Drug Delivery System
Mostrando 13-24 de 226 artigos, teses e dissertações.
-
13. Synthesis of ordered mesoporous silica MCM-41 with controlled morphology for potential application in controlled drug delivery systems
Resumo O MCM-41 é uma das cerâmicas mesoporosas mais estudadas para sistemas de liberação controlada de fármacos. Sua elevada área superficial específica e mesoporosidade permitem alta capacidade de adsorção. Apesar dos inúmeros trabalhos publicados na área biomédica, até o presente momento não há relatos de aplicações comerciais do MCM-41.
Cerâmica. Publicado em: 06/06/2019
-
14. Drug use in delivery hospitalization: Pelotas births cohort, 2015
RESUMO OBJETIVO: Identificar o padrão de uso dos medicamentos durante a internação para o parto. MÉTODO: Estudo transversal realizado de junho a outubro de 2015, inserido na coorte de nascimentos de Pelotas de 2015. Todas as mulheres residentes na zona urbana da cidade que foram internadas para o parto fizeram parte da amostra. Foram coletadas informa�
Rev. Saúde Pública. Publicado em: 30/05/2019
-
15. Carregamento e caracterização do fármaco carboplatina na microestrutura microporosa do biomaterial granulado bifásico micro e nanoestruturado de fosfato de cálcio
RESUMO As biocerâmicas bifásicas hidroxiapatita/fosfato tricálcico-beta (HA/TCP-β) microporosas são pesquisadas e se destacam em aplicações biomédicas como substitutos dos tecidos ósseos. Estes biomateriais são biocompatíveis e apresentam microestruturas microporosas interconectadas, que permitem sua utilização no reparo do tecido ósseo. Devido
Matéria (Rio J.). Publicado em: 20/05/2019
-
16. Preparation and physicochemical characterization of prazosin conjugated PLGA nanoparticles for drug delivery of flutamide
In the current work, a sustained drug delivery system of flutamide (FLT) was developed using Poly(D,L-lactide-co-glycolide) (PLGA) decorated bypoly(ethylene glycol) (PEG) grafted prazosin (PLGA-PEG-Praz) as a targeting moiety. In a multi-step reaction, PLGA was linked to PEG and prazosin. The structure of the synthesized polymers was confirmed by FTIR and 1H
Braz. J. Pharm. Sci.. Publicado em: 08/04/2019
-
17. Development and evaluation of multiparticulate biphasic system for the treatment of circadian diseases
Multiparticulate systems have biopharmaceutical advantages when compared to the monolithic systems, once they allow different patterns of drug release and can be used in different treatments. The aim of the present work was to develop a biphasic controlled release delivery system, using propranolol hydrochloride (PROP) that can be used for the treatment of c
Braz. J. Pharm. Sci.. Publicado em: 08/04/2019
-
18. Influence of different formulation variables on the performance of transdermal drug delivery system containing tizanidine hydrochloride: in vitro and ex vivo evaluations
The present study was aimed at preparation of transdermal patches of tizanidine HCl, evaluation of the effect of polymers on in vitro release pattern of the drug, and the effect of permeation enhancers on the penetration of the drug through the rabbit skin. Various proportions of hydrophilic (HPMC) and hydrophobic (Eudragit L-100) polymers were used with PEG
Braz. J. Pharm. Sci.. Publicado em: 08/04/2019
-
19. Physicochemical Characterizations and Antioxidant Property of Copaiba Oil Loaded into SNEDDS Systems
Self-nanoemulsion drug delivery systems (SNEDDS) represent a potential carrier to improve solubility and bioavailability of health care products. In this sense, copaiba oil (CO) loaded on cosurfactant-free SNEDDS formulations (CO-SNEDDS) were obtained by using phase diagram performed on different concentrations of constituents (oil, surfactant and water). Th
J. Braz. Chem. Soc.. Publicado em: 2019-02
-
20. Matéria Evaluation of zinc oxide nanoparticles influence on hydrophilic polymer matrix systems
ABSTRACT Hydrophilic polymer matrix systems (HPMSs) are a highly relevant tool for drugs delivery whose bioavailability is impaired by low hydrosolubility. Besides this, when associated with nanoparticles these systems can provide better control over release profile of the active drug, maintaining the posology. Since polyvinylpyrrolidone (PVP) and zinc oxide
Matéria (Rio J.). Publicado em: 06/12/2018
-
21. Acute toxicity study of a polysaccharide based hydrogel from linseed for potential use in drug delivery system
ABSTRACT Linseed hydrogel (LSH) was evaluated by acute toxicity for its potential application in oral drug delivery design. White albino mice and rabbits were divided in four groups (I-IV) and different doses of LSH (1, 2 and 5 g/kg body weight) were given except to the control group (I) that was left untreated. Rabbits were monitored for eye irritation, acu
Braz. J. Pharm. Sci.. Publicado em: 26/07/2018
-
22. Antinociceptive local effect of the combination of dexketoprofen trometamol and chlorhexidine gluconate in a formalin test: an additive effect
ABSTRACT A drug delivery system (DDS) with analgesic and antibacterial properties would be desirable for the local control of post-operatory pain and the prevention for surgical site infection (SSI). The objective of the present study was to evaluate the antinociceptive effect of the combination between dexketoprofen trometamol (DXT) and chlorhexidine glucon
Braz. J. Pharm. Sci.. Publicado em: 26/07/2018
-
23. Preparation, characterization, and antiproliferative activities of biotin-decorated docetaxel-loaded bovine serum albumin nanoparticles
ABSTRACT The aim of the present study was to characterize biotin-decorated docetaxel-loaded bovine serum albumin nanoparticles (DTX-BIO-BSA-NPs) and evaluate their antiproliferative activity in vitro. The particle size of prepared DTX-BIO-BSA-NPs was found to be always lower than 200 nm, with sizes of 166.9, 160.3, 159.0, 176.1 and 184.8 nm and the zeta pote
Braz. J. Pharm. Sci.. Publicado em: 26/07/2018
-
24. Development of self-nanoemulsifying tablet (SNET) for bioavailability enhancement of sertraline
Abstract The purpose of the study was to combine the advantages of self-nanoemulsifying drug delivery systems and tablets as a conventional dosage form. Self-nanoemulsifying drug delivery system (SNEDDS) was prepared to enhance the solubility and thus oral bioavailability of sertraline. Aqueous titration method was used to prepare the liquid SNEDDS; ternary
Braz. J. Pharm. Sci.. Publicado em: 07/06/2018