نتایج جستجو برای: drug loading

تعداد نتایج: 660466  

2014
María Alba Pilar Formentín Josep Ferré-Borrull Josep Pallarès Lluís F Marsal

We report on the fabrication of polyelectrolyte multilayer-coated hollow silicon dioxide micropillars as pH-responsive drug delivery systems. Silicon dioxide micropillars are based on macroporous silicon formed by electrochemical etching. Due to their hollow core capable of being loaded with chemically active agents, silicon dioxide micropillars provide additional function such as drug delivery...

Journal: :Circulation 2005
Nicolas von Beckerath Dirk Taubert Gisela Pogatsa-Murray Edgar Schömig Adnan Kastrati Albert Schömig

BACKGROUND For patients undergoing percutaneous coronary intervention, the administration of a clopidogrel loading dose ranging from 300 to 600 mg is currently recommended. It is unknown, though, whether loading doses higher than 600 mg exert additional suppression of platelet function. METHODS AND RESULTS Sixty patients with suspected or documented coronary artery disease admitted to our hos...

Objective(S): In this work, paclitaxel (PX), a promising anticancer drug, was loaded in the basil seed mucilage (BSM) aerogels by implementation of supercritical carbon dioxide (SC-CO2) technology. Then, the effects of operating conditions were studied on the PX mean particle size (MPS), particle size distribution (PSD) and drug loading efficiency (DLE). <stron...

2006
M. Agüeros M. A. Campanero J. M. Irache

Introduction Oral delivery is the most convenient and desired way for drug delivery. The major factor determinant for bioavailability of orally administered drug is the membrane permeability and drug solubility in the intestinal lumen. Many drugs show bioavailability problems due to their low water solubility, slow dissolution rate and instability in the gastrointestinal tract. One possibility ...

2010
M. Agüeros M. A. Campanero J. M. Irache

Oral delivery is the most convenient and desired way for drug delivery. The major factor determinant for bioavailability of orally administered drug is the membrane permeability and drug solubility in the intestinal lumen. Many drugs show bioavailability problems due to their low water solubility, slow dissolution rate and instability in the gastrointestinal tract. One possibility to enhance dr...

Journal: :Acta biomaterialia 2012
Danya M Lavin Robert M Stefani Linda Zhang Stacia Furtado Richard A Hopkins Edith Mathiowitz

The strength and stability of hybrid fiber delivery systems, ones that perform a mechanical function and simultaneously deliver drug, are critical in the design of surgically implantable constructs. We report the fabrication of drug-eluting microfibers where drug loading and processing conditions alone increase microfiber strength and stability partially due to solvent-induced crystallization. ...

Journal: :Journal of controlled release : official journal of the Controlled Release Society 2006
Igor V Zhigaltsev Norbert Maurer Katarina Edwards Göran Karlsson Pieter R Cullis

The development of procedures to enhance drug retention in liposomes is important in order to achieve therapeutically optimized rates of drug release from liposomal carriers. In this study, the ability of lipophilic weak base drugs to complex with arylsulfonates resulting in formation of intravesicular precipitates is investigated as a means to enhance drug retention. It is shown that the aryls...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2005
Tariq Ashraf Munir Ahmed M Saeed Talpur Asadullah Kundi Azhar Masood A Faruqui Abdul Hafeez Jaffery Aslam Fareed

OBJECTIVE The primary objective of this study was to test the hypothesis that the antiplatelet effects of loading dose of locally manufactured clopidogrel Lowplat referred as drug (B) 600 mg (8 tablets) given once is comparable to the antiplatelet effects of loading dose of foreign manufactured clopidogrel Plavix referred as drug (A) 600 mg (8 tablets) given once in patients with suspected isch...

2011
G. Devanand Venkatasubbu S. Ramasamy V. Ramakrishnan J. Kumar

In bone disorders infections are common. The concentration of majority of antibiotics is very low in the bone tissue. A high local dose can be obtained from the ciprofloxacin-loaded hydroxyapatite nanoparticles. The present study is aimed at developing the use of hydroxyapatite and zinc-doped hydroxyapatite nanoparticles as a carrier for ciprofloxacin drug delivery system. The ciprofloxacin-loa...

2017
Liwei Tan Jinrong Peng Qian Zhao Lan Zhang Xichuan Tang Lijuan Chen Minyi Lei Zhiyong Qian

Satisfactory drug loading capacity and stability are the two main factors that determine the anti-cancer performance. In general, the stability of the micelles is reduced when the drug loading (DL) is increased. Therefore, it was a challenge to have high drug loading capacity and good stability. In this study, we introduced a hydrophilic poly (L-Lysine) (PLL) segment with different molecular-we...

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