Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Ross A. KENNEDY"'
Publikováno v:
Pharmaceutics, Vol 13, Iss 7, p 974 (2021)
Context: Overcoming the intestinal mucosal barrier can be a challenge in drug delivery. Nanoemulsions with negative zeta potentials can effectively permeate the mucus layer, but those with positive zeta potentials are better taken up by cells; a nano
Externí odkaz:
https://doaj.org/article/0764389c79704f32a113cb00e2e06a9f
Publikováno v:
Indonesian Journal of Pharmacy. :353-365
Patients in intensive care units have a critical problem with Intravenous (IC) drug administration. The effort to decrease incompatibility or manage the incompatibility risks is paramount significant to reduce morbidity and mortality. This review col
Publikováno v:
Journal of Research in Pharmacy. 26:1955-1959
Autor:
Ross A. Kennedy
Publikováno v:
First World War Studies. :1-2
Autor:
Aamir Jalil, Ahmad Malkawi, Barbara Matuszczak, Andreas Bernkop-Schnürch, Imran Nazir, Ross A. Kennedy
Publikováno v:
Molecular Pharmaceutics
The aim of this study was to develop hydrophobic ionic drug polymer complexes in order to provide sustained drug release from self-emulsifying drug delivery systems (SEDDS). Captopril (CTL) was used as an anionic model drug to form ionic complexes wi
Autor:
Ross A. Kennedy
Publikováno v:
A Companion to U.S. Foreign Relations
Autor:
Ross S. Kennedy
Publikováno v:
The Journal of Ecclesiastical History. 73:871-872
Publikováno v:
Pharmaceutics
Volume 13
Issue 7
Pharmaceutics, Vol 13, Iss 974, p 974 (2021)
Volume 13
Issue 7
Pharmaceutics, Vol 13, Iss 974, p 974 (2021)
Context: Overcoming the intestinal mucosal barrier can be a challenge in drug delivery. Nanoemulsions with negative zeta potentials can effectively permeate the mucus layer, but those with positive zeta potentials are better taken up by cells
a
a
Autor:
Ross A. Kennedy
Publikováno v:
The Journal of Interdisciplinary History. 53:360-361
Publikováno v:
Journal of Pharmaceutical Sciences.
The mucolytic function of N-acetylcysteine (NAC) is necessary for the diffusion of mucoactive self-nanoemulsifying drug delivery systems (SEDDS) through the intestinal mucus gel layer. NAC instantly released from SEDDS leads to nonsignificant mucolyt