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50results about How to "Meet release requirements" patented technology

PH response four-arm star block copolymer and preparation method and application thereof

The invention discloses pH response four-arm star block copolymer and a preparation method and application thereof. According to the copolymer, pentaerythritol is used as an inner core, each arm is connected with a hydrophobic group, a pH response group and a hydrophilic group; and the preparation method comprises the following steps of: performing ring opening polymerization on pentaerythritol to obtain hydrophobic group copolymer, performing acylation on the tail end of the hydrophobic group copolymer, and sequentially initiating pH response monomer and the hydrophilic group to perform electron transfer activating agent regeneration-atom transfer radical polymerization by using hydrophobic group copolymer of which the tail end is subjected to acylation and which is used as macroinitiator to obtain the pH response four-arm star block copolymer. The copolymer is self-assembled into nano micelle in an aqueous solution, so that insoluble medicines can be effectively solubilized; the copolymer is used for preparing a micelle medicine carrying system for insoluble anti-cancer medicines, and the medicines can be kept to be slowly released when pH of normal tissues is 7.4, and can be quickly released in a controllable way under the faintly acid condition that pH of cancer cells is 5 to 6; and the proportion of foundational groups of the copolymer is easy to control, and the copolymer is simple in synthesis process and high in yield.
Owner:SOUTH CHINA UNIV OF TECH

pH-responsive 6-arm star block copolymer and preparation method and application thereof

The invention discloses a pH-responsive 6-arm star block copolymer and a preparation method and application thereof. In the structure of the copolymer, pentaerythritol is adopted as a kernel, and each arm is connected with a hydrophobic group, a pH-responsive group and a hydrophilic group. The preparation method comprises the steps of: carrying out ring opening polymerization of the pentaerythritol to obtain a hydrophobic group polymer, carrying out acylation of the end of the hydrophobic group polymer to prepare a macromolecular initiator, carrying out sequential initiation of regeneration of an electron transfer activator for a pH-responsive monomer and the hydrophilic group, i.e. radical polymerization for atom transfer, thereby obtaining the pH-responsive 6-arm star block copolymer. The polymer is self-assembled into nano micelles in aqueous solution, the dissolution of water-insoluble drugs can be enhanced effectively, the polymer can be applied in preparation of a micelle carrying system for water-insoluble anticancer drugs, and the drugs can be released slowly when the pH of normal tissues is 7.4 and rapidly in a controlled way under acidic conditions when the pH of tumor cells is 5-6; and the proportion of functional groups can be easily adjusted, the synthesis process is simple, and the yield is higher.
Owner:SOUTH CHINA UNIV OF TECH

Cholesterol modified amphiphilic pH response pennicuius copolymer as well as preparation and micelle of copolymer

The invention belongs to the technical field of preparation of biomedical high molecular polymer materials and discloses a cholesterol modified amphiphilic pH response pennicuius copolymer and a preparation method and a micelle system prepared based thereof. The copolymer has a structure shown in the formula I in the specification, wherein x is 10-36, y is 15-40 and z is 8-30. The copolymer is obtained by virtue of irregular copolymerization of a hydrophilic block hydroxyethyl methylacrylate, hydrophobic cholesterol and pH response block methacrylic acid N, N-diethyl aminoethyl combined with hydrophilic poly(ethylene glycol) methyl ether methacrylate. The copolymer is dissolved in a solvent to obtain a nanoscale micelle system, wherein the inner layer is a cholesterol modified hydrophobic chain segment, the middle layer is a pH response chain segment and the shell is a hydrophilic chain segment, so that the function of high entrapment performance, stable existence of a neutral condition and quick release in a weak acidic condition is achieved. By adjusting the proportions of the blocks in the polymer, the release rates of medicines can be regulated to satisfy the release requirements on different drugs.
Owner:SOUTH CHINA UNIV OF TECH

Amphipathic four-arm star-like polymer and shell reversible crosslinked micelle system based on same, and preparation method and application of amphipathic four-arm star-like polymer

The invention belongs to the technical field of biological medical macromolecule polymer materials, and discloses an amphipathic four-arm star-like polymer and a shell reversible crosslinked micelle system based on the same, and a preparation method and an application of the amphipathic four-arm star-like polymer. The polymer specifically has a structure shown by a formula (I) as shown in the specification, wherein x=10-30, y=5-20, and z=5-20. The invention also provides the shell reversible crosslinked micelle system based on the amphipathic four-arm star-like polymer. For the polymer disclosed by the invention, under the condition that the pH value is 6.5 and a catalyst namely aniline exists, an aldehyde group at a shell crosslinked site reacts with a crosslinking agent 3,3'-dithio-bis(propionic acid dihydrazide) to form a reversible crosslinked structure containing a disulfide bond and an acylhydrazone bond, and the reversible crosslinked structure has good stability and significantly-improved dilution resistance; and when the polymer is applied to loading water-insoluble medicines, controllable and rapid release of the water-insoluble medicines in different environments can be realized, efficient delivery release of medicines is realized, and the treatment efficiency of cancers is improved.
Owner:SOUTH CHINA UNIV OF TECH

Double-pH-response amphiphilic copolymer and preparation method and application thereof

The invention relates to double-pH-response amphiphilic copolymer, the molecular formula of the double-pH-response amphiphilic copolymer is MPEG-Dliable-PAE-g-Chol, and the structure of the double-pH-response amphiphilic copolymer is as shown in formula I. The double-pH-response amphiphilic copolymer is copolymerized by hydrophilic block methoxy polyethylene glycol, hydrophobic cholesterol and pH response block poly(beta-amino ester). The double-pH-response amphiphilic copolymer has the advantages that the double-pH-response amphiphilic copolymer can self-assemble in an aqueous solution to obtain a nanoscale micellar system, the inner layer of the nanoscale micellar system is a hydrophobic core modified by cholesterol, the middle of the nanoscale micellar system is a pH-sensitive-response PAE layer, the shell of the nanoscale micellar system is hydrophilic block MPEG, the hydrophilic shell is connected sensitive middle layer through a pH-sensitive benzimide bond, the cell intake of a micelle drug-loading system is increased effectively while the requirements of high entrapment performance, stable system structure, long in-vivo circulation time, stability under neutral conditions and controllable drug release under weak acid conditions of hydrophobic drugs are satisfied, and accordingly drug bioavailability is increased, and a tumor treatment effect is optimized.
Owner:THE NAT CENT FOR NANOSCI & TECH NCNST OF CHINA

Amphiphilic pH-responsive 4/6 heteroarm star-shaped copolymer and preparation method thereof

The invention belongs to the technical field of high molecular polymer materials for biomedicine, and discloses an amphiphilic pH-responsive 4 / 6 heteroarm star-shaped copolymer of which the number-average molecular weight is 30000-54000g / mol. The invention also discloses a preparation method of the amphiphilic pH-responsive 4 / 6 heteroarm star-shaped copolymer, which comprises the following steps: mixing epsilon-caprolactone, stannous octoate and low molecular initiator, reacting at 110-140 DEG C for 24-48 hours, performing reduced pressure distillation, precipitating, filtering, and drying to obtain polycaprolactone high molecular initiator; dissolving the polycaprolactone high molecular initiator, 2-diethylaminoethyl methacrylate, hexamethyltriethylenetetramine and copper bromide in toluene, stirring, then adding stannous octoate, and reacting at 60-90 DEG C for 5-12 hours; and adding methoxy polyoxyethylene methacrylate, continuously polymerizing for 5-12 hours, removing a catalyst, filtering, and performing posttreatment on the filtrate to obtain the amphiphilic pH-responsive 4 / 6 heteroarm star-shaped copolymer. The amphiphilic pH-responsive 4 / 6 heteroarm star-shaped copolymer is used for preparation of a micelle system for carrying water insoluble medicaments.
Owner:SOUTH CHINA UNIV OF TECH

PH response/membrane adhesive amphiphilic block copolymer as well as preparation method and application thereof

The invention discloses a pH response/membrane adhesive amphiphilic block copolymer as well as a preparation method and application thereof. According to the preparation method, methacrylic acid with an isoelectric point of 5.0-6.5 is utilized as a pH response monomer, methacrylic aminoethyl ester with pH-insensitive hydrophilia is utilized as a membrane-adhesive monomer, an electron transfer activator regeneration-atom transfer free radical active polymerization method is adopted, a pH response monomer and hydrophobic monomer block copolymer is firstly prepared; and by taking the pH response monomer and hydrophobic monomer block copolymer as a macroinitiator, the membrane-adhesive monomer, namely the methacrylic aminoethyl ester is polymerized, and finally acidolysis reaction is performed, so that the pH response/membrane adhesive amphiphilic block copolymer is prepared. The pH response/membrane adhesive amphiphilic block copolymer is capable of being self-assembled to form a core-shell structure micelle in an aqueous solution, has favorable pH sensibility and membrane adhesion property, lower critical micelle concentration and relaively small micelle particle size, and can be used in drug delivery systems for oral medication application of polypeptide or proteinic drugs.
Owner:XIANGTAN UNIV

Cholesterol modification based pH response polypeptide polymer as well as preparation method and application thereof

The invention belongs to the technical field of high-molecular polymer materials for biological medicines, and discloses a cholesterol modification based pH response polypeptide polymer as well as a preparation method and application thereof. The polypeptide polymer has a structure shown in a formula (1): mPEG-R-Chol (1). The polypeptide polymer disclosed by the invention is a polypeptide pH response amphiphilic tri-block polymer material which is hydrophilically modified by methoxy polyethylene glycol and is hydrophobically modified by cholesterol, can be self-assembled to be nano-micelles in an aqueous solution, can be used for effectively encapsulating water-insoluble medicines, can be applied to the field of medicines, and is particularly suitable for preparing a targeted medicine delivery system of water-insoluble anti-cancer medicines. Moreover, the polypeptide polymer is adjustable and controllable in topological structure and simple in synthesis process, and can be used for adjusting and controlling the release rate of the medicines by adjusting the content of polypeptide with pH response so as to ensure that the release requirements of different medicines can be met. The polypeptide polymer disclosed by the invention has relatively low critical aggregation concentration, and the critical aggregation concentration is only 1.8-4.8mg / L, so that high stability of the medicine delivery micelles can be achieved.
Owner:SOUTH CHINA UNIV OF TECH

Easily degradable responsive core-crosslinkable amphiphilic block polymer, preparation method thereof and application of amphiphilic block polymer as drug carrier

The invention discloses an easily degradable response type core-crosslinkable amphiphilic block polymer, a preparation method thereof and an application of the amphiphilic block polymer as a drug carrier. According to the amphiphilic block polymer, methoxypolyethylene glycol-b-polylactide serves as a main chain, and a side chain is modified with carboxyl and a dithiopyridine group; the amphiphilic block polymer and a water-insoluble drug can easily form a response type core cross-linked micelle, and the micelle is stable in a normal physiological environment, and is easy to be stimulated by environment after reaching tumour cells, and then, the cross-linked structure is damaged, so that the controlled release of the medicine is realized, the utilization rate of the medicine is improved, and the toxic and side effects of the loaded medicine are reduced; theamphiphilic block polymer is easy to degrade, so thatlong-term toxicity caused by accumulation of micelles in human tissues and organs is avoided; the amphiphilic block polymer has goodbiocompatibility, and has wide potential application prospects in the field of cancer chemotherapy; and the synthetic method of the amphiphilic block polymer is simple, mild in condition, few in side reaction and beneficial to expanded production.
Owner:XIANGTAN UNIV

Sodium alginate and preparation method and application of sodium alginate

The invention discloses sodium alginate and a preparation method and an application of the sodium alginate. The preparation method comprises the following steps: (1) soaking water to soak and wash brown algae, mixing and digesting with an alkaline agent, adding water to dilute, adding kieselguhr, filtering, and obtaining an alginic acid monomer according to a calcium coagulation acidification method; (2) degrading the alginic acid monomer at the temperature of 30-50 DEG C; (3) taking solid sodium carbonate as a neutralizer, mixing with the alginic acid, stirring, carrying out a reaction to obtain a semi-finished product of sodium alginate, then adding an ethanol solution, stirring to disperse the semi-finished product of sodium alginate into a powder, pelleting, drying and crushing to obtain the sodium alginate. The viscosity of the sodium alginate is 200-700 mpas, the viscosity drop rate is lower than 5%, the Mw / Mn is less than 1.85, the water content is less than 11%, the transparency is more than 30 cm, the specific gravity of a powder is 0.65-0.75 g / cm<3>, the granularity is 120 meshes, and the distribution of the powder granularity is narrow. The sodium alginate can be used ina slow release formulation, and the slow release effect is stable.
Owner:QINGDAO BRIGHT MOON SEAWEED GROUP

A kind of ph response/membrane adhesion amphiphilic block copolymer and preparation method thereof

The invention discloses a pH response / membrane adhesive amphiphilic block copolymer as well as a preparation method and application thereof. According to the preparation method, methacrylic acid with an isoelectric point of 5.0-6.5 is utilized as a pH response monomer, methacrylic aminoethyl ester with pH-insensitive hydrophilia is utilized as a membrane-adhesive monomer, an electron transfer activator regeneration-atom transfer free radical active polymerization method is adopted, a pH response monomer and hydrophobic monomer block copolymer is firstly prepared; and by taking the pH response monomer and hydrophobic monomer block copolymer as a macroinitiator, the membrane-adhesive monomer, namely the methacrylic aminoethyl ester is polymerized, and finally acidolysis reaction is performed, so that the pH response / membrane adhesive amphiphilic block copolymer is prepared. The pH response / membrane adhesive amphiphilic block copolymer is capable of being self-assembled to form a core-shell structure micelle in an aqueous solution, has favorable pH sensibility and membrane adhesion property, lower critical micelle concentration and relaively small micelle particle size, and can be used in drug delivery systems for oral medication application of polypeptide or proteinic drugs.
Owner:XIANGTAN UNIV

Energy accumulator liquid filling integrated valve

The invention belongs to the technical field of hydraulic control and specifically relates to an energy accumulator liquid filling integrated valve. The energy accumulator liquid filling integrated valve comprises a flow priority valve, a liquid filling valve and an electromagnetic switching valve set. The flow priority valve comprises a three-position four-way valve and a damping II. An oil inletof the three-position four-way valve is connected with an oil port P. The liquid filling valve comprises a one-way valve, a two-position two-way valve I, an overflow valve and an adjustable throttling valve II. An oil port A of the three-position four-way valve communicates with an oil inlet of the one-way valve. An oil outlet of the one-way valve is connected with an oil port P3. The oil port Pis connected with an oil inlet of the two-position two-way valve I through the damping II. An oil outlet of the two-position two-way valve I is connected with an oil port T1. A spring cavity of the three-position four-way valve is connected with an oil inlet of the two-position two-way valve I. The overflow valve and the adjustable throttling valve II are connected between the oil port T1 and theoil port P3 in parallel. An oil port B of the three-position four-way valve is connected with an oil port P1. Through the integrated flow priority valve of the energy accumulator liquid filling integrated valve, switching and synchronous operating of an energy accumulator and a tamping device main valve can be realized.
Owner:XCMG XUZHOU TRUCK MOUNTED CRANE

Ginkgo leaf total flavone controlled-release tablet and preparation method thereof

The invention belongs to the technical field of medicines, and particularly discloses a ginkgo leaf total flavone controlled-release tablet and a preparation method thereof. The controlled-release tablet disclosed by the invention is a tablet which is prepared by combining polyoxyethylene and a controlled-release skeleton material and adopting a conventional tablet preparation technology and has the zero-order release behavior characteristic. The controlled-release tablet consists of an active ingredient ginkgo leaf total flavone, a high polymer material polyoxyethylene (PEO), the controlled-release skeleton material and a certain amount of release rate conditioning agent. The active ingredients of the ginkgo leaf total flavone mainly comprise isorhamnetin, kaempferide and quercetin, and the total flavonoid glycoside content of the quercetin is not lower than 20%. Compared with a common tablet, the ginkgo leaf total flavone controlled-release tablet has the advantages that the controlled-release tablet can be used for maintaining the constancy of the blood concentration, reducing the adverse reactions of the medicines and improving the compliance of the patients. The preparation method is simple in technological operation, low in cost, easy to control and suitable for industrial large-scale production.
Owner:SHENYANG PHARMA UNIVERSITY

An amphiphilic four-armed star polymer and its shell-based reversible cross-linked micelle system, preparation method and application

The invention belongs to the technical field of biological medical macromolecule polymer materials, and discloses an amphipathic four-arm star-like polymer and a shell reversible crosslinked micelle system based on the same, and a preparation method and an application of the amphipathic four-arm star-like polymer. The polymer specifically has a structure shown by a formula (I) as shown in the specification, wherein x=10-30, y=5-20, and z=5-20. The invention also provides the shell reversible crosslinked micelle system based on the amphipathic four-arm star-like polymer. For the polymer disclosed by the invention, under the condition that the pH value is 6.5 and a catalyst namely aniline exists, an aldehyde group at a shell crosslinked site reacts with a crosslinking agent 3,3'-dithio-bis(propionic acid dihydrazide) to form a reversible crosslinked structure containing a disulfide bond and an acylhydrazone bond, and the reversible crosslinked structure has good stability and significantly-improved dilution resistance; and when the polymer is applied to loading water-insoluble medicines, controllable and rapid release of the water-insoluble medicines in different environments can be realized, efficient delivery release of medicines is realized, and the treatment efficiency of cancers is improved.
Owner:SOUTH CHINA UNIV OF TECH

Ph-responsive polypeptide polymer based on cholesterol modification, preparation method and application

The invention belongs to the technical field of high-molecular polymer materials for biological medicines, and discloses a cholesterol modification based pH response polypeptide polymer as well as a preparation method and application thereof. The polypeptide polymer has a structure shown in a formula (1): mPEG-R-Chol (1). The polypeptide polymer disclosed by the invention is a polypeptide pH response amphiphilic tri-block polymer material which is hydrophilically modified by methoxy polyethylene glycol and is hydrophobically modified by cholesterol, can be self-assembled to be nano-micelles in an aqueous solution, can be used for effectively encapsulating water-insoluble medicines, can be applied to the field of medicines, and is particularly suitable for preparing a targeted medicine delivery system of water-insoluble anti-cancer medicines. Moreover, the polypeptide polymer is adjustable and controllable in topological structure and simple in synthesis process, and can be used for adjusting and controlling the release rate of the medicines by adjusting the content of polypeptide with pH response so as to ensure that the release requirements of different medicines can be met. The polypeptide polymer disclosed by the invention has relatively low critical aggregation concentration, and the critical aggregation concentration is only 1.8-4.8mg / L, so that high stability of the medicine delivery micelles can be achieved.
Owner:SOUTH CHINA UNIV OF TECH

pH-responsive 6-arm star block copolymer and preparation method and application thereof

The invention discloses a pH-responsive 6-arm star block copolymer and a preparation method and application thereof. In the structure of the copolymer, pentaerythritol is adopted as a kernel, and each arm is connected with a hydrophobic group, a pH-responsive group and a hydrophilic group. The preparation method comprises the steps of: carrying out ring opening polymerization of the pentaerythritol to obtain a hydrophobic group polymer, carrying out acylation of the end of the hydrophobic group polymer to prepare a macromolecular initiator, carrying out sequential initiation of regeneration of an electron transfer activator for a pH-responsive monomer and the hydrophilic group, i.e. radical polymerization for atom transfer, thereby obtaining the pH-responsive 6-arm star block copolymer. The polymer is self-assembled into nano micelles in aqueous solution, the dissolution of water-insoluble drugs can be enhanced effectively, the polymer can be applied in preparation of a micelle carrying system for water-insoluble anticancer drugs, and the drugs can be released slowly when the pH of normal tissues is 7.4 and rapidly in a controlled way under acidic conditions when the pH of tumor cells is 5-6; and the proportion of functional groups can be easily adjusted, the synthesis process is simple, and the yield is higher.
Owner:SOUTH CHINA UNIV OF TECH
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