Results 21 to 30 of about 5,586,070 (250)

3DP Printing of Oral Solid Formulations: A Systematic Review

Pharmaceutics, 2021
Three-dimensional (3D) printing is a recent technology, which gives the possibility to manufacture personalised dosage forms and it has a broad range of applications.
Chiara R. M. Brambilla, Ogochukwu Lilian Okafor-Muo, Hany Hassanin, Amr ElShaer   +3 more
doaj   +1 more source

The Role of Oral Controlled Release Matrix Tablets in Drug Delivery Systems [PDF]

, 2012
Formulations that are able to control the release of drug have become an integral part of the pharmaceutical industry. In particular oral drug delivery has been the focus of pharmaceutical research for many years.
Raja, Shaista, Ali Nokhodchi, Shaista Raja, Pryia Patel, Asare-Addo, Kofi, Patel, Pryia, Kofi Asare-Addo, Shaista Raja (16203524), Nokhodchi, Ali, Priya Patel (679595), Ali Nokhodchi (4465915), Kofi Asare-Addo (4172488)   +11 more
core   +1 more source

Rational dispensing of oral dosage forms of medicines to children at a teaching hospital in Sri Lanka

BMC Health Services Research, 2020
Background Good dispensing practice is vital for rational use of medicines. There are many paediatric specific challenges when maintaining good dispensing practices to children.
Abarna Nadeshkumar, Gitanjali Sathiadas, Shalini Sri Ranganathan   +2 more
doaj   +1 more source

Importance of Appropriate Medication Administration in Patients with Nasogastric Feeding Tube

Journal of Pharmaceutical Research, 2023
Solid dosage forms like modified release and enteric coated formulations are considered inappropriate for nasogastric feeding tube (NGFT) administration due to varying pharmacokinetics which could lead to inadequate therapeutic responses or ...
L A Pradeep Rajkumar, Sujith J Chandy, Heber Rew Bright, V J Hema Jiji, Judith Basker, K Gunaraj   +5 more
doaj   +1 more source

Biowaiver monographs for immediate release solid oral dosage forms: prednisolone. [PDF]

, 2007
Literature data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage forms containing prednisolone are reviewed.
Barends, D M, Midha, K K, Stavchansky, S, Shah, V P, Vogt, M, Derendorf, H, Junginger, HE, Midha, KK, Shah, VP, Dressman, JB, Dressman, J B, Krämer, J, Barends, DM, Junginger, H E   +13 more
core   +1 more source

Consumer Preferences and Perceptions towards the use Colored Oral Solid Dosage Forms in Baghdad [PDF]

Archives of Pharmacy Practice, 2010
Objective: The main aims of this study were to determine consumers’ preferences and perceptions in Baghdad towards the color of Oral Solid Dosage Form.Materials and Methods: A cross sectional study was conducted using a self–administered questionnaire. A
Inas Rifaat Ibrahim,*, Mohamed Izham M.I & Mahmoud Al-Haddad
doaj   +2 more sources

Herbal medicinal products in the treatment of pain as a symptom of osteoarthritis [PDF]

Arhiv za farmaciju, 2016
Herbal medicinal products which are used perorally in the treatment of minor articular pain include those obtained from willow bark, Salicis cortex, devil's claw root, Harpagophyti radix, nettle leaf and herb, Urticae folium/herba, meadowsweet flower and
Maksimović Zoran, Samardžić Stevan
doaj   +1 more source

Comparing Multi-Label Classification Methods for Provisional Biopharmaceutics Class Prediction. [PDF]

, 2014
The biopharmaceutical classification system (BCS) is now well established and utilized for the development and biowaivers of immediate oral dosage forms. The prediction of BCS class can be carried out using multilabel classification.
Taravat Ghafourian, Ghafourian, Taravat, Danielle Newby (1695076), Newby, D., Danielle Newby, Taravat Ghafourian (4466557), Alex Freitas (3762685), Freitas, Alex A., Alex. A. Freitas   +8 more
core   +1 more source

A Survey of the Regulatory Requirements for the Waiver of In Vivo Bioequivalence Studies of Generic Products in Certain Dosage Forms by Participating Regulators and Organisations of the International Pharmaceutical Regulators Programme

Journal of Pharmacy & Pharmaceutical Sciences, 2021
The requirements to waive in vivo bioequivalence studies for immediate release solid oral dosage forms based on the Biopharmaceutics Classifications System (BCS) are well known, and biowaivers[1] for other types of oral dosage forms based on pre-defined ...
Alfredo Garcia Arieta, Craig Simon, Andrew Tam, Gustavo Mendes Lima Santos, Eduardo Agostinho Freitas Fernandes, Zulema Rodríguez Martínez, Clare Rodrigues, Sang Aeh Park, JaYoung Kim, Kwansoo Kim, Ryosuke Kuribayashi, Aya Myoenzono, Kohei Shimojo, Chantal Walther, Matthias S. Roost, Wen-Yi Hung, Li-feng Hsu, Christopher Crane, April C. Braddy, Joy van Oudtshoorn, Diego Alejandro Gutierrez Triana, Erwin Guzmán Aurela, Ben Jones, Henrike Potthast, Ivana Abalos   +24 more
doaj   +1 more source

Oral medicines for children in the European paediatric investigation plans. [PDF]

PLoS ONE, 2014
INTRODUCTION: Pharmaceutical industry is no longer allowed to develop new medicines for use in adults only, as the 2007 Paediatric Regulation requires children to be considered also.
Diana A van Riet-Nales, Erwin G A W Römkens, Agnes Saint-Raymond, Piotr Kozarewicz, Alfred F A M Schobben, Toine C G Egberts, Carin M A Rademaker   +6 more
doaj   +1 more source