in:(Chandrasekaran Santosh K.(Moraga,CA))

Topical ophthalmic suspensions NCL 29 ECL 1 COD 02 RLAP COD 72 APN 544518 APD 19900627 PSC 03 RLAP COD 82 APN 537005 APD 19900612 PSC 03 RLAP COD 81 APN 301114 APD 19890125 PSC 03 RLAP COD 82 APN 153762 APD 19880208 PSC 03 RLAP COD 75 APN 429770 APD 19891031 PSC 03 CLAS EDF 5 US07/549093
[Chandrasekaran Santosh K.(Moraga,CA), Reents Margaret J.(Alameda,CA), Babcock John C.(Olga,WA), Bowman Lyle M.(Pleasanton,CA), Archibald Roy D.(Fremont,CA), Robinson Joseph R.(Madison,WI)] A topical, aqueous ophthalmic gel suspension for dry eye is administrable to the eye in drop form, remains as a gel in the eye for a prolonged time, and releases water and one or more ophthalmic demulcents or vasoconstrictors. It comprises water and from 0.1% to 6.5% by weight of lightly cross-linked carboxyl-containing polymer having a particle size of not more than about 50 .mu.m in equivalent spherical diameter. The suspension is at a pH of from 6.6 to 8.0, has an osmolality of from 50 to 400 mOsM, and a viscosity of from about 500 to about 4,000 centipoise (0.5 to 4 Pa.s).
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Aminosteroids for ophthalmic use NCL 20 ECL 1 COD 02 RLAP COD 71 APN 838875 APD 19920219 PSC 03 RLAP COD 84 APN 537062 APD 19900612 PSC 01 PNO 5124154 CLAS EDF 5 US07/933574
[Babcock John C.(Olga,WA), Polansky Jon R.(Mill Valley,CA), Bowman Lyle M.(Pleasanton,CA), Tsao Sheng-Wan(San Carlos,CA), Si Erwin C.(Alameda,CA), Chandrasekaran Santosh K.(Moraga,CA)] Methods and compositions for preventing or treating ophthalmic diseases or disorders wherein an ophthalmically effective amount of the C.sub.20 through C.sub.26 aminosteroids of formula XI and their pharmaceutical, acceptable salts, hydrates or solvates is administered in an inert vehicle to arrest oxidation processes damaging to the eye.
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Aminosteroids for ophthalmic use NCL 9 ECL 1 COD 02 RLAP COD 74 APN 537062 APD 19900612 PSC 01 PNO 5124154 CLAS EDF 5 US07/836888
[Babcock John G.(Olga,WA), Polansky Jon R.(Mill Valley,CA), Bowman Lyle M.(Pleasanton,CA), Tsao Sheng-Wan(San Carlos,CA), Si Erwin C.(Alameda,CA), Chandrasekaran Santosh K.(Moraga,CA)] Methods and compositions for preventing or treating ophthalmic diseases or disorders wherein an ophthalmically effective amount of the C.sub.20 through C.sub.26 aminosteroids of formula XI and their pharmaceutical, acceptable salts, hydrates or solvates is administered in an inert vehicle to arrest oxidation processes damaging to the eye.
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Aminosteroids for ophthalmic use NCL 17 ECL 1 COD 02 RLAP COD 74 APN 537062 APD 19900612 PSC 01 PNO 5124154 CLAS EDF 5 US07/836866
[Babcock John C.(Olga,WA), Polansky Jon R.(Mill Valley,CA), Bowman Lyle M.(Pleasanton,CA), Tsao Sheng-Wan(San Carlos,CA), Si Erwin C.-C.(Almeda,CA), Chandrasekaran Santosh K.(Moraga,CA)] Methods and compositions for preventing or treating ophthalmic diseases or disorders wherein an ophthalmically effective amount of the C.sub.20 through C.sub.26 aminosteroids of formula XI and their pharmaceutical, acceptable salts, hydrates or solvates is administered in an inert vehicle to arrest oxidation processes damaging to the eye.
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Stabilization of aminosteroids for topical ophthalmic and other applications NCL 36 ECL 1 DCD 20090623 COD 02 RLAP COD 72 APN 933574 APD 19920824 PSC 01 PNO 5209926 RLAP COD 81 APN 838875 APD 19920219 PSC 03 RLAP COD 84 APN 537062 APD 19900612 PSC 01 PNO 5124154 CLAS EDF 5 US07/984445
[Babcock John C.(Olga,WA), Polansky Jon R.(Mill Valley,CA), Bowman Lyle M.(Pleasanton,CA), Tsao Sheng-Wan(San Carlos,CA), Si Erwin C.(Alameda,CA), Chandrasekaran Santosh K.(Moraga,CA)] The invention provides methods for stabilizing amino-substituted steroid therapeutic agents in topical ophthalmic and other pharmaceutical formulations using effective stabilizing amounts of lightly cross-linked carboxy-containing polymers; Stabilized and stabilized/solubilized pharmaceutical compositions adapted for various routes of administration are also described.
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Stabilization of aminosteroids for topical ophthalmic and other applications NCL 7 ECL 1 COD 02 RLAP COD 74 APN 984445 APD 19921202 PSC 01 PNO 5332582 RLAP COD 82 APN 933574 APD 19920824 PSC 01 PNO 5209926 RLAP COD 81 APN 838875 APD 19920219 PSC 03 RLAP COD 84 APN 537062 APD 19900612 PSC 01 PNO 5124154 CLAS EDF 6 US08/202469
[Babcock John C.(Olga,WA), Polansky Jon R.(Mill Valley,CA), Bowman Lyle M.(Pleasanton,CA), Tsao Sheng-Wan(San Carlos,CA), Si Erwin C. C.(Alameda,CA), Chandrasekaran Santosh K.(Moraga,CA)] The invention provides methods for stabilizing amino-substituted steroid therapeutic agents in topical ophthalmic and other pharmaceutical formulations using effective stabilizing amounts of lightly cross-linked carboxy-containing polymers; and methods for stabilizing and solubilizing amino-substituted steroid therapeutic agents in such pharmaceutical formulations using effective stabilizing amounts of lightly cross-linked carboxy-containing polymers and amounts of selected cyclodextrin derivatives sufficient to at least partially solubilize the therapeutic agents. The cyclodextrin derivatives are selected from the group consisting of the hydroxypropyl, hydroxyethyl, glucosyl, maltosyl and maltotriosyl derivatives of .beta.- and .gamma.-cyclodextrin. Stabilized and stabilized/solubilized pharmaceutical compositions adapted for various routes of administration are also described.
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Ophthalmic suspensions NCL 35 ECL 1 COD 02 RLAP COD 72 APN 537005 APD 19900612 PSC 03 RLAP COD 81 APN 301114 APD 19890125 PSC 03 RLAP COD 82 APN 153762 APD 19880208 PSC 03 CLAS EDF 5 US07/544518
[Davis Jeffrey P.(Madison,WI), Chandrasekaran Santosh K.(Moraga,CA), Su Yansheng(Shandong,CNX), Archibald Roy D.(Fremont,CA), Robinson Joseph R.(Madison,WI)] Lightly crosslinked polymers, preferably ones prepared by suspension or emulsion polymerizing at least about 90% by weight of a carboxyl-containing monoethylenically unsaturated monomer such as acrylic acid with from about 0.1% to about 5% by weight of a polyfunctional, and preferably difunctional, crosslinking agent such as divinyl glycol (3,4-dihydroxy-1,5-hexadiene), having a particle size of not more than about 50 .mu.m in equivalent spherical diameter, when formulated with an ophthalmic medicament, e.g., fluorometholone, into suspensions in aqueous medium in which the amount of polymer ranges from about 0.1% to about 6.5% by weight, based on the total weight of the aqueous suspension, the pH is from about 3.0 to about 6.5, and the osmotic pressure (osmolality or tonicity) is from about 10 mOsM to about 400 mOsM, provide new topical ophthalmic medicament delivery systems having suitably low viscosities which permit them to be easily administered to the eye in drop form, and hence be comfortably administrable in consistent, accurate dosages. These suspension will rapidly gel in the eye after coming into contact with the eye's tear fluid to a substantially greater viscosity than that of the originally-introduced suspension and thus remain in place for prolonged periods of time to provide sustained release of the ophthalmic medicament.
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Liquid droplet dispensing apparatus NCL 35 ECL 1 NDR 2 NFG 6 COD 02 CLAS EDF 5 US07/324793
[Davis Jeffrey P.(Madison,WI), Archibald Roy D.(Fremont,CA), Nicholas Christa D.(Alameda,CA), Chandrasekaran Santosh K.(Moraga,CA)] A disposable unit- or multi-dose liquid dispensing container device, particularly adapted for delivery of ophthalmic liquid medicament in the form of discrete droplets to the eye. The structural configuration of the device including an angularly offset leading end permits the user to employ a free hand for manipulation of the eyelid to enhance reception of the discharge opening of the dispenser into the conjunctival cul-de-sac while at the same time, enabling the user to look directly into a wall-mounted mirror for accurate placement of the medicament. A small capacity reservoir and ease of control of accurate orifice size enables the application of uniform liquid-ejection pressure by the user to deliver droplets of reproducible dosage size with the multi-dose embodiment.
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