Patel, Ahmedabad
Aditya Patel, Ahmedabad IN
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20160058865 | STABLE TIGECYCLINE COMPOSITION - The present invention relates to a stable pharmaceutical composition of Tigecycline and process for the preparation of the same. The composition comprises Tigecycline and maltose wherein the pH of the bulk solution or solution after reconstitution is in between 3-6. | 03-03-2016 |
Amrish Patel, Ahmedabad IN
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20160132648 | Data Processing System and Method for Computer-Assisted Coding of Natural Language Medical Text - A system and method utilizing deep clinical knowledge represented as a knowledge-graph to complement and enhance Natural Language Processing (NLP) for efficient and high-quality computer assisted coding of medical text. One embodiment utilizes the International Classification of Diseases version-10 Procedural Coding System (ICD-10-PCS). The system uses multiple knowledge bases combined with direct mapping provided by the ICD-10-PCS standard to enhance the coverage of assigned code. The system identifies ICD-10-PCS code considering hierarchical mapping and identifies the code by individual ICD-10-PCS character. | 05-12-2016 |
Arvindbhai Lavjibhai Patel, Ahmedabad IN
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20160139058 | METHOD AND DEVICE FOR GEMSTONE EVOLUTION - The present invention relates to the method and device to determination of the properties of gemstones and more particularly evolution of gemstone by detection of internal and external structure of gemstone. In particular, the present invention methods and device is used to identify the size, location of impurities/defects in raw gemstone with the help of optimize spectroscopy scanning. The present invention method and device is used for precise automatic evolution of gemstones and possibilities (estimation) of final value of planned gemstone after remaining gemstone processing cycle. | 05-19-2016 |
Bhavesh Patel, Ahmedabad IN
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20090275647 | TAXANE DERIVATIVE COMPOSITION - A stable, absolutely ethanol free composition of docetaxel that prevents alcoholic intoxication or anaphylactic shock. The composition can be in the form of a stable injectable composition that includes a taxane derivative, wherein the composition includes a mixture of docetaxel, one or more stabilizer, one or more surfactant, or more co-solvent and water for injection wherein the composition is absolutely free of ethanol. | 11-05-2009 |
20120252835 | STABLE TEMSIROLIMUS COMPOSITION AND PROCESS OF PREPARING SAME - The present disclosure describes a stable composition of Temsirolimus for parenteral administration. The composition includes BHA or BHT as anti-oxidants and alcoholic solvent. The pH of the composition is below 5.0. The composition also can include a chelating agent and/or a surfactant. A method of producing the composition is also described. | 10-04-2012 |
20130303464 | STABLE READY-TO-USE CETRORELIX INJECTION - The present invention discloses a stable ready-to-use aqueous pharmaceutical preparation containing Cetrorelix or its pharmaceutically acceptable salt, wherein the preparation does not contain any surfactant. Further, the present invention discloses process for the preparation of said stable ready-to-use aqueous pharmaceutical preparation. | 11-14-2013 |
Bhavesh Vallabhabhai Patel, Ahmedabad IN
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20100248376 | IN-VITRO METHOD FOR TESTING BIOEQUIVALENCE OF IRON-SUCROSE FORMULATION - The present disclosure relates to an in vitro method for measuring the T | 09-30-2010 |
20100267824 | STABLE OXALIPLATIN COMPOSITION FOR PARENTERAL ADMINISTRATION - The present invention relates to a stable parenteral composition of oxaliplatin having pH range in between 3 to 4.5, which comprises of a solution of oxaliplatin in water wherein the said pH is attained by sparging of carbon dioxide in the composition. Further, a method for the preparation of oxaliplatin composition of the present invention is also disclosed. | 10-21-2010 |
Chaitanya A. Patel, Ahmedabad IN
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20120247793 | MULTI DRILL CULTIVATOR - An improved multi drill cultivator which mainly consists of octagonal central drum ( | 10-04-2012 |
Chetan Patel, Ahmedabad IN
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20140006930 | SYSTEM AND METHOD FOR INTERNET PUBLISHING | 01-02-2014 |
20150156226 | SYSTEM AND METHOD FOR INTERNET PUBLISHING - Disclosed herein are systems and methods for internet publishing. In some aspects, the systems and methods may be implemented by software designed for users such as, for example, small businesses, to manage and implement an online digital strategy. A digital web-based platform, for example, may be used to establish and expand the online presence of a brand. In some aspects, the systems and methods may be implemented to publish, syndicate, and monetize content in an automated and seamless manner from a single interface as well as to monitor and respond to information relevant to such content. | 06-04-2015 |
20150213561 | SYSTEM AND METHOD FOR INTERNET PUBLISHING - Disclosed herein are systems and methods for internet publishing. In some aspects, the systems and methods may be implemented by software designed for users such as, for example, small businesses, to manage and implement an online digital strategy. A digital web-based platform, for example, may be used to establish and expand the online presence of a brand. In some aspects, the systems and methods may be implemented to publish, syndicate, and monetize content in an automated and seamless manner from a single interface as well as to monitor and respond to information relevant to such content. | 07-30-2015 |
Chintan G. Patel, Ahmedabad IN
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20150071936 | PHARMACEUTICAL FORMULATIONS OF TNF-ALPHA ANTIBODIES - The present invention provides certain improved formulations of proteins. Specifically, the present invention provides use of certain excipients that are useful for stabilization of antibody preparations. Additionally, the novel formulations of the present invention prevents the formation of aggregates or fragments or modifications of protein in solution. | 03-12-2015 |
Dhaval J Patel, Ahmedabad IN
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20140148593 | PROCESS FOR PREPARING FLUTICASONE PROPIONATE/FUROATE - The present invention relates to an improved process for the preparation of substituted Fluticasone derivatives. The invention also reveals the processes for the purification of Fluticasones and related intermediates to provide the highly pure product. | 05-29-2014 |
Dhaval Jashvantbhai Patel, Ahmedabad IN
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20150087834 | PROCESS FOR THE PREPARATION OF SITAGLIPTIN PHOSPHATE - The present invention relates to a method for the preparation of sitagliptin phosphate and sitagliptin phosphate anhydrous of Formula (I′) and monohydrate of Formula (I), | 03-26-2015 |
Dhaval P Patel, Ahmedabad IN
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20140148593 | PROCESS FOR PREPARING FLUTICASONE PROPIONATE/FUROATE - The present invention relates to an improved process for the preparation of substituted Fluticasone derivatives. The invention also reveals the processes for the purification of Fluticasones and related intermediates to provide the highly pure product. | 05-29-2014 |
Dhimant Jasubhai Patel, Ahmedabad IN
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20100190999 | PROCESS FOR THE PREPARATION OF AMORPHOUS ATORVASTATIN CALCIUM - The present invention also provides the amorphous form of hemi-calcium salt of atorvastatin with high purity and processes for preparation thereof. | 07-29-2010 |
20130059885 | Method For Preparation Of Pitavastatin and Pharmaceutical Acceptable Salts Thereof - The present invention discloses a compound, which is alkali or alkaline earth metal salts of pitavastatin, wherein the alkali or earth metal comprise one or more of magnesium, zinc, potassium, strontium and barium. | 03-07-2013 |
20140148481 | PITAVASTATIN CALCIUM AND PROCESS FOR ITS PREPARATION - The invention provides the process for the preparation of pitavastatin and its pharmaceutically acceptable salts thereof. In particular, the invention provides a process for the preparation of stable pitavastatin calcium in crystalline form having water content less than 5% wt/wt. The present invention also provides stable crystalline form of pitavastatin calcium substantially free from crystal Form-A and use thereof for pharmaceutical compositions. | 05-29-2014 |
Hamish Patel, Ahmedabad IN
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20150254414 | MOBILE DEVICE CASING FOR HEALTH MONITORING - A casing adapted to use with a mobile device for monitoring health condition of a user is provided. The casing includes (a) a memory unit, (b) a sensor unit at a surface of the casing, (c) a plurality of health parameter measuring sensors embedded within the sensor unit for measuring raw health parameters data of the user, (d) a processor which is activated from a sleep mode based on a user input including contacting at least one predetermined sensor surface on the casing for a predetermined period, and (e) a power unit for controllably supplying power to the sensors and the processor upon detecting the user input. The processor (i) initializes and configures the sensors, and (ii) receives the raw health parameters data from the sensors. The casing further includes a communication unit for communicating the raw health parameters data to a mobile device for processing. | 09-10-2015 |
Hemantkumar H. Patel, Ahmedabad IN
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20130317078 | PHENYLALKYL N-HYDROXYUREAS FOR TREATING LEUKOTRIENE RELATED PATHOLOGIES - The method of treating patients by administering N-[3-[5-[(4-fluorophenyl)methyl]-2-thienyl]-1-methyl-2-propynyl]-N-hydroxyurea for treatment of leukotriene related pathologies, and compositions for this use. | 11-28-2013 |
Hiren Patel, Ahmedabad IN
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20100075933 | INJECTABLE COMPOSITIONS OF VITAMIN D COMPOUNDS - Pharmaceutical injectable compositions comprising at least one vitamin D compound as an active agent, processes for preparing such compositions, and methods of using such compositions. | 03-25-2010 |
Jagdish Maganlal Patel, Ahmedabad IN
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20160002275 | PROCESS FOR PREPARATION AND PURIFICATION OF CANAGLIFLOZIN - The present invention provides a canagliflozin complex. The complex is provided with an adsorbent selected from activated carbon, silica gel, ionic or non-ionic polymer and a cyclodextrin or derivatives thereof. The invention also provides a process for the preparation of canagliflozin and its intermediates thereof. The invention further provides a process for the purification of canagliflozin. | 01-07-2016 |
20160083345 | POLYMORPHIC FORMS OF LOMITAPIDE AND ITS SALTS AND PROCESSES FOR THEIR PREPARATION - The present invention relates to various polymorphic forms of lomitapide or its salts and processes for preparation thereof. The present invention provides Lomitapide mesylate in solid amorphous form and process for preparation thereof. The invention also provides an amorphous solid dispersion of lomitapide mesylate. Further, various crystalline forms of lomitapide mesylate like A, B and C and process for preparation thereof are provided. The invention also provides crystalline forms of lomitapide free base, in particular Form I and Form-II and their preparation. The invention further provides compositions comprising various forms of lomitapide and its salts. | 03-24-2016 |
Jayantibhai Prabhuram Patel, Ahmedabad IN
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20100327597 | SYSTEM FOR GENERATING POWER USING FLOW OF WATER - Disclosed is a system for generating electrical power using flowing water in canals, rivers and the like water streams. The system comprising: plurality of circular structures, each having a bore at the center and plurality of elongated arms being fixed on the outer periphery of said structure; plurality of blades being fitted on said plurality of elongated arms; a rotating shaft for rotatably accommodating in space apart relationship said circular structures over outer body of said shaft through said bore; an electrical generator for converting the mechanical energy generated by rotation of said shaft into electrical energy to produce electrical power; and a transmission device for transmitting the mechanical energy generated by rotation of said shaft from shaft to said electrical generator; wherein said circular structures along with blades are kept across the flow of water, the blades of said structure get rotation due to force of flowing water and generate energy which rotates said shaft which in turn generate mechanical energy and finally said mechanical energy is transmitted to electrical generator through transmission device for generating electrical power. | 12-30-2010 |
Jitendra Patel, Ahmedabad IN
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20120093882 | STABLE PHARMACEUTICAL COMPOSITIONS OF DICLOFENAC - The present invention discloses a stable pharmaceutical composition of diclofenac or salts thereof comprising nano size droplets of diclofenac or salts thereof, wherein the composition exhibits a significant difference in one or both of the rate and extent of absorption of diclofenac or salts thereof as compared to formulation of diclofenac marketed under the trade name Voveran® | 04-19-2012 |
Jitendra Dasharathlal Patel, Ahmedabad IN
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20130273172 | TOPICAL PHARMACEUTICAL COMPOSITIONS CONTAINING NANODROPLETS FOR THE TREATMENT PSORIASIS - The present invention relates to stable topical pharmaceutical compositions for the treatment of psoriasis. Disclosed are in particular nonoemulsions comprising nano size droplets of one or more anti-psoriasis agents, e.g. clobetasol and/or salicylic acid. These compositions exhibit greater permeability, and improved bioavailability. The invention also relates to processes for the preparation of such compositions. | 10-17-2013 |
20130287825 | PHARMACEUTICAL COMPOSITIONS COMPRISING NANO SIZE DROPLETS OF SKIN WHITENING AGENTS - The present invention relates to pharmaceutical compositions comprising mono size droplets of skin whitening agents or salts thereof. In particular, the present invention relates to a stable pharmaceutical composition comprising skin whitening agents or salts thereof along with other pharmaceutically acceptable excipients which possess substantially improved skin whitening effects and also exhibits greater skin permeability. The invention also relates to processes for the preparation of such compositions. | 10-31-2013 |
20130295145 | TOPICAL PHARMACEUTICAL COMPOSITIONS COMPRISING ETODOLAC - The present invention relates to stable pharmaceutical compositions comprising nano size droplets of etodolac or salts thereof along with other pharmaceutically acceptable excipients. These compositions exhibit greater permeability, and improved bioavailability leading to enhanced therapeutic activity. The invention also relates to processes for the preparation of such compositions. | 11-07-2013 |
Jitendra Rameshchandra Patel, Ahmedabad IN
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20150072014 | Pharmaceutical Compositions of Sodium Picosulfate, Magnesium Oxide and Citric Acid - The present invention relates to pharmaceutical compositions of sodium picosulfate, magnesium oxide and citric acid. In particular, the invention relates to pharmaceutical compositions comprise granules having a layer of sodium picosulfate on neutral carrier/s. The invention also relates to processes for the preparation of such compositions and use thereof for bowel cleansing. | 03-12-2015 |
Kalpesh Mahendrabhai Patel, Ahmedabad IN
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20110282094 | PROCESS FOR PREPARATION OF PHENOLIC MONOESTERS OF HYDROXYMETHYL PHENOLS - A process for the preparation of phenolic monoesters of 2-(3-diisopropylamino-1-phenylpropyl)-4-(hydroxymethyl)phenol by converting (±)6-halo-4-phenylchroman-2-one to (±)4-halo-2-(3-hydroxy-1-phenylpropyl)phenol. The two hydroxyl groups are protected and the protected compound is reacted with diisopropylamine to give (±)[3-(2-benzyloxy-5-halophenyl)-3-phenylpropyl]diisopropylamine. The halo substituent on the benzene ring is converted to corresponding benzyl alcohol and then the protection is removed to give racemic 5-HMT. Racemic 5-HMT is converted R enantiomer and then it is esterified. | 11-17-2011 |
Keyur Patel, Ahmedabad IN
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20100248376 | IN-VITRO METHOD FOR TESTING BIOEQUIVALENCE OF IRON-SUCROSE FORMULATION - The present disclosure relates to an in vitro method for measuring the T | 09-30-2010 |
Manish C. Patel, Ahmedabad IN
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20120253540 | ENERGY GRID DEVICE COMMISSIONING METHOD AND SYSTEM - A commissioning method and system. The method includes receiving details of a configuring process enabled by a power grid monitoring/control device associated with a power grid network topology comprising monitoring points associated and a power distribution grid. The power grid network topology is validated with respect to a configuration of measurement types, event types, and controls of the power distribution grid. Network point identifiers for each of the monitoring points are retrieved and a mapping report associating the power grid monitoring/control device with the power grid network topology using the network point identifiers is generated. The power grid monitoring/control device is registered for remote operation functionality and multiple grid events. The power grid monitoring/control device is commissioned into the power distribution grid. | 10-04-2012 |
20140207295 | ENERGY GRID DEVICE COMMISSIONING - A commissioning method and system. The method includes receiving details of a configuring process enabled by a power grid monitoring/control device associated with a power grid network topology comprising monitoring points associated and a power distribution grid. The power grid network topology is validated with respect to a configuration of measurement types, event types, and controls of the power distribution grid. Network point identifiers for each of the monitoring points are retrieved and a mapping report associating the power grid monitoring/control device with the power grid network topology using the network point identifiers is generated. The power grid monitoring/control device is registered for remote operation functionality and multiple grid events. The power grid monitoring/control device is commissioned into the power distribution grid. | 07-24-2014 |
Manish Popatlal Patel, Ahmedabad IN
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20090281323 | PROCESS FOR THE MANUFACTURE OF MONTELUKAST SODIUM - Process for the manufacture of 1-[[[(1R)-1-[3-[(1E)-2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]cyclopropane acetic acid, sodium salt [montelukast sodium (I)] consisting of: i. Converting methyl 1-(mercaptomethyl)-cyclopropaneacetate to a metal salt (X) using a metal hydroxide, ii. Subjecting the metal salt (X) to monometallation to provide a dimetallide (XI). iii. Converting a diol of formula (II) to a mesylate of formula (III) and reacting (III) in situ with (XI) affordin the metal salt of 1-[[[(1R)-1-[3-[(1E)-2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]cyclopropane acetic acid. iv. Reacting the metal salt in-situ with a base and purifying to afford an amine salt (XII). v. Treating (XII) with a sodium base and precipitating out montelukast sodium (I). | 11-12-2009 |
Mayur Ramnikbhai Patel, Ahmedabad IN
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20130190366 | SUBSTANTIALLY PURE SALTS OF FEBUXOSTAT AND PROCESSES FOR PREPARATION THEREOF - Substantially pure salts of febuxostat of Formula (IA): wherein Y is Na | 07-25-2013 |
Naitik Bharatbhai Patel, Ahmedabad IN
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20140378682 | PROCESSES AND INTERMEDIATES FOR PREPARING RIVAROXABAN - The invention discloses processes for the preparation of rivaroxaban and its pharmaceutically acceptable salts, solvates, and hydrates thereof. The invention also relates to novel intermediates for the preparation of rivaroxaban. | 12-25-2014 |
Nilamkumari Somalal Patel, Ahmedabad IN
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20120027849 | STABLE PHARMACEUTICAL COMPOSITION FOR ATHEROSCLEROSIS - The present invention relates to a stable solid oral pharmaceutical multi-component composition comprising combination of blood pressure lowering drugs with lipid lowering agent/s and optionally a platelet aggregation inhibitor in a single dosage form. The blood pressure lowering agents are selected from β-adrenergic receptor blocking agent, ACE inhibitor and diuretic. The lipid lowering agent is selected from HMG Co-enzyme-A reductase inhibitor. The pharmaceutical composition made as per present invention a) overcomes any drug-drug interactions, b) exhibits pharmacokinetic and pharmacodynamic profile of individual therapeutic agent, c) has minimal side effects. The invention provides multi-component composition (MCC) to increase adherences to therapy. The MCC as per present invention provides compositions that maintain activity of all active ingredients without significant increase in adverse event profile. The present invention further relates to a method of preparing the said pharmaceutical composition. | 02-02-2012 |
Pankaí R. Patel, Ahmedabad IN
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20120108496 | SHORT-CHAIN PEPTIDES AS PARATHYROID HORMONE (PTH) RECEPTOR AGONIST - The present invention provides novel short-chain peptides, which primarily act as parathyroid hormone (PTH/PTH-1) receptor agonist. These short-chain peptides exhibit increased stability to proteolytic cleavage. Most of short-chain peptides were found to be stable in rat plasma up to 24 hours (in vitro), showed increased stability against GIT enzymes such as pepsin and acidic stomach pH and also against liver microsomes (in vitro). Due to increased metabolic stability, other than parenteral route of administration, some of the short-chain peptides can also be delivered by oral routes of administration, for the treatment/prevention of hypoparathyroidism and diseases characterized by bone mass reduction, such as osteoporosis, postmenopausal osteoporosis and for stimulating bone repair. A-Z | 05-03-2012 |
Pankaj R. Patel, Ahmedabad IN
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20120184544 | SUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS - The present invention relates to substituted benzamide derivatives of the general Formula I and their pharmaceutically acceptable salts, pharmaceutically acceptable solvates, enantiomers, diastereomers, prodrugs, metabolites, and polymorphs and can be useful for treating disease states mediated by glucokinase. Compounds disclosed herein can be used for reducing blood glucose levels and for increasing insulin secretion for treating type II diabetes. The invention also relates to processes for the preparation of the compounds of invention, pharmaceutical compositions containing the compounds, and their use. | 07-19-2012 |
20150291603 | SUBSTITUTED PHTHALAZIN-1 (2H)-ONE DERIVATIVES AS SELECTIVE INHIBITORS OF POLY (ADP-RIBOSE) POLYMERASE-1 - The present invention relates to novel compounds of general formula (I), their stereoisomers, regioisomers, tautomeric forms and novel intermediates involved in their synthesis, their pharmaceutically acceptable salts, pharmaceutically acceptable solvates and pharmaceutical compositions containing them. The present invention also relates to a process of preparing novel compounds of general formula (I), their stereoisomers, regioisomers, their tautomeric forms, their pharmaceutically acceptable salts, pharmaceutically acceptable solvates, pharmaceutical compositions containing them, and novel intermediates involved in their synthesis. | 10-15-2015 |
Parixit Amrutbhai Patel, Ahmedabad IN
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20120126036 | NON PRESSURE COMPENSATED DRIP IRRIGATION EMITTER WITH MULTIFLOW FACILITY - Described is a non pressure compensated drip emitter with multiflow facility, the drip emitter being placed inside a pipe of a drip irrigation system, the drip emitter comprising: a housing; a filter system being fitted at each inlet to ensure pure supply of water inside the emitter; three pools of water from only one of which water get discharged out of emitter and from emitter to the land to be irrigated, the third pool in the middle; a labyrinth in fluid communication with each pool and the filter system, the labyrinth comprises zigzag water paths; wherein the labyrinth connects middle pool with remaining two pools through the zigzag water path in such a way that even in case of partial clogging of the zigzag water path, the remaining partial zigzag water path remain active and ensure the discharge of water at a selected flow rate from the emitter. | 05-24-2012 |
Prashant Yogesh Patel, Ahmedabad IN
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20110020440 | STABLE SOLUTIONS OF SPARINGLY SOLUBLE ACTIVES - The present invention relates to a stable pharmaceutical composition comprising soft gelatin capsules containing at least one sparingly soluble active drug (singly or in combination with sparingly soluble and/or soluble drugs) and a solvent system, wherein the solvent system comprises of solvent, co-solvent, solubilizer(s), surfactant, aqueous solution of alkali and crystal growth inhibitor. The present invention further relates to process for preparing a stable pharmaceutical composition of sparingly soluble active drug(s) in soft gelatin capsules. | 01-27-2011 |
Raghvendra Jayantibhai Patel, Ahmedabad IN
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20150307468 | PROCESS FOR THE PREPARATION OF CABAZITAXEL AND ITS INTERMEDIATES - The present invention relates to a novel process for preparation of cabazitaxel (I) starting from 10-Deacetyl baccatin or derivative that involves methylation of 7, 10 —OH groups. Also provided is a novel process using chiral bis-lactam linker for the synthesis of cabazitaxel. | 10-29-2015 |
Rajeshkumar Naranbhai Patel, Ahmedabad IN
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20130118888 | DESALINATION UNIT FOR THE PRODUCTION OF POTABLE WATER FROM SUB-SOIL BRINE - A desalination unit for production of potable water from sub-soil brine including in combination a trapezoidal basin, a condenser, a feed tank, a header, a heat exchanger, a flush valve, a sprinkling system, exhaust heat pipe and water collecting channel; where the exhaust heat pipe is connected to a heat source at one end and to the header at the another end, the header being coupled with the heat exchanger to provide the heat flow, and the heat exchanger being fitted at the inner portion of the trapezoidal basin to heat the sub-soil brine. | 05-16-2013 |
Sanjay Ghanshyambhai Patel, Ahmedabad IN
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20160095925 | STABLE FORMULATION OF AZACITIDINE OR SALTS THEREOF AND THEIR PROCESS FOR PREPARATION - The present invention relates to a stable pharmaceutical composition comprising azacitidine or its pharmaceutically acceptable salts, one or more sugar alcohols and one or more pharmaceutically acceptable excipients, wherein said composition is suitable for parenteral administration. The invention also relates to processes for preparing the preparation of such reconstitutable formulations. The invention also relates to therapeutic methods of use of such formulations and to use of such formulations in the manufacture of medicaments. | 04-07-2016 |
Sanjay Maganbhai Patel, Ahmedabad JP
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20110177137 | NOVEL DOSAGE FORM OF PALIPERIDONE AND PROCESS FOR PREPARING THE SAME - The present invention relates to an extended release composition of paliperidone for oral administration comprising paliperidone and at least one matrixing agent. The said extended release composition maintains desired therapeutic drug effect over a prolonged period of time and thereby reduces the side effects resulting due to excess drug blood plasma concentration. Further, the invention also relates to process for the preparation of an extended release oral composition of paliperidone. | 07-21-2011 |
Vimal Ashwinkumar Patel, Ahmedabad IN
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20150309813 | A System for analyzing applications in order to find security and quality issues - The present invention relates to field of application and more specifically to analysis of applications for determining security and quality issues. The present invention describes an application analysis system providing a platform for analyzing applications which is useful in finding security and quality issues in an application. In particular, the present invention is composed of an advanced fusion analyzer which gains an understanding of the application behavior by using a multi-way coordination and orchestration across components used in the present invention to build an continuously refine a model representing knowledge and behavior of the application as a large network of objects across different dimensions and using reasoning and learning logic on this model along with information and events received from the components to both refine and model further as well as drive the components further by sending information and events to them and again using the information and events received as a result to further trigger the entire process until the system stabilizes. The present invention is useful in analysis of internet/intranet based web applications, desktop applications, mobile applications and also embedded systems as well as for hardware, equipment and machines controlled by software. | 10-29-2015 |
Vishnu Jagdishbhai Patel, Ahmedabad IN
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20100304321 | FIVE SEGMENT ORTHODONTIC ARCH WIRE AND ORTHODONTIC APPARATUS MADE THEREOF - The present invention relates to an arch wire that is used during orthodontic treatment. In accordance to the present invention a five segment orthodontic arch wire to provide a track for movement of teeth for correcting misalignment of teeth, said arch wire generally having ‘U’ shape and having same longitudinal axis through out the length, said arch wire characterized by: first segment having rectangular cross section and being provided for the posterior, 2nd premolar and molar region in left side of the jaw; second segment having rectangular cross section with rounded off corners, said second segment is followed by said first segment and provided for the canine and first premolar region in left side of the jaw; third segment having rectangular cross section, said third segment is followed by said second segment and provided for the anterior, incisor region; fourth segment having rectangular cross section with rounded off corners, said fourth segment is followed by said third segment and provided for the canine and 1st premolar region in right side of the jaw; and fifth segment having rectangular cross section, said fifth segment is followed by said fourth segment and provided for the posterior, 2nd premolar and molar region in right side of the jaw, wherein said arch wire is single piece and continuous in construction. Also an orthodontic apparatus comprising a five segment orthodontic arch wire in accordance with the present invention along with slotted bracket is also provided. | 12-02-2010 |