COMPOSITIONS AND METHODS FOR SUSTAINED TREATMENT OF PAIN

    公开(公告)号:US20220241200A1

    公开(公告)日:2022-08-04

    申请号:US17589639

    申请日:2022-01-31

    发明人: William J. Taylor

    摘要: Disclosed herein is a composition for treating post-surgical pain comprising: an aqueous carrier; and a lipid phase comprising an anesthetic agent, the lipid phase dispersed within the aqueous carrier. In certain aspects, the aqueous carrier is hydrogel comprised of tyramine substituted hyaluronic acid. In certain embodiments, the hydrogel is formed through di-tyramine crosslinking. In certain embodiments, the degree of tyramine substitution of hyaluronic acid hydroxyl groups is about 0.5% to about 3%. In further aspects, the lipid phase is comprised of a plurality of lipid microparticles. According to certain embodiments, a salt form of the anesthetic unbound by the plurality of lipid microparticles is dissolved in the aqueous carrier.

    HYDROGEL-BASED BIOLOGICAL DELIVERY VEHICLE
    2.
    发明申请

    公开(公告)号:US20190175495A1

    公开(公告)日:2019-06-13

    申请号:US16300660

    申请日:2017-05-12

    摘要: A hydrogel-based biological delivery vehicle used to effectively deliver drug and biological material to tissue or organ sites. More specifically, a hydrogel binding matrix having a biopolymer backbone containing carboxyl groups. Tyramine may be substituted for at least a portion of the carboxyl groups, so that, when hydrogen peroxide is added, it causes creation of covalent bonds between tyramine molecules and cross-links the hydrogel binding matrix, thereby enabling the hydrogel binding matrix to transition from liquid to gel state. The hydrogel binding matrix, in its liquid form, is capable of encapsulating drug reservoirs to create a homogenous liquid with evenly distributed particles containing drugs or target molecules. As the hydrogel binding matrix solidifies into a gel state, the newly created cross-links do not disrupt or react with the drugs or target molecules contained within the drug reservoirs. This hydrogel-based biological delivery vehicle can be used in several medical applications.

    SUSTAINED RELEASE STABLE EMULSION PHARMACEUTICAL FORMULATIONS

    公开(公告)号:US20240335437A1

    公开(公告)日:2024-10-10

    申请号:US18631935

    申请日:2024-04-10

    摘要: Disclosed herein is composition for treating pain in a subject in need thereof that comprises an emulsion comprising: an aqueous carrier; and liquid lipid phase dispersed into droplets within the aqueous carrier, and a first anesthetic agent within the lipid phase. In certain embodiments, the first anesthetic agent comprises a first plurality of anesthetic agent crystals. In certain alternative embodiments, the first anesthetic agent is dissolved with the lipid phase. In certain implementations, the composition further comprises a second plurality of anesthetic agent crystals within the aqueous carrier, but not the lipid phase and wherein the second plurality of anesthetic agent crystals dissolves and elutes from the emulsion at a faster rate than the first plurality anesthetic agent crystals. In certain implementations, the composition further comprises one or more additional anesthetic agents, different from the first anesthetic agent.

    SUSTAINED RELEASE CANCER THERAPEUTICS FORMULATIONS

    公开(公告)号:US20240315968A1

    公开(公告)日:2024-09-26

    申请号:US18615846

    申请日:2024-03-25

    摘要: Disclosed herein is composition for treating a tumor in a subject in need thereof that comprises an emulsion comprising: an aqueous carrier; and liquid lipid phase dispersed into droplets within the aqueous carrier, and a first chemotherapeutic agent within the lipid phase. In certain embodiments, the first chemotherapeutic agent comprises a first plurality of chemotherapeutic agent crystals. In certain alternative embodiments, the first chemotherapeutic agent is dissolved with the lipid phase. In certain implementations, the composition further comprises a second plurality of chemotherapeutic agent crystals within the aqueous carrier, but not the lipid phase and wherein the second plurality of chemotherapeutic agent crystals dissolves and elutes from the emulsion at a faster rate than the first plurality chemotherapeutic agent crystals. In certain implementations, the composition further comprises one or more additional chemotherapeutic agents, different from the first chemotherapeutic agent.

    HYDROGEL-BASED BIOLOGICAL DELIVERY VEHICLE

    公开(公告)号:US20230080761A1

    公开(公告)日:2023-03-16

    申请号:US17946849

    申请日:2022-09-16

    摘要: A hydrogel-based biological delivery vehicle used to effectively deliver drug and biological material to tissue or organ sites. More specifically, a hydrogel binding matrix having a biopolymer backbone containing carboxyl groups. Tyramine may be substituted for at least a portion of the carboxyl groups, so that, when hydrogen peroxide is added, it causes creation of covalent bonds between tyramine molecules and cross-links the hydrogel binding matrix, thereby enabling the hydrogel binding matrix to transition from liquid to gel state. The hydrogel binding matrix, in its liquid form, is capable of encapsulating drug reservoirs to create a homogenous liquid with evenly distributed particles containing drugs or target molecules. As the hydrogel binding matrix solidifies into a gel state, the newly created cross-links do not disrupt or react with the drugs or target molecules contained within the drug reservoirs. This hydrogel-based biological delivery vehicle can be used in several medical applications.

    Hydrogel-based biological delivery vehicle

    公开(公告)号:US11471402B2

    公开(公告)日:2022-10-18

    申请号:US16300660

    申请日:2017-05-12

    摘要: A hydrogel-based biological delivery vehicle used to effectively deliver drug and biological material to tissue or organ sites. More specifically, a hydrogel binding matrix having a biopolymer backbone containing carboxyl groups. Tyramine may be substituted for at least a portion of the carboxyl groups, so that, when hydrogen peroxide is added, it causes creation of covalent bonds between tyramine molecules and cross-links the hydrogel binding matrix, thereby enabling the hydrogel binding matrix to transition from liquid to gel state. The hydrogel binding matrix, in its liquid form, is capable of encapsulating drug reservoirs to create a homogenous liquid with evenly distributed particles containing drugs or target molecules. As the hydrogel binding matrix solidifies into a gel state, the newly created cross-links do not disrupt or react with the drugs or target molecules contained within the drug reservoirs. This hydrogel-based biological delivery vehicle can be used in several medical applications.