摘要:
The present invention is concerned with a pharmacuetical formulation comprising an amylin agonist and optionally a buffer, a tonicifier or stabilizer, and a preservative in a container, for example, a vial prefilled syringe or disposable pen. The formulation may be liquid, gel, solid or powdered form for delivery, for example,via nasal, oral, subligual, buccal, transdermal, or parental routes. Formulation with biocompatible polymers and release modifiers, such as sugars, can facilitate controlled release after injection, minimizing the number of administrations to a patient. These formulations maintain stability upon storage under refrigerated or room temperature conditions. Such formulations can be further combined with insulin for administration to a patient.
摘要:
The invention provides methods and kits to form water swellable gel coatings, preferably lubricious coatings, on substrates, and coated substrates thus formed. The coatings contain one or more antimicrobial metals formed with atomic disorder, together with one or more antimicrobial metals formed with atomic disorder such that the coatings provide an antimicrobial and anti-inflammatory effect when wet. The invention also provides a method to produce metal powders by sputtering a coating onto a moving surface, and then scraping the coating with one or more scrapers to produce the metal powder. The method is particularly useful for producing large amounts of nanocrystalline antimicrobial metal powders formed with atomic disorder, useful in the water swellable gel coatings on this invention.
摘要:
The present invention is directed to methods and compositions for treating skin disorders. The present invention is easily administered and can be used for both humans and animals. The compositions of the present invention comprise borate compounds and provide relief from skin disorder symptoms and lesions. Additionally, the present invention can be used to provide long term maintenance of symptom-free skin.
摘要:
The invention concerns novel heteroethynylene compounds of general formula (I) and their use in pharmaceutical compositions for use in human or veterinary medicine (dermatologic, rheumatic, respiratory, cardiovascular and ophthalmologic affections in particular), or for cosmetic compositions.
摘要:
The invention relates to a topical, foamable composition including at least one antifungal agent, said composition characterised in that said at least one antifungal agent is able to penetrate the upper layers of skin and is retained in or on an area to be treated for a prolonged period of time, and in that it has a residual non-volatile component content of less than 25 %. The invention furthermore relates to a method of treating fungal diseases including jock itch, tinea, dandruff and sebborheic dermatitis by applying to the affected area of a patient requiring such treatment the antifungal composition as claimed in any one of claims 1-29.
摘要:
Use of stereoisomeric glycosidic compounds of formula (I) as phar maceutical agents against psoriasis, compounds therefor and pharmaceutical formulation thereof wherein R and R are independently selected from H, -OH, (1) and (2) and related esters and ethers thereto; R is selected from -OH, (3), (4), (5), (6), (7) and (8) and related esters and ethers thereto; R is (9); R is selected from the group -CH, -CHO, -COOH, -CH OH and related esters and ethers thereto; R is selected from OH, (10), (11), (12), (13) and (14) in the preparation of a medicament for the treatment of disease involving hyperproliferation of dermis cells.
摘要翻译:使用式(I)的立体异构糖苷化合物作为抗银屑病的药物,其化合物及其药物组合物,其中R 1和R 2独立地选自H,-OH,(1)和(2)和 相关的酯和醚; R 3选自-OH,(3),(4),(5),(6),(7)和(8)及其相关的酯和醚; R 4为(9); R 5选自-CH,-CHO,-COOH,-CHOH和相关的酯和醚; R 6选自OH,(10),(11),(12),(13)和(14)在制备用于治疗涉及真皮细胞过度增殖的疾病的药物中的用途。
摘要:
The first invention provides an external preparation for treating dermatoses comprising vitamin E and squalane, which has an efficacy at least equivalent to that of external preparations containing adrenocortical hormones as the active ingredient. The second invention provides an external preparation for treating dermatoses comprising an adrenocortical hormone, vitamin E and squalane, which is reduced in adrenocortical hormone content as compared with conventional preparations, is also reduced in side effects, and has high clinical efficacy. The third invention provides an external preparation for treating dermatoses comprising a nonsteroidal antiinflammatory agent, vitamin E, and squalane and/or squalene, which is reduced in side effects and is highly efficacious. The fourth invention provides an external preparation for treating dermatoses comprising an antihistaminic agent, vitamin E, and squalane and/or squalene, which is reduced in side effects and is highly efficacious like the above preparation. The fifth invention provides an external preparation for treating dermatoses comprising vitamin E, squalene and squalane, which is reduced in side effects and is highly efficacious.
摘要:
A method for the preparation of Mycobacteria from any liquid, semisolid or exotic source is described. The extracted Mycobacterial sample is suitable for detection by culture and amplification.
摘要:
Autoimmune diseases are controlled by the administration of non-methylene-interrupted fatty acids of formula (I) in which R is alkyl or alkenyl. A preferred compound within the scope of this formula is 5,11,14-eicosatrienoic acid.
摘要:
Inhibitors of testosterone 5 alpha -reductase activity, for example those of formula (I) wherein novel substituents are provided at the R , R , R , R and/or R positions are useful for the treatment of diseases whose progress is aided by activation of androgen receptors, e.g., prostate cancer, benign prostatic hyperplasia, acne, seborrhea, hirsutism, androgenic alopecia and the like.