Atherosclerosis-targeted liposome nanocarrier delivery system and preparation method therefor
US-2024424132-A1 · Dec 26, 2024 · US
US12310934B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12310934-B2 |
| Application number | US-202017440178-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 20, 2020 |
| Priority date | Mar 20, 2019 |
| Publication date | May 27, 2025 |
| Grant date | May 27, 2025 |
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Spontaneous preterm birth (sPTB) is premature delivery prior to 37 weeks of pregnancy and is a leading cause of infant mortality worldwide. sPTB is associated with a unique gene expression profile. Identified herein are numerous safe and proven therapeutic compositions used for unrelated indications that have the biological effect of reversing, in part, the gene expression profile of sPTB and which can be used in preventative or interventional treatments to prevent, delay, or ameliorate sPTB. The repurposed drugs include several Class A and Class B therapeutics that are regarded as safe or low risk in pregnant subjects.
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The invention claimed is: 1. A method of treating spontaneous preterm birth in a subject in need of treatment therefor by the administration to the subject of a therapeutic composition comprising a therapeutically effective amount of one or more agents that partially reverse the gene expression profile associated with spontaneous preterm birth. 2. The method of claim 1 , wherein the subject is a subject at any stage of pregnancy. 3. The method of claim 1 , wherein the subject is a subject having one or more risk factors or symptoms of spontaneous preterm birth. 4. The method of claim 1 , wherein the treatment is a preventative treatment. 5. The method of claim 1 , wherein the therapeutic composition comprises an agent that partially reverses the gene expression profile associated with spontaneous preterm birth selected from the group consisting of: naproxen, cefotaxime, levopropoxyphene, prednisone, vorinostat, brompheniramine, genistein, valproic acid, cefoperazone, alprostadil, lansoprazole, iopamidol, letrozole, molindone, fluticasone, estradiol, isoxicam, thiamphenicol, guanabenz, isometheptene, isoniazid, sulfadimethoxine, ribavirin, pioglitazone, benzocaine, pentoxifylline, meclofenamic acid, rosiglitazone, methotrexate, domperidone, amitriptyline, vinblastine, naringenin, fulvestrant, sodium phenylbutyrate, haloperidol, zalcitabine, zuclopenthixol, iohexol, adenosine phosphate, iodixanol, viomycin, nimodipine, ciclosporin, rifabutin, podophyllotoxin, ceforanide, sirolimus, ajmaline, diloxanide, chlortalidone, trimethobenzamide, timolol, tenoxicam, ketotifen, geldanamycin, dantrolene, dapsone, streptozocin, raloxifene, ambroxol, benzathine benzylpenicillin, finasteride, trifluoperazine, vanoxerine, thiamazole, homosalate, levomepromazine, co-dergocrine mesilate, oxyphenbutazone, promazine, carisoprodol, niclosamide, methoxamine, tocainide, cefotiam, maprotiline, resveratrol, and nadolol. 6. The method of claim 5 , wherein the therapeutic composition comprises lansoprazole. 7. The method of claim 5 , wherein the therapeutic composition comprises cefotaxime. 8. The method of claim 5 , wherein the therapeutic composition comprises rifabutin. 9. The method of claim 5 , wherein the therapeutic composition comprises chlortalidone. 10. The method of claim 5 , wherein the therapeutic composition comprises benzathine benzylpenicillin. 11. The method of claim 5 , wherein the therapeutic composition comprises maprotiline. 12. The method of claim 5 , wherein the therapeutic composition comprises naproxen.
having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid {(cannabinoids A61K31/658)} · CPC title
substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone · CPC title
containing further heterocyclic rings, e.g. cephalothin · CPC title
containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole (nicotine A61K31/465) · CPC title
only substituted in position 2, e.g. pheniramine, bisacodyl · CPC title
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