Development and evaluation of pediatric orally disintegrating paracetamol tablets [PDF]
The limitations of commercially available paracetamol formulations specifically: 1)stability and portability (commercial paracetamol suspensions) and 2) non-pediatric friendly excipients and expensive manufacturing processes (commercially available ...
Ngugi, S.G., Nyamweya, N.N.M.
core +2 more sources
Design, formulation, and physicochemical evaluation of montelukast orally disintegrating tablet
Background: Orally disintegrating tablets (ODTs) are a modern form of tablets that when placed in the oral cavity, disperses rapidly. These tablets have advantages, particularly good applications for children and old patients who have a complication in ...
Abolfazl Aslani, Maryam Beigi
doaj +1 more source
Patient centric formulations for paediatrics and geriatrics: Similarities and differences [PDF]
Paediatrics and geriatrics both represent highly heterogenous populations and require special consideration when developing appropriate dosage forms. This paper discusses similarities, differences and considerations with respect to the development of ...
Ernest, TB +5 more
core +1 more source
Pengaruh Komposisi Campuran Fisik Crospovidone-Sodium Starch Glycolate (1:1, 1:2, dan 1:3) terhadap Karakteristik Fisikokimia Sediaan Tablet Orodispersible Atenolol [PDF]
Penggunaan tablet konvensional atenolol menimbulkan masalah dalam hal kepatuhan minum obat pada pasien geriatri. Hal ini disebabkan terjadinya perubahan fisiologis pada pasien geriartri seperti susah menelan dan tremor.
Parfati, Nani +2 more
core +2 more sources
Formulation and Evaluation of Loperamide HCl Oro Dispersible Tablets
This work proposes the design of novel oral disintegrating tablets (ODTs) of loperamide HCl with special emphasis on disintegration and dissolution studies. The main goal was augmenting the adherence to treatment of diseases which happen with diarrhea in
Blasco Alejandro +2 more
doaj +1 more source
Dissolution testing of orally disintegrating tablets
Abstract For industrially manufactured pharmaceutical dosage forms, product quality tests and performance tests are required to ascertain the quality of the final product. Current compendial requirements specify a disintegration and/or a dissolution test to check the quality of oral solid dosage forms.
Johannes, Kraemer +4 more
openaire +2 more sources
Abstract Background Pill‐swallowing difficulty is common yet under‐recognised, and patients rarely seek or receive support from healthcare professionals. Lubricating jelly pastes are widely available in Japan, yet evidence for their effectiveness in pill administration remains limited. The PILL‐5 enables validated, self‐reported screening of clinically
Yoko Inamoto +8 more
wiley +1 more source
Non-human tools for the evaluation of bitter taste in the design and development of medicines: a systematic review [PDF]
Taste evaluation is a crucial factor for determining acceptance of medicines by patients. The human taste panel test is the main method used to establish the overall palatability and acceptability of a drug product to a patient towards the end of ...
Ernest, T +3 more
core +2 more sources
Oral Disintegrating Tablets – An Updated Patent Perspective
Current Development in drug delivery system has been employed with an endeavour to enhance the bioavailability of the drug, mask its taste, induce the rapid onset of action and improve patient compliance. An alternative approach to the conventional dosage form is being employed to triumph over all these issues named as Orodispersible system. Over the
Shailesh Sharma, Kuljit Singh
openaire +3 more sources
Active packaging offers an effective approach to extending food shelf life. This review summarizes the past decade of progress in metal‐organic framework (MOF)‐based active food packaging, highlighting material selection, characterization, challenges, and future prospects.
Belladini Lovely +4 more
wiley +1 more source

