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93results about How to "Minimize irritation" patented technology

Biodegradable low molecular weight triblock poly(lactide-co- glycolide) polyethylene glycol copolymers having reverse thermal gelation properties

InactiveUS6201072B1Difficult to formulateDifficult to administerOrganic active ingredientsPowder deliverySolubilityPolymer science
A water soluble, biodegradable ABA- or BAB-type tri-block polymer is disclosed that is made up of a major amount of a hydrophobic A polymer block made of a biodegradable polyester and a minor amount of a hydrophilic polyethylene glycol(PEG) B polymer block, having an overall average molecular weight of between about 2000 and 4990, and that possesses reverse thermal gelation properties. Effective concentrations of the tri-block polymer and a drug may be uniformly contained in an aqueous phase to form a drug delivery composition. At temperatures below the gelation temperature of the tri-block polymer the composition is a liquid and at temperatures at or above the gelation temperature the composition is a gel or semi-solid. The composition may be administered to a warm-blooded animal as a liquid by parenteral, ocular, topical, inhalation, transdermal, vaginal, transurethral, rectal, nasal, oral, pulmonary or aural delivery means and is a gel at body temperature. The composition may also be administered as a gel. The drug is released at a controlled rate from the gel which biodegrades into non-toxic products. The release rate of the drug may be adjusted by changing various parameters such as hydrophobic/hydrophilic component content, polymer concentration, molecular weight and polydispersity of the tri-block polymer. Because the tri-block polymer is amphiphilic, it functions to increase the solubility and/or stability of drugs in the composition.
Owner:KIM PH D SUNG WAN +2

Biodegradable low molecular weight triblock poly (lactide-co-glycolide) polyethylene glycol copolymers having reverse thermal gelation properties

A water soluble biodegradable ABA- or BAB-type triblock polymer is disclosed that is made up of a major amount of a hydrophobic polymer made of a poly(lactide-co-glycolide) copolymer or poly(lactide) polymer as the A-blocks and a minor amount of a hydrophilic polyethylene glycol polymer B-block, having an overall weight average molecular weight of between about 2000 and 4990, and that possesses reverse thermal gelation properties. Effective concentrations of the triblock polymer and a drug may be uniformly contained in an aqueous phase to form a drug delivery composition. At temperatures below the gelation temperature of the triblock polymer the composition is a liquid and at temperatures at or above the gelation temperature the composition is a gel or semi-solid. The composition may be administered to a warm-blooded animal as a liquid by parenteral, ocular, topical, inhalation, transdermal, vaginal, transurethral, rectal, nasal, oral, pulmonary or aural delivery means and is a gel at body temperature. The composition may also be administered as a gel. The drug is released at a controlled rate from the gel which biodegrades into non-toxic products. The release rate of the drug may be adjusted by changing various parameters such as hydrophobic/hydrophilic componenet content, polymer concentration, molecular weight and polydispersity of the triblock polymer. Because the triblock polymer is amphiphilic, it functions to increase the solubility and/or stability of drugs in the composition.
Owner:BTG INT LTD +2

Intraocular lens with accommodative properties

InactiveUS6200342B1Focus assistPrevent excessive lateral movement and luxationIntraocular lensPupil diameterIntraocular lens
A new lens design and method of implantation uses the change in pupil diameter of the eye concurrent with the changes induced by a contraction of the ciliary muscle during the accommodative reflex, in order to assist in focusing of nearby objects. This new intraocular lens consists of two parts. The posterior part or haptic part is inserted behind the iris and in front of the natural lens or artificial implant. Its main purpose is to participate in the accommodative mechanism and to prevent excessive lateral movement and luxation of the lens. An anterior or optical part is made of flexible material and is placed before the iris. Its diameter is variable but should be large enough to cover the pupillary margins to some degree under various conditions of natural dilation. The anterior and posterior part of the lens are separated by a compressible circular groove in which the iris will settle. The diameter of this groove is slightly larger than the pupillary diameter measured under normal photopic daylight conditions and for distance vision. Since the pupil becomes smaller in near vision, the iris will exert a slight pressure at the level of the groove of the lens which will cause a progressive and evenly distributed flexing of the anterior part of the intraocular lens, as the diameter of the compressible circular groove slightly decreases. This flexing will induce an increase in refractive power which corresponds to a variable part of the amount necessary for focusing nearby objects.
Owner:TASSIGNON MARIE JOSE B

Interbody fusion system with intervertebral implant retention assembly

ActiveUS20100217393A1Eliminating exacerbation of instabilityImprove stabilitySpinal implantsFastenersPosterior instrumentationCorpectomy
The present disclosure is directed towards a biomechanical implant and anterior, lateral or posterior instrumentation construct. The construct may be of unitary or modular construction, whereby a single molded construction can form the entire assembly, in which case the through holes may be adapted to receive a metallic insert for screw fixation; or alternatively be of a modular construction wherein the anterior/lateral instrumentation and intervertebral spacer are designed for removable locking engagement, one with the other, for insertion by the surgeon as a unitary construct. A unique feature of the construct resides within the instrumentation construction, whereby a single opening formed therein permits two bone screws, or the like fastener device, to be positioned within both the superior and inferior vertebral bodies surrounding the spacer implant, or, for example in the case of a corpectomy or diskectomy with cage insertion, wherein two screws can be fixed within a single vertebral body through a single through hole, and wherein the bone screws are constructed and arranged to cooperate with the retention plate so as to provide locking engagement, one to the other, with the retention plate, upon final fixation thereof. Screw retention elements of alternative shape, based upon the choice of vertical or horizontal orientation, based upon an opened figure eight design, are provided for insertion in a groove formed in the borehole of the instrumentation plate which allows insertion of each fixation element but will prevent a loosened fixation element from falling out of the plate.
Owner:SPARTAN CAGE HLDG

Interbody fusion system with intervertebral implant retention assembly

ActiveUS8187329B2Effective protectionLower profile of implantSpinal implantsFastenersPosterior instrumentationEngineering
The present disclosure is directed towards a biomechanical implant and anterior, lateral or posterior instrumentation construct. The construct may be of unitary or modular construction, whereby a single molded construction can form the entire assembly, in which case the through holes may be adapted to receive a metallic insert for screw fixation; or alternatively be of a modular construction wherein the anterior / lateral instrumentation and intervertebral spacer are designed for removable locking engagement, one with the other, for insertion by the surgeon as a unitary construct. A unique feature of the construct resides within the instrumentation construction, whereby a single opening formed therein permits two bone screws, or the like fastener device, to be positioned within both the superior and inferior vertebral bodies surrounding the spacer implant, or, for example in the case of a corpectomy or diskectomy with cage insertion, wherein two screws can be fixed within a single vertebral body through a single through hole, and wherein the bone screws are constructed and arranged to cooperate with the retention plate so as to provide locking engagement, one to the other, with the retention plate, upon final fixation thereof. Screw retention elements of alternative shape, based upon the choice of vertical or horizontal orientation, based upon an opened figure eight design, are provided for insertion in a groove formed in the borehole of the instrumentation plate which allows insertion of each fixation element but will prevent a loosened fixation element from falling out of the plate.
Owner:SPARTAN CAGE HLDG

Long-acting oxytocin analogues for the treatment and prevention of breast cancer and psychiatric disorders

InactiveUS6894026B1Prevent and alleviate symptomInhibit initiation and growthOrganic active ingredientsNervous disorderDiseaseVein
Methods and compositions are provided for prophylaxis and treatment of breast cancer involving administration of a therapeutically effective amount of carbetocin and/or other long-acting oxytocin analogues. 1-Butanoic acid-2-(O-methyl-L-tyrosine)-1-carbaoxytocin (carbetocin) and/or other long-acting oxytocin analogues are formulated with a pharmaceutically acceptable carrier and administered in an amount sufficient to inhibit initiation or growth of breast cancer in the patient. The carbetocin and/or other long-acting oxytocin analogues may also be formulated with a pharmaceutically acceptable carrier and administered in an amount sufficient to treat, prevent or alleviate the symptoms of a psychiatric disorder in the patient. Carbetocin may be administered prophylactically or to treat existing conditions in patients by a variety of administration modes, including intramuscular, intravenous, intranasal, intrapulmonary, subcutaneous, parenteral, oral, or transdermal delivery methods and formulations. Preferably, the carbetocin is administered to a mucosal surface of the patient via intranasal delivery. For this purpose, pharmaceutical compositions are provided for intranasal delivery that incorporate carbetocin in a powder or aqueous formulation for intranasal delivery.
Owner:KYALIN BIOSCI
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