نتایج جستجو برای: encapsulating

تعداد نتایج: 3757  

Background: Eptifibatide (Integrilin) is an intravenous (IV) peptide drug that selectively inhibits ligand binding to the platelet GP IIb/IIIa receptor. It is an efficient peptide drug, however has a short half-life. Therefore, antithrombotic agents like eptifibatide are required to become improved with a protected and targeted delivery system such as using nano-liposomes to the site of thrombu...

Asmita Gajbhiye, Naina Dubey, Sapna Patel, Shailendra Patil,

Carvedilol (CVD) is an antihypertensive agent with a short half-life, pH-dependent solubility, and narrow absorption window. The purpose of this research was to prepare a floating-drug delivery-system of carvedilol to increase its half-life. The present study investigates the preparation of carvedilol-floating microspheres, evaluates the floating-drug delivery-system (FDDS) (by scanning electro...

1995
Dirk Riehle

In: Pattern Languages of Programm Design 2. Chapter 6. Edited by John M. Vlissides, James O. Coplien and Norman L. Kerth. Reading, Massachusetts: Addison-Wesley, 1996. Good object-oriented design firmly relies on abstract classes. They define the interface to work with subclasses that implement them. If clients directly name these subclasses, they become dependent on them. This complicates both...

Journal: :International Journal of Nanomedicine 2007
Rohan Bhavane Efstathios Karathanasis Ananth V Annapragada

Nanostructured agglomerated vesicles encapsulating ciprofloxacin were evaluated for modulated delivery from the lungs in a healthy rabbit model. An aliphatic disulfide crosslinker, cleavable by cysteine was used to form cross-links between nanosized liposomes to form the agglomerates. The blood levels of drug after pulmonary instillation of free ciprofloxacin, liposomal ciprofloxacin, and the a...

2015
Neha N Parayath Hayley Nehoff Philipp Müller Sebastien Taurin Khaled Greish

Drug delivery systems could potentially overcome low bioavailability and gastrointestinal toxicity, which are the major challenges for the development of oral anticancer drugs. Herein, we demonstrate the ability of styrene maleic acid (SMA) nanomicelles encapsulating epirubicin to traverse in vitro and ex vivo models of the intestinal epithelium without affecting the tissue integrity. Further, ...

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