About: Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension

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About: Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 1961

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1961 (uk) im Oktober 1961 veröffentlichter wissenschaftlicher Artikel (de) 1961 թվականի հոկտեմբերի 1-ին հրատարակված գիտական հոդված (hy) scientific article published on 01 October 1961 (en) artículu científicu espublizáu n'ochobre de 1961 (ast)
publication date	wds:Q63918425-FE60180E-C23D-45D9-AFB0-D6BE8E68AA61
publication date	1961-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q63918425-600DA2B8-DBA6-4951-8BD7-AB5C26256F04
language of work or name	English
author name string	wds:Q63918425-954B748A-276B-45CA-8F65-06F758BBD64F
author name string	T HIGUCHI
rdfs:label	Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension (en) Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension (nl)
skos:prefLabel	Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension (en) Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension (nl)
name	Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension (en) Rate of Release of Medicaments from Ointment Bases Containing Drugs in Suspension (nl)
title	wds:Q63918425-DF65A876-A4EE-4F38-987B-0374E590A075
title	Rate of release of medicaments from ointment bases containing drugs in suspension (en)
page(s)	wds:Q63918425-940DF0B4-2D4D-4119-8731-03ACEDD29562
page(s)	874-875
instance of	wds:Q63918425-192D8CC9-7F98-4596-B39C-3D9EF2AD5813
instance of	scholarly article
main subject	wds:Q63918425-DFDD2584-6987-4EDF-AF5C-11D871EE7D34
main subject	ointment
PubMed ID	wds:Q63918425-74465DF2-493E-4F01-AA1F-C93146FB7733
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13907269
PubMed ID	13907269
published in	wds:Q63918425-9D2257F0-58B1-418A-B48B-47A46DBC31DF
published in	Journal of Pharmaceutical Sciences
issue	wds:Q63918425-100E097C-5150-4E0F-92E7-48D1F1A7E5CD
volume	wds:Q63918425-91A8F81F-BAA6-443C-9B7F-C1787BC27D5D
issue	10
volume	50
DOI	wds:Q63918425-D0CACBF4-8BFC-4EB1-9C61-D617F1663B7C
DOI	http://dx.doi.org/10.1002/JPS.2600501018
DOI	10.1002/JPS.2600501018
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q63918425
is cites work of	On the importance and mechanisms of burst release in matrix-controlled drug delivery systems Poly(lactic-co-glycolic) acid-controlled-release systems: experimental and modeling insights Mass transport Phenomena and Models: Theoretical Concepts Polymer micelles with cross-linked polyanion core for delivery of a cationic drug doxorubicin. Sustained-release effervescent floating matrix tablets of baclofen: development, optimization and in vitro-in vivo evaluation in healthy human volunteers Development and in vitro evaluation of an oral floating matrix tablet formulation of diltiazem hydrochloride Release kinetics and up-take studies of model fluoroquinolones from carbomer hydrogels Therapeutic applications of implantable drug delivery systems DDSolver: an add-in program for modeling and comparison of drug dissolution profiles Modeling and comparison of dissolution profiles Vehicle Design for a New Tropical Steroid, Fluocinonide Mathematical models of skin permeability: an overview Modeling of supersaturated dissolution data. (-)-Hinokinin-loaded poly(D,-lactide-co-glycolide) microparticles for Chagas disease. Hydrocortisone Diffusion Through Synthetic Membrane, Mouse Skin, and Epiderm™ Cultured Skin Novel mathematical method for quantitative expression of deviation from the higuchi model Effects of Polyoxypropylene 15 Stearyl Ether and Propylene Glycol on Percutaneous Penetration Rate of DiflorasoneDiacetate Drug physical state and drug-polymer interaction on drug release from chitosan matrix films Entrapment and release of quinoline derivatives using a hydrogel of a low molecular weight gelator Percutaneous Absorption Phospholipase A2-responsive antibiotic delivery via nanoparticle-stabilized liposomes for the treatment of bacterial infection Physicochemical characterization of hexetidine-impregnated endotracheal tube poly(vinyl chloride) and resistance to adherence of respiratory bacterial pathogens Encapsulation of docetaxel in oily core polyester nanocapsules intended for breast cancer therapy A thermosensitive chitosan-based hydrogel for the local delivery of paclitaxel In vitro release studies of piroxicam from oil-in-water creams and hydroalcoholic gel topical formulations Antimicrobial activity of silicone rubber used in hydrocephalus shunts, after impregnation with antimicrobial substances. A simple in vitro model to study the release kinetics of liposome encapsulated material Zero order drug delivery from double-layered porous films: release rate profiles from ethyl cellulose, hydroxypropyl cellulose and polyethylene glycol mixtures The in vitro release of some antimuscarinic drugs from monoolein/water lyotropic liquid crystalline gels Lidocaine loaded biodegradable nanospheres. II. Modelling of drug release PLGA-based microparticles: elucidation of mechanisms and a new, simple mathematical model quantifying drug release. Evaluation of transcutol as a clonazepam transdermal permeation enhancer from hydrophilic gel formulations K88 Fimbrial Adhesin Targeting of Microspheres Containing Gentamicin Made with Albumin Glycated with Lactose Real time in vitro studies of doxorubicin release from PHEMA nanoparticles Terminalia gum as a directly compressible excipient for controlled drug delivery Gastroretentive drug delivery system of ranitidine hydrochloride: formulation and in vitro evaluation Studies on rifampicin release from ethylcellulose coated nonpareil beads The effect of rheological behaviour of a topical anaesthetic formulation on the release and permeation rates of the active compound Preparation and comparative clinical evaluation of liposomal gel of benzoyl peroxide for acne. Synthetic hydrogels as drug delivery systems Long-term sustained release of ganciclovir from biodegradable scleral implant for the treatment of cytomegalovirus retinitis Dissolution testing of acetylsalicylic acid by a channel flow method-correlation to USP basket and intrinsic dissolution methods Compressed matrix core tablet as a quick/slow dual-component delivery system containing ibuprofen Relationship between swelling, erosion and drug release in hydrophillic natural gum mini-matrix formulations An alternative method to the evaluation of similarity factor in dissolution testing Solution-Solubility Dependency of Controlled Release of Drug from Polymer Matrix: Mathematical Analysis Hydrogel containing nanoparticle-stabilized liposomes for topical antimicrobial delivery A mucoadhesive in situ gel delivery system for paclitaxel The power law can describe the 'entire' drug release curve from HPMC-based matrix tablets: a hypothesis. Formulation of controlled-release baclofen matrix tablets: influence of some hydrophilic polymers on the release rate and in vitro evaluation Enhanced Controlled Transdermal Delivery of Mexazolam Using Ethylene-vinyl Acetate. In vitro evaluation of sustained drug release from biodegradable elastomer Microstructure and release characteristics of the minipellet, a collagen-based drug delivery system for controlled release of protein drugs Preclinical evaluation of thermoreversible triamcinolone acetonide hydrogels for drug delivery to the inner ear. The release and percutaneous permeation of anthralin products, using clinically involved and uninvolved psoriatic skin In vitro permeation profile of a local anaesthetic compound from topical formulations with different rheological behaviour--verified by in vivo efficacy data A general approach to describe the antimicrobial agent release from highly swellable films intended for food packaging applications. Guar gum, xanthan gum, and HPMC can define release mechanisms and sustain release of propranolol hydrochloride Influence of Shape Factors on Kinetics of Drug Release from Matrix Tablets I: Theoretical Evaluation of Lanolin Alcohol Films and Kinetics of Triamcinolone Acetonide Release

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