Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Manish Ghimire"'
Autor:
Stefania Marano, Manish Ghimire, Shahrzad Missaghi, Ali Rajabi-Siahboomi, Duncan Q. M. Craig, Susan A. Barker
Publikováno v:
Pharmaceutics, Vol 15, Iss 3, p 802 (2023)
Fibre-based oral drug delivery systems are an attractive approach to addressing low drug solubility, although clear strategies for incorporating such systems into viable dosage forms have not yet been demonstrated. The present study extends our previ
Externí odkaz:
https://doaj.org/article/6f11552e4240407b8c625e3eaf1e9e00
Publikováno v:
Journal of Nepal Medical Association, Vol 59, Iss 234 (2021)
Introduction: Elderly population is more likely to suffer from malnutrition due to aging-associated factors that influence nutritional status like loss of appetite, swallowing difficulties, digestive problems, and chronic illness. There is insufficie
Externí odkaz:
https://doaj.org/article/60e067922bed4dbf8ebae76320c46446
Autor:
Manish Ghimire
Publikováno v:
British Journal of Pharmacy, Vol 2, Iss 2 (2018)
Raman microscopy was used to visualize the integrity of a barrier membrane coating at the various stage of chewable tablets development. The effect of substrate morphology and particle characteristics was found to be important in maintaining the inte
Externí odkaz:
https://doaj.org/article/46c4034e51a84044a5f89e19d298bd65
Autor:
Zarina Ali, Catherine Tuleu, Alexander Keeley, Mine Orlu, Manish Ghimire, Minyi Teo, John Frost, Ali R. Rajabi-Siahboomi
Publikováno v:
Molecular Pharmaceutics. 16:2095-2105
The majority of active pharmaceutical ingredients (APIs) are bitter. Therefore, compliance can be a problem where adequate taste masking has not been achieved; this is most problematic in pediatrics. Taste masking is thus a key stage during pharmaceu
Autor:
Ana Patricia Ferreira, Charles Vesey, Jane Lightfoot, Mike Tobyn, Elaine Martin, Ali R. Rajabi-Siahboomi, Manish Ghimire, Andrea Kasuboski-Freeman
Publikováno v:
Pharmaceutical development and technology. 23(10)
A key part of the Risk Assessment of excipients is to understand how raw material variability could (or does) contribute to differences in performance of the drug product. Here we demonstrate an approach which achieves the necessary understanding for
Autor:
Janet Band, Lee Ann Hodges, Bridget O'Mahony, Howard N.E. Stevens, Manish Ghimire, Alexander B. Mullen, Fiona J. McInnes
Publikováno v:
Journal of Controlled Release. 147:70-75
The purpose of this study was to evaluate and compare the in-vitro and in-vivo erosion profiles of two tablet formulations primarily consisting of hydroxypropylmethylcellulose (HPMC) and lactose. HPMC was used at concentrations below and above the re
Publikováno v:
European Journal of Pharmaceutics and Biopharmaceutics. 67:515-523
The aim of the current study was to investigate the in-vitro and in-vivo performance of a press-coated tablet (PCT) intended for time delayed drug release, consisting of a rapidly disintegrating theophylline core tablet, press-coated with barrier gra
Autor:
Marano, Stefania1 (AUTHOR), Ghimire, Manish2 (AUTHOR), Missaghi, Shahrzad2 (AUTHOR), Rajabi-Siahboomi, Ali2 (AUTHOR), Craig, Duncan Q. M.1 (AUTHOR), Barker, Susan A.1 (AUTHOR) s.barker@greenwich.ac.uk
Publikováno v:
Pharmaceutics. Mar2023, Vol. 15 Issue 3, p802. 28p.
Autor:
Manish Ghimire
Raman microscopy was used to visualize the integrity of a barrier membrane coating at the various stage of chewable tablets development. The effect of substrate morphology and particle characteristics was found to be important in maintaining the inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee2c1305bac61a14e7e312d1a7a377f9
Autor:
Tobyn, Mike1 mike.tobyn@bms.com, Ferreira, Ana Patricia1, Lightfoot, Jane2, Martin, Elaine B.2, Ghimire, Manish3, Vesey, Charles4, Kasuboski-Freeman, Andrea5, Rajabi-Siahboomi, Ali4
Publikováno v:
Pharmaceutical Development & Technology. Dec2018, Vol. 23 Issue 10, p1146-1155. 10p.