Abstract:
The present invention relates to a nanoparticulate topical composition comprising (i) nanoparticles of a water soluble and water susceptible active ingredient or its pharmaceutically acceptable salt, having a particle size distribution such that 90% of the particles are less than 1000 nm, (ii) one or more wetting agent and (iii) a non-aqueous liquid vehicle, wherein the composition is free of water. The present invention also relates to a method of treating acne, rosacea, impetigo or a skin disease caused by a bacteria, by topical application of a nanoparticulate topical composition comprising nanoparticles of a water soluble and water susceptible active ingredient or its pharmaceutically acceptable salt, having a particle size distribution such that 90% of the particles are less than 1000 nm.
Abstract:
A compound of formula (I), formula (I) or pharmaceutically acceptable salt thereof, as renin inhibitor, process of preparation thereof, and to the use of the compounds in the preparation of pharmaceutical compositions for the therapeutic treatment of cardiovascular disorders related to hypertension, in warm-blooded animals. Further the present invention also provides a method for treatment of disorders like congestive heart failure, cardiac hypertrophy, cardiac fibrosis, coronary artery disease, vasculopathy, neuropathy, intraocular hypertension, glaucoma, diabetic nephropathy, abnormal vascular growth, hyperaldosteronism etc.
Abstract:
An ophthalmic solution comprising therapeutically effective amount of a prostaglandin or its analog and water soluble excipient(s) dissolved in a pharmaceutically acceptable vehicle, wherein the solution is free of a surfactant.
Abstract:
The present invention relates to a metered dose inhaler comprising an actuator being controlled by locking means. Locking means comprises a pendulum rod (6) which is operated by shaking movement of the inhaler.
Abstract:
The present invention discloses a method of treating a disease condition susceptible to baclofen therapy, said method comprising orally administering once-a-day in the evening a controlled release drug delivery system comprising baclofen or its pharmaceutically acceptable salt or its derivatives and pharmaceutically acceptable excipients.
Abstract:
The present invention relates to coated capsules comprising therapeutically active ingredient and pharmaceutically acceptable carrier and the coating composition (4) comprising a hydrophobic polymer and a hydrophilic substance, wherein the said coating composition is applied directly to the capsule and wherein the coated capsules upon contact with the aqueous environment (1) break open into the cap (2) and the body (3) and thereby providing a programmed release of the therapeutically active ingredient.
Abstract:
The present invention relates to compounds of formula I or salts thereof, wherein, R 1 is selected from the group consisting of hydrogen and R 4 ; R 2 is selected from the group consisting of hydrogen, acetyl and R 4 ; R 3 is selected from the group consisting of alkyl, -O-alkyl,-NH-alkyl, aryl and heterocyclyl; R 4 represents a moiety (A) wherein, X is selected from the group consisting of a single bond, alkylene, alkenylene, alkynylene, arylene or a heterocyclylene moiety; R 5 and R 6 are same or different and are independently selected from hydrogen, alkyl, aryl or heterocyclyl; or R 5 and R 6 may form together with the nitrogen atom to which they are attached a heterocyclyl ring system.
Abstract:
The present invention relates to compounds of formula (I), and salts thereof, wherein P represents a 5 or 6-membered heteroaryl ring; R 1 is aryl or unsaturated heterocyclyl radical optionally substituted by one or more identical or different radicals R 5.
Abstract translation:本发明涉及式(I)化合物及其盐,其中P表示5或6元杂芳基环; R 1是任选被一个或多个相同或不同基团R 5取代的芳基或不饱和杂环基。
Abstract:
This invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof (wherein X, Y, Z and n are defined herein). These compounds are useful in the treatment of diseases mediated by topoisomerase I enzyme such as cancers. The present invention also provides processes for the preparation of compounds of Formula I. The compounds of the present invention are more water soluble, stable in buffer solution at various pH, and exhibit better anti-tumor activity and rapid release of SN-38 in tumor microenvironments.
Abstract:
The present invention relates to a method of loading an ionizable drug having a group selected from (Formule I or Formule II) or pharmaceutically acceptable salts thereof into a liposome and the liposomal composition of drug produced therewith.