نتایج جستجو برای: among powder formulations

تعداد نتایج: 1234364  

M Motavali Emami M Yazdi MA Nilforoosh Zadeh

Background: Increasing in the prevalence of pediculosis among school students and upward trend of pesticide marketing with evidence of resistance to them, indicate the possibility of lice resistance. Objective: To compare 3 drug formulations including: Lindan shampoo 1%, permethrin shampoo 1% and Copex powder 0.5% in the treatment of head lice infestation. Patients and Methods: Ninety stu...

Journal: :Clinical and vaccine immunology : CVI 2009
Joanne Huang Ajit J D'Souza Jason B Alarcon John A Mikszta Brandi M Ford Matthew S Ferriter Michelle Evans Todd Stewart Kei Amemiya Robert G Ulrich Vincent J Sullivan

The potential use of Yersinia pestis as a bioterror agent is a great concern. Development of a stable powder vaccine against Y. pestis and administration of the vaccine by minimally invasive methods could provide an alternative to the traditional liquid formulation and intramuscular injection. We evaluated a spray-freeze-dried powder vaccine containing a recombinant F1-V fusion protein of Y. pe...

2010
Thatiana TERROSO Irene C. KÜLKAMP Denise S. JORNADA Adriana R. POHLMANN Sílvia S. GUTERRES

Nanocapsule suspensions containing coenzyme Q10 were prepared by interfacial deposition. The nanocapsules showed characteristics compatible with dermal application: slightly acid pH, drug content close to 100%, particle size between 213 and 248 nm with low polydispersity and negative zeta potential. Three cosmetic formulations for skin application were developed, one with the free-coenzyme Q10,...

Journal: :nanomedicine journal 0
eskandar moghimipour nanotechnology research center, jundishapur university of medical sciences, ahvaz, iran department of pharmaceutics, school of pharmacy, jundishapur university of medical sciences, ahvaz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی جندی شاپور اهواز (ahvaz jundishapur university of medical sciences) anayatollah salimi nanotechnology research center, jundishapur university of medical sciences, ahvaz, iran department of pharmaceutics, school of pharmacy, jundishapur university of medical sciences, ahvaz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی جندی شاپور اهواز (ahvaz jundishapur university of medical sciences) hassan dagheri department of pharmaceutics, school of pharmacy, jundishapur university of medical sciences, ahvaz, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی جندی شاپور اهواز (ahvaz jundishapur university of medical sciences)

objective(s): the purpose of the present study was to prepare and to evaluate a novel niosome as transdermal drug delivery system for propranolol hydrochloride and to compare the in vitro efficiency of niosome by either thin film hydration or hand shaking method. materials and methods: niosomes were prepared by thin film hydration (tfh) or hand shaking (hs) method. propranolol niosomes were pre...

2012
Sergey V. Dorozhkin

In early 1980s, researchers discovered self-setting calcium orthophosphate cements, which are a bioactive and biodegradable grafting material in the form of a powder and a liquid. Both phases after mixing form a viscous paste that after being implanted sets and hardens within the body as either a non-stoichiometric calcium deficient hydroxyapatite (CDHA) or brushite, sometimes blended with un-r...

2011
Y. A. Batta

Formulations of Metarhizium anisopliae conidia with oven ash, chalk powder, charcoal and wheat flour at a ratio of 1:4 (W/W) were prepared. Formulations containing charcoal and oven ash had a conidial viability half-life of 4.1–4.3 months at 2071!C. In comparison, unformulated conidia held under the same conditions had a viability half-life of 0.9 month. Bioassays carried out at 2872!C and 7075...

2015
Nilesh S Kulkarni Nisharani S Ranpise Govind Mohan

Purpose: To develop rosuvastatin calcium-loaded self-nanoemulsifying powder for improved oral delivery of the drug. Methods: Solubility study was carried out in different oils, surfactants and co-surfactants. Based on the solubility study, liquid formulations were prepared using LAS/Capryol 90: Maisine 35-1 as oil phase and Tween 20 with Lutrol E400 as surfactant mixture (Smix). The liquid form...

2014
Mohamed A. Etman Mona Gamal Aly H. Nada Mohamed A. Shams-Eldeen

Article history: Received on: 13/08/2014 Revised on: 09/09/2014 Accepted on: 15/10/2014 Available online: 27/11/2014 Desloratadine (DS) is a tricyclic antihistaminic, characterized by bitter taste and slight water solubility. The aim of this study is to prepare DS as orally disintegrating tablets (ODT) to mask the bitter taste and improve compliance. Twelve different placebo ODT (F1-F12) were p...

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