Innovations in chewable formulations: the novelty and applications of 3D printing in drug product design

L Rodríguez-Pombo, A Awad, AW Basit… - Pharmaceutics, 2022 - mdpi.com
Since their introduction, chewable dosage forms have gained traction due to their ability to
facilitate swallowing, especially in paediatric, geriatric and dysphagia patients. Their benefits …

[PDF][PDF] A REVIEW ON: FLOATING DRUG DELIVERY SYSTEM

VS Vasave - World Journal of Pharmaceutical …, 2023 - wjpr.s3.ap-south-1.amazonaws.com
Floating drug delivery systems (FDDS) have a lower bulk density than gastric fluids,
consequently they float in the stomach for longer decades of time without altering the gastric …

A multivariate data analysis approach to tablet sticking on an industrial scale: a qualitative case study of an ibuprofen-based formulation

M Dembélé, S Hudon, JS Simard… - Pharmaceutical …, 2022 - Taylor & Francis
Objectives Sticking is one of the most common and damaging issues that occur during tablet
manufacturing. Sticking is the adhesion of powder onto tooling surfaces during compression …

Polyethylene oxide and its controlled release properties in hydrophilic matrix tablets for oral administration

JD Vanza, RB Patel, RR Dave… - Pharmaceutical …, 2020 - Taylor & Francis
Polymers are excipients that modify the rate of drug release from pharmaceutical dosage
forms. Hydrophilic polymer-based controlled drug delivery system is more advantageous as …

Role of cyclodextrins and drug solid state properties on flufenamic acid dissolution performance from tablets

F Maestrelli, M Cirri, E De Luca, D Biagi, P Mura - Pharmaceutics, 2022 - mdpi.com
Flufenamic acid (FFA) is a non-steroidal anti-inflammatory drug characterised by a low
solubility and problems of variable dissolution rate and bio-inequivalence. Different FFA …

[PDF][PDF] Rosuvastatin-Excipient Compatibility Studies for Advanced Drug delivery Systems Development

MM Alburyhi, MA Noman, AA Saif… - World Journal of …, 2024 - researchgate.net
The safety, efficacy, quality and stability of a formulation are major concepts of any API
development process. In API development process, a detailed characterization of the API …

[PDF][PDF] Diclofenac-Excipient Compatibility Studies for Advanced Drug delivery Systems Development

MM Alburyhi, MA Noman, AA Saif… - World Journal of …, 2024 - academia.edu
WORLD JOURNAL OF PHARMACEUTICAL RESEARCH Page 1 Alburyhi et al. World Journal of
Pharmaceutical Research www.wjpr.net │ Vol 13, Issue 14, 2024. │ ISO 9001: 2015 Certified …

Characterization and evaluation of the performance of different calcium and magnesium salts as excipients for direct compression

P Mura, M Valleri, S Baldanzi, N Mennini - International journal of …, 2019 - Elsevier
The performance of a series of inorganic salts as direct compression excipients was
systematically evaluated. The physical-chemical and technological properties of the different …

Designing high‐performance colour cosmetics through optimization of powder flow characteristics

X Liu, C Drakontis, S Amin - International Journal of Cosmetic …, 2020 - Wiley Online Library
Objective Explore the impact of powder flow properties such as flow energy and
compressibility on the performance characteristics of foundation powders such as cake …

Formulation and evaluation of proliposomal tablet of Diclofenac sodium

A Nagarsheth, D Patel, H Thakkar - Journal of Drug Delivery Science and …, 2022 - Elsevier
Proliposomes were successfully formulated using film deposition on carrier technique and
characterized for percentage yield, drug content, size, PDI, zeta potential, flow properties …