Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Modified Release Dosage Form"'
Autor:
Senthilkumar Murugesan, Veera Venkata Satyanarayana Reddy Karri, Kaviarasan Lakshmanan, B. Gowramma, Arun Radhakrishnan
Publikováno v:
Current Drug Research Reviews. 12:16-25
Oral drug delivery is the most widely utilized route of administration among all the routes that have been explored for systemic delivery of drugs via pharmaceutical products of different dosage form and this oral route provides maximum active surfac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf72d1500223738463b001af238eecba
https://doi.org/10.2174/2589977511666191121094520
https://doi.org/10.2174/2589977511666191121094520
Publikováno v:
Journal of Pharmaceutical Innovation. 16:419-438
The present study was aimed to formulate and evaluate fast-disintegrating tablets (FDTs) having Flurbiprofen (FP) and Metoclopramide HCl (MHCl) in combination. Direct compression was used to formulate FDTs of FP and MHCl as a combination regimen in s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e188fd2730f6057836b099e26f31e3f7
https://doi.org/10.1007/s12247-020-09455-z
https://doi.org/10.1007/s12247-020-09455-z
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Relatório de Estágio do Mestrado Integrado em Ciências Farmacêuticas apresentado à Faculdade de Farmácia Atualmente a indústria farmacêutica passou por uma grande revolução, nomeadamente devido ao avanço do conhecimento em tecnologia farma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::03db31bf7944e61443941234872f3eb5
Gastro-retentive oral drug delivery systems: a promising approach for narrow absorption window drugs
Publikováno v:
Journal of advanced Biomedical and Pharmaceutical Sciences.
Drugs with narrow absorption window (NAW) are those drugs that are absorbed from a specific region (most notably first part) of the gastrointestinal tract. Therefore, typical modified/sustained release formulations of those drugs cannot provide a tru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c328a6b4649bbd50bce6fcf2ad8657f
https://doi.org/10.21608/jabps.2019.11357.1042
https://doi.org/10.21608/jabps.2019.11357.1042
Autor:
Saqiba Zulfiqar, Muhammad Jamshaid, Irfan Bashir, Muhammad Bilal Hassan Mahboob, Tehseen Riaz
Publikováno v:
International Current Pharmaceutical Journal. 5:111-117
In the late 1970s, rapid disintegrating drug delivery system was developed as an alternative to capsules, tablets and syrups for geriatric and pediatric patients having problems in swallowing. To overcome the need, number of orally disintegrating tab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff15f628d072c3700422faf473459467
https://doi.org/10.3329/icpj.v5i12.30413
https://doi.org/10.3329/icpj.v5i12.30413
Publikováno v:
AAPS Introductions in the Pharmaceutical Sciences ISBN: 9783030317447
This chapter presents an extensive overview of the concepts of delayed-release, sustained-release, and pulsatile-release for drug delivery. Formulation approaches and delivery technologies are discussed in detail, along with the required performance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45595e92cad9ae66f2a98220225f2a9d
https://doi.org/10.1007/978-3-030-31745-4_4
https://doi.org/10.1007/978-3-030-31745-4_4
Autor:
Mohammed S. Jabbar, Yehia I. Khalil
Publikováno v:
Iraqi Journal of Pharmaceutical Sciences, Vol 19, Iss 1 (2017)
Metoprolol is a β1 adrenergic blocker used in treatment of heart diseases. Metoprolol (100mg) tablets was formulated as a modified release oral system utilizing the concept of bilayer system, first layer contained (30mg) as immediate release and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58c5d185a602df2581b236ed16bdd582
https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/185
https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/185
Autor:
Constantinos Markopoulos, Xavier Pepin, Maria Vertzoni, Jennifer B. Dressman, Cord J. Andreas, Christos Reppas
Publikováno v:
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences. 102
When administered orally as either an immediate or modified release dosage form, zolpidem demonstrates a negative food effect, i.e. decrease in CPharmacokinetic profiles of zolpidem are presented from a bioavailability (8mg intravenous; 10mg immediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::211623e90806b77463ebf27ab855b3c6
https://pubmed.ncbi.nlm.nih.gov/28286289
https://pubmed.ncbi.nlm.nih.gov/28286289
Publikováno v:
Colloids and Surfaces B: Biointerfaces. 89:182-187
Zolpidem tartarate is a non-benzodiazepine, sedative-hypnotic, which finds its major use in various types of insomnia. The present work relates to development of multiparticulate floating drug delivery system based on gas generation technique to prol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeeb50586ecfe77fd0f865890a67e89b
https://doi.org/10.1016/j.colsurfb.2011.09.011
https://doi.org/10.1016/j.colsurfb.2011.09.011
Autor:
Stephan Maus, Oliver Thews, Nicole Bausbacher, Peter Langguth, Eva Hühn, Mathias Schreckenberger, Frank Rösch, Gamal A. Shazly, Hans-Georg Buchholz
Publikováno v:
European Journal of Pharmaceutical Sciences. 41:71-77
This study aimed to predict the in vivo performance from the in vitro release of a low-molecular weight model compound, [(18)F]-2-fluoro-2-deoxy-d-glucose ([(18)F]FDG), from liposomes and by means of positron emission tomography (PET). Liposomes comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aad5f04734f26bfa06fd7bd4dc43730a
https://doi.org/10.1016/j.ejps.2010.05.020
https://doi.org/10.1016/j.ejps.2010.05.020