are also provided.
Owner:UNIV OF SOUTHERN CALIFORNIA

A kind of liposome drug carrier and its preparation method and application

The invention belongs to the technical field of drug preparation development, in particular to a liposome drug carrier and a preparation method and application thereof. The liposome drug carrier includes the following ingredients: cetylic acid and cholesterol. By freeze drying or rotary drying the ingredients transform into membranes. Through the subsequent hydration and filming the final products are acquired. The liposome drug carrier can automatically form lipid microspheres which are quite stable. At the same time the drug carrier preserves the advantages of traditional liposome, namely, the drug carrier has a structure similarity to the bimolecular lamellar membrane structure of biological plasma membrane. The drug carrier has the advantages of excellent biological adaptability, stability, simple production and high encapsulation efficiency and the like. The liposome drug carrier can be used to carry biphosphonate drugs with a consistent and unified particle diameter, high encapsulation efficiency and high stability. The carrier has negative charges and can further enhance the ability that the drug enters cells. Compared with traditional lecithin liposome the carrier enhances the effects on macrophages.
Owner:SHANGHAI JIAO TONG UNIV
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